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MINI REVIEW article

Front. Cell. Neurosci., 16 May 2017
Sec. Cellular Neurophysiology
This article is part of the Research Topic Demystifying Serotonin: Molecules, Circuits, and Behaviors View all 15 articles

The Effect of Serotonin-Targeting Antidepressants on Neurogenesis and Neuronal Maturation of the Hippocampus Mediated via 5-HT1A and 5-HT4 Receptors

  • Department of Biological Science and Technology, Faculty of Industrial Science and Technology, Tokyo University of Science, Tokyo, Japan

Antidepressant drugs such as selective serotonin reuptake inhibitors (SSRIs) specifically increase serotonin (5-HT) levels in the synaptic cleft and are widely used to treat mood and anxiety disorders. There are 14 established subtypes of 5-HT receptors in rodents, each of which has regionally different expression patterns. Many preclinical studies have suggested that the hippocampus, which contains abundant 5-HT1A and 5-HT4 receptor subtypes in the dentate gyrus (DG), is critically involved in the mechanisms of action of antidepressants. This review article will analyze studies demonstrating regulation of hippocampal functions and hippocampus-dependent behaviors by SSRIs and similar serotonergic agents. Multiple studies indicate that 5-HT1A and 5-HT4 receptor signaling in the DG contributes to SSRI-mediated promotion of neurogenesis and increased neurotrophic factors expression. Chronic SSRI treatment causes functions and phenotypes of mature granule cells (GCs) to revert to immature-like phenotypes defined as a “dematured” state in the DG, and to increase monoamine reactivity at the dentate-to-CA3 synapses, via 5-HT4 receptor signaling. Behavioral studies demonstrate that the 5-HT1A receptors on mature GCs are critical for expression of antidepressant effects in the forced swim test and in novelty suppressed feeding; such studies also note that 5-HT4 receptors mediate neurogenesis-dependent antidepressant activity in, for example, novelty-suppressed feeding. Despite their limitations, the collective results of these studies describe a potential new mechanism of action, in which 5-HT1A and 5-HT4 receptor signaling, either independently or cooperatively, modulates the function of the hippocampal DG at multiple levels, any of which could play a critical role in the antidepressant actions of 5-HT-enhancing drugs.

Introduction

Serotonin (5-hydroxytryptamine, 5-HT) is a monoamine neurotransmitter that plays important roles in physiological and pathophysiological functions in the brain. Serotonergic neurons from the dorsal and median raphe project throughout the brain, including sending afferents to the hippocampus, one of the stress-sensitive limbic structures implicated in the pathophysiology of mood and anxiety disorders (Pittenger and Duman, 2008; Kheirbek et al., 2012). Drugs such as selective serotonin reuptake inhibitors (SSRIs) specifically increase 5-HT levels in the synaptic cleft and are widely used to treat mood and anxiety disorders. Preclinical studies demonstrate that stress leads to the atrophy and loss of hippocampal neurons (Pittenger and Duman, 2008; McEwen et al., 2016). In addition, many, but not all, neuroimaging studies report that the hippocampal volume is relatively small in patients with depression (MacQueen and Frodl, 2011). Conversely, chronic SSRI treatment increases the dendritic spine density of neurons in the CA pyramidal cell subfields and stimulates adult neurogenesis in the dentate gyrus (DG; Malberg et al., 2000; Santarelli et al., 2003; Bessa et al., 2009). Recent reports also indicate that chronic SSRI treatment significantly changes the physiological and functional properties of mature granule cells (GCs), the primary cell type of the DG (Kobayashi et al., 2010). These findings demonstrate that enhancing serotonergic activity with antidepressants modulates hippocampal function. Therefore, newer research has been focused on the signaling pathways activated by SSRIs in the hippocampus.

At least 14 different 5-HT receptor types and subtypes have been identified (Hoyer et al., 2002). Among them, 5-HT1A, 5-HT1B, 5-HT2B, 5-HT4 and 5-HT7 receptors are expressed in the DG of the hippocampus (Pompeiano et al., 1992; Grossman et al., 1993; Bruinvels et al., 1994; Vilaró et al., 1996; Klempin et al., 2010; Tanaka et al., 2012; Diaz et al., 2013). Although there are some cell-type-related exceptions, the 5-HT1A and the 5-HT1B receptors generally couple to Gi/o proteins, the 5-HT2B receptor couples to Gq/11 proteins, and the 5-HT4 and the 5-HT7 receptors couple to Gs proteins (Bockaert et al., 2008; Polter and Li, 2010).

This review article discusses studies demonstrating multiple forms of regulation of hippocampal functions mediated by SSRIs and serotonergic agents. A recent review has addressed the general roles of 5-HT1A and 5-HT4 receptors in the actions of antidepressants (Samuels et al., 2016), but this mini-review article focuses specifically on the contribution of 5-HT1A and 5-HT4 receptor activity to functional modulation of GCs in the DG. It will also briefly discuss the involvement of 5-HT1A and 5-HT4 receptors in hippocampus-dependent antidepressant and anxiolytic behavioral effects.

