GDNF-based therapies, GDNF-producing interneurons, and trophic support of the dopaminergic nigrostriatal pathway. Implications for Parkinson’s disease

The glial cell line-derived neurotrophic factor (GDNF) is a well-established trophic agent for dopaminergic (DA) neurons in vitro and in vivo. GDNF is necessary for maintenance of neuronal morphological and neurochemical phenotype and protects DA neurons from toxic damage. Numerous studies on animal models of Parkinson’s disease (PD) have reported beneficial effects of GDNF on nigrostriatal DA neuron survival. However, translation of these observations to the clinical setting has been hampered so far by side effects associated with the chronic continuous intra-striatal infusion of recombinant GDNF. In addition, double blind and placebo-controlled clinical trials have not reported any clinically relevant effect of GDNF on PD patients. In the past few years, experiments with conditional Gdnf knockout mice have suggested that GDNF is necessary for maintenance of DA neurons in adulthood. In parallel, new methodologies for exogenous GDNF delivery have been developed. Recently, it has been shown that a small population of scattered, electrically interconnected, parvalbumin positive (PV+) GABAergic interneurons is responsible for most of the GDNF produced in the rodent striatum. In addition, cholinergic striatal interneurons appear to be also involved in the modulation of striatal GDNF. In this review, we summarize current knowledge on brain GDNF delivery, homeostasis, and its effects on nigrostriatal DA neurons. Special attention is paid to the therapeutic potential of endogenous GDNF stimulation in PD.

Introduction

Parkinson’s disease (PD) is a progressive, mainly idiopathic and age-related, neuronal disorder that affects as much as 1% of the population over 60 years (de Lau and Breteler, 2006). PD causes severe postural, motor, and physiological impairments that can reduce life expectancy. Although PD is a systemic disease, affecting central and peripheral neurons, the most disabling motor symptoms are due to the progressive death of dopaminergic (DA) neurons in the substantia nigra pars compacta (SNpc), a mesencephalic nucleus that sends projections to the striatum (caudate nucleus (Cd) and putamen) and is involved in motor control. Although pharmacological (pro-DA drugs) and surgical (deep brain stimulation) therapies exist to alleviate PD symptoms (see Tarazi et al., 2014), to date there is no cure for PD despite intense efforts made to develop new protocols, particularly cell replacement therapy, to substitute or protect nigrostriatal cells affected by the disease. The discovery by Lin et al. (1993) of a specific DA neurotrophic factor secreted by rat glial cells -the glial cell line-derived neurotrophic factor (GDNF)- opened a new perspective for PD pathogenesis and therapy. This review will discuss the pros and cons of using GDNF as a treatment for PD, highlighting the potential therapeutic applicability of endogenous brain GDNF activation.

GDNF Administration for Treatment of Parkinson’s Disease: Early Observations and Clinical Trials

GDNF and its structurally related trophic proteins artemin, neurturin and persephin, are distant member of the transforming growth factor-β superfamily (Airaksinen and Saarma, 2002). A wealth of papers based on rodent and non-human primate models have described the benefits of GDNF treatment on nigrostriatal neurons. In early studies, GDNF showed a specific action on survival of rat E16 midbrain DA neurons in culture and proved to be a potent and selective stimulator of dopamine uptake and neurite outgrowth in tyrosine hydroxylase positive (TH+) neurons (Lin et al., 1993). These initial in vitro observations led to immediate testing of GDNF effects on PD animal models based on toxin-induced destruction of midbrain DA neurons. Hoffer et al. (1994) used rats unilaterally injected with 6-hydroxydopamine (6-OHDA) in the nigrostriatal pathway. This procedure elicits a rapid and permanent ipsilateral destruction of DA neurons that is manifested by a contralateral rotation pattern in response to low doses of amphetamines, thus accurately reflecting the degree of DA neuronal loss. In 6-OHDA-treated animals, intranigral injection of 100 μg of recombinant human GDNF reduced the rotations by ~4-fold (Hoffer et al., 1994). Similar rescue effects of GDNF were reported in an independent study on the same rat model (Winkler et al., 1996). In 1995, four articles described the potent neurotrophic effects of GDNF on mesencephalic DA (Beck et al., 1995; Tomac et al., 1995a) as well as motor (Oppenheim et al., 1995; Yan et al., 1995) neurons in vivo; a year later the first non-human primate data in a 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-induced parkinsonian monkey model was published (Gash et al., 1996). GDNF-treated monkeys showed functional improvement of parkinsonian features along with increased levels of striatal dopamine. The benefits claimed by GDNF use were unanimous, although when it came to human patients the initial elation dissipated.

Several human studies have been performed to test the effect of striatal delivery of GDNF through a permanently implanted cannula. The degree of symptomatic relief in these clinical trials has varied from major improvement (Gill et al., 2003; Love et al., 2005; Patel et al., 2005; Slevin et al., 2005) to no benefit at all (Lang et al., 2006). Some patients enrolled in these studies developed neutralizing antibodies as part of an immune response to the recombinant human GDNF treatment (Lang et al., 2006; Tatarewicz et al., 2007), whereas others simply reacted to the placebo in a randomized trial (Lang et al., 2006). In another study, intraventricular GDNF delivery resulted in strong adverse effects (Nutt et al., 2003). A phase II clinical trial, based on improved bilateral intra-putaminal GDNF injection, has recently been launched at the Frenchay Hospital in Bristol (UK) to overcome the inconsistent results previously obtained. Progress to a treatment is hampered by the problem of delivering GDNF to brain cells across the blood-brain barrier (Boado and Pardridge, 2009). Thus, it seems that the simple administration of the GDNF protein does not represent a sustainable treatment for PD and alternative options have to be tested to exploit the benefit of the potent trophic action of GDNF on DA neurons.

Alternative GDNF-Based Therapies

Overcoming the blood-brain-barrier (BBB) obstacle for GDNF delivery to the brain using a systemic route has became a major technological objective (see Figure 1). Trojan horse approaches were tested by the mean of systemic administration of nanoliposomes engulfing a GDNF plasmid and engineered to cross the BBB via trancytosis after coupling to the transferrin receptor. This resulted to a near complete rescue of the nigrostriatal system from 6-OHDA neurotoxicity in the rat brain (Xia et al., 2008; Zhang and Pardridge, 2009). An attempt to fuse GDNF to a monoclonal immunoglobulin (GDNF-IgG) directed against the BBB cellular component proved to be potent in mice (Fu et al., 2010), but this method failed when it was tested on monkeys as no behavioral improvements were observed (Ohshima-Hosoyama et al., 2012). Biodegradable GDNF-loaded microspheres implanted in the striatum are an interesting alternative to overcome the BBB problem since they sustainably release recombinant GDNF for at least 8 weeks (Jollivet et al., 2004a; Garbayo et al., 2009; Herrán et al., 2013), with long protective effects lasting up to 24 weeks (Jollivet et al., 2004b). Finally, the administration of GDNF by nasal route, using cationic liposomes to increase their residence time through electrostatic interactions at the olfactory epithelium, has recently been tested. Intranasal GDNF given to rats, immediately prior to 6-OHDA lesion, provided significant protection of striatal DA neurons (Migliore et al., 2014).

FIGURE 1

Figure 1. Schematic summary of GDNF-delivery strategies tested in human PD patients and rodent models. AAV, adeno-associated virus; Ad, adenovirus; LV, lentivirus; Lf, lactoferrin; SNpc, substantia nigra pars compacta; DA, dopamine; Cd, caudate nucleus; Put, putamen; BBB, blood-brain-barrier.

In parallel with the studies based on the delivery of GDNF peptide, considerable efforts have been made towards the development of in vivo gene transfer by recombinant viral vectors expressing the Gdnf gene (Figure 1). Bilateral intranigral delivery of adenoviral vector constructs carrying the GDNF sequence (Ad-Gdnf) to adult rats prior to 6-OHDA lesion protected DA neurons from toxin-induced cell death (Choi-Lundberg et al., 1997). Although the experimental design was criticized (Pallini et al., 1997), this landmark attempt was encouraging and thus followed by several other studies based on viral vector-driven GDNF strategy in rodent and monkey models (reviewed by Kordower and Bjorklund, 2013). A key study reported that adeno-associated virus (AAV)-Gdnf promoted motor recovery of parkinsonian rats when injected in the striatum rather than in the SN region (Kirik et al., 2000). Furthermore, intranigral AAV-Gdnf exhibited histological neuroprotection on DA neuronal bodies but DA fibers sprouting and functional recovery occurred only when AAV-Gdnf was transduced in the striatum (Kirik et al., 2000, 2004). Several viral vector based strategies have been developed to optimize GDNF production, in particular inducible vectors in order to control the timely expression of GDNF. For instance, injection of a synthetic steroid mifepristone lead to highly increased levels of GDNF expression from the inducible AAV-Gdnf. This allowed the recovery of motor function in 6-OHDA lesioned rats, and was associated to DA neuron protection in the SN (Tereshchenko et al., 2014). Another newly reported approach used lentivirus (LV) vectors transgenes fused with a destabilizing domain (DD). The resulting fusion protein is unstable and rapidly cleared by the proteasome unless it is stabilized by trimethoprim (TMP). Thus, peripheral injection of TMP allows DD-GDNF stabilization in the striatum (Tai et al., 2012). When applied to 6-OHDA lesioned rats, the TMP-stabilized DD-GDNF protects the DA nigrostriatal pathway and associated functional behavior (Quintino et al., 2013). Pharmacological modulation of GDNF-expressing viral vectors, still in initial stage of development, is particularly attractive when considering new therapeutic approaches in early disease stages to protect nigrostriatal degeneration and concomitantly prevent adverse effects from sustained high GDNF delivery. Biodegradable nanoparticles encompassing a plasmid DNA coding for GDNF can get through the plasma membrane of neurotensin receptor-expressing cells, such as DA neurons. This non-viral targeted transfection has proved to be efficient when used in rat PD models (Gonzalez-Barrios et al., 2006). A set of experiments combining non-viral gene delivery with systemic route of administration gave promising results. Multiple intravenous injections of a lactoferrin (Lf)-modified vector, expressing human GDNF, protected DA neurons and highly reduced the amphetamine-induced rotational behavior that normally occurs after lesion by 6-OHDA intrastriatal injection (Huang et al., 2009).

Evidently, not all studies have systematically reported positive effect of viral GDNF vectors. Indeed, an herpes simplex virus (HSV)-derived vector overexpressing GDNF presented toxic effects while masking the potential benefits of GDNF (Monville et al., 2004). Intranigral lentiviral injection of a vector expressing the A30P mutant human α-synuclein provoked a selective and progressive degeneration of the nigrostriatal DA neurons in the treated rats (Lo Bianco et al., 2002). Preventive treatment by LV-GDNF vector, successfully used in a monkey PD model (Palfi et al., 2002), failed to modulate nigrostriatal degeneration induced by the α-synuclein toxicity (Lo Bianco et al., 2004). Surprisingly, the use of a tetracyclin-dependent LV-GDNF expression in the striatum in normal rats provoked a dramatic down-regulation of TH protein expression (Georgievska et al., 2004).