Enhancement of Adult Neurogenesis in the Hippocampus by SSRIs and Relative Involvement of 5-HT Receptor Subtypes in the DG

Hippocampal neurogenesis is a dynamic process that is controlled by various factors, including environmental stimuli. In the mammalian DG, new neurons are generated from neural stem cells and progenitors in the subgranular zone (SGZ) of the DG throughout life (Ming and Song, 2005). Hippocampal neurogenesis is enhanced by active environmental stimulation such as learning, exercise and rich environmental conditions. Conversely, stress exposure or aversive stimulation suppresses this process. Preclinical studies demonstrate that exposure to chronic stress reduces proliferation of neuronal progenitors in the DG, resulting in decreased neurogenesis (Fuchs et al., 2006). Many, but not all, clinical studies also show reductions in hippocampal volume under depression and stress conditions (MacQueen and Frodl, 2011); together, these findings suggest that the reduction of neurogenesis by stress may be one of the cellular mechanisms underlying hippocampal structural changes in patients with depression.

Studies performed over the past 20 years provide evidence that SSRI-mediated acceleration of neurogenesis is one of the cellular mechanisms underlying antidepressant efficacy. Chronic administration of SSRIs such as fluoxetine facilitates each stage of neurogenesis, including progenitor proliferation, survival, and the early phase of maturation (Encinas et al., 2006; Wang et al., 2008). Fluoxetine administration also restores neurogenesis decreased by stress exposure. Inescapable electrical shock stress reduces cell proliferation in the adult rat hippocampus in a manner reversed by chronic fluoxetine treatment (Malberg and Duman, 2003). Chronic corticosterone treatment in mice, a model of anxiety and depression, also reduces proliferation of progenitor cells. In this model, the effect of fluoxetine at each stage of neurogenesis including proliferation, differentiation, and survival is more pronounced than that in control mice (David et al., 2009), suggesting that corticosterone treatment increases the sensitivity of hippocampal neurogenesis to fluoxetine. In humans, the number of neuronal progenitors in the DG of SSRI-treated patients with major depressive disorder is higher than that in untreated patients (Boldrini et al., 2009). Consistent with this report, the number of mature GCs in the DG of SSRI-treated patients with major depressive disorder is also higher than that in untreated patients (Boldrini et al., 2013).

Multiple evidences have demonstrated that the 5-HT1A receptor in mature GCs contribute to the promotion of hippocampal neurogenesis by SSRIs. In situ hybridization studies demonstrate abundant 5-HT1A mRNA expression in mouse GCs (Pompeiano et al., 1992; Tanaka et al., 2012; Diaz et al., 2013). Pharmacological studies show that a 5-HT1A receptor agonist, 8-OH-DPAT, increased proliferation in the DG upon short-term administration in mice or rats (Banasr et al., 2004; Klempin et al., 2010; Arnold and Hagg, 2012; reviewed in Alenina and Klempin, 2015). Conversely, chronic treatment with 5-HT1A receptor antagonists (WAY100135 or NAN-190) decreases proliferation and survival of newborn cells in the DG in some studies, but not all (Radley and Jacobs, 2002; Zhang et al., 2016). Furthermore, germline 5-HT1A receptor knockout mice show lack of effects of the SSRIs on cell proliferation in the DG (Santarelli et al., 2003). However, since the 5-HT1A receptor is expressed not only in GCs as a heteroreceptor but also in serotonergic raphe neurons as an autoreceptor, it is unclear whether 5-HT1A signaling in GCs directly influences neurogenesis. Recently, the function of the 5-HT1A receptor in the hippocampal DG was examined using mice lacking the 5-HT1A receptor specific to GCs (Samuels et al., 2015). Fluoxetine-induced facilitation in cell proliferation and early neural maturation in the DG are attenuated in mice lacking GC-specific 5-HT1A receptor, demonstrating that postsynaptic 5-HT1A signaling in GCs is involved in hippocampal neurogenesis induced by fluoxetine.

Recent studies have also implicated that the 5-HT4 receptor signaling contributes to the promotion of hippocampal neurogenesis by SSRIs. Specific ligand binding and in situ hybridization studies demonstrate abundant 5-HT4 expression in mouse or rat DG (Grossman et al., 1993; Vilaró et al., 1996; Tanaka et al., 2012; Diaz et al., 2013; Imoto et al., 2015). Pharmacological studies demonstrate that the proliferative effect of a 5-HT4 agonist (RS67333) is observed in the rat DG following a short term administration protocol (Lucas et al., 2007; Pascual-Brazo et al., 2012). Chronic activation of the 5-HT4 receptor facilitates not only proliferation, but also maturation in newborn neurons, and chronic inhibition of 5-HT4 receptor partially blocks the neurogenic effect of chronic fluoxetine (Mendez-David et al., 2014). Another line of study also demonstrates that germline 5-HT4 receptor knockout mice of the C57BL/6J strain are resistant to the effects of fluoxetine on the proliferation of newborn cells and the number of immature neurons in the DG (Imoto et al., 2015). Since there is no report of GC-specific 5-HT4 receptor knockout mice, it is unknown whether 5-HT4 receptors act specifically in the GCs to contributes to neurogenesis therein. However, several evidences indicate that the 5-HT4 receptor activates the intracellular signaling of GCs. For example, the short-term stimulation of 5-HT4 receptors increases cAMP response element binding protein (CREB) activation and brain derived neurotrophic factor (BDNF) expression in the DG (Lucas et al., 2007; Pascual-Brazo et al., 2012). Thus, increased 5-HT4 activity in mature GCs may directly facilitate gene expression of neurotrophic factors in the DG, and contribute to the hippocampal neurogenesis. It is still possible that 5-HT4 receptors expressed in other brain regions could affect neurogenesis. For example, the 5-HT4 receptor in the prefrontal cortex is found to increase the activity of dorsal raphe serotonergic neurons (Lucas and Debonnel, 2002; Compan et al., 2004).

It is also important to note that serotonergic activity is critical for exercise-induced adult hippocampal neurogenesis (Klempin et al., 2013). It would be interesting to investigate the 5-HT receptor subtypes and mechanisms involved in exercise-induced neurogenesis and then to compare the results with those of SSRI-induced neurogenesis. Interestingly, neither the 5-HT1A receptor- nor the 5-HT4 receptor-deficient mice have changes in basal hippocampal neurogenesis (Santarelli et al., 2003; Imoto et al., 2015), suggesting that neither 5-HT1A nor the 5-HT4 activity is necessary for the maintenance of neurogenesis. Therefore, these signals may play an important role in regulating hippocampal activity in response to environmental and pharmacological stimuli.

Ssri-Related Functional and Phenotypic Changes in Mature Granule Neurons and the Involvement of Specific 5-HT Receptor Subtypes

Mature GCs in the DG, which is positioned at the entrance of the hippocampal excitatory trisynaptic circuit, play a critical role in regulating hippocampal function. The majority of neurons in the adult DG are mature GCs. Electrophysiological studies show that GC mossy fibers regulate associative synaptic plasticity in the hippocampal CA3 region (Contractor et al., 2000; Lauri et al., 2001; Feng et al., 2003; Kobayashi and Poo, 2004). The abundant expression of 5-HT1A and 5-HT4 receptors in mature GCs suggests that serotonergic afferents regulate the function of the DG. However, it remains to be explained how sustained elevation of 5-HT levels in the synaptic cleft by chronic SSRI treatment affects the function and phenotypes of mature GCs.

The mature state of GCs is characterized by several distinct molecular and physiological features (Figure 1). Recent reports demonstrate that chronic treatment of SSRIs such as fluoxetine and paroxetine in adult mice changes several features of mature GCs, essentially transforming the cells into an immature-like phenotype defined here as a “dematured” state (Kobayashi et al., 2010, 2013). Electrophysiological analysis shows that fluoxetine-treated GCs are more easily excited by somatic current injection, and demonstarate markedly reduced synaptic facilitation in dentate-to-CA3 signal transmission, a condition characterizing the immature GC-to-CA3 synapse (Marchal and Mulle, 2004). In contrast, fluoxetine-treated GCs have unaltered input resistance and membrane time constant, indicating that fluoxetine did not induce drastic changes in the cell size or morphology in mature GCs (Kobayashi et al., 2010). Chronic fluoxetine also reduces expression of mature GC markers, such as calbindin and tryptophan-2,3-dioxygenase, which are normally highly expressed (Yamasaki et al., 2008). Several animal mutation-based models, including SNAP-25 mutant mice and Schnurri-2 knockout mice, possess “immature” cellular phenotypes in the DG (Ohira et al., 2013; Takao et al., 2013). A transcriptome analysis in the hippocampus shows that gene expression patterns are significantly similar between SNAP-25 mutant mice and fluoxetine-treated mice (Ohira et al., 2013), suggesting that fluoxetine-treated mice and SNAP-25 mutant mice demonstrate a similar immature GC phenotype. Many studies have shown that chronic fluoxetine treatment accelerates the early maturation process, including the corresponding increase in dendritic complexity (Wang et al., 2008) and decrease in the proportion of expression of the immature GC marker, calretinin, to newborn neurons (Klempin et al., 2010). These data suggest that chronic fluoxetine may have different effects on immature differentiating neurons and mature neurons, depending on the state of differentiation and maturation (Figure 1).

FIGURE 1
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Figure 1. Model of bidirectional effects of chronic serotonin (5-HT) reuptake inhibitors (SSRIs) exposure on the regulation of the state of maturation in the granule cells (GCs). Developmental stages of GCs in the dentate gyrus (DG) can be identified by stage marker expression and neural function. Chronic SSRI administration may have bidirectional effects on differentiating immature neurons and mature neurons, depending on the state of differentiation and maturation.

In a mouse model of depression and anxiety generated by chronic corticosterone treatment, changes in the maturation phenotypes of GCs can be induced at serum concentrations of fluoxetine that are close to those observed in patients during fluoxetine treatment (Kobayashi et al., 2013). Furthermore, electroconvulsive stimulation in animals, which simulates electroconvulsive therapy (a highly effective and fast-acting treatment for depression) in people, rapidly induces dematuration changes in GCs (Imoto et al., 2017). Together, these data imply a degree of clinical relevance for these phenotypic changes in GCs. Indeed, they suggest that dematuration of neurons in the DG could be a common cellular basis for the therapeutic effects of pharmacological and non-pharmacological antidepressant treatments. It is possible that the alteration in maturation phenotypes in GCs following antidepressant treatment may restore cell function; that is, it may act as a “reset” button for GCs. 5-HT4 receptor activity contributes to fluoxetine-induced maturation phenotype changes in GCs in addition to facilitation of neurogenesis (Kobayashi et al., 2010). The fluoxetine-induced expression of BDNF in the DG is associated with dematuration (Imoto et al., 2015). These studies suggest that sustained elevation of 5-HT levels in the synaptic cleft by chronic fluoxetine changes the phenotypes of GCs via the 5-HT4 receptor, which may alter the transcriptome pattern of the GCs and subsequently contribute to an increase in neurogenesis in the dentate SGZ.