Cell-based GDNF therapy, i.e., transplantation of GDNF-expressing cells, has also been extensively tested. Two main strategies have been used so far: (i) introduction of GDNF-secreting cells in the lesioned nigrostriatal system; and (ii) transplantation of DA-producing cells in association with GDNF treatment to protect and to increase survival of grafted cells. Successful intrastriatal transplantation of primary astrocytes engineered to express GDNF prevented 6-OHDA-induced DA neuronal death (Cunningham and Su, 2002). Interestingly, low levels of GDNF released by these astrocytes (~5 pg/g of striatum) provided a remarkable robust neuroprotection. Neural stem cells engineered to synthesize GDNF were also successfully used to limit DA neuron degeneration in a 6-OHDA lesion mouse model (Åkerud et al., 2001). Encapsulated GDNF-producing cells may represent a valuable option since they will not migrate out of the targeted region, the caudate-putamen, and can still be removed in the event that some adverse effects may occur (reviewed by Lindvall and Wahlberg, 2008). Pioneer work from Tseng et al. (1997) used polymer-encapsulated fibroblasts engineered to overexpress GDNF prior to be transplanted next to the SN. Nanogram levels of continuous GDNF release completely prevented degeneration of DA neurons induced by medial forebrain bundle axotomy. Alternatively, trophic factors-producing tissues, such as the carotid body (CB), have been used as a source of GDNF. The CB is highly DA, bilateral, O₂-sensing organ that contains cells which produce unusual high levels of GDNF (López-Barneo et al., 1999; Villadiego et al., 2005). Intrastriatal transplantation of CB cells produces clear neuroprotective effects on DA neurons in rodent parkinsonian models (Espejo et al., 1998; Muñoz-Manchado et al., 2013), and amelioration, with indications of biological effects, in PD patients (Mínguez-Castellanos et al., 2007). However, the therapeutic action of CB is limited by the small amount of tissue available. To overcome this limitation, new stem cell-based procedures are being assayed to expand CB tissue before transplatation (see Pardal et al., 2007; Platero-Luengo et al., 2014). The combination of GDNF delivery and fetal DA grafts, to improve survival of transplanted cells, has been largely tested in animal models (Rodriguez-Pallares et al., 2012; Kauhausen et al., 2013), as well as in PD patients (Mendez et al., 2000). GDNF promoted survival of fetal mesencephalic cell transplants in the striatum of 6-OHDA-lesioned rats, which was associated with functional improvement (Yurek et al., 2009). However, this beneficial effect was limited in time, as 6 months later the association of grafted cells/LV-GDNF failed to support DA neuron survival. Moreover, LV-GDNF induced some down regulation of TH in the grafted cells. In similar experimental conditions, GDNF had no effect on fetal mesencephalic graft outgrowth when compared to other growth factors such as bFGF (Törnqvist et al., 2000). GDNF has also been used to increase DA differentiation and survival of embryonic (Buytaert-Hoefen et al., 2004) or bone marrow stromal (Dezawa et al., 2004) stem cell-derived DA neurons prior to transplantation. This procedure, that represents an indirect use of GDNF, substantially alleviated the rotation behavior induced by amphetamines in 6-OH dopamine-lesioned rats. However, the use of GDNF to drive stem cell-derived neuronal cells to produce DA is a procedure that calls for caution, as safety of progenitor cell transplants is always a key concern. Optimization of DA neuron maintenance and GDNF delivery protocols has permitted recent preclinical advances in the field. DA cells from ventral mesencephalon of young donors (embryonic day 10) transplanted homotopically in the nigral region, combined with the intrastriatal injection of a AAV-GDNF, allowed graft survival, integration into the medial forebrain bundle circuitry to innervate the striatum, and functional motor recovery (Kauhausen et al., 2013). Together, the data summarized in this section support a beneficial neuroprotective action of exogenous GDNF on DA nigrostriatal neurons.

GDNF Signaling on Dopaminergic Neurons

GDNF shares the receptor tyrosine kinase rearranged during transcription (Ret) with artemin, neurturin and persephin. Ret activation requires association to a second glycosylphosphatidyl inositol-anchored protein named GDNF family receptor α (GFRα), of which four subtypes have been identified with different affinities for ligands of the GDNF-family. The GDNF homodimer specifically binds to two GFRα1 to form a high affinity complex with the recruitment of Ret proteins (Bespalov and Saarma, 2007). GDNF displays lower affinity for GFRα2 and GFRα3. The Ret-GFRα1 complex formation induces transphosphorylation of Ret tyrosine kinase residues which, in turn, activates downstream signaling molecules (Figure 2) such as the mitogen-activated protein kinase (MAPK) and the phosphatidylinositol 3-kinase (PI3K)/Akt (Airaksinen and Saarma, 2002). In vitro studies suggest that the protective effect of GDNF on DA neurons involves the activation of the MAPK and PI3K intracellular pathways (Ugarte et al., 2003; Onyango et al., 2005). Aging mice (26 months) carrying a partial deletion of Gfrα1 (heterozygous), show a decrease in TH fiber density in the striatum accompanied by a lower number of TH+ neurons in the SN. Additionally, these mice exhibit increased sensitivity of nigrostriatal DA neurons to MPTP toxicity (Boger et al., 2008). These observations suggest a pivotal role of GFRα1 in the trophic protection by GDNF signaling. Specific ablation of Ret in DA neurons (using a dopamine transporter-Cre/Ret-flox mice) results in progressive loss of nigrostriatal DA neurons. Spontaneous decrease of TH+ cells in the SNpc and striatal innervation occurred in these mice and this was associated with increased number of activated glial cells, a sign of CNS injury (Kramer et al., 2007). GDNF signaling also utilizes c-Src kinase to promote neurites outgrowth (Encinas et al., 2001). Although the GFRα1/Ret complex is the most studied GDNF receptor, it is known that this trophic factor can also bind to alternative signaling system, e.g., NCAM (Paratcha et al., 2003). This would explain why ablation of Ret does not produce a phenotype similar to GDNF-deficiency (see Pascual et al., 2011).

FIGURE 2

Figure 2. Schematic representation of the main signaling pathways involved in the neuroprotective action of GDNF on dopaminergic neurons. GDNF principally stimulates the binding of GFRα1 and Ret to trigger intracellular signaling cascades leading to pro-survival genes expression, calcium signaling and pro-apoptosis factors inhibition. Akt, protein kinase B; Bcl-2, B cell lymphoma 2; Casp-3, caspase 3; c-Src, proto-oncogene tyrosine-protein kinase Src; ERK, extracellular signal-regulated kinase; HO1, heme oxygenase 1; IP3, inositol tris-phosphate; JNK, c-Jun N-terminal kinase; MEK, mitogen extracellular signal-regulated kinase; NF-κB, nuclear factor kappa B; PI-3K, phosphatidylinositol 3 kinase; Raf, Raf kinase; ROS, reactive oxygen species. Dashed arrows indicate indirect stimulation or inhibition.

The data summarized in the previous paragraph strongly suggest the requirement of direct GDNF trophic signaling to the DA neurons for their survival. Ret and GFRα1 mRNA expressions are up-regulated in the SNpc shortly after 6-OHDA lesion, a trophic response to drug toxicity. After 3 to 6 days, the level of expression of both Ret and GFRα1 mRNA decreased dramatically, which could be explained by the loss of DA neurons observed after 6 days in this rat PD model (Marco et al., 2002). Ret is not specific to GDNF but its activation is also enhanced by other ligands such as GM1 ganglioside (Newburn et al., 2014). This observation denotes a possible pharmacological induction of the GDNF signaling cascade to promote a trophic response. The canonical neurotrophic factor action requires retrograde communication from the axon terminals to neuron cell bodies, partly explained by the “signaling endosome hypothesis” where the activated receptor is internalized and transported via the microtubules machinery for cytosolic and nuclear signaling (Howe and Mobley, 2005; Ibáñez, 2007). GDNF is no exception to this rule as it has been demonstrated that ¹²⁵I-GDNF injected into the rat striatum is retrogradely transported to the cell body of SNpc neurons (Tomac et al., 1995b).

The use of Gdnf-null mice has provided valuable data regarding the role of endogenous GDNF on DA neuron survival. Mice carrying GDNF deletion do not survive after birth due to lack of the entire enteric nervous system and kidney agenesis (Moore et al., 1996; Pichel et al., 1996; Sánchez et al., 1996). However, embryonic development of the midbrain DA nigrostriatal pathway is not affected by the lack of GDNF (Sánchez et al., 1996). Mice with partial deletion of Gdnf (Gdnf^+/–) suffer from higher neuro-inflammation and loss of TH-positive neurons with aging (Boger et al., 2006) or following lipopolysaccharide (LPS) treatment (Granholm et al., 2011). However, whether GDNF might serve as an important target-derived neurotrophic factor for adult nigral DA neurons has remained unknown until conditional GDNF-KO mice were generated. Inducible CRE-LoxP Gdnf-null mice were engineered to bypass the developmental lethality caused by GDNF loss. In this model, a floxed-Gdnf allele was deleted in adulthood by tamoxifen-induced Cre recombinase activation, leading to a marked decrease of GDNF expression in the striatum (Pascual et al., 2008). Strikingly, these mice showed a progressive and selective death of the catecholaminergic neuronal population in the substantia nigra (SN), ventral tegmental area, and locus coeruleus with associated locomotor dysfunction (Pascual et al., 2008). These data further support the notion that adult mammalian mesencephalic catecholaminergic neurons rely on the continuous input of endogenous GDNF, an observation that remains to be demonstrated with other animals models and in the human brain.

Mechanisms Involved in the Protective Effect of GDNF

It is postulated that GDNF protects the DA nigrostriatal system by interacting with several cellular pathways involved in apoptosis, metabolism, and redox homeostasis (see Figure 2). GDNF may prevent apoptosis in the DA neuron population by directly up-regulating the anti-apoptotic proteins B cell lymphoma 2 (Bcl-2) and Bcl-X via PI3K signaling (Sawada et al., 2000). The neuroprotective action by GDNF on the nigrostriatal system might also involve the activation of protein kinase CK2 as demonstrated in parkinsonian rats (Chao et al., 2006). Moreover, GDNF induces nuclear factor κB (NF-κB) pathways to promote neuronal survival from toxic insults (Cao et al., 2008). Other targets of GDNF are caspase-3 and the endoplasmic reticulum stress-related genes. Treatment of primary mesencephalic rat cultures with lactacystin inhibits the ubiquitin-proteasome system and leads to apoptosis of DA neurons. However, pretreatment with GDNF prevents DA neuronal death by suppressing caspase-3 activation and endoplasmic reticulum stress (Li et al., 2007). Intrastriatal infusion of GDNF prevents lactacystin-induced DA neuron loss by inhibiting the pro-apoptotic molecules Jun N-terminal kinase (JNK) and p38 and activating the pro-survival Akt and MAPK pathways (Du et al., 2008).

As it occurs in the classical neurotrophic models, GDNF promotes the DA phenotype in DA neurons, and in this way exerts some of its neuroprotective actions. GDNF seems to increase cellular levels of transcription factors, such as Nurr1 and Pitx3, involved in the expression of a set of genes—TH, vesicular monoamine transporter (Vmat2), dopamine transporter (Dat) and aromatic L-amino acid decarboxylase (Aadc)—involved in dopamine metabolism, (Lei et al., 2011). When added to the culture medium of midbrain-derived neural stem cells (mdNSCs), GDNF induced a DA phenotype associated with Nurr1 and Pitx3 up-regulation. Transplantation of these cells into the striatum of 6-OHDA-injected rats greatly prevented the amphetamine-induced contralateral rotation in the lesioned animals (Lei et al., 2011).

Although the causes of DA neuron degeneration in PD remain unclear, mitochondrial dysfunction and oxidative stress induced by reactive oxygen species (ROS) are known to have a pathogenic role early in the disease process (Subramaniam and Chesselet, 2013). Interestingly, striatal GDNF administration moderately enhances the activity of certain enzymes involved in the enzymatic detoxification of ROS: superoxide dismutase, catalase and glutathione peroxidase (Chao and Lee, 1999). Moreover, GDNF administration in the rat striatum prevents 6-OHDA-induced ROS formation, evidenced by protein carbonyls and 4-hydroxynonenal, and thus protects DA neurons from oxidative stress (Smith and Cass, 2007). GDNF seems to negatively regulate the expression of heme oxygenase-1 (HO-1) to reduce oxidative stress (Saavedra et al., 2005).

A proteomic analysis revealed 46 specifically regulated proteins in the striatum of MPTP mice 4 and 72 h after striatal GDNF injection. These proteins are related to cell differentiation, system development, cell structure and motility, energy pathways, transport, apoptosis, cell proliferation and response to stress-regulating genes (Hong et al., 2009). However, none of them are involved in GFRα1-Ret downstream-activated pathways. Taking into account that post-transcriptional modification, such as phosphorylation, were not detected with the aforementioned method, a thorough proteomic examination of posttranslational modifications elicited by GDNF on DA neurons would probably provide relevant information for understanding the neuroprotective action of GDNF. It has been reported that striatal GDNF inhibits Shh production by DA neurons and, in turn, Shh released at the striatal DA terminals down-regulates Gdnf gene expression (Gonzalez-Reyes et al., 2012). This concept is attractive, as the mutual repression of Shh and GDNF would allow DA neurons to dynamically control neurotrophic factor production in the striatum. The level of striatal Gdnf mRNA, and the number of GDNF-expressing parvalbumin-positive (PV+) interneurons (see below) do not seem to be affected by MPTP-derived lesions of nigrostriatal neurons (Hidalgo-Figueroa et al., 2012). However, to what extent the integrity of the DA nigrostriatal pathway modulates the survival and activity of GDNF-producing striatal interneurons is under debate. Although much progress has been done regarding the molecular mechanism of GDNF neurotrophic/neuroprotective action, whether the intracellular pathways involved are the same in normal and lesioned cells and to what extent GDNF production is cell autonomous or depend on the activity of the relevant neuronal networks are fundamental questions yet to be resolved.

In addition to its well-established neurotrophic role, GDNF may also modulate the activity of DA nerve terminals at the basal ganglia. Amperometric recordings from midbrain DA neurons showed that exposure to GDNF increases quantal release of catecholamines as well as the density of axonal varicosities (Pothos et al., 1998). GDNF enhances basal levels and release of DA and DA metabolites evoked by potassium or amphetamine in primary cultured ventral midbrain (VM) DA neurons (Wang et al., 2001), striatal slices (Gomes et al., 2006), and striatal synaptosomes (Gomes et al., 2009). Similar effects of GDNF have also been observed in vivo by microdialysis measurements (Hebert et al., 1996; Xu and Dluzen, 2000; Cass and Peters, 2010). Therefore, GDNF may not only prevent DA neurons from degeneration but also potentiate DA release and turnover by some as yet unknown mechanism.

Endogenous GDNF Expression: Striatum

Knowledge of where and when GDNF is expressed in the adult brain is fundamental to understand the physiological role of this trophic factor and the mechanisms that regulate its synthesis. Eventually, this could make it possible to pharmacologically stimulate endogenous GDNF production as a way to increase the level of GDNF available at the striatal DA nerve terminals. Unfortunately, studies on GDNF expression performed with antibodies are challenged by specificity considerations. However, there are several studies in which either Gdnf mRNA expression was analyzed by in situ hybridization (ISH), or mouse models with reporter genes were used to estimate Gdnf promoter activity. In rodents, Gdnf mRNA is broadly expressed in the developing embryo (Golden et al., 1999), although in adult mice its expression is rather limited to few organs, with the highest content found in the ovary and testis. In the adult rodent brain, Gdnf mRNA expression is consistently observed in restricted discrete cells of the striatum, thalamic structures, nucleus accumbens, cerebellum and hippocampus (Schaar et al., 1993; Nosrat et al., 1996; Trupp et al., 1997). Using a β-gal reporting mouse model (Sánchez et al., 1996), GDNF expression in adult mice brain was restricted to the dorsal and ventral striatum, the anteroventral nucleus of the thalamus, the septum and, interestingly, the subcommissural organ (Pascual et al., 2008). Curiously, GFRα1 and Ret do not share the same expression pattern than GDNF and are broadly expressed in the adult CNS. Noteworthy, GDNF receptor mRNAs are not detected in the striatum, but highly expressed in the SNpc (Trupp et al., 1997), which again supports that GDNF may specifically act on SNpc DA neurons that project to the striatum. This also indicates that no other striatal cells could benefit from its trophic action. GDNF protein levels have been measured by enzyme-linked immunosorbant assay (ELISA) in lysates of caudate/putamen, SN, cerebellum, frontal cortex, and the cerebrospinal fluid (CSF) of PD and non-PD postmortem human brains. GDNF concentration in the range of 40–70 pg/mg total protein was relatively constant between control and PD patients in the SN and Cd and putamen, with lower concentrations reported in the cerebellum and the frontal cortex (10–15 pg/mg). However, GDNF was no detected in the CSF (Mogi et al., 2001). Additionally, polymorphisms in the GDNF gene have been found in PD and non PD patients with no apparent correlation between mutation and disease (Wartiovaara et al., 1998). In another study, depletion of GDNF, but no other neurotrophic factors, was detected in the SN of parkinsonian patients (Chauhan et al., 2001). Although these results must be taken with caution as they are based on immunohistochemical analyses, they suggest that down regulation of GDNF might participate in the onset of PD pathophysiology. However, whether alterations in GDNF synthesis and release have any causative pathogenic role in PD is for the moment unknown.

There are few studies focused on the cell distribution of striatal GDNF. In an ISH-based study over 60% of the choline acetyl-transferase (ChAT) positive interneurons were reported to express Gdnf mRNA (Bizon et al., 1999). In the same study, a significant fraction (17–42%) of GABAergic neurons expressed Gdnf mRNA, however it did not discriminate between the medial spiny neurons (the most abundant cells in the striatum) and the GABAergic interneurons. As PV+ interneurons represent only a small fraction of GABA-positive cells, it could be concluded from these data that PV+ neurons account for a small proportion of striatal cells expressing GDNF (Bizon et al., 1999). However, in this study a majority of PV+ cells expressed NGF and acidic fibroblast growth factor (FGF1), which are thought to provide trophic protection to excitotoxic insult. Interestingly, some cells were found highly co-expressing GDNF and FGF1 (Bizon et al., 1999). In contrast with these observations, the use of a Gdnf-LacZ mouse model (Sánchez et al., 1996) unveiled a different population of GDNF-expressing cells in the striatum. Gdnf promoter-driven LacZ expression, revealed by β-galactosidase activity (XGal staining), demonstrates that Gdnf is expressed in more than 80% of striatal PV+ GABAergic interneurons. Moreover, ~95% of the GDNF-positive striatal neurons are PV+, while the remaining GDNF+ cells are either cholinergic (ACh) or somatostatinergic (SS) interneurons (Hidalgo-Figueroa et al., 2012; see Figure 3). As yet there is no explanation for the discrepancy between these two studies performed in different models of rat (Bizon et al., 1999) and mouse (Hidalgo-Figueroa et al., 2012). However the particularly scattered distribution of PV+ cells throughout the mouse striatum, their electrical coupling by dendro-dendritic gap junctions (Fukuda, 2009) and their high resistance to excitotoxicity, make them a target of choice for pharmacological modulation. On the other hand, although the number of ACh+ and GDNF+ cells does not seem to be too high, they may have a significant contribution to striatal GDNF homeostasis, as degeneration of cholinergic interneurons following the injection of the cholinotoxin AF64α results in a 30% reduction in striatal GDNF protein content (Gonzalez-Reyes et al., 2012). This decrease of GDNF production might be directly inferred to the loss of ACh+ interneurons, or a consequence of a drop of cholinergic input to the PV+ interneurons (Chang and Kita, 1992). Despite these recent advances in the identification of GDNF-producing interneurons in the rodent striatum, the nature of the cells that produce GDNF in the human striatum remains as yet unidentified.

FIGURE 3

Figure 3. Protection of the dopaminergic nigrostriatal pathway by striatal GDNF and activation of endogenous GDNF production. Dopaminergic (DA) neurons (green) located in the substantia nigra pars compacta (SNpc) innervate the caudate-putamen to modulate the activity of GABAergic medium spiny neurons (gray), parvalbumin (PV)-positive interneurons (red) and other cholinergic (ACh) or somatostatin (SS) interneurons (brown). PV neurons form an ensemble of synchronized cells through multiple dendrodendritic electrical synapses (resistance in the scheme), and release GDNF at the nerve terminals to provide trophic support to DA neurons via retrograde signaling (dotted arrow). Proposed strategies to enhance the endogenous GDNF production are summarized in the purple box (right).

In the lesioned striatum, reactive astrocytosis occurs in parallel to an increase in GDNF expression (Nakajima et al., 2001). Similarly, in the DA-depleted striatum, reactive astrocytes results in expression of Gdnf mRNA, as shown by both quantitative RT-PCR and ISH (Nakagawa and Schwartz, 2004). However, in the Gdnf-LacZ mice, none of the GDNF expressing cells are of astrocyte or microglia origin 7 and 21 days post-MPTP, despite a significant increase of the astrocytic population occurred (Hidalgo-Figueroa et al., 2012). Unilateral nigrostriatal lesions with 6-OHDA produce a 50% decrease in the number of PV+ neurons in the ipsilateral side in comparison with the contralateral side (Proschel et al., 2014). This brings an interesting contradiction with the MPTP-treated Gdnf-LacZ mice that displayed no difference in PV/GDNF expression in the injured striatum (Hidalgo-Figueroa et al., 2012). These differences may be due to the use of rats vs. mice and distinct parkinsonian models (neurotoxic drugs and route of administration).

Stimulation of Striatal Endogenous GDNF Production

Since GDNF has a potent neurotrophic effect on DA neurons and it is highly expressed in the striatum, pharmacological or physical interventions aiming at up-regulating endogenous GDNF production are of major potential medical relevance. Several drugs have been tested to boost striatal GDNF expression thus far (see Table 1). For instance, a weeklong systemic injection of 1,25-dihydroxyvitamin D3 (calcitriol) induced Gdnf mRNA and protein expression in the rat striatum, presumably via the activation of vitamin D receptors. Longer treatment with calcitriol prevented DA neuron loss in 6-OHDA-lesionned rats (Smith et al., 2006). Monoamine oxidase (MAO) inhibitors rasagiline and selegiline, broadly used to treat PD patients, up-regulate in vitro GDNF expression via NF-κB internalization (Mizuta et al., 2000; Maruyama et al., 2004; Bar-Am et al., 2005). It would be interesting to test these MAO inhibitors in vivo. Valproic acid, an anti-epileptic drug, induces GDNF secretion in the culture medium of rat astrocytes, which partially prevents DA cell loss after LPS or MPTP treatment (Chen et al., 2006). Valproate is a powerful histone deacetylase inhibitor, therefore facilitating chromatin relaxation and transcriptional activation, which is suggested to facilitate transcription of neurotrophic factors (Harrison and Dexter, 2013). Indeed, treatment with histone deacetylase inhibitors increased Gdnf and Bdnf expression and preserved DA neuronal function from MPTP injury. Moreover, valproate induced a marked increase in Gdnf promoter activity and promoter-associated histone H3 acetylation (Wu et al., 2008). Other mood stabilizer drugs have been reported to trigger GDNF release by rat glioblastoma cell line (see Table 1 for details). In any case, these data must be interpreted cautiously, as rat cortical primary astrocyte and cell line cultures used in these studies are experimental models very different from the striatum in situ.