Recent studies also demonstrate that fluoxetine enhances monoamine reactivity at the synapses formed by GC-derived mossy fibers. 5-HT and dopamine potentiate mossy fiber-CA3 pyramidal cell synaptic transmission in mouse hippocampal slices (Kobayashi et al., 2010, 2012); chronic fluoxetine or paroxetine treatment induces a prominent increase in the magnitude of such potentiation. Synaptic potentiation by dopamine is mediated via D1-like receptors whose expression in the DG is upregulated by chronic fluoxetine, indicating their potential involvement in enhanced dopamine sensitivity mediated by fluoxetine. Synaptic potentiation by 5-HT is mediated via 5-HT4 receptors; however, chronic fluoxetine does not increase the expression of the 5-HT4 receptor in the DG, suggesting that the increase in 5-HT sensitivity is likely mediated by downstream intracellular signaling (e.g., second messenger signaling). Both 5-HT4 and D1-like receptors are cAMP-dependent (via Gs coupling). This enhanced monoaminergic modulation would greatly increase excitatory drive to the hippocampal circuit through the DG. Although the influence of 5-HT1A signaling on the function and phenotypes of mature GCs is unclear, studies using non-neuronal and neuronal cell lines indicate that 5-HT1A signal transduction is linked to not only the conventional Gi/o-mediated signaling pathway, but also to the mitogen-activated protein kinase (MAPK) and Akt signaling pathways. The latter pathways are thought to be associated with neurotrophic or growth factor expression in GCs (see description below, Samuels et al., 2015; Rojas and Fiedler, 2016). Taken together, functional and phenotypic changes by SSRIs in the mature GCs modulate hippocampal function, and this effect may contribute, in part, to their behavioral actions (Figure 2).

FIGURE 2
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Figure 2. Model of 5-HT1A and 5-HT4 receptor-mediated modulation of hippocampal function. The higher level of 5-HT in synaptic cleft in the DG induces increase in expression of neurotrophic factors such as brain derived neurotrophic factor (BDNF), facilitation of hippocampal neurogenesis, and dematuration of GCs via the 5-HT1A and 5-HT4 receptors in the DG. The signals of 5-HT1A and 5-HT4 receptors in the DG contribute to several antidepressant and anxiolytic behaviors.

Hippocampal-Dependent Behavioral Changes by SSRIs Mediated by Specific 5-HT Receptor Subtypes

Recent evidence suggests that the DG plays an important role in antidepressive and anxiolytic behavioral changes. Using optogenetic manipulation, increased ventral DG activity suppresses innate anxiety in mice (Kheirbek et al., 2013), while re-activating GCs in the DG that were previously active during a positive experience suppress depression-like behaviors (Ramirez et al., 2015). These findings indicate that functional regulation of the DG by SSRIs could contribute to their behavioral actions.

A recent study shows that the 5-HT1A receptor on mature GCs is critical for several antidepressant effects induced by chronic fluoxetine treatment (Samuels et al., 2015). Mice lacking GC-specific 5-HT1A receptors exhibit deficits in the antidepressant and anxiolytic effects of fluoxetine when tested with the forced swim test, novelty-suppressed feeding, and elevated plus maze. In contrast, 5-HT1A receptor missing from only young adult-born GCs produces normal fluoxetine-mediated responses, indicating the important role of the 5-HT1A signal in mature GCs. Fluoxetine-induced increases in BDNF and vascular endothelial growth factor (VEGF) expression levels in the DG are also attenuated in mice lacking GC-specific 5-HT1A receptors.

The 5-HT4 receptor is also thought to contribute to the behavioral effects of fluoxetine. In a model of anxiety and/or depression, antidepressant and anxiolytic effects caused by fluoxetine treatment are attenuated by administration of a 5-HT4 receptor antagonist; the same result is found in 5-HT4 receptor knockout mice (Mendez-David et al., 2014; Amigó et al., 2016). Since the 5-HT4 receptor antagonist suppresses the effect of fluoxetine on novelty-suppressed feeding, which is a neurogenesis-dependent antidepressant behavior, the 5-HT4 receptor-mediated increase of neurogenesis in the DG appears to be involved in the behavioral actions of fluoxetine. The functional and phenotypic changes in mature GCs due to 5-HT4 receptor activity may also have an influence on mature GC-dependent behaviors. Chronic fluoxetine treatment with high doses induces behavioral destabilization that is characterized by alternating between hypoactivity and hyperactivity within a few days; this behavioral destabilization by fluoxetine is tightly associated with fluoxetine-induced dematuration of the GCs and is attenuated in mice lacking 5-HT4 receptors (Kobayashi et al., 2011). Although behavioral destabilization may be caused by an increase in hippocampal excitability, it is unknown whether this behavioral change is involved in antidepressant activity. In a depression model in which hippocampal activity is suppressed, SSRI-induced functional and phenotypic changes of GC by the 5-HT4 receptor would hypothetically correct some of the hippocampally mediated, depression-like behaviors.