TABLE 1

Table 1. In vivo and in vitro pharmacological tests employed to modulate the endogenous GDNF production.

Noribogaine, a metabolite of the naturally occurring alkaloid ibogaine, bears anti-addictive effects on alcohol and other drugs consumption. In rats, the effect of ibogaine on the reduction of ethanol intake is located in the ventral tegmental area a DA mesencephalic region medial to the SN. Systemic injection of ibogaine stimulates Gdnf mRNA expression in the midbrain of both rats and mice, and when added to the SH-SY5Y adrenergic cell line (He et al., 2005; Carnicella et al., 2010). Although ibogaine/noribogaine is known to act as an agonist to 5-HT2A and κ-opioid receptors and as an antagonist to NMDA receptors, the mechanism by which it induces Gdnf mRNA expression remains to be deciphered. Another potential stimulant of Gdnf mRNA and protein expression in mouse striatal neurons is the metabotropic glutamate receptor 3 agonist LY379268 (Battaglia et al., 2009). The organotellurium compound AS101 exerts diverse biologic activities and holds great potential in PD. Systemic application of this immunomodulator prevents neurotoxicity and behavioral deficits induced by 6-OHDA striatal injections in rats. Besides activation of the Ras-Raf-MEK-Erk cascade leading to cell growth and survival, AS101 up-regulates GDNF levels by inhibiting interleukin-10 in primary astrocyte cultures as well as in the rat SN (Sredni et al., 2007). It is surprising, however, that this compound has not been further studied in regard to its potential effect on GDNF expression.

Chinese medicinal plants also bring interesting molecules such as echinacoside, a polyphenol natural product that when injected peripherally alleviates MPTP-induced DA neuronal loss. Echinacoside stimulates GDNF and BDNF and prevents MPTP-induced apoptosis (Zhao et al., 2010). Puerarin, from the roots of a kudzu plant Pueraria lobata, partially prevents the chemically-induced DA neurodegeneration in mice and rats, and stimulates striatal GDNF (Zhu et al., 2010, 2014). Naringin is another recent example of a plant pigment (flavonoid) present in grapefruits that seems to stimulate GDNF in the SN of MPTP-treated mice (Jung et al., 2014; Leem et al., 2014).

An elegant strategy used to activate endogenous GDNF is based on an engineered zinc-finger protein (ZFP) that specifically activates the GDNF promoter (Laganiere et al., 2010). In this work, a six ZFPs sequence carried by an AAV vector was designed to target rat, human and monkey Gdnf promoters (hGDNF-ZFP). Microarray data from in vitro assays showed a very specific increase of Gdnf mRNA expression while the rest of the genomic activity remained unchanged. hGDNF-ZFP infused into the striatum of normal adult rats 4 weeks before triggering neurotoxicity by a 6-OHDA striatal injection, increased GDNF production in the striatum and improved motor activity in lesioned rats (Laganiere et al., 2010). This methodology could be potentially applicable to prevent DA neuron degeneration in genetic cases in which the disease can be diagnosed before appearance of the clinical symptoms. Whether hGDNF-ZFP induces GDNF expression in the striatal cells that normally synthetize the trophic factor, or if other cell types are also put to contribution, is a point that needs to be clarified. Recently, stimulation of the intracellular Sigma-1 receptor (Sig-1R) by the agonist PRE-084 (Su et al., 1991) showed neurorestorative properties in 6-OHDA-treated mice (Francardo et al., 2014). PRE-084 also induced a moderate, but significant, increase of GDNF protein in the striatum (~6% over vehicle treatment) and in the SN (~14%) whereas no difference was observed in the Sig-1R-null mice (Francardo et al., 2014). Quantification with inadequately characterized anti-GDNF antibodies remains a weak point in several of these studies (Battaglia et al., 2009; Di Liberto et al., 2011; Campos et al., 2012; Lee et al., 2013; Francardo et al., 2014). Such antibodies need to be tested on GDNF-KO tissue extracts as they may give false positive bands of the expected molecular size (authors’ unpublished observation), and this may contribute to overstatement on the efficiency of certain drugs in stimulating GDNF expression.

In parallel to the pharmacological agents, noninvasive approaches are also being considered to stimulate endogenous brain GDNF production. In vitro analysis has revealed that GDNF is secreted both tonically and after depolarization of cells with high K⁺, suggesting that in vivo GDNF could be released in an activity dependent manner (Lonka-Nevalaita et al., 2010). Transcranial magnetic stimulation (TMS) has been used for some time with little insights regarding its actual effect on neurons. A recent study made an attempt to use TMS on rats to assess the effect on GDNF production. Repeated TMS (rTMS), at 10 Hz, during 20 min for 4 weeks proved to be beneficial to unilaterally 6-OHDA-lesioned rats with improvement of behavioral test scores, increase of SNpc TH+ neuron number and fiber density as well as GDNF, NGF and PDGF levels in the striatum (Lee et al., 2013). However, the mechanisms leading to the positive action of rTMS on striatal neurotrophin expression and the associated neurorestorative effect are unknown. Electroconvulsive shock (ECS), a standard psychiatric therapy provoking seizures to provide relief from psychiatric illnesses, is known to improve motor function in PD animal models. ECS prevents neurodegeneration of the DA nigrostriatal pathway observed after 6-OHDA injections. Daily ECS treatment to healthy rats for 7 days stimulates GDNF protein expression in the SN but not in the striatum (Anastasia et al., 2007). Moreover, anti-GDNF IgG inhibits the neuroprotective effect of chronic ECS treatment (Anastasía et al., 2011). It is however not clear how GDNF is up-regulated in the SN since its expression is located in the striatum where no change in protein expression is observed after ECS. A far-fetched explanation would involve the participation of a large ECS-induced glutamate release, which may stimulate GDNF expression and release by the surrounding astrocytes (Yamagata et al., 2002).

Finally, physical exercise (Zigmond et al., 2009), and food restriction diets (Maswood et al., 2004), have both been suggested to have a neuroprotective effect. For example in rats, placing a cast to immobilize the limb ipsilateral to the 6-OHDA injection, thus forcing the use of the contralateral limb, reduces behavioral deficits and DA neuron loss in the lesioned striatum. This also increases GDNF protein content in the striatum (Cohen et al., 2003). Protective effect of exercise on the nigrostriatal DA system associated to an increase of GDNF protein in the 6-OHDA lesioned striatum has been reported in other studies (Tajiri et al., 2010; Lau et al., 2011). Yet, it remains unexplained how exercise can positively modulate GDNF expression, as well as other growth factors, in the striatum and SN. Altogether, the data summarized in this section demonstrate that activation of endogenous GDNF is feasible and therefore further research should be done to determine what methodology, or combination of techniques, can produce more consistent protection for DA neurons and terminals (Figure 1).

Concluding Remarks

Two decades have passed since the discovery of GDNF and much advance has been produced regarding its cellular effects and neuroprotective action on DA neurons. However, it still remains unclear which are the main factors determining GDNF production by brain cells and whether GDNF can effectively be used as a therapeutic agent for PD. Despite intense preclinical research and some clinical studies have been performed, intrastriatal delivery or systemic administration of GDNF have failed so far to provide robust and reproducible methodologies applicable to a large number of PD patients. Intrastriatal transplantation of GDNF-producing cells has worked well in animal models but is still confronted with several limitations (e.g., graft stability, cell survival, and sufficient cell number) for its translation to the clinical setting. The discovery of a specific set of striatal PV+ neurons, organized as a functional ensemble, responsible for production of most of the striatal GDNF, offers a well-identified target to stimulate endogenous production of GDNF. This electrically (gap-junction) interconnected PV+ neuronal pool is particularly attractive, as stimulation of a few of these cells could induce a synchronized activation of the whole population. However, the actual role of PV+ cells in nigrostriatal protection and the functional relations between the different subclasses of interneurons (GABAergic and cholinergic) need to be evaluated by selective deletion of the Gdnf gene in each one of these cell types. In addition to the striatum, PV+ neurons are also present in other parts of the brain, in particular in the cerebral cortex. As cortical PV+ neurons do not significantly produce GDNF, it would be interesting to investigate molecular differences between cortical and striatal PV+ neurons that make the latter capable of producing GDNF. Most of the research on GDNF has been done on non-human samples and models. The actual role of human striatal GDNF and the identification of human striatal cells producing this trophic factor are questions that should be urgently addressed by experimental work. GDNF therapy holds much hope and still remains an important field of investigation in PD. Combined with early diagnosis, neuroprotection by endogenous GDNF stimulation may be a potential preventive therapy to PD patients.

Conflict of Interest Statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Acknowledgments

Xavier d’Anglemont de Tassigny was supported by the Miguel Servet program (grant CP12-03217) from the Health Institute Carlos III. Research by Alberto Pascual and Jose López-Barneo was supported by the Botín Foundation, the Spanish Ministry of Science and Innovation (SAF program) and the Andalusian Government. We would like to thank Janine Michaels for editing comments on the manuscript.

References

Airaksinen, M. S., and Saarma, M. (2002). The GDNF family: signalling, biological functions and therapeutic value. Nat. Rev. Neurosci. 3, 383–394. doi: 10.1038/nrn812

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Åkerud, P., Canals, J. M., Snyder, E. Y., and Arenas, E. (2001). Neuroprotection through delivery of glial cell line-derived neurotrophic factor by neural stem cells in a mouse model of Parkinson’s disease. J. Neurosci. 21, 8108–8118.