Conclusions

In summary, a large body of evidence indicates that 5-HT signaling regulates hippocampal function and changes several antidepressant and anxiolytic behaviors through activity at both 5-HT1A and 5-HT4 receptors. It will be necessary to investigate how the 5-HT1A and the 5-HT4 receptors cooperate to activate downstream signals in the dentate GCs. In particular, identifying molecular changes that are induced by prolonged serotonin elevation is important for the development of new antidepressant drugs with a more rapid onset of action. Recent studies also indicate that chronic treatment with SSRIs not only promotes generation of new neurons, but also induces dematuration in existing GCs in the hippocampal DG, implicating that sustained elevation of serotonin levels in the synaptic cleft by chronic SSRIs may have bidirectional effects on GC maturation depending on the maturational stage of the cells. Although there are some limitations to these data, the results of these studies suggest that in addition to the 5-HT1A receptor, 5-HT4 receptor-mediated dematuration in mature GCs, as well as 5-HT4 receptor-mediated neurogenic effects, are responsible for the modulation of hippocampal function by SSRIs (Figure 2). Furthermore, these activities probably affect hippocampal-dependent behaviors and could play an important role in the actions of antidepressant treatment.

Author Contributions

ES-N planned, organized and wrote the review article.

Funding

This work was supported in part by MEXT KAKENHI (Grant Number 25460096, 17K08316, ES-N), grants from the Naito Foundation (ES-N), the foundation of Pharmaceutical Sciences (ES-N), and Astellas Foundation (ES-N).

Conflict of Interest Statement

The author declares 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

I thank Dr. Katsunori Kobayashi for his helpful advice and Editage (www.editage.jp) for English language editing.

References

Alenina, N., and Klempin, F. (2015). The role of serotonin in adult hippocampal neurogenesis. Behav. Brain Res. 277, 49–57. doi: 10.1016/j.bbr.2014.07.038

PubMed Abstract | CrossRef Full Text | Google Scholar

Amigó, J., Díaz, A., Pilar-Cuéllar, F., Vidal, R., Martín, A., Compan, V., et al. (2016). The absence of 5-HT4 receptors modulates depression- and anxiety-like responses and influences the response of fluoxetine in olfactory bulbectomised mice: adaptive changes in hippocampal neuroplasticity markers and 5-HT1A autoreceptor. Neuropharmacology 111, 47–58. doi: 10.1016/j.neuropharm.2016.08.037

PubMed Abstract | CrossRef Full Text | Google Scholar

Arnold, S. A., and Hagg, T. (2012). Serotonin 1A receptor agonist increases species- and region-selective adult CNS proliferation, but not through CNTF. Neuropharmacology 63, 1238–1247. doi: 10.1016/j.neuropharm.2012.07.047

PubMed Abstract | CrossRef Full Text | Google Scholar

Banasr, M., Hery, M., Printemps, R., and Daszuta, A. (2004). Serotonin-induced increases in adult cell proliferation and neurogenesis are mediated through different and common 5-HT receptor subtypes in the dentate gyrus and the subventricular zone. Neuropsychopharmacology 29, 450–460. doi: 10.1038/sj.npp.1300320

PubMed Abstract | CrossRef Full Text | Google Scholar

Bessa, J. M., Ferreira, D., Melo, I., Marques, F., Cerqueira, J. J., Palha, J. A., et al. (2009). The mood-improving actions of antidepressants do not depend on neurogenesis but are associated with neuronal remodeling. Mol. Psychiatry 14, 764–773, 739. doi: 10.1038/mp.2008.119

PubMed Abstract | CrossRef Full Text | Google Scholar

Bockaert, J., Claeysen, S., Compan, V., and Dumuis, A. (2008). 5-HT4 receptors: history, molecular pharmacology and brain functions. Neuropharmacology 55, 922–931. doi: 10.1016/j.neuropharm.2008.05.013

PubMed Abstract | CrossRef Full Text | Google Scholar

Boldrini, M., Santiago, A. N., Hen, R., Dwork, A. J., Rosoklija, G. B., Tamir, H., et al. (2013). Hippocampal granule neuron number and dentate gyrus volume in antidepressant-treated and untreated major depression. Neuropsychopharmacology 38, 1068–1077. doi: 10.1038/npp.2013.5

PubMed Abstract | CrossRef Full Text | Google Scholar

Boldrini, M., Underwood, M. D., Hen, R., Rosoklija, G. B., Dwork, A. J., John Mann, J., et al. (2009). Antidepressants increase neural progenitor cells in the human hippocampus. Neuropsychopharmacology 34, 2376–2389. doi: 10.1038/npp.2009.75

PubMed Abstract | CrossRef Full Text | Google Scholar

Bruinvels, A. T., Landwehrmeyer, B., Gustafson, E. L., Durkin, M. M., Mengod, G., Branchek, T. A., et al. (1994). Localization of 5-HT1B, 5-HT1Dα, 5-HT1E and 5-HT1F receptor messenger RNA in rodent and primate brain. Neuropharmacology 33, 367–386. doi: 10.1016/0028-3908(94)90067-1

PubMed Abstract | CrossRef Full Text | Google Scholar

Compan, V., Zhou, M., Grailhe, R., Gazzara, R. A., Martin, R., Gingrich, J., et al. (2004). Attenuated response to stress and novelty and hypersensitivity to seizures in 5-HT4 receptor knock-out mice. J. Neurosci. 24, 412–419. doi: 10.1523/JNEUROSCI.2806-03.2004

PubMed Abstract | CrossRef Full Text | Google Scholar

Contractor, A., Swanson, G. T., Sailer, A., O’Gorman, S., and Heinemann, S. F. (2000). Identification of the kainate receptor subunits underlying modulation of excitatory synaptic transmission in the CA3 region of the hippocampus. J. Neurosci. 20, 8269–8278.