Pubmed Abstract | Pubmed Full Text | Google Scholar

Anastasia, A., de Erausquin, G. A., Wojnacki, J., and Mascó, D. H. (2007). Protection of dopaminergic neurons by electroconvulsive shock in an animal model of Parkinson’s disease. J. Neurochem. 103, 1542–1552. doi: 10.1111/j.1471-4159.2007.04856.x

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Anastasía, A., Wojnacki, J., de Erausquin, G. A., and Mascó, D. H. (2011). Glial cell-line derived neurotrophic factor is essential for electroconvulsive shock-induced neuroprotection in an animal model of Parkinson’s disease. Neuroscience 195, 100–111. doi: 10.1016/j.neuroscience.2011.08.019

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Bar-Am, O., Weinreb, O., Amit, T., and Youdim, M. B. H. (2005). Regulation of Bcl-2 family proteins, neurotrophic factors and APP processing in the neurorescue activity of propargylamine. FASEB J. 19, 1899–1901. doi: 10.1096/fj.05-3794fje

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Battaglia, G., Molinaro, G., Riozzi, B., Storto, M., Busceti, C. L., Spinsanti, P., et al. (2009). Activation of mGlu3 receptors stimulates the production of GDNF in striatal neurons. PLoS One 4:e6591. doi: 10.1371/journal.pone.0006591

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Beck, K. D., Valverde, J., Alexi, T., Poulsen, K., Moffat, B., Vandlen, R. A., et al. (1995). Mesencephalic dopaminergic neurons protected by GDNF from axotomy-induced degeneration in the adult brain. Nature 373, 339–341. doi: 10.1038/373339a0

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Bespalov, M. M., and Saarma, M. (2007). GDNF family receptor complexes are emerging drug targets. Trends Pharmacol. Sci. 28, 68–74. doi: 10.1016/j.tips.2006.12.005

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Bizon, J. L., Lauterborn, J. C., and Gall, C. M. (1999). Subpopulations of striatal interneurons can be distinguished on the basis of neurotrophic factor expression. J. Comp. Neurol. 408, 283–298. doi: 10.1002/(sici)1096-9861(19990531)408:2<283::aid-cne9>3.3.co;2-u

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Boado, R. J., and Pardridge, W. M. (2009). Comparison of blood-brain barrier transport of glial-derived neurotrophic factor (GDNF) and an IgG-GDNF fusion protein in the Rhesus monkey. Drug Metab. Dispos. 37, 2299–2304. doi: 10.1124/dmd.109.028787

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Boger, H. A., Middaugh, L. D., Huang, P., Zaman, V., Smith, A. C., Hoffer, B. J., et al. (2006). A partial GDNF depletion leads to earlier age-related deterioration of motor function and tyrosine hydroxylase expression in the substantia nigra. Exp. Neurol. 202, 336–347. doi: 10.1016/j.expneurol.2006.06.006

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Boger, H. A., Middaugh, L. D., Zaman, V., Hoffer, B., and Granholm, A.-C. (2008). Differential effects of the dopamine neurotoxin MPTP in animals with a partial deletion of the GDNF receptor, GFR alpha1, gene. Brain Res. 1241, 18–28. doi: 10.1016/j.brainres.2008.09.011

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Buytaert-Hoefen, K. A., Alvarez, E., and Freed, C. R. (2004). Generation of tyrosine hydroxylase positive neurons from human embryonic stem cells after coculture with cellular substrates and exposure to GDNF. Stem Cells 22, 669–674. doi: 10.1634/stemcells.22-5-669

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Campos, F. L., Cristovão, A. C., Rocha, S. M., Fonseca, C. P., and Baltazar, G. (2012). GDNF contributes to oestrogen-mediated protection of midbrain dopaminergic neurones. J. Neuroendocrinol. 24, 1386–1397. doi: 10.1111/j.1365-2826.2012.02348.x

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Cao, J. P., Wang, H. J., Yu, J. K., Liu, H. M., and Gao, D. S. (2008). The involvement of NF-kappaB p65/p52 in the effects of GDNF on DA neurons in early PD rats. Brain Res. Bull. 76, 505–511. doi: 10.1016/j.brainresbull.2008.03.007

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Carnicella, S., He, D.-Y., Yowell, Q. V., Glick, S. D., and Ron, D. (2010). Noribogaine, but not 18-MC, exhibits similar actions as ibogaine on GDNF expression and ethanol self-administration. Addict. Biol. 15, 424–433. doi: 10.1111/j.1369-1600.2010.00251.x

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Cass, W. A., and Peters, L. E. (2010). Neurturin effects on nigrostriatal dopamine release and content: comparison with GDNF. Neurochem. Res. 35, 727–734. doi: 10.1007/s11064-010-0128-0

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Chang, H. T., and Kita, H. (1992). Interneurons in the rat striatum: relationships between parvalbumin neurons and cholinergic neurons. Brain Res. 574, 307–311. doi: 10.1016/0006-8993(92)90830-3

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Chao, C. C., Chiang, C. H., Ma, Y. L., and Lee, E. H. Y. (2006). Molecular mechanism of the neurotrophic effect of GDNF on DA neurons: role of protein kinase CK2. Neurobiol. Aging 27, 105–118. doi: 10.1016/j.neurobiolaging.2005.01.009

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Chao, C. C., and Lee, E. H. (1999). Neuroprotective mechanism of glial cell line-derived neurotrophic factor on dopamine neurons: role of antioxidation. Neuropharmacology 38, 913–916. doi: 10.1016/s0028-3908(99)00030-1

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Chauhan, N. B., Siegel, G. J., and Lee, J. M. (2001). Depletion of glial cell line-derived neurotrophic factor in substantia nigra neurons of Parkinson’s disease brain. J. Chem. Neuroanat. 21, 277–288. doi: 10.1016/s0891-0618(01)00115-6

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Chen, P.-S., Peng, G.-S., Li, G., Yang, S., Wu, X., Wang, C.-C., et al. (2006). Valproate protects dopaminergic neurons in midbrain neuron/glia cultures by stimulating the release of neurotrophic factors from astrocytes. Mol. Psychiatry 11, 1116–1125. doi: 10.1038/sj.mp.4001893

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Choi-Lundberg, D., Lin, Q., Chang, Y., Chiang, Y., Hay, C., Mohajeri, H., et al. (1997). Dopaminergic neurons protected from degeneration by GDNF gene therapy. Science 275, 838–841. doi: 10.1126/science.275.5301.838

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Cohen, A. D., Tillerson, J. L., Smith, A. D., Schallert, T., and Zigmond, M. J. (2003). Neuroprotective effects of prior limb use in 6-hydroxydopamine-treated rats: possible role of GDNF. J. Neurochem. 85, 299–305. doi: 10.1046/j.1471-4159.2003.01657.x

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Cunningham, L. A., and Su, C. (2002). Astrocyte delivery of glial cell line-derived neurotrophic factor in a mouse model of Parkinson’s disease. Exp. Neurol. 174, 230–242. doi: 10.1006/exnr.2002.7877

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

de Lau, L. M. L., and Breteler, M. M. B. (2006). Epidemiology of Parkinson disease. Lancet Neurol. 5, 525–535. doi: 10.1016/S1474-4422(06)70471-9

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Dezawa, M., Kanno, H., Hoshino, M., Cho, H., Matsumoto, N., Itokazu, Y., et al. (2004). Specific induction of neuronal cells from bone marrow stromal cells and application for autologous transplantation. J. Clin. Invest. 113, 1701–1710. doi: 10.1172/jci200420935

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Di Liberto, V., Mudò, G., and Belluardo, N. (2011). mGluR2/3 agonist LY379268, by enhancing the production of GDNF, induces a time-related phosphorylation of RET receptor and intracellular signaling Erk1/2 in mouse striatum. Neuropharmacology 61, 638–645. doi: 10.1016/j.neuropharm.2011.05.006

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Du, Y., Li, X., Yang, D., Zhang, X., Chen, S., Huang, K., et al. (2008). Multiple molecular pathways are involved in the neuroprotection of GDNF against proteasome inhibitor induced dopamine neuron degeneration in vivo. Exp. Biol. Med. (Maywood) 233, 881–890. doi: 10.3181/0712-rm-329

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Encinas, M., Tansey, M. G., Tsui-Pierchala, B. A., Comella, J. X., Milbrandt, J., and Johnson, E. M. (2001). c-Src is required for glial cell line-derived neurotrophic factor (GDNF) family ligand-mediated neuronal survival via a phosphatidylinositol-3 kinase (PI-3K)-dependent pathway. J. Neurosci. 21, 1464–1472.

Pubmed Abstract | Pubmed Full Text | Google Scholar

Espejo, E. F., Montoro, R. J., Armengol, J. A., and López-Barneo, J. (1998). Cellular and functional recovery of parkinsonian rats after intrastriatal transplantation of carotid body cell aggregates. Neuron 20, 197–206. doi: 10.1016/s0896-6273(00)80449-3

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Francardo, V., Bez, F., Wieloch, T., Nissbrandt, H., Ruscher, K., and Cenci, M. A. (2014). Pharmacological stimulation of sigma-1 receptors has neurorestorative effects in experimental parkinsonism. Brain 137, 1998–2014. doi: 10.1093/brain/awu107

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Fu, A., Zhou, Q.-H., Hui, E. K.-W., Lu, J. Z., Boado, R. J., and Pardridge, W. M. (2010). Intravenous treatment of experimental Parkinson’s disease in the mouse with an IgG-GDNF fusion protein that penetrates the blood-brain barrier. Brain Res. 1352, 208–213. doi: 10.1016/j.brainres.2010.06.059

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Fukuda, T. (2009). Network architecture of gap junction-coupled neuronal linkage in the striatum. J. Neurosci. 29, 1235–1243. doi: 10.1523/jneurosci.4418-08.2009

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Garbayo, E., Montero-Menei, C. N., Ansorena, E., Lanciego, J. L., Aymerich, M. S., and Blanco-Prieto, M. J. (2009). Effective GDNF brain delivery using microspheres—a promising strategy for Parkinson’s disease. J. Control. Release 135, 119–126. doi: 10.1016/j.jconrel.2008.12.010

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Gash, D. M., Zhang, Z., Ovadia, A., Cass, W. A., Yi, A., Simmerman, L., et al. (1996). Functional recovery in parkinsonian monkeys treated with GDNF. Nature 380, 252–255. doi: 10.1038/380252a0

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Georgievska, B., Jakobsson, J., Persson, E., Ericson, C., Kirik, D., and Lundberg, C. (2004). Regulated delivery of glial cell line-derived neurotrophic factor into rat striatum, using a tetracycline-dependent lentiviral vector. Hum. Gene Ther. 10, 934–944. doi: 10.1089/hum.2004.15.934

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Gill, S. S., Patel, N. K., Hotton, G. R., O’Sullivan, K., McCarter, R., Bunnage, M., et al. (2003). Direct brain infusion of glial cell line-derived neurotrophic factor in Parkinson disease. Nat. Med. 9, 589–595. doi: 10.1038/nm850

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Golden, J. P., DeMaro, J. A., Osborne, P. A., Milbrandt, J., and Johnson, E. M. (1999). Expression of neurturin, GDNF and GDNF family-receptor mRNA in the developing and mature mouse. Exp. Neurol. 158, 504–528. doi: 10.1006/exnr.1999.7127

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Gomes, C. A. R. V., Simões, P. F., Canas, P. M., Quiroz, C., Sebastião, A. M., Ferré, S., et al. (2009). GDNF control of the glutamatergic cortico-striatal pathway requires tonic activation of adenosine A receptors. J. Neurochem. 108, 1208–1219. doi: 10.1111/j.1471-4159.2009.05876.x

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Gomes, C. A. R. V., Vaz, S. H., Ribeiro, J. A., and Sebastião, A. M. (2006). Glial cell line-derived neurotrophic factor (GDNF) enhances dopamine release from striatal nerve endings in an adenosine A2A receptor-dependent manner. Brain Res. 1113, 129–136. doi: 10.1016/j.brainres.2006.07.025

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Gonzalez-Barrios, J. A., Lindahl, M., Bannon, M. J., Anaya-Martínez, V., Flores, G., Navarro-Quiroga, I., et al. (2006). Neurotensin polyplex as an efficient carrier for delivering the human GDNF gene into nigral dopamine neurons of hemiparkinsonian rats. Mol. Ther. 14, 857–865. doi: 10.1016/j.ymthe.2006.09.001

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Gonzalez-Reyes, L. E., Verbitsky, M., Blesa, J., Jackson-Lewis, V., Paredes, D., Tillack, K., et al. (2012). Sonic hedgehog maintains cellular and neurochemical homeostasis in the adult nigrostriatal circuit. Neuron 75, 306–319. doi: 10.1016/j.neuron.2012.05.018

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Granholm, A.-C., Zaman, V., Godbee, J., Smith, M., Ramadan, R., Umphlet, C., et al. (2011). Prenatal LPS increases inflammation in the substantia nigra of Gdnf heterozygous mice. Brain Pathol. 21, 330–348. doi: 10.1111/j.1750-3639.2010.00457.x

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Harrison, I. F., and Dexter, D. T. (2013). Epigenetic targeting of histone deacetylase: therapeutic potential in Parkinson’s disease? Pharmacol. Ther. 140, 34–52. doi: 10.1016/j.pharmthera.2013.05.010

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

He, D.-Y., McGough, N. N. H., Ravindranathan, A., Jeanblanc, J., Logrip, M. L., Phamluong, K., et al. (2005). Glial cell line-derived neurotrophic factor mediates the desirable actions of the anti-addiction drug ibogaine against alcohol consumption. J. Neurosci. 25, 619–628. doi: 10.1523/jneurosci.3959-04.2005

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Hebert, M., Van Horne, C., Hoffer, B., and Gerhardt, G. (1996). Functional effects of GDNF in normal rat striatum: presynaptic studies using in vivo electrochemistry and microdialysis. J. Pharmacol. Exp. Ther. 279, 1181–1190.

Pubmed Abstract | Pubmed Full Text | Google Scholar

Herrán, E., Ruiz-Ortega, J. Á., Aristieta, A., Igartua, M., Requejo, C., Lafuente, J. V., et al. (2013). In vivo administration of VEGF- and GDNF-releasing biodegradable polymeric microspheres in a severe lesion model of Parkinson’s disease. Eur. J. Pharm. Biopharm. 85, 1183–1190. doi: 10.1016/j.ejpb.2013.03.034

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Hidalgo-Figueroa, M., Bonilla, S., Gutiérrez, F., Pascual, A., and López-Barneo, J. (2012). GDNF is predominantly expressed in the PV+ neostriatal interneuronal ensemble in normal mouse and after injury of the nigrostriatal pathway. J. Neurosci. 32, 864–872. doi: 10.1523/jneurosci.2693-11.2012

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Hisaoka, K., Nishida, A., Koda, T., Miyata, M., Zensho, H., Morinobu, S., et al. (2001). Antidepressant drug treatments induce glial cell line-derived neurotrophic factor (GDNF) synthesis and release in rat C6 glioblastoma cells. J. Neurochem. 79, 25–34. doi: 10.1046/j.1471-4159.2001.00531.x

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Hisaoka, K., Nishida, A., Takebayashi, M., Koda, T., Yamawaki, S., and Nakata, Y. (2004). Serotonin increases glial cell line-derived neurotrophic factor release in rat C6 glioblastoma cells. Brain Res. 1002, 167–170. doi: 10.1016/j.brainres.2004.01.009

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Hoffer, B. J., Hoffman, A., Bowenkamp, K., Huettl, P., Hudson, J., Martin, D., et al. (1994). Glial cell line-derived neurotrophic factor reverses toxin-induced injury to midbrain dopaminergic neurons in vivo. Neurosci. Lett. 182, 107–111. doi: 10.1016/0304-3940(94)90218-6

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Hong, Z., Liu, J., Xia, L., Pan, J., Xiao, Q., Lu, G., et al. (2009). Identification of glial-cell-line-derived neurotrophic factor-regulated proteins of striatum in mouse model of Parkinson disease. Proteomics. Clin. Appl. 3, 1072–1083. doi: 10.1002/prca.200800234

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Howe, C. L., and Mobley, W. C. (2005). Long-distance retrograde neurotrophic signaling. Curr. Opin. Neurobiol. 15, 40–48. doi: 10.1016/j.conb.2005.01.010

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Huang, R., Han, L., Li, J., Ren, F., Ke, W., Jiang, C., et al. (2009). Neuroprotection in a 6-hydroxydopamine-lesioned Parkinson model using lactoferrin-modified nanoparticles. J. Gene Med. 11, 754–763. doi: 10.1002/jgm.1361

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Ibáñez, C. F. (2007). Message in a bottle: long-range retrograde signaling in the nervous system. Trends Cell Biol. 17, 519–528. doi: 10.1016/j.tcb.2007.09.003

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Jollivet, C., Aubert-Pouessel, A., Clavreul, A., Venier-Julienne, M.-C., Montero-Menei, C. N., Benoit, J.-P., et al. (2004b). Long-term effect of intra-striatal glial cell line-derived neurotrophic factor-releasing microspheres in a partial rat model of Parkinson’s disease. Neurosci. Lett. 356, 207–210. doi: 10.1016/j.neulet.2003.11.051

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Jollivet, C., Aubert-Pouessel, A., Clavreul, A., Venier-Julienne, M., Remy, S., Montero-Menei, C., et al. (2004a). Striatal implantation of GDNF releasing biodegradable microspheres promotes recovery of motor function in a partial model of Parkinson’s disease. Biomaterials 25, 933–942. doi: 10.1016/s0142-9612(03)00601-x

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Jung, U. J., Leem, E., and Kim, S. R. (2014). Naringin: a protector of the nigrostriatal dopaminergic projection. Exp. Neurobiol. 23, 124–129. doi: 10.5607/en.2014.23.2.124

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Kauhausen, J., Thompson, L. H., and Parish, C. L. (2013). Cell intrinsic and extrinsic factors contribute to enhance neural circuit reconstruction following transplantation in Parkinsonian mice. J. Physiol. 591, 77–91. doi: 10.1113/jphysiol.2012.243063

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Kirik, D., Georgievska, B., and Björklund, A. (2004). Localized striatal delivery of GDNF as a treatment for Parkinson disease. Nat. Neurosci. 7, 105–110. doi: 10.1038/nn1175

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Kirik, D., Rosenblad, C., Bjo, A., and Mandel, R. J. (2000). Long-Term rAAV-mediated gene transfer of GDNF in the rat Parkinson’s model: intrastriatal but not intranigral transduction promotes functional regeneration in the lesioned nigrostriatal system. J. Neurosci. 20, 4686–4700.

Pubmed Abstract | Pubmed Full Text | Google Scholar

Kordower, J. H., and Bjorklund, A. (2013). Trophic factor gene therapy for Parkinson’s disease. Mov. Disord. 28, 96–109. doi: 10.1002/mds.25344

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Kramer, E. R., Aron, L., Ramakers, G. M. J., Seitz, S., Zhuang, X., Beyer, K., et al. (2007). Absence of Ret signaling in mice causes progressive and late degeneration of the nigrostriatal system. PLoS Biol. 5:e39. doi: 10.1371/journal.pbio.0050039

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Laganiere, J., Kells, A. P., Lai, J. T., Guschin, D., Paschon, D. E., Meng, X., et al. (2010). An engineered zinc finger protein activator of the endogenous glial cell line-derived neurotrophic factor gene provides functional neuroprotection in a rat model of Parkinson’s disease. J. Neurosci. 30, 16469–16474. doi: 10.1523/jneurosci.2440-10.2010

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Lang, A. E., Gill, S., Patel, N. K., Lozano, A., Nutt, J. G., Penn, R., et al. (2006). Randomized controlled trial of intraputamenal glial cell line-derived neurotrophic factor infusion in Parkinson disease. Ann. Neurol. 59, 459–466. doi: 10.1002/ana.20737

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Lau, Y.-S., Patki, G., Das-Panja, K., Le, W.-D., and Ahmad, S. O. (2011). Neuroprotective effects and mechanisms of exercise in a chronic mouse model of Parkinson’s disease with moderate neurodegeneration. Eur. J. Neurosci. 33, 1264–1274. doi: 10.1111/j.1460-9568.2011.07626.x

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Lee, J. Y., Kim, S. H., Ko, A.-R., Lee, J. S., Yu, J. H., Seo, J. H., et al. (2013). Therapeutic effects of repetitive transcranial magnetic stimulation in an animal model of Parkinson’s disease. Brain Res. 1537, 290–302. doi: 10.1016/j.brainres.2013.08.051

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Leem, E., Nam, J. H., Jeon, M.-T., Shin, W.-H., Won, S.-Y., Park, S.-J., et al. (2014). Naringin protects the nigrostriatal dopaminergic projection through induction of GDNF in a neurotoxin model of Parkinson’s disease. J. Nutr. Biochem. 25, 801–806. doi: 10.1016/j.jnutbio.2014.03.006

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Lei, Z., Jiang, Y., Li, T., Zhu, J., and Zeng, S. (2011). Signaling of glial cell line-derived neurotrophic factor and its receptor GFRα1 induce Nurr1 and Pitx3 to promote survival of grafted midbrain-derived neural stem cells in a rat model of Parkinson disease. J. Neuropathol. Exp. Neurol. 70, 736–747. doi: 10.1097/nen.0b013e31822830e5

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Li, X., Peng, C., Li, L., Ming, M., Yang, D., and Le, W. (2007). Glial cell-derived neurotrophic factor protects against proteasome inhibition-induced dopamine neuron degeneration by suppression of endoplasmic reticulum stress and caspase-3 activation. J. Gerontol. A Biol. Sci. Med. Sci. 62, 943–950. doi: 10.1093/gerona/62.9.943

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Lin, H. F., Doherty, D. H., Lile, J. D., Bektesh, S., and Collins, F. (1993). GDNF: a glial cell line-derived neurotrophic factor for midbrain dopaminergic neurons. Science 260, 1130–1132. doi: 10.1126/science.8493557

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Lindvall, O., and Wahlberg, L. U. (2008). Encapsulated cell biodelivery of GDNF: a novel clinical strategy for neuroprotection and neuroregeneration in Parkinson’s disease? Exp. Neurol. 209, 82–88. doi: 10.1016/j.expneurol.2007.08.019

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Lo Bianco, C., Déglon, N., Pralong, W., and Aebischer, P. (2004). Lentiviral nigral delivery of GDNF does not prevent neurodegeneration in a genetic rat model of Parkinson’s disease. Neurobiol. Dis. 17, 283–289. doi: 10.1016/j.nbd.2004.06.008

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Lo Bianco, C., Ridet, J. L., Schneider, B. L., Déglon, N., and Aebischer, P. (2002). Alpha-Synucleinopathy and selective dopaminergic neuron loss in a rat lentiviral-based model of Parkinson’s disease. Proc. Natl. Acad. Sci. U S A 99, 10813–10818. doi: 10.1073/pnas.152339799

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Lonka-Nevalaita, L., Lume, M., Leppänen, S., Jokitalo, E., Peränen, J., and Saarma, M. (2010). Characterization of the intracellular localization, processing and secretion of two glial cell line-derived neurotrophic factor splice isoforms. J. Neurosci. 30, 11403–11413. doi: 10.1523/jneurosci.5888-09.2010

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

López-Barneo, J., Pardal, R., Montoro, R. J., Smani, T., García-Hirschfeld, J., and Ureña, J. (1999). K+ and Ca 2+ channel activity and cytosolic [Ca 2+] in oxygen-sensing tissues. Respir. Physiol. 115, 215–227. doi: 10.1016/s0034-5687(99)00016-x