PubMed Abstract | Google Scholar

David, D. J., Samuels, B. A., Rainer, Q., Wang, J. W., Marsteller, D., Mendez, I., et al. (2009). Neurogenesis-dependent and -independent effects of fluoxetine in an animal model of anxiety/depression. Neuron 62, 479–493. doi: 10.1016/j.neuron.2009.04.017

PubMed Abstract | CrossRef Full Text | Google Scholar

Diaz, S. L., Narboux-Nême, N., Trowbridge, S., Scotto-Lomassese, S., Kleine Borgmann, F. B., Jessberger, S., et al. (2013). Paradoxical increase in survival of newborn neurons in the dentate gyrus of mice with constitutive depletion of serotonin. Eur. J. Neurosci. 38, 2650–2658. doi: 10.1111/ejn.12297

PubMed Abstract | CrossRef Full Text | Google Scholar

Encinas, J. M., Vaahtokari, A., and Enikolopov, G. (2006). Fluoxetine targets early progenitor cells in the adult brain. Proc. Natl. Acad. Sci. U S A 103, 8233–8238. doi: 10.1073/pnas.0601992103

PubMed Abstract | CrossRef Full Text | Google Scholar

Feng, L., Molnár, P., and Nadler, J. V. (2003). Short-term frequency-dependent plasticity at recurrent mossy fiber synapses of the epileptic brain. J. Neurosci. 23, 5381–5390.

PubMed Abstract | Google Scholar

Fuchs, E., Flugge, G., and Czeh, B. (2006). Remodeling of neuronal networks by stress. Front. Biosci. 11, 2746–2758. doi: 10.2741/2004

PubMed Abstract | CrossRef Full Text | Google Scholar

Grossman, C. J., Kilpatrick, G. J., and Bunce, K. T. (1993). Development of a radioligand binding assay for 5-HT4 receptors in guinea-pig and rat brain. Br. J. Pharmacol. 109, 618–624. doi: 10.1111/j.1476-5381.1993.tb13617.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Hoyer, D., Hannon, J. P., and Martin, G. R. (2002). Molecular, pharmacological and functional diversity of 5-HT receptors. Pharmacol. Biochem. Behav. 71, 533–554. doi: 10.1016/s0091-3057(01)00746-8

PubMed Abstract | CrossRef Full Text | Google Scholar

Imoto, Y., Kira, T., Sukeno, M., Nishitani, N., Nagayasu, K., Nakagawa, T., et al. (2015). Role of the 5-HT4 receptor in chronic fluoxetine treatment-induced neurogenic activity and granule cell dematuration in the dentate gyrus. Mol. Brain 8:29. doi: 10.1186/s13041-015-0120-3

PubMed Abstract | CrossRef Full Text | Google Scholar

Imoto, Y., Segi-Nishida, E., Suzuki, H., and Kobayashi, K. (2017). Rapid and stable changes in maturation-related phenotypes of the adult hippocampal neurons by electroconvulsive treatment. Mol. Brain 10:8. doi: 10.1186/s13041-017-0288-9

PubMed Abstract | CrossRef Full Text | Google Scholar

Kheirbek, M. A., Drew, L. J., Burghardt, N. S., Costantini, D. O., Tannenholz, L., Ahmari, S. E., et al. (2013). Differential control of learning and anxiety along the dorsoventral axis of the dentate gyrus. Neuron 77, 955–968. doi: 10.1016/j.neuron.2012.12.038

PubMed Abstract | CrossRef Full Text | Google Scholar

Kheirbek, M. A., Klemenhagen, K. C., Sahay, A., and Hen, R. (2012). Neurogenesis and generalization: a new approach to stratify and treat anxiety disorders. Nat. Neurosci. 15, 1613–1620. doi: 10.1038/nn.3262

PubMed Abstract | CrossRef Full Text | Google Scholar

Klempin, F., Babu, H., De Pietri Tonelli, D., Alarcon, E., Fabel, K., and Kempermann, G. (2010). Oppositional effects of serotonin receptors 5-HT1a, 2, and 2c in the regulation of adult hippocampal neurogenesis. Front. Mol. Neurosci. 3:14. doi: 10.3389/fnmol.2010.00014

PubMed Abstract | CrossRef Full Text | Google Scholar

Klempin, F., Beis, D., Mosienko, V., Kempermann, G., Bader, M., and Alenina, N. (2013). Serotonin is required for exercise-induced adult hippocampal neurogenesis. J. Neurosci. 33, 8270–8275. doi: 10.1523/JNEUROSCI.5855-12.2013

PubMed Abstract | CrossRef Full Text | Google Scholar

Kobayashi, K., Haneda, E., Higuchi, M., Suhara, T., and Suzuki, H. (2012). Chronic fluoxetine selectively upregulates dopamine D1-like receptors in the hippocampus. Neuropsychopharmacology 37, 1500–1508. doi: 10.1038/npp.2011.335

PubMed Abstract | CrossRef Full Text | Google Scholar

Kobayashi, K., Ikeda, Y., Asada, M., Inagaki, H., Kawada, T., and Suzuki, H. (2013). Corticosterone facilitates fluoxetine-induced neuronal plasticity in the hippocampus. PLoS One 8:e63662. doi: 10.1371/journal.pone.0063662

PubMed Abstract | CrossRef Full Text | Google Scholar

Kobayashi, K., Ikeda, Y., Sakai, A., Yamasaki, N., Haneda, E., Miyakawa, T., et al. (2010). Reversal of hippocampal neuronal maturation by serotonergic antidepressants. Proc. Natl. Acad. Sci. U S A 107, 8434–8439. doi: 10.1073/pnas.0912690107

PubMed Abstract | CrossRef Full Text | Google Scholar

Kobayashi, K., Ikeda, Y., and Suzuki, H. (2011). Behavioral destabilization induced by the selective serotonin reuptake inhibitor fluoxetine. Mol. Brain 4:12. doi: 10.1186/1756-6606-4-12

PubMed Abstract | CrossRef Full Text | Google Scholar

Kobayashi, K., and Poo, M.-M. (2004). Spike train timing-dependent associative modification of hippocampal CA3 recurrent synapses by mossy fibers. Neuron 41, 445–454. doi: 10.1016/s0896-6273(03)00873-0

PubMed Abstract | CrossRef Full Text | Google Scholar

Lauri, S. E., Bortolotto, Z. A., Bleakman, D., Ornstein, P. L., Lodge, D., Isaac, J. T., et al. (2001). A critical role of a facilitatory presynaptic kainate receptor in mossy fiber LTP. Neuron 32, 697–709. doi: 10.1016/s0896-6273(01)00511-6

PubMed Abstract | CrossRef Full Text | Google Scholar

Lucas, G., and Debonnel, G. (2002). 5-HT4 receptors exert a frequency-related facilitatory control on dorsal raphé nucleus 5-HT neuronal activity. Eur. J. Neurosci. 16, 817–822. doi: 10.1046/j.1460-9568.2002.02150.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Lucas, G., Rymar, V. V., Du, J., Mnie-Filali, O., Bisgaard, C., Manta, S., et al. (2007). Serotonin4 (5-HT4) receptor agonists are putative antidepressants with a rapid onset of action. Neuron 55, 712–725. doi: 10.1016/j.neuron.2007.07.041

PubMed Abstract | CrossRef Full Text | Google Scholar

MacQueen, G., and Frodl, T. (2011). The hippocampus in major depression: evidence for the convergence of the bench and bedside in psychiatric research? Mol. Psychiatry 16, 252–264. doi: 10.1038/mp.2010.80

PubMed Abstract | CrossRef Full Text | Google Scholar

Malberg, J. E., and Duman, R. S. (2003). Cell proliferation in adult hippocampus is decreased by inescapable stress: reversal by fluoxetine treatment. Neuropsychopharmacology 28, 1562–1571. doi: 10.1038/sj.npp.1300234

PubMed Abstract | CrossRef Full Text | Google Scholar

Malberg, J. E., Eisch, A. J., Nestler, E. J., and Duman, R. S. (2000). Chronic antidepressant treatment increases neurogenesis in adult rat hippocampus. J. Neurosci. 20, 9104–9110.

PubMed Abstract | Google Scholar

Marchal, C., and Mulle, C. (2004). Postnatal maturation of mossy fibre excitatory transmission in mouse CA3 pyramidal cells: a potential role for kainate receptors. J. Physiol. 561, 27–37. doi: 10.1113/jphysiol.2004.069922

PubMed Abstract | CrossRef Full Text | Google Scholar

McEwen, B. S., Nasca, C., and Gray, J. D. (2016). Stress effects on neuronal structure: hippocampus, amygdala, and prefrontal cortex. Neuropsychopharmacology 41, 3–23. doi: 10.1038/npp.2015.171

PubMed Abstract | CrossRef Full Text | Google Scholar

Mendez-David, I., David, D. J., Darcet, F., Wu, M. V., Kerdine-Römer, S., Gardier, A. M., et al. (2014). Rapid anxiolytic effects of a 5-HT4 receptor agonist are mediated by a neurogenesis-independent mechanism. Neuropsychopharmacology 39, 1366–1378. doi: 10.1038/npp.2013.332

PubMed Abstract | CrossRef Full Text | Google Scholar

Ming, G. L., and Song, H. (2005). Adult neurogenesis in the mammalian central nervous system. Annu. Rev. Neurosci. 28, 223–250. doi: 10.1146/annurev.neuro.28.051804.101459

PubMed Abstract | CrossRef Full Text | Google Scholar

Ohira, K., Kobayashi, K., Toyama, K., Nakamura, H. K., Shoji, H., Takao, K., et al. (2013). Synaptosomal-associated protein 25 mutation induces immaturity of the dentate granule cells of adult mice. Mol. Brain 6:12. doi: 10.1186/1756-6606-6-12

PubMed Abstract | CrossRef Full Text | Google Scholar

Pascual-Brazo, J., Castro, E., Díaz, A., Valdizán, E. M., Pilar-Cuéllar, F., Vidal, R., et al. (2012). Modulation of neuroplasticity pathways and antidepressant-like behavioural responses following the short-term (3 and 7 days) administration of the 5-HT4 receptor agonist RS67333. Int. J. Neuropsychopharmacol. 15, 631–643. doi: 10.1017/s1461145711000782

PubMed Abstract | CrossRef Full Text | Google Scholar

Pittenger, C., and Duman, R. S. (2008). Stress, depression, and neuroplasticity: a convergence of mechanisms. Neuropsychopharmacology 33, 88–109. doi: 10.1038/sj.npp.1301574

PubMed Abstract | CrossRef Full Text | Google Scholar

Polter, A. M., and Li, X. (2010). 5-HT1A receptor-regulated signal transduction pathways in brain. Cell Signal 22, 1406–1412. doi: 10.1016/j.cellsig.2010.03.019

PubMed Abstract | CrossRef Full Text | Google Scholar

Pompeiano, M., Palacios, J. M., and Mengod, G. (1992). Distribution and cellular localization of mRNA coding for 5-HT1A receptor in the rat brain: correlation with receptor binding. J. Neurosci. 12, 440–453.