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Love, S., Plaha, P., Patel, N., Hotton, G., Brooks, D., and Gill, S. (2005). Glial cell line-derived neurotrophic factor induces neuronal sprouting in human brain. Nat. Med. 11, 703–704. doi: 10.1038/nm0705-703

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Marco, S., Saura, J., Pérez-Navarro, E., José Martí, M., Tolosa, E., and Alberch, J. (2002). Regulation of c-Ret, GFRalpha1 and GFRalpha2 in the substantia nigra pars compacta in a rat model of Parkinson’s disease. J. Neurobiol. 52, 343–351. doi: 10.1002/neu.10082

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Maruyama, W., Nitta, A., Shamoto-Nagai, M., Hirata, Y., Akao, Y., Yodim, M., et al. (2004). N-Propargyl-1 (R)-aminoindan, rasagiline, increases glial cell line-derived neurotrophic factor (GDNF) in neuroblastoma SH-SY5Y cells through activation of NF-κB transcription factor. Neurochem. Int. 44, 393–400. doi: 10.1016/j.neuint.2003.08.005

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Maswood, N., Young, J., Tilmont, E., Zhang, Z., Gash, D. M., Gerhardt, G. A., et al. (2004). Caloric restriction increases neurotrophic factor levels and attenuates neurochemical and behavioral deficits in a primate model of Parkinson’s disease. Proc. Natl. Acad. Sci. U S A 101, 18171–18176. doi: 10.1073/pnas.0405831102

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Mendez, I., Dagher, A., Hong, M., Hebb, A., Gaudet, P., Law, A., et al. (2000). Enhancement of survival of stored dopaminergic cells and promotion of graft survival by exposure of human fetal nigral tissue to glial cell line—derived neurotrophic factor in patients with Parkinson’s disease report of two cases and technical considerations. J. Neurosurg. 92, 863–869. doi: 10.3171/jns.2000.92.5.0863

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Migliore, M. M., Ortiz, R., Dye, S., Campbell, R. B., Amiji, M. M., and Waszczak, B. L. (2014). Neurotrophic and neuroprotective efficacy of intranasal GDNF in a rat model of Parkinson’s disease. Neuroscience 274, 11–23. doi: 10.1016/j.neuroscience.2014.05.019

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Mínguez-Castellanos, A., Escamilla-Sevilla, F., Hotton, G. R., Toledo-Aral, J. J., Ortega-Moreno, A., Méndez-Ferrer, S., et al. (2007). Carotid body autotransplantation in Parkinson disease: a clinical and positron emission tomography study. J. Neurol. Neurosurg. Psychiatry 78, 825–831. doi: 10.1136/jnnp.2006.106021

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Mizuta, I., Ohta, M., Ohta, K., Nishimura, M., Mizuta, E., Hayashi, K., et al. (2000). Selegiline and desmethylselegiline stimulate NGF, BDNF and GDNF synthesis in cultured mouse astrocytes. Biochem. Biophys. Res. Commun. 279, 751–755. doi: 10.1006/bbrc.2000.4037

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Mogi, M., Togari, A., Kondo, T., Mizuno, Y., Kogure, O., Kuno, S., et al. (2001). Glial cell line-derived neurotrophic factor in the substantia nigra from control and parkinsonian brains. Neurosci. Lett. 300, 179–181. doi: 10.1016/s0304-3940(01)01577-4

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Monville, C., Torres, E., Thomas, E., Scarpini, C. G., Muhith, J., Lewis, J., et al. (2004). HSV vector-delivery of GDNF in a rat model of PD: partial efficacy obscured by vector toxicity. Brain Res. 1024, 1–15. doi: 10.1016/j.brainres.2004.06.082

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Moore, M., Klein, R., Fariñas, I., Sauer, H., Armanini, M., Phillips, H., et al. (1996). Renal and neuronal abnormalities in mice lacking GDNF. Nature 382, 76–79. doi: 10.1038/382076a0

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Muñoz-Manchado, A. B., Villadiego, J., Suárez-Luna, N., Bermejo-Navas, A., Garrido-Gil, P., Labandeira-García, J. L., et al. (2013). Neuroprotective and reparative effects of carotid body grafts in a chronic MPTP model of Parkinson’s disease. Neurobiol. Aging 34, 902–915. doi: 10.1016/j.neurobiolaging.2012.06.001

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Nakagawa, T., and Schwartz, J. P. (2004). Gene expression profiles of reactive astrocytes in dopamine-depleted striatum. Brain Pathol. 14, 275–280. doi: 10.1111/j.1750-3639.2004.tb00064.x

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Nakajima, K., Hida, H., Shimano, Y., Fujimoto, I., Hashitani, T., Kumazaki, M., et al. (2001). GDNF is a major component of trophic activity in DA-depleted striatum for survival and neurite extension of DAergic neurons. Brain Res. 916, 76–84. doi: 10.1016/s0006-8993(01)02866-9

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Newburn, E. N., Duchemin, A.-M., Neff, N. H., and Hadjiconstantinou, M. (2014). GM1 ganglioside enhances Ret signaling in striatum. J. Neurochem. 130, 541–554. doi: 10.1111/jnc.12760

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Nosrat, C. A., Tomac, A., Lindqvist, E., Lindskog, S., Humpel, C., Strömberg, I., et al. (1996). Cellular expression of GDNF mRNA suggests multiple functions inside and outside the nervous system. Cell Tissue Res. 286, 191–207. doi: 10.1007/s004410050688

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Nutt, J. G., Burchiel, K. J., Comella, C. L., Jankovic, J., Lang, A. E., Laws, E. R. Jr., et al. (2003). Randomized, double-blind trial of glial cell line-derived neurotrophic factor (GDNF) in PD. Neurology 60, 69–73. doi: 10.1212/wnl.60.1.69

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Ohshima-Hosoyama, S., Simmons, H. A., Goecks, N., Joers, V., Swanson, C. R., Bondarenko, V., et al. (2012). A monoclonal antibody-GDNF fusion protein is not neuroprotective and is associated with proliferative pancreatic lesions in parkinsonian monkeys. PLoS One 7:e39036. doi: 10.1371/journal.pone.0039036

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Onyango, I. G., Tuttle, J. B., and Bennett, J. P. Jr. (2005). Brain-derived growth factor and glial cell line-derived growth factor use distinct intracellular signaling pathways to protect PD cybrids from H2O2-induced neuronal death. Neurobiol. Dis. 20, 141–154. doi: 10.1016/j.nbd.2005.02.009

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Oppenheim, R. W., Houenou, L. J., Johnson, J. E., Lin, L. F., Li, L., Lo, A. C., et al. (1995). Developing motor neurons rescued from programmed and axotomy-induced cell death by GDNF. Nature 373, 344–346. doi: 10.1038/373344a0

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Palfi, S., Leventhal, L., Chu, Y., Ma, S. Y., Emborg, M., Bakay, R., et al. (2002). Lentivirally delivered glial cell line-derived neurotrophic factor increases the number of striatal dopaminergic neurons in primate models of nigrostriatal degeneration. J. Neurosci. 22, 4942–4954.

Pubmed Abstract | Pubmed Full Text | Google Scholar

Pallini, R., Consales, A., Lauretti, L., and Fernandez, E. (1997). Experiments in a Parkinson’s rat model. Science 277, 389–390. doi: 10.1126/science.277.5324.389

CrossRef Full Text | Google Scholar

Paratcha, G., Ledda, F., and Ibáñez, C. F. (2003). The neural cell adhesion molecule NCAM is an alternative signaling receptor for GDNF family ligands. Cell 113, 867–879. doi: 10.1016/s0092-8674(03)00435-5

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Pardal, R., Ortega-Sáenz, P., Durán, R., and López-Barneo, J. (2007). Glia-like stem cells sustain physiologic neurogenesis in the adult mammalian carotid body. Cell 131, 364–377. doi: 10.1016/j.cell.2007.07.043

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Pascual, A., Hidalgo-Figueroa, M., Gómez-Díaz, R., and López-Barneo, J. (2011). GDNF and protection of adult central catecholaminergic neurons. J. Mol. Endocrinol. 46, R83–R92. doi: 10.1530/jme-10-0125

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Pascual, A., Hidalgo-Figueroa, M., Piruat, J. I., Pintado, C. O., Gómez-Díaz, R., and López-Barneo, J. (2008). Absolute requirement of GDNF for adult catecholaminergic neuron survival. Nat. Neurosci. 11, 755–761. doi: 10.1038/nn.2136

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Patel, N. K., Bunnage, M., Plaha, P., Svendsen, C. N., Heywood, P., and Gill, S. S. (2005). Intraputamenal infusion of glial cell line-derived neurotrophic factor in PD: a two-year outcome study. Ann. Neurol. 57, 298–302. doi: 10.1002/ana.20374

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Pichel, J., Shen, L., Sheng, H. Z., Granholm, A. C., Drago, J., Grinberg, A., et al. (1996). Defects in enteric innervation and kidney development in mice lacking GDNF. Nature 382, 73–76. doi: 10.1038/382073a0

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Platero-Luengo, A., González-Granero, S., Durán, R., Díaz-Castro, B., Piruat, J. I., García-Verdugo, J. M., et al. (2014). An O2-sensitive glomus cell-stem cell synapse induces carotid body growth in chronic hypoxia. Cell 156, 291–303. doi: 10.1016/j.cell.2013.12.013

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Pothos, E. N., Davila, V., and Sulzer, D. (1998). Presynaptic recording of quanta from midbrain dopamine neurons and modulation of the quantal size. J. Neurosci. 18, 4106–4118.

Pubmed Abstract | Pubmed Full Text | Google Scholar

Proschel, C., Stripay, J. L., Shih, C.-H., Munger, J. C., and Noble, M. D. (2014). Delayed transplantation of precursor cell-derived astrocytes provides multiple benefits in a rat model of Parkinsons. EMBO Mol. Med. 6, 504–518. doi: 10.1002/emmm.201302878

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Quintino, L., Manfré, G., Wettergren, E. E., Namislo, A., Isaksson, C., and Lundberg, C. (2013). Functional neuroprotection and efficient regulation of GDNF using destabilizing domains in a rodent model of Parkinson’s disease. Mol. Ther. 21, 2169–2180. doi: 10.1038/mt.2013.169

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Rodriguez-Pallares, J., Joglar, B., Muñoz-Manchado, A. B., Villadiego, J., Toledo-Aral, J. J., and Labandeira-Garcia, J. L. (2012). Cografting of carotid body cells improves the long-term survival, fiber outgrowth and functional effects of grafted dopaminergic neurons. Regen. Med. 7, 309–322. doi: 10.2217/rme.12.22

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Saavedra, A., Baltazar, G., Carvalho, C. M., and Duarte, E. P. (2005). GDNF modulates HO-1 expression in substantia nigra postnatal cell cultures. Free Radic. Biol. Med. 39, 1611–1619. doi: 10.1016/j.freeradbiomed.2005.08.005

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Sánchez, M. P., Silos-Santiago, I., Frisén, J., He, B., Lira, S. A., and Barbacid, M. (1996). Renal agenesis and the absence of enteric neurons in mice lacking GDNF. Nature 382, 70–73. doi: 10.1038/382070a0

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Sawada, H., Ibi, M., Kihara, T., Urushitani, M., Nakanishi, M., Akaike, A., et al. (2000). Neuroprotective mechanism of glial cell line-derived neurotrophic factor in mesencephalic neurons. J. Neurochem. 74, 1175–1184. doi: 10.1046/j.1471-4159.2000.741175.x

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Schaar, D. G., Sieber, B. A., Dreyfus, C. F., and Black, I. B. (1993). Regional and cell-specific expression of GDNF in rat brain. Exp. Neurol. 124, 368–371. doi: 10.1006/exnr.1993.1207

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Shao, Z., Dyck, L. E., Wang, H., and Li, X. M. (2006). Antipsychotic drugs cause glial cell line derived neurotrophic factor secretion from C6 glioma cells. J. Psychiatry Neurosci. 31, 32–37.