PubMed Abstract | Google Scholar

Radley, J. J., and Jacobs, B. L. (2002). 5-HT1A receptor antagonist administration decreases cell proliferation in the dentate gyrus. Brain Res 955, 264–267. doi: 10.1016/s0006-8993(02)03477-7

PubMed Abstract | CrossRef Full Text | Google Scholar

Ramirez, S., Liu, X., MacDonald, C. J., Moffa, A., Zhou, J., Redondo, R. L., et al. (2015). Activating positive memory engrams suppresses depression-like behaviour. Nature 522, 335–339. doi: 10.1038/nature14514

PubMed Abstract | CrossRef Full Text | Google Scholar

Rojas, P. S., and Fiedler, J. L. (2016). What do we really know about 5-HT1A receptor signaling in neuronal cells? Front. Cell. Neurosci. 10:272. doi: 10.3389/fncel.2016.00272

PubMed Abstract | CrossRef Full Text | Google Scholar

Samuels, B. A., Anacker, C., Hu, A., Levinstein, M. R., Pickenhagen, A., Tsetsenis, T., et al. (2015). 5-HT1A receptors on mature dentate gyrus granule cells are critical for the antidepressant response. Nat. Neurosci. 18, 1606–1616. doi: 10.1038/nn.4116

PubMed Abstract | CrossRef Full Text | Google Scholar

Samuels, B. A., Mendez-David, I., Faye, C., David, S. A., Pierz, K. A., Gardier, A. M., et al. (2016). Serotonin 1A and serotonin 4 receptors: essential mediators of the neurogenic and behavioral actions of antidepressants. Neuroscientist 22, 26–45. doi: 10.1177/1073858414561303

PubMed Abstract | CrossRef Full Text | Google Scholar

Santarelli, L., Saxe, M., Gross, C., Surget, A., Battaglia, F., Dulawa, S., et al. (2003). Requirement of hippocampal neurogenesis for the behavioral effects of antidepressants. Science 301, 805–809. doi: 10.1126/science.1083328

PubMed Abstract | CrossRef Full Text | Google Scholar

Takao, K., Kobayashi, K., Hagihara, H., Ohira, K., Shoji, H., Hattori, S., et al. (2013). Deficiency of schnurri-2, an MHC enhancer binding protein, induces mild chronic inflammation in the brain and confers molecular, neuronal, and behavioral phenotypes related to schizophrenia. Neuropsychopharmacology 38, 1409–1425. doi: 10.1038/npp.2013.38

PubMed Abstract | CrossRef Full Text | Google Scholar

Tanaka, K. F., Samuels, B. A., and Hen, R. (2012). Serotonin receptor expression along the dorsal-ventral axis of mouse hippocampus. Philos. Trans. R. Soc. Lond. B Biol. Sci. 367, 2395–2401. doi: 10.1098/rstb.2012.0038

PubMed Abstract | CrossRef Full Text | Google Scholar

Vilaró, M. T., Cortés, R., Gerald, C., Branchek, T. A., Palacios, J. M., and Mengod, G. (1996). Localization of 5-HT4 receptor mRNA in rat brain by in situ hybridization histochemistry. Mol. Brain Res. 43, 356–360. doi: 10.1016/s0169-328x(96)00248-3

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, J. W., David, D. J., Monckton, J. E., Battaglia, F., and Hen, R. (2008). Chronic fluoxetine stimulates maturation and synaptic plasticity of adult-born hippocampal granule cells. J. Neurosci. 28, 1374–1384. doi: 10.1523/JNEUROSCI.3632-07.2008

PubMed Abstract | CrossRef Full Text | Google Scholar

Yamasaki, N., Maekawa, M., Kobayashi, K., Kajii, Y., Maeda, J., Soma, M., et al. (2008). Alpha-CaMKII deficiency causes immature dentate gyrus, a novel candidate endophenotype of psychiatric disorders. Mol. Brain 1:6. doi: 10.1186/1756-6606-1-6

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhang, J., Cai, C. Y., Wu, H. Y., Zhu, L. J., Luo, C. X., and Zhu, D. Y. (2016). CREB-mediated synaptogenesis and neurogenesis is crucial for the role of 5-HT1a receptors in modulating anxiety behaviors. Sci. Rep. 6:29551. doi: 10.1038/srep29551

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: antidepressant, neurogenesis, 5-HT4 receptor, hippocampus, maturation, granule cell

Citation: Segi-Nishida E (2017) The Effect of Serotonin-Targeting Antidepressants on Neurogenesis and Neuronal Maturation of the Hippocampus Mediated via 5-HT1A and 5-HT4 Receptors. Front. Cell. Neurosci. 11:142. doi: 10.3389/fncel.2017.00142

Received: 02 March 2017; Accepted: 28 April 2017;
Published: 16 May 2017.

Edited by:

Yu-Qiang Ding, Tongji University, China

Reviewed by:

Nicola Berretta, Fondazione Santa Lucia (IRCCS), Italy
Friederike Klempin, Max Delbrück Center for Molecular Medicine (HZ), Germany

Copyright © 2017 Segi-Nishida. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Eri Segi-Nishida, eri.segi.nishida@rs.tus.ac.jp

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