Pubmed Abstract | Pubmed Full Text | Google Scholar

Slevin, J. T., Gerhardt, G. A., Smith, C. D., Gash, D. M., Kryscio, R., and Young, B. (2005). Improvement of bilateral motor functions in patients with Parkinson disease through the unilateral intraputaminal infusion of glial cell line-derived neurotrophic factor. J. Neurosurg. 102, 216–222. doi: 10.3171/jns.2005.102.2.0216

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Smith, M. P., and Cass, W. A. (2007). GDNF reduces oxidative stress in a 6-hydroxydopamine model of Parkinson’s disease. Neurosci. Lett. 412, 259–263. doi: 10.1016/j.neulet.2006.11.017

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Smith, M. P., Fletcher-Turner, A., Yurek, D. M., and Cass, W. A. (2006). Calcitriol protection against dopamine loss induced by intracerebroventricular administration of 6-hydroxydopamine. Neurochem. Res. 31, 533–539. doi: 10.1007/s11064-006-9048-4

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Sredni, B., Geffen-Aricha, R., Duan, W., Albeck, M., Shalit, F., Lander, H. M., et al. (2007). Multifunctional tellurium molecule protects and restores dopaminergic neurons in Parkinson’s disease models. FASEB J. 21, 1870–1883. doi: 10.1096/fj.06-7500com

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Su, T.-P., Wu, X. Z., Cone, E. J., Shukla, K., Gund, T. M., Dodge, A. L., et al. (1991). Sigma compounds derived from phencyclidine: identification of PRE-084, a new, selective sigma ligand. J. Pharmacol. Exp. Ther. 259, 543–550.

Pubmed Abstract | Pubmed Full Text | Google Scholar

Subramaniam, S. R., and Chesselet, M.-F. (2013). Mitochondrial dysfunction and oxidative stress in Parkinson’s disease. Prog. Neurobiol. 106–107, 17–32. doi: 10.1016/j.pneurobio.2013.04.004

CrossRef Full Text | Google Scholar

Tai, K., Quintino, L., Isaksson, C., Gussing, F., and Lundberg, C. (2012). Destabilizing domains mediate reversible transgene expression in the brain. PLoS One 7:e46269. doi: 10.1371/journal.pone.0046269

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Tajiri, N., Yasuhara, T., Shingo, T., Kondo, A., Yuan, W., Kadota, T., et al. (2010). Exercise exerts neuroprotective effects on Parkinson’s disease model of rats. Brain Res. 1310, 200–207. doi: 10.1016/j.brainres.2009.10.075

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Tang, Y. P., Ma, Y. L., Chao, C. C., Chen, K. Y., and Lee, E. H. Y. (1998). Enhanced glial cell line-derived neurotrophic factor mRNA expression upon (-)-deprenyl and melatonin treatments. J. Neurosci. Res. 53, 593–604. doi: 10.1002/(sici)1097-4547(19980901)53:5<593::aid-jnr9>3.3.co;2-7

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Tarazi, F. I., Sahli, Z. T., Wolny, M., and Mousa, S. A. (2014). Emerging therapies for Parkinson’s disease: from bench to bedside. Pharmacol. Ther. 144, 123–133. doi: 10.1016/j.pharmthera.2014.05.010

CrossRef Full Text | Google Scholar

Tatarewicz, S. M., Wei, X., Gupta, S., Masterman, D., Swanson, S. J., and Moxness, M. S. (2007). Development of a maturing T-cell-mediated immune response in patients with idiopathic Parkinson’s disease receiving r-metHuGDNF via continuous intraputaminal infusion. J. Clin. Immunol. 27, 620–627. doi: 10.1007/s10875-007-9117-8

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Tereshchenko, J., Maddalena, A., Bähr, M., and Kügler, S. (2014). Pharmacologically controlled, discontinuous GDNF gene therapy restores motor function in a rat model of Parkinson’s disease. Neurobiol. Dis. 65, 35–42. doi: 10.1016/j.nbd.2014.01.009

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Tomac, A., Lindqvist, E., Lin, L. F., Ogren, S. O., Young, D., Hoffer, B. J., et al. (1995a). Protection and repair of the nigrostriatal dopaminergic system by GDNF in vivo. Nature 373, 335–339. doi: 10.1038/373335a0

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Tomac, A., Widenfalk, J., Lin, L. F., Kohno, T., Ebendal, T., Hoffer, B. J., et al. (1995b). Retrograde axonal transport of glial cell line-derived neurotrophic factor in the adult nigrostriatal system suggests a trophic role in the adult. Proc. Natl. Acad. Sci. U S A 92, 8274–8278. doi: 10.1073/pnas.92.18.8274

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Törnqvist, N., Björklund, L., Almqvist, P., Wahlberg, L., and Strömberg, I. (2000). Implantation of bioactive growth factor-secreting rods enhances fetal dopaminergic graft survival, outgrowth density and functional recovery in a rat model of Parkinson’s disease. Exp. Neurol. 164, 130–138. doi: 10.1006/exnr.2000.7411

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Trupp, M., Belluardo, N., Funakoshi, H., and Ibáñez, C. F. (1997). Complementary and overlapping expression of glial cell line-derived neurotrophic factor (GDNF), c-ret proto-oncogene and GDNF receptor-alpha indicates multiple mechanisms of trophic actions in the adult rat CNS. J. Neurosci. 17, 3554–3567.

Pubmed Abstract | Pubmed Full Text | Google Scholar

Tseng, J. L., Baetge, E. E., Zurn, A. D., and Aebischer, P. (1997). GDNF reduces drug-induced rotational behavior after medial forebrain bundle transection by a mechanism not involving striatal dopamine. J. Neurosci. 17, 325–333.

Pubmed Abstract | Pubmed Full Text | Google Scholar

Ugarte, S. D., Lin, E., Klann, E., Zigmond, M. J., and Perez, R. G. (2003). Effects of GDNF on 6-OHDA-induced death in a dopaminergic cell line: modulation by inhibitors of PI3 kinase and MEK. J. Neurosci. Res. 73, 105–112. doi: 10.1002/jnr.10632

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Villadiego, J., Méndez-Ferrer, S., Valdés-Sánchez, T., Silos-Santiago, I., Fariñas, I., López-Barneo, J., et al. (2005). Selective glial cell line-derived neurotrophic factor production in adult dopaminergic carotid body cells in situ and after intrastriatal transplantation. J. Neurosci. 25, 4091–4098. doi: 10.1523/jneurosci.4312-04.2005

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Wang, C. Y., Yang, F., He, X., Chow, A., Du, J., Russell, J. T., et al. (2001). Ca2+ binding protein frequenin mediates GDNF-induced potentiation of Ca2+ channels and transmitter release. Neuron 32, 99–112. doi: 10.1016/s0896-6273(01)00434-2

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Wartiovaara, K., Hytönen, M., Vuori, M., Paulin, L., Rinne, J., and Sariola, H. (1998). Mutation analysis of the glial cell line-derived neurotrophic factor gene in Parkinson’s disease. Exp. Neurol. 152, 307–309. doi: 10.1006/exnr.1998.6857

CrossRef Full Text | Google Scholar

Winkler, C., Sauer, H., Lee, C. S., and Björklund, A. (1996). Short-term GDNF treatment provides long-term rescue of lesioned nigral dopaminergic neurons in a rat model of Parkinson’s disease. J. Neurosci. 16, 7206–7215.

Pubmed Abstract | Pubmed Full Text | Google Scholar

Wu, X., Chen, P. S., Dallas, S., Wilson, B., Block, M. L., Wang, C.-C., et al. (2008). Histone deacetylase inhibitors up-regulate astrocyte GDNF and BDNF gene transcription and protect dopaminergic neurons. Int. J. Neuropsychopharmacol. 11, 1123–1134. doi: 10.1017/s1461145708009024

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Xia, C.-F., Boado, R. J., Zhang, Y., Chu, C., and Pardridge, W. M. (2008). Intravenous glial-derived neurotrophic factor gene therapy of experimental Parkinson’s disease with Trojan horse liposomes and a tyrosine hydroxylase promoter. J. Gene Med. 10, 306–315. doi: 10.1002/jgm.1152

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Xu, K., and Dluzen, D. E. (2000). The effect of GDNF on nigrostriatal dopaminergic function in response to a two-pulse K(+) stimulation. Exp. Neurol. 166, 450–457. doi: 10.1006/exnr.2000.7515

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Yamagata, K., Tagami, M., Ikeda, K., Tsumagari, S., Yamori, Y., and Nara, Y. (2002). Differential regulation of glial cell line-derived neurotrophic factor (GDNF) mRNA expression during hypoxia and reoxygenation in astrocytes isolated from stroke-prone spontaneously hypertensive rats. Glia 37, 1–7. doi: 10.1002/glia.10003

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Yan, Q., Matheson, C., and Lopez, O. T. (1995). In vivo neurotrophic effects of GDNF on neonatal and adult facial motor neurons. Nature 373, 341–344. doi: 10.1038/373341a0

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Yurek, D. M., Flectcher, A. M., Kowalczyk, T. H., Padegimas, L., and Cooper, M. J. (2009). Compacted DNA nanoparticle gene transfer of GDNF to the rat striatum enhances the survival of grafted fetal dopamine neurons. Cell Transplant. 18, 1183–1196. doi: 10.3727/096368909x12483162196881

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Zhang, Y., and Pardridge, W. M. (2009). Near complete rescue of experimental Parkinson’s disease with intravenous, non-viral GDNF gene therapy. Pharm. Res. 26, 1059–1063. doi: 10.1007/s11095-008-9815-9

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Zhao, Q., Gao, J., Li, W., and Cai, D. (2010). Neurotrophic and neurorescue effects of Echinacoside in the subacute MPTP mouse model of Parkinson’s disease. Brain Res. 1346, 224–236. doi: 10.1016/j.brainres.2010.05.018

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Zhu, G., Wang, X., Chen, Y., Yang, S., Cheng, H., Wang, N., et al. (2010). Puerarin protects dopaminergic neurons against 6-hydroxydopamine neurotoxicity via inhibiting apoptosis and upregulating glial cell line-derived neurotrophic factor in a rat model of Parkinson’s disease. Planta Med. 76, 1820–1826. doi: 10.1055/s-0030-1249976

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Zhu, G., Wang, X., Wu, S., Li, X., and Li, Q. (2014). Neuroprotective effects of puerarin on 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine induced Parkinson’s disease model in mice. Phytother. Res. 28, 179–186. doi: 10.1002/ptr.4975

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar

Zigmond, M. J., Cameron, J. L., Leak, R. K., Mirnics, K., Russell, V. A., Smeyne, R. J., et al. (2009). Triggering endogenous neuroprotective processes through exercise in models of dopamine deficiency. Parkinsonism Relat. Disord. 15(Suppl. 3), S42–S45. doi: 10.1016/s1353-8020(09)70778-3

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar