Siru Qin1†
Zichen Zhang1†
Yadan Zhao1
Jingyi Liu1
Jiwen Qiu1,2,3
Yinan Gong1,2Wen Fan4Yongming Guo1,2,3
Yi Guo1,3,5
Zhifang Xu1,2,3*
Yang Guo3,6*- 1Research Center of Experimental Acupuncture Science, Tianjin University of Traditional Chinese Medicine, Tianjin, China
- 2School of Acupuncture & Moxibustion and Tuina, Tianjin University of Traditional Chinese Medicine, Tianjin, China
- 3National Clinical Research Center for Chinese Medicine Acupuncture and Moxibustion, Tianjin, China
- 4Department of Rehabilitation Physical Therapy Course, Faculty of Health Science, Suzuka University of Medical Science, Suzuka, Japan
- 5School of Traditional Chinese Medicine, Tianjin University of Traditional Chinese Medicine, Tianjin, China
- 6Acupuncture Department, First Teaching Hospital of Tianjin University of Traditional Chinese Medicine, Tianjin, China
Ischemic stroke is common in the elderly, and is one of the main causes of long-term disability worldwide. After ischemic stroke, spontaneous recovery and functional reconstruction take place. These processes are possible thanks to neuroplasticity, which involves neurogenesis, synaptogenesis, and angiogenesis. However, the repair of ischemic damage is not complete, and neurological deficits develop eventually. The WHO recommends acupuncture as an alternative and complementary method for the treatment of stroke. Moreover, clinical and experimental evidence has documented the potential of acupuncture to ameliorate ischemic stroke-induced neurological deficits, particularly sequelae such as dyskinesia, spasticity, cognitive impairment, and dysphagia. These effects are related to the ability of acupuncture to promote spontaneous neuroplasticity after ischemic stroke. Specifically, acupuncture can stimulate neurogenesis, activate axonal regeneration and sprouting, and improve the structure and function of synapses. These processes modify the neural network and function of the damaged brain area, producing the improvement of various skills and adaptability. Astrocytes and microglia may be involved in the regulation of neuroplasticity by acupuncture, such as by the production and release of a variety of neurotrophic factors, including brain-derived neurotrophic factor (BDNF) and nerve growth factor (NGF). Moreover, the evidence presented indicates that acupuncture promotes neuroplasticity by modulating the functional reconstruction of the whole brain after ischemia. Therefore, the promotion of neuroplasticity is expected to become a new target for acupuncture in the treatment of neurological deficits after ischemic stroke, and research into the mechanisms responsible for these actions will be of significant clinical value.
Introduction
Ischemic stroke is common in the elderly, and its incidence increases with age. It is one of the leading causes of long-term disability worldwide (Go et al., 2014). The primary cause of ischemic stroke is the interruption of blood flow by cerebral vascular occlusion. Acutely and sub-acutely lack of blood supply produces metabolic acidosis, excitotoxicity, inflammation, oxidative stress, and cytotoxic edema, resulting in necrosis or apoptosis of neurons. However, spontaneous recovery appears in the brain damaged by an ischemic stroke. For instance, in the subacute stage of stroke, neurotrophic factors (NTFs) and associated signaling pathways, such as protein-serine-threonine kinase (Akt) pathway, trigger the neuroprotective effect. In the chronic phase, neurogenesis, angiogenesis, and synaptogenesis are the main processes of spontaneous neuroplasticity, but the repair is often incomplete due to the limited regenerative capacity of neurons (Chavez et al., 2017). Therefore, understanding the mechanisms of promoting spontaneous and therapeutic neuroplasticity-mediated structural reconstruction and functional recovery is of great significance for the treatment and prognosis of ischemic stroke (Cassidy and Cramer, 2017).
Brain neuroplasticity refers to the ability of the brain to modify its morphological structure and functional activity in response to internal or external stimuli (Carey et al., 2019). It occurs throughout the entire lifespan, and the structural and functional plasticity may be enhanced after brain injury. Brain neuroplasticity can be observed at different levels, such as changes in the structure and function of synapses, cells, and regions, subsequent modifications in the communication and networks among cells and regions, and, ultimately, changes in neurologic behavior and function, such as sensory perception, motor behavior, and cognition (Murphy and Corbett, 2009; Pekna et al., 2012). Since the brain has a remarkable capacity for plasticity and reorganization, it would be useful to exploit these properties to improve the clinical efficacy of ischemic stroke therapy.
Acupuncture, a process of inserting fine needles into the skin or deep tissues of specific parts (acupoints) of the body, is an essential component of Traditional Chinese Medicine. Acupuncture can be applied by hand, electric stimulation, or heating (Li and Wang, 2013), and is characterized by a safe, efficient, economical, and simple operation. Lines of clinical and experimental evidence have demonstrated that acupuncture can improve ischemic stroke-induced neurological deficits, especially for the sequelae of stroke (World Health Organization, 2002; Li et al., 2021; Shao et al., 2021). The effect of acupuncture starts from the stimulation of the acupoints, i.e., excitable complexes of muscle and skin nerves with a high density of nerve endings (Li et al., 2004). After converting physical or chemical information to electrical activity in acupoints, the signal is sent along afferent fibers to the spinal cord and brain (Zhao, 2008). There is evidence that acupuncture can modulate neuroplasticity in central nervous system (CNS) by modifying neural structure and function (Chavez et al., 2017). However, the detailed mechanisms of the effect of acupuncture on brain neuroplasticity in ischemic stroke have not been systematically reviewed.
This review analyzes neuroplasticity as the basis for the discussion of the effects of acupuncture on ischemic stroke and their potential mechanisms. The understanding of how acupuncture promotes and modulates neurogenesis, axonal regeneration and sprouting, synaptic plasticity, neuroglial crosstalk, and functional reconstruction reviewed in this work provides novel insights into the therapeutic mechanism of this procedure on ischemic stroke. It is hoped that the information provided will promote the clinical application of acupuncture for the functional recovery of ischemic stroke worldwide.
Methods
Search strategy
We searched the PubMed database for studies published between January 2010 and April 2021 using the MeSH terms “Acupuncture,” “Ischemic Stroke” and relevant entry terms. The search identified 211 relevant articles.
Study selection
We developed the following study inclusion criteria to study the treatment of ischemic stroke by acupoint stimulation via regulating neuroplasticity: stimulation methods included manual acupuncture, electroacupuncture, and moxibustion, and the research topics were related to neuroplasticity, specifically, neurogenesis, axon sprouting, axon regeneration, synaptic plasticity, and functional reorganization of the brain regions. Following the identification of 211 articles by the search engine, we performed a manual search of the reference lists of articles to identify further relevant articles that met the inclusion criteria based on the titles and abstracts. We excluded 62 articles due to duplication, the lack of an abstract or lack of relevance to ischemic stroke before conducting full-text assessments. This left 149 articles, including 66 basic research articles, 54 clinical research articles, and 29 review articles or meta-analyses. The full texts of the 66 basic research and 54 clinical research articles were obtained and evaluated carefully. Of the 66 basic research articles, 35 were selected and 31 were excluded as they did not focus on neuroplasticity. Of the 54 clinical studies, 12 were selected and 42 were excluded as they described single case reports, editorials, incomplete or uncontrolled trials, or were irrelevant to neuroplasticity. Thus, a total of 47 articles were included in our review. A flowchart of this search process is illustrated in Figure 1.
Figure 1. A flowchart of this search process.
Data extraction
Two authors independently evaluated the titles and abstracts of the retrieved articles and assessed the full texts of the articles. All of the 47 articles were finally included in the review, from which the data were extracted and listed according to the prespecified criteria, to analyze the mechanisms of acupuncture in regulating neuroplasticity in the treatment of ischemic stroke. Any disagreement was resolved by discussion between the authors.
Clinical Effect of Acupuncture on Ischemic Stroke
Neurological deficits after ischemic stroke can be self-repaired to varying degrees, which may be due to the plasticity of the remaining brain tissue. Despite this, damage to the functional areas of the brain may persist in areas responsible for motion, cognition, sensation, vision, and language (Rathore et al., 2002). Therefore, a wide range of rehabilitation treatments for stroke recovery has been developed, including the use of drugs, stem cells, behavioral therapy, robotics, and acupuncture (Cramer, 2008). Of these types of therapy, many systematic reviews have indicated that acupuncture can improve the neurological function of patients with ischemic stroke (Liu et al., 2015; Yang et al., 2016; Hung et al., 2019). A Cochrane review included 31 trials with a total of 2,257 participants in the subacute or chronic stages of stroke, and found that compared with no acupuncture, acupuncture was beneficial for the improvement of dependency, global neurological deficiency, and specific neurological impairments including motor, cognitive, and swallowing functions, as well as depression and pain (Yang et al., 2016). Four trials in this systematic review and other randomized controlled trials (RCTs) used the Fugl-Meyer Assessment scale (FMI) to evaluate the impact of acupuncture therapy after an ischemic stroke on the motor function of the upper and lower limbs. The results showed greater improvement in motor function in the acupuncture group compared with the non-acupuncture group (Li et al., 2015; Yang et al., 2016; Wu J. et al., 2017). The results of 11 trials in this review and other following RCTs found that the dependence measured by continuous scales [Barthel Index (BI), Modified Barthel Index and Activity of Daily Living Scale] in the acupuncture group was significantly improved compared with the control group (Yang et al., 2016; Wu J. et al., 2017; Wu et al., 2018). Furthermore, in this review, 13 trials were conducted to evaluate the improvement of cognitive function by acupuncture, using the Mini-Mental State Examination, Montreal Cognitive Assessment Scale, and Revised Hasegawa Dementia Scale. The results showed that acupuncture was superior to non-acupuncture in the improvement of cognitive function in convalescent stroke patients. The authors also concluded that acupuncture is most beneficial in the first 3 months with reduced benefit after 6 months. However, in terms of long-term follow-up, including mortality and quality of life, there is a lack of data from RCTs on the clinical outcomes of acupuncture in the treatment of stroke (Yang et al., 2016). The analysis of the recurrence of ischemic stroke treated with or without acupuncture has shown that patients treated with both medications and acupuncture had a lower rate of recurrence than patients treated only pharmaceutically (Shih et al., 2015). However, we still need more reliable evidence of major outcomes from more stringent RCTs, including the setting of grouping concealment, to draw conclusions about the efficacy of acupuncture on stroke.
RCTs focused on the use of acupuncture for the treatment of stroke have shown satisfactory results when acupuncture is applied at acupoints to treat various stroke sequelae, such as hemiplegia, dysphagia, and cognitive impairment. For hemiplegia, the most commonly used acupoints include Baihui (GV20), Yintang (EX-HN3), and the anterior oblique line of vertex-temporal of the head, Jianyu (LI15), Quchi (LI11), Shousanli (LI10), Waiguan (TB5), Hegu (LI4) of upper limbs, Liangqiu (ST34), Zusanli (ST36), Yanglingquan (GB34), Sanyinjiao (SP6), Fenglong (ST40), Jiexi (ST41), and Taichong (LR3) of lower limbs. These acupoints are important to inhibit muscle spasm, restore the coordination function of extensors and flexors, and inhibit their synergic movement, improving in this manner the limb function in hemiplegia (Chen J. et al., 2014; Wang et al., 2017). For aphasia, No. 1, 2, and 3 language sections of the head are selected according to the type of aphasia, in which language section No. 1 is for motor aphasia, No. 2 is for anomic aphasia, No. 3 is for sensory aphasia, and No. 1 combined with No. 2 is for mixed aphasia. In addition, Fengchi (GB20), Yamen (GV15), Jinjin (EX-HN12), Yuye (EX-HN13), Tongli (HT5), and Lianquan (CV23) acupoints are used, which are located near the tongue and above the Heart Meridian of Hand-shaoyin associated with the tongue (Sun et al., 2012). For a mild cognitive impairment, GV20, Shenting (GV24), Benshen (GB13), Taiyang (EX-HN5), Touwei (ST8), Sishencong (EX-HN1) are employed. Among them, EX-HN5, ST8, and EX-HN1 acupoints are located in the anterior and medial sides of the temporal lobe and adjacent areas, which control memory function and mental activity (Chen J. et al., 2014; Kalaria et al., 2016). Although acupuncture protocols differ according to the different impaired functions, they all conform to the principle of the of integral-local combined selection, i.e., matching the acupoints of brain functional areas with those of specific lesion areas.
Acupuncture Modulates Neuroplasticity
Recovery of lost functions after ischemic stroke is thought to depend on neuroplasticity, that is, the ability of the brain to restructure and reconstruct in response to endogenous and exogenous stress and injuries (Murphy, 2015; Dąbrowski et al., 2019). Neuroplasticity manifests in short-term functional changes and long-term structural changes. Short-term functional changes consist of modifications of synaptic efficiency, while the long-term structural changes reflect adaptations of neural connections. The core components of neuroplasticity are neurogenesis, axon sprouting, axon regeneration, and synaptic plasticity (Hickmott and Ethell, 2006; Lillard and Erisir, 2011). These processes and the potential mechanisms by which acupuncture can affect them are reviewed below and summarized in Table 1.
Table 1. The mechanisms of acupuncture on regulating neuroplasticity in the treatment of ischemic stroke.
Acupuncture promotes endogenous neurogenesis
The neurogenesis of the adult mammalian brain continues throughout the lifespan of an organism. The main neurogenic niches are located in the subventricular zone (SVZ) of the lateral ventricle and the subgranular zone (SGZ) of the dentate gyrus in the hippocampus. Neural stem cells (NSCs) and neural precursor cells (NPCs) from SVZ migrate to the olfactory bulb through the rostral migratory stream and are thought to be responsible for the maintenance and reorganization of the interneuron system within the olfactory bulb. The cells from the SGZ migrate to the granule cell layer and differentiate into granulosa cells that form synapses with existing neurons and have an important function in neuroplasticity (Merson and Bourne, 2014; Xiao et al., 2018). Increasing evidence suggests that adult neurogenesis also occurs in several other regions of the CNS, including the spinal cord, striatum, neocortex, cerebellum, substantia nigra, amygdala, and hypothalamus, particularly following a CNS injury (Martino et al., 2011; Sandvig et al., 2018).
Cell death occurs immediately in the ischemic core of the cerebral infarction, followed by the spread of injury to the ischemic penumbra. Therefore, enhancing the survival, proliferation, and migration of endogenous NSCs to the injured region by upregulating local secretion of NTFs facilitates the formation of new synapses and circuits and the restoration of the structure and function of the brain. NSCs can differentiate into neurons, astrocytes, oligodendrocytes, and other neural cells, which gradually migrate to target areas (Yamashita et al., 2006; Brouns and De Deyn, 2009). Since the number of endogenous NSCs and NPCs is too small to sustain the recovery of neurologic functions after ischemic stroke, strategies aiming at the promotion of their proliferation and directional differentiation into neurons with normal functions are the focus of intense research. At the same time, the transformation of astrocytes into neurons to assume neuronal functions after brain injury is also a new research hotspot (Magnusson et al., 2014).
Many studies have suggested that acupuncture can promote the proliferation, migration, and differentiation of NSCs, protecting the brain from ischemic damage and improving neurological deficits. For instance, the study conducted by Luo et al. (2014) demonstrated that middle cerebral artery occlusion (MCAO) in rats produced a large number of cells positive for nestin (a specific marker of NSCs), 5-bromo-2’-dexoyuridine (BrdU, a marker of cell proliferation), and cells double-positive for both markers in the brain, while cells positive for these markers were absent in control non-MCAO mice, and acupuncture at Shuigou (GV26) further increased the number of nestin/BrdU positive regenerative cells in MCAO mice. These results indicated that a certain extent of “self-healing” takes place after brain damage induced by focal cerebral ischemia, and acupuncture treatment promotes the proliferation of NSCs. This study also demonstrated that the expression of nestin mRNA in the cortex in the acupuncture group was much higher than in the non-MCAO and non-acupuncture groups. Moreover, with acupuncture, nestin expression increased slightly in the hippocampus and decreased in the striatum, indicating that acupuncture at GV26 promoted more extensive proliferation and/or migration of new neurons to the cortex than to the hippocampus and striatum (Luo et al., 2014). In another study, electroacupuncture (EA) was applied to the acupoints ST36 and LI11 at 1/20 Hz to treat MCAO rats. At 7 and 14 days after the induction of ischemia, the number of BrdU/glial fibrillary acidic protein (GFAP, a marker of astrocyte activation) double-positive cells in SVZ and BrdU/NeuN (a marker of mature neurons) and double-positive cells in the striatum was higher in EA-treated rats (Tao et al., 2010). Liao et al. (2017) also obtained similar results by applying 2 Hz EA in ST36 and ST37 for cerebral infarction rats with ischemia reperfusion injury. These results suggest that EA therapy can induce cell proliferation and differentiation into astrocytes and mature neurons.
Acupuncture mediates the upregulation of neurogenesis-related factors and the activation of related cell signaling pathways that promote the proliferation, migration, and differentiation of NSCs. Tan et al. (2018) found that stimulation at GV20 and Dazhui (GV14) by 5/20 Hz EA induced the proliferation and differentiation of endogenous NSCs in MCAO rats, together with upregulating the expression of plasticity-related gene 5 (PRG5, a key factor of neurogenesis) and downregulating the expression of three neurogenesis inhibitors, including the neurite outgrowth inhibitor NogoA, lysophosphatidic acid, and Ras homolog family member A (RhoA), indicating that EA may promote the proliferation and differentiation of endogenous NSCs by regulating PRG5/RhoA signaling. Stimulation with 2 Hz EA at the same acupoints led to the promotion of NSC proliferation and differentiation by brain-derived neurotrophic factor (BDNF), together with vascular endothelial growth factor (VEGF)-mediated angiogenesis of downstream phosphatidylinositol 3-kinase (PI3K) signaling. Specifically, EA increased both proliferation and differentiation in the hippocampus and SVZ and the mRNA and protein levels of BDNF and VEGF in the ipsilateral hippocampus and SVZ, as well as enhancing the levels of phosphorylated PI3K in the newly formed neuroblasts. In addition, the levels of various neurogenesis-related factors were up-regulated, including forkhead box protein G1 (FOXG1), nuclear receptor subfamily 4, group A, member 3 (NR4R3) protein, and zinc finger protein 423 (ZNF423; Wang et al., 2012; Kim et al., 2014). Kim et al. (2018) transplanted bone marrow mesenchymal stem cells (MSCs) into the striata of MCAO mice and stimulated them with 2 Hz EA at GV20 and GV14. The treatment reduced the atrophy of the striatum and promoted the proliferation of NPCs in the SVZ and peristriatal area. Increased numbers of BDNF and neurotrophin-4 (NT-4)-positive neurons were detected in the peristriatal area and the hippocampus. These results indicated that the combined treatment of MSCs and EA could promote neurogenesis in the ischemic brain by upregulating the expression of neurotrophic factors such as BDNF and NT-4, thus improving the motor function of MCAO mice (Kim et al., 2018). Another study in MCAO rats showed that after 1/20 Hz EA at ST36 and LI11 in the affected limb, the number of nestin/GFAP-positive cells was increased in the cortex, as well as the gene and protein levels of Wnt1 and β-catenin, while the transcription of glycogen synthase kinase 3 (GSK3) was inhibited, which suggested that EA may promote the proliferation of nerve stem/progenitor cells in the area around the cortical infarction after stroke through the Wnt/β-catenin pathway, thereby reducing the infarct volume and improving the neurological impairment (Chen et al., 2015). It was also observed that EA significantly enhanced the activity of the neurogenic locus notch homolog protein 1 (Notch1) signaling pathway and its downstream transcription target Hes1, leading to increased NSC proliferation and differentiation (Zhao et al., 2015). Studies have shown that Retinoic Acid (RA) is a key factor in regulating the proliferation of adult hippocampal nerve stem/progenitor cells (Mishra et al., 2018). Hong et al. (2013) found that 5/20 Hz EA at ST36 and LI11 may reduce the infarct volume and promote the recovery of neurological function by regulating the RA pathway in the ischemic brain.
MicroRNAs (miRNAs, miRs) are involved in the post-transcriptional modification of gene expression. In cerebral ischemia/reperfusion injury, acupuncture can promote the regeneration and repair of damaged nerves by regulating miRNAs. Sha et al. found that in rats with cerebral ischemia/reperfusion injury, stimulation with 20 Hz EA at Waiguan (TE5) and ST36 on the affected limb increased the expression of miR-223 and reduced the expression of phosphatase and tensin homolog deleted on chromosome ten (PTEN) in the SVZ and hippocampus by activating the Notch1 signaling pathway, thereby increasing the numbers of NSCs (Sha et al., 2019). Another study, in vivo and in vitro, revealed that EA regulated endogenous neurogenesis through the action of exosomal miRNAs. Specifically, 1/20 Hz EA at ST36 and LI11 on the affected limb induced the differentiation of endogenous NSCs into neurons in the ischemic striatum and SVZ by promoting the release of exosomes containing miR-146b in the ischemic striatum, thereby improving neurological impairment in MCAO rats (Zhang et al., 2020).
Therefore, acupuncture can indeed activate endogenous neurogenesis by stimulating proliferation and differentiation of NSCs in the SVZ and SGZ through activation of related cell-signaling pathways and upregulation of neurogenesis-related factors. It is also worth exploring which acupoints and stimulation parameters are optimal for the induction of neurogenesis. Furthermore, the number of endogenous NSCs is limited and not adequate to generate a sufficient number of differentiated functional neurons, and resolving this obstacle needs further innovative research.
Acupuncture promotes axonal regeneration and sprouting
Ischemic stroke is characterized acutely by a massive and rapid loss of axons, and recovery depends on axonal regeneration and sprouting, which constitute the compensatory mechanism to establish the new functional connections and strengthen the communication between neurons (Hinman, 2014). Axonal regeneration involves the regrowth of injured axons that is initiated by the formation of the growth cone at the broken ends, while axonal sprouting is the process of collateral sprouting and elongation of uninjured axons (Darian-Smith, 2009). Therefore, promoting axonal regeneration and the development of sprouting in the right direction contributes to the recovery of ischemic stroke patients.
Growth-associated protein-43 (GAP-43) is a growth cone-associated protein that promotes neurite outgrowth by regulating cytoskeletal organization via protein kinase C signaling. The expression of GAP-43 decreases with nerve development, but when the brain is damaged, the neurons adjacent to the injured area compensate for the loss of cells by collateral sprouting and reactive axon regeneration. Under these conditions, the local expression of GAP-43 is again upregulated. Therefore, GAP-43 is considered to represent a molecular marker of axonal growth and plasticity (Felling and Song, 2015). It has been documented that EA at ST36 and Neiguan (PC6), performed daily for 20 min, can improve the neurological function in rats with cerebral infarction. The mechanism may be related to the statistically significant upregulation of GAP-43 in the ischemic region, from the 7th day after the injury (Zhou et al., 2011). A similar effect was also obtained by applying acupuncture on both sides of PC6 and GV26 for 7 days (Xu et al., 2017). A study performed in rats showed that bilateral EA at LI11 and ST36 (5 Hz/10 Hz, 2 mA) improved the neurobehavioral score after ischemic stroke more than a unilateral EA, and the expression level of GAP-43 was increased in the CA3 of the hippocampus by EA (Qing et al., 2016). These findings may be explained by the structural organization of the innervation of the limbs. The cerebral cortex innervates the activity of bilateral limbs because 80% of the nerve fibers from the anterior central gyrus innervate the movement of the contralateral limbs, and a small fraction of them, which are not crossed, descend directly to form the anterior corticospinal tract and innervate the movement of the ipsilateral limbs. The secondary fibers of some posterior root fibers are combined with the ascending fibers of the ipsilateral spinothalamic tract, and the bilateral projection effect of the upper and lower fibers of the brain stem network determine the effect of acupuncture signals on the bilateral cerebral cortex. Thus, the cerebral cortex acts as the master center that dominates the movement and sensation of the bilateral limbs (Qing et al., 2016). In addition, another study revealed that 2 Hz EA stimulation of GV20 can not only promote nerve regeneration by upregulating GAP-43 and BDNF after cerebral ischemia but can also reduce inhibition of axon regeneration by downregulation of myelin-associated inhibitors and the RhoA/Rho-associated coiled-coil-containing protein kinase (ROCK) signaling pathway after cerebral ischemia, thus reducing the size of the cerebral infarction and improving neuronal function and hippocampal ultrastructural damage (Chen S. Q. et al., 2020).
MiRNAs are also involved in acupuncture-promoted axonal regeneration. Zhao et al. (2018) have shown that the expression of miR-132 was downregulated after MCAO, and that EA inhibited the transcription of SRY-box transcription factor 2 (SOX2) by upregulating miR-132. These changes resulted in the promotion of axonal sprouting and alleviation of neurological deficits, suggesting that neurobehavioral functional recovery after ischemic injury depends on axonal sprouting enabled by the inhibition of SOX2 translation via miR-132 (Zhao et al., 2018). Moreover, it was found that within 28 days after reperfusion in MCAO rats, after 2/10 Hz EA stimulation of GV20, the expressions of paired immunoglobulin-like receptor B (PirB), RhoA, and GAP-43 were regulated by modulating miR-181b directly targeting Pirb mRNA in the penumbra, promoting axon regeneration and new projections of corticospinal tracts after oxygen-glucose deprivation injury, which improved the neurological deficits (Deng et al., 2016).
Acupuncture modulates synaptic plasticity
Synapse is not only the specific site of intercellular information transmission but also a sensitive site of neuroplasticity. Synaptic plasticity mostly refers to morphological and functional modifications of synaptic connections, including long-term changes in synaptic structure and number, as well as the short-term changes in the strength and efficiency of neurotransmission (Neves et al., 2008).
Plasticity of synaptic structure
The plasticity of the synapsis depends on the modification of its ultrastructure, which includes the following aspects: (1) contact area (total number of synapses, number density of synapses, area density of synapses, average area of single synapse; Mundy et al., 2008); (2) content of active substances, such as synaptophysin (SYN), in synaptic contact area (Kwon and Chapman, 2011); (3) synapse-related subcellular structure, such as the postsynaptic density (PSD)-95 (Xie et al., 2019); and (4) synaptic gap width and interface curvature (Xiao et al., 2018).
Acupuncture has been demonstrated to modify the synaptic structure and promote the synaptic plasticity in rodent models of stroke by upregulating SYN and increasing PSD (Xia et al., 2017; Xiao et al., 2018). After 5 weeks of EA with a 5/10 Hz wave at GV20 and GV14, the thickness of synaptic PSD, and the number and surface densities of synapses were increased in MCAO rats, without significant changes in other indices of synaptic ultrastructure, such as volume density and synaptic curvature. These modifications were accompanied by the upregulation of P38, GAP-43, nerve growth factor (NGF), and BDNF in the ischemic cerebral cortex, indicating that EA could protect synaptic ultrastructure by increasing the level of these proteins (Yi et al., 2006). However, another study found that after 2 weeks of acupuncture in Taixi (KI3) and LR3, motor and cognitive deficits were noticeably improved compared with the untreated group at the 7th and 14th day after ischemic stroke. The improvement was accompanied by an increase in BDNF, SYN, PSD, and synaptic curvatures, and a smaller width of the synapse cleft. These results suggested the possibility that the inconsistency in the modifications of the synaptic structure might be caused by differences in acupoints, parameters, target brain areas, and observation points (Xia et al., 2017). Xie et al. (2019) demonstrated that the MCAO injury reduced the number of PSD-95/SYN double-positive cells in the hippocampal CA1 area, and 14 days of EA stimulation of GV20 and GV24 points reversed this trend, thus affecting synaptic plasticity. Activation of the Janus-activated kinase 2 (JAK2)/signal transducer and activator of transcription 3 (STAT3) signaling has been proved to induce spatial learning and memory impairment by inhibiting synaptic plasticity in the hippocampal CA1 region. EA treatment decreased the levels of phosphorylation of JAK2 and STAT3 in the CA1, indicating that the intervention at GV20 and GV24 improved synaptic plasticity by inhibiting the JAK2/STAT3 signaling pathway (Xie et al., 2019). In addition, after 1/20 Hz EA at the same acupoints, it was found that the density of dendritic spines was increased and the cognitive function of MCAO rats was improved. It was suggested that the mechanism may be related to the upregulation of Cdc42, RAS-related C3 botulinus toxin substrate 1 (Rac1), and Filamentous actin (F-actin) in the hippocampus, as well as down-regulation of RhoA expression (Lin et al., 2016).
Plasticity of synaptic function
It has been proposed that the plasticity of synaptic function is dependent on its structural plasticity. Functional plasticity is mostly related to the strength of synaptic transmission efficiency in the form of long-term potentiation (LTP) and long-term depression (LTD), which are prevalent paradigms of micro-neuroplasticity (Matsuzaki et al., 2004). LTP facilitates synaptic transmission, amplifies presynaptic signals, and enhances the persistence of postsynaptic potentials, thereby appearing more relevant to synaptic remodeling than LTD (Kim E. et al., 2012; Stewart and Dringenberg, 2016). Cognitive impairment often occurs after ischemic stroke and leads to difficulties in memory, learning, analysis, organization, interpretation, and concentration, decreasing the quality of life (Liu F. et al., 2014), which is the main cause of persistent sequelae of ischemic stroke. In these processes, LTP can enhance long-term memory through acquisition, consolidation, and storage of information, while LTD can verify the memory content and regulate LTP (Neves et al., 2008; Xiao et al., 2018).
Dendritic spines contribute to the spread of information via deformation and control synaptic efficacy by modulating LTP and LTD that are related to learning and memory (Schacher and Hu, 2014; Park et al., 2015). It has been reported that LIM domain kinase 1 (LIMK1) regulates LTP and long-term memory by activating cyclic adenylate monophosphate response element-binding protein (CREB), and LIMK1 knockout mice suffer from the severe damage of dendritic spines and LTP in the hippocampus. MiRNAs, which play important roles in learning and memory formation, can regulate LIMK1 expression to induce synaptic-dendritic plasticity. Therefore, the modulation of miRNA-LIMK1 represents a potential target for the treatment of cognitive deficit. Liu et al. (2017) demonstrated by T2-weighted imaging that EA at GV20 and GV24 alleviated cognitive impairment and reduced the volume of multiple brain lesions. Importantly, synaptic-dendritic loss in hippocampal CA1 pyramidal cells could be rescued by EA. This effect was associated with the suppression of the increase in the expression of miR-134 and LIMK1, indicating that these molecules might mediate the induction of hippocampal synaptic plasticity by EA, which contributed to the improvement of learning and memory during the recovery from ischemic stroke (Liu et al., 2017). In addition, acupuncture could lead to lasting changes in cortical excitability by affecting the activity of neurosynapses (Yang et al., 2017). For instance, a study in which 18 healthy subjects were subjected to acupuncture at the LI11 and TB5 acupoints showed an increased muscle excitability that lasted for 20 min after the needle was pulled out, proving the existence of a time-dependent effect of acupuncture on the excitability of bilateral primary motor cortex, which can induce LTP-like plasticity and increase motor learning (He et al., 2019).
Numerous studies have demonstrated that acupuncture enhances LTP in rats subjected to MCAO. For example, EA at GV20 for 6 days can reverse the MCAO-induced impairment of memory and decrease in hippocampal LTP, and inhibit the overexpression of N-methyl-d-aspartate receptor subtype 1 (NR1) and transient receptor potential vanilloid subtype 1 (TRPV1) receptors in the CA1 area of the hippocampus, indicating that NR1 and TRPV1 may mediate the effect of EA on MCAO-induced behavioral defects and LTP damage (Lin and Hsieh, 2010). Ye et al. (2017) have documented that acupuncture at GV20 and ST36 restored cognitive dysfunction in the rat two-vessel occlusion (2VO) model. The primary mechanism underlying this acupuncture effect was the improvement of decreased LTP by promoting the release of dopamine and its main metabolites and reversing the decline in dopamine D1/D5 receptors (Ye et al., 2017).
This section summarized the evidence that acupuncture regulates structural plasticity after stroke, that is, acupuncture can stimulate neurogenesis, axonal regeneration and sprouting, improve the structure and function of the synapse, to provide a theoretical basis for the improvement of the neurological deficits of ischemic stroke by acupuncture.
Glial Cells Play A Key Role in The Regulation of Neuroplasticity by Acupuncture
Glial cells, including astrocytes, oligodendrocytes, and microglia, play a key role in acupuncture’s regulation of neuroplasticity. By interacting with neurons, they regulate the formation and remodeling of synapses and neural circuits, thus contributing to the reconstruction of the functional brain (Stogsdill and Eroglu, 2017). Acupuncture can regulate neuroplasticity through glial cells, and the evidence is shown in Table 2.
Table 2. The mechanisms of glial cells in the regulation of neuroplasticity by acupuncture in the treatment of ischemic stroke.
Glial cells regulate neuroplasticity by secreting NTFs
It is well documented that NTFs are required for neurogenesis, axonal regeneration, synaptic activity and plasticity, and other neuroplasticity processes in CNS diseases, and can improve neurological deficits. NGF, BDNF, neurotrophin-3, and NT-4 are four members of the mammalian neurotrophin family (Gibon and Barker, 2017).
BDNF
The role of BDNF in neuroplasticity makes it an excellent candidate for stroke treatment (Mang et al., 2013). Additionally, BDNF acts on NSCs, promoting their survival, proliferation, and differentiation by interacting with TrkB and initiating downstream pathways, such as mitogen-activated protein kinase (MAPK)/extracellular signal-regulated kinase (ERK) and PI3K/Akt cascades. MAPK/ERK and PI3K/Akt signaling can reduce neuronal death induced by excitotoxicity in the ischemic penumbra (Tejeda et al., 2019). BDNF can also increase the formation of dendrite branches and connections between dendrites and promote the development and maturation of the CNS (Song et al., 2017). BDNF is directly involved in angiotensin-1 receptor blocker-mediated functional recovery, angiogenesis, and synaptic formation (Fouda et al., 2017). Finally, BDNF can provide local anti-inflammatory effect by downregulating the expression of tumor necrosis factor alpha (TNF-α) and upregulating the expression of interleukin-10 (IL-10), to promote nerve repair. BDNF increases the number of activated and phagocytic microglia via the increase in intracellular Ca2+. Once activated, microglia can further secrete BDNF and other NTFs, generating a positive feedback loop (Jiang et al., 2010).
In animal models of MCAO, acupuncture utilizing different parameters, such as acupoints, frequency, and intervention time, produces distinct effects on BDNF in the brain. The EA treatment at the GV20 and Qubin (GB7) acupoints for 14 days after MCAO, utilizing a bipolar waveform current of 3 Hz applied for bursts of 5 s and 2 s intervals, increased the levels of BDNF in the ischemic lobe and improved functional and motor recovery (Kim M. W. et al., 2012). Similarly, EA at GV20 and GV14 for two times with 5 Hz/10 Hz enhanced the expression of BDNF in the ischemic area (Cheng et al., 2014; Chavez et al., 2017). In MCAO mice, the expression of BDNF mRNA in the hippocampus was upregulated by EA applied for seven consecutive days at the Shenshu (BL23), Geshu (BL17), and GV20 acupoints (Zhao et al., 2013). Furthermore, EA at the GV20 once a day for 2 weeks improved motor function, elevated BDNF in the ischemic hemisphere, and increased the number of BDNF-positive cells and the expression of TrkB (Kim M. W. et al., 2012). Thus, acupuncture may play a neuroprotective role in ischemic stroke by modulating the expression of BDNF, but the functional verification of this possibility remains to be obtained.
NGF
NGF is the first NTF identified by Rita Levi-Montalcini and Viktor Hamburger in mouse sarcoma in vitro in the 1950s. Subsequent studies have established that NGF binds to the tropomyosin-related kinase A (TrkA) and p75NTR receptors to activate downstream signaling cascades, such as MAPK/ERK and PI3K/Akt. The stimulation of these pathways modulates the transcription of neurite outgrowth inhibition protein A, Nogo receptor, Rho family small GTPases A, Rho-associated kinase 2, thus promoting the differentiation and survival of neurons and growth of axon growths (Chang et al., 2016; Keefe et al., 2017). Furthermore, NGF exhibits neuroprotective activity by reducing intracellular calcium overload and antagonizing the excitotoxicity of amino acids after cerebral ischemia (Keefe et al., 2017).
Yi et al. (2006) demonstrated that EA at the GV20 and GV14 points increased the expression of NGF after ischemic brain injury. A higher level of NGF was essential to protect neurons by promoting synaptic plasticity and axonal regeneration, reflected by the increase of numerical density, surface density, volume density, and gap width of cortical synapses, as well as PSD and GAP-43 expression in the ischemic area. The results also documented an increase in expression of NGF from 2 to 5 weeks after EA intervention, indicating that acupuncture can not only increase NGF but also maintain its expression at a high level for a prolonged time, achieving a long-lasting protective effect (Yi et al., 2006).
Other NTFs, such as glial cell line-derived neurotrophic factor (GDNF; Manni et al., 2011), VEGF, insulin-like growth factor (IGF; Liu S. J. et al., 2014), stromal cell-derived factor-1a, and ciliary neurotrophic factor (Kim et al., 2013), have also been demonstrated to mediate the regulatory effects of acupuncture on neuroplasticity. Therefore, the ability of acupuncture to enhance neuroplasticity and improve neural function defects appears to be dependent on the NTFs family of growth factors (Manni et al., 2010; Xiao et al., 2018). In addition to the secretion of neurotrophic factors, other mechanisms by which astrocytes and microglia influence neuroplasticity are also worthy of attention.
Mechanisms of astrocyte regulation of neuroplasticity
Astrocytes have an important effect on neuroplasticity. In addition to secreting NTFs, astrocytes can also secrete or express specific mediators that regulate the number, morphology, and function of synapses, such as Maverick (a member of TGF-β superfamily), Hevin/Sparcl1, and thrombospondin. Cholesterol synthesized by astrocytes can significantly enhance the transmission efficiency of synapses, which is also promoted by glutamic acid and homocysteine released by astrocytes. D-serine plays an essential role in the induction of LTP without apparent effects on normal synaptic transmission (Allen and Eroglu, 2017). On the other hand, reactive astrocytes subsets residing within hundreds of microns from the infarcted area are involved in the formation of glial scar separating the infarct from the surrounding intact brain tissue. However, the overgrowth of astrocytes is detrimental because the upregulation of extracellular matrix proteins and other inhibitors of cell growth can prevent the effective regeneration of axons (Silver and Miller, 2004). For example, the deposition of chondroitin sulfate proteoglycans released by astrocytes via RhoA/ROCK-mediated pathways restricts neuroplasticity in the proximity of the glial scar, permitting the reconstruction of the neural circuit only distal sites (Carmichael et al., 2005; Sims and Yew, 2017).
The number of cells double-positive for GFAP/BrdU, GFAP/vimentin (expressed in radial neuroglia cells and neural and glial precursors), and GFAP/nestin in the cortex and striatum of MCAO rats was further increased 3 days after the EA of LI11 and ST36, indicating that EA can promote the proliferation of astrocytes in the cortex and striatum. At the same time, increased expression of cyclins, including cyclin Dl, cyclin-dependent kinase 4 (CDK4), and phospho-Rb, in the cortex and striatum regulates the activation of the G1-to-S transition, suggesting reactive astrocyte proliferation. In addition, EA enhanced the local expression of BDNF in the cortex and striatum. Together, these results indicated that EA plays a neuroprotective role by stimulating the proliferation of GFAP/vimentin/nestin-positive reactive astrocytes, which, in turn, secrete BDNF (Tao et al., 2016). It may be reflected in improving the structural characteristics of the synaptic interface, including numerical density, surface density, volume density, and gap width of the cortical synapse, enhancing the transmission function of the synapse, and modifying its structure and function, thus stimulating the regeneration of nerves and repair of the injury (Allen and Eroglu, 2017). At a later stage, acupuncture can increase the formation of new neurons and inhibit the excessive proliferation and differentiation of astrocytes, preventing the inhibition of axon regeneration by the excess of harmful substances (Jiang et al., 2016). It has been demonstrated that in the traumatic brain injury model not in cerebral infarction model, the number of BrdU/GFAP double-positive cells in the rats after acupuncture at GV20, GV26, Fengfu (GV16), GV15, and bilateral LI4 acupoints was significantly higher than that in the untreated group, which decreased to the same level as that in the untreated group at 7 days, reaching the same value as that of the sham-operated rats at 14 days, while the level remained higher in the injured animals not treated with acupuncture. These investigations demonstrated that acupuncture is conducive to the moderate proliferation and differentiation of astrocytes.
Mechanisms of microglia regulating neuroplasticity
Resident microglia perform a variety of functions in response to the pathological changes associated with the ischemic injury. They can rapidly change their morphology and migrate to the site of injury, affecting the integrity of neurons, changing synaptic input and activity, and activating neurogenesis. All these processes are beneficial to the recovery and reconstruction of neural function (Pocock and Kettenmann, 2007; Morrison and Filosa, 2013). Activated microglia complement receptor 3 can trigger LTD of peripheral neurons by regulating nicotinamide adenine dinucleotide phosphate oxidase, one of the main mediators of stroke neurotoxicity (Zhang et al., 2014). Another study showed that after cerebral ischemia, the activity-dependent connection between microglia and synapses was significantly prolonged for approximately 1 h, while the connection in the intact brain was maintained for approximately 5 min, suggesting that microglia can regulate LTP. This ability of microglia is critical for the reconstruction of the neural circuit after cerebral ischemic injury (Wake et al., 2009). Stimulation of microglia with low levels of interferon-gamma (IFN-γ) promotes early neurogenesis after stroke (Butovsky et al., 2006). In the chronic stage of ischemia, 16 weeks, the expression of IGF-1, GDNF, and BDNF in the M2 microglia in the ipsilateral SVZ (Ekdahl et al., 2009), generates conditions conducive to the continuous neurogenesis and recovery of function (Neumann et al., 2006; Nakajima et al., 2008). Additionally, microglia secrete chemokines, such as stromal cell-derived factor-1 α, which can bind to its receptor C-X-C chemokine receptor 4 (CXCR4) that is highly expressed in neural progenitor cells, promoting the migration of NSCs to the infarcted area.
At present, most of the research on the action of acupuncture on the neurological deficits of ischemic stroke has been from the perspective of reducing neuroinflammation, represented by reducing microglial activation and the release of proinflammatory mediators and neurotoxic substances. For example, Huang et al. (2017) performed EA on GV20 and GV24 for 7 days, and the results showed that EA could improve the neurological deficits and motor function of MCAO rats, as well as playing an anti-inflammatory role by reducing the secretion of interleukin-1beta (IL-1β) and promoting the release of IL-10 (Huang et al., 2017). However, there is little clinical and experimental evidence of the role of microglia in the acupuncture-mediated modulation of neuroplasticity after ischemic stroke, and this should be addressed in future research.
In conclusion, the role of glial cells in neuroplasticity has become an important research topic. These cells not only secrete NTFs and other factors but also transmit signals through their interaction with neurons. However, much is still not understood, specifically, the involvement of glial-neuronal interactions on the regulation of neuroplasticity by acupuncture.
Acupuncture Promotes The Functional Reorganization of Different Brain Regions
The functional reorganization of different brain regions after cerebral ischemic injury depends on the plasticity of both individual neurons and the functional networks of the brain, including contralateral transfer, ipsilateral functional compensation, and the activation of latent pathways. Experimental models of stroke in mice, rats, and monkeys allowed the identification of new connections formed in the ipsilateral cerebral hemisphere between the motor, somatosensory, and premotor areas of the cerebral cortex adjacent to the stroke. Stroke can also induce new connections between frontal motor regions and parts of the brainstem or spinal cord that have lost their projections from the stroke region in the contralateral hemisphere (Carmichael et al., 2017). At the same time, increased cerebral blood flow and excitability in the contralateral cortex contribute to recovery from stroke. There is simultaneous compensation within the ipsilateral and contralateral hemispheres, although this is dependent on the dominant hemisphere. For example, when a cortical lesion is large, the compensatory effect of the ipsilateral residual cortex is weakened, while the contralateral compensatory effect is enhanced (Fang et al., 2012). The functional compensation of both the tissue surrounding the lesion and the contralateral hemisphere may be explained by the activation of latent pathways or dormant synapses (Xiao et al., 2017). Acupuncture has been suggested to be complementary to mainstream rehabilitation after stroke, promoting the improvement of motor, sensory, cognitive, and other impairments, and is closely related to the activation of the corresponding brain areas (Li et al., 2015; Wu J. et al., 2017; Wen et al., 2018). This section explains the underlying functional plasticity mechanism activated by acupuncture during the regulation of neurological deficits after stroke, as shown in Table 3.
Table 3. The mechanisms of acupuncture on regulating functional reorganization in the treatment of ischemic stroke.
Numerous imaging studies have revealed that acupuncture can induce changes in bilateral brain regions or functional connections between brain regions by stimulating unilateral limbs, thus improving sensorimotor disorders after ischemic stroke. Animal experiments showed that after EA treatment at the LI11 and ST36 acupoints of the affected limbs, the infarct volume of MCAO rats was significantly reduced and motor function was recovered. It has been suggested that the possible reason for this is that neural activity and functional connections among brain regions related to motor function were stimulated by EA, including the caudate putamen, motor cortex, somatosensory cortex, dorsal thalamus, and striatum (Liang et al., 2017; Wu P. et al., 2017; Li et al., 2021). Using regional homogeneity (ReHo) analysis in a resting state in patients, it was found that the ReHo values of the right precentral gyrus and superior frontal gyrus were increased, and the ReHo values of the right superior parietal lobule, left fusiform gyrus, and left supplementary motor area were decreased after needling LI11 and ST36 of the right (healthy) limb, indicating that needling one side could stimulate changes in neuronal activity in bilateral brain regions (Chen S. et al., 2020). Acupuncture at the TE5 acupoint can regulate the sensorimotor network of the ipsilateral hemisphere, stimulate the contralateral sensorimotor network, enhance the synergy of the bilateral sensorimotor network, and alter the synchronicity between the cerebellum and the brain (Chen L. et al., 2014). The application of acupuncture together with twisting manipulation affected broad areas of the brain, influencing the contralateral intact hemisphere in patients with unilateral cerebral apoplexy of the primary sensorimotor area and the medial frontal cortex, which suggested that the effects of acupuncture are redistributed throughout the cortex, including the unaffected hemisphere, thereby enhancing the effect of the compensatory process (Huang et al., 2013). For example, the brain region responsible for motor execution and the limbic system of the affected hemisphere were activated by acupuncture at TE5, as well as the brain region related to motor execution and the cerebellum of the unaffected hemisphere. At the same time, improving glucose metabolism in the affected hemisphere also contributes to brain compensation (Huang et al., 2012). EA at GV20 and right GB7 resulted in immediate changes in glucose metabolism in both hemispheres in response to excitatory changes in various brain regions, including bilateral effects in the primary motor area (M1), premotor cortex, and superior parietal lobule (LPs), as well as the supplementary motor area in the unaffected hemisphere. The effect was still apparent 3 weeks after the acupuncture treatment with significant changes observed in glucose metabolism in bilateral M1 and LPs, as well as in other sites such as the insula, putamen, and cerebellum (Fang et al., 2012). These studies show that acupuncture activated bilateral motor areas of the brain, as well as neural tissues related to motor activity, to promote motor function after ischemic stroke. There is, thus, functional reorganization of multiple affected and unaffected areas of the cerebral cortex, and activation of potential functional areas to enhance compensation, especially in the unaffected hemisphere.
EA at GV20 and GV24 can improve cognitive dysfunction in rats after ischemic stroke, and its protective effect may be related to the activation of cognition-related brain regions, such as the hippocampus, retrosplenial cortex, cingulate gyrus, prelimbic cortex, and sensory cortex (Wen et al., 2018), as well as increasing the functional connectivity of these regions (Zhang et al., 2021). Other studies have reported that acupuncture can cause the structural restructuring of the network of the frontal lobe and default mode network (Wu et al., 2018). These brain regions may be the potential therapeutic targets and mechanisms for acupuncture to promote motor and cognitive recovery. In addition to movement, sensation, and cognition, acupuncture can also regulate brain regions related to visual function. For example, acupuncture at TE5 resulted in modulation of brain regions such as BA18 and BA19 (Chen et al., 2013). The International Standard Scalp Acupuncture, namely, acupuncture of the parietal midline (MS5) and left anterior/posterior parietal-temporal oblique lines (MS6 and MS7), can regulate functional brain connections in the dominant hemisphere of patients with acute middle cerebral artery infarction, and specifically strengthen the connections among vision-related brain regions such as BA18 and BA19, and the calcarine, fusiform, and lingual gyri (Liu et al., 2020). At present, most of the imaging studies on the use of acupuncture in the treatment of ischemic stroke have focused on improving the relationships between motor, sensory, and cognitive impairment, and functional compensation in bilateral brain regions, while the neurophysiological mechanism underlying the functional integration of the various CNS components after ischemic stroke remains to be investigated.
Discussion and Conclusion
The selection of acupoints is critical to the acupuncture process. Clinical investigations have emphasized specific treatments and have aimed to verify the effectiveness of acupuncture for the different sequelae of ischemic stroke, such as hemiplegia, dysphagia, and cognitive impairment. Although acupuncture treatments may vary according to the different types of functional impairment, they all comply with the principle of integral-local combination, that is, the acupoints in the functional areas of the brain are matched with those in specific lesion areas. These acupoints are located on yang meridians, especially Yangming and Shaoyang meridians, which have been verified by Dr. Zhang et al. (2018) through data mining technology (Zhang et al., 2018). Basic research solves a specific scientific question and emphasizes standardized acupuncture techniques and repeatability, resulting in differences between the treatment protocols in clinical and basic research. The selection of acupoints in basic research partially follows the clinical principle of integral-local combination, and many studies use head or body acupoints alone. Single or no more than five acupoints are generally used in basic research, with most of the selected acupoints used being acupoints that have been found to be effective in clinical practice, such as GV24, GV20, ST36, LI11, and TE5.
The neuroprotective effect was influenced by the different frequencies and waveforms of EA. Through the analysis of the data, we found that density-sparse waves were the most used, such as 1/20 Hz and 2/10 Hz. Previous studies have shown that the neuroprotective effect generated by density-sparse waves is the most marked, followed by intermittent waves, with continuous waves performing the worst. The reason may be that the density-sparse wave can activate different signaling pathways through conversion between low-, medium-, and high-frequency stimuli, to stimulate the release of different types of neurochemicals, leading to the neuroprotective effect, while the continuous wave can induce tolerance to electrical stimulation (Li and Wang, 2013). In addition, the acupuncture period is also one of the important factors affecting the curative effect of acupuncture. We observed that EA for 5 and 30 min has a superior effect in reducing the sizes of the ischemic cerebral infarction and neurological deficits, consistent with the conclusions of previous studies (Zhou et al., 2013).
The intervention time window of acupuncture is of great significance to the prognosis of ischemic stroke. In this review, most of the acupuncture intervention time point in the included basic studies was 24 h following the induction of MCAO, but a few studies carried out acupuncture intervention at 3 and 5 days after modeling. The duration of acupuncture ranged from 3 to 21 days. In terms of clinical research, a systematic review and network meta-analysis on the efficacy and safety of dissimilar acupuncture intervention time-points in treating stroke found that the faster the acupuncture intervention, the more effective it is in improving FMA score and BI. The optimal time point for acupuncture intervention is within 48 h after stroke, and the significant validity period lasts until 15 days after onset (Zhuo et al., 2021). Therefore, both clinical and basic studies suggest that acupuncture treatment within 24 and 48 h after cerebral infarction is more beneficial. The period of acupuncture treatment was less than 3 weeks due to greater self-recovery ability in animal models of cerebral infarction. Comparatively speaking, the clinical stroke patients have a longer course of disease, so in addition to giving acupuncture as early as possible, longer acupuncture period can be implemented to promote neuroplasticity and improve the sequelae of ischemic stroke.
In conclusion, spontaneous recovery takes place in the damaged brain due to neuroplasticity after ischemic stroke. However, the recovery is often incomplete, eventually leading to neurological deficit. Several lines of clinical evidence have shown that acupuncture can improve neurological deficits induced by ischemic stroke, particularly dyskinesia, spasticity, cognitive impairment, and dysphagia. Acupuncture plays a key role in regulating neuroplasticity, as shown in Figure 2. Specifically, acupuncture promotes the replacement of functional cells that have died after stroke by stimulating nerve cell regeneration, laying the structural foundation for the establishment of contacts and synapses between the cells by promoting the growth of new nerve processes or the regeneration of damaged axons, and thus ultimately promoting information transfer by enhancing structural connections and transmission by individual synapses, neural networks, and brain regions, leading to neuroplasticity-mediated structural reconstruction and functional recovery. Glial cells represented by astrocytes and microglia, as well as the NTFs secreted by them, such as BDNF and NGF, play important roles in supporting and promoting the neuroplasticity regulated by acupuncture. However, many factors have not been discussed in depth in this review due to the lack of direct evidence, for example, there are few studies on the role of M2 microglia in acupuncture-regulated post-stroke neural plasticity, which will be the focus of future research. In addition, high-quality clinical trials and systematic investigation of relevant mechanisms are needed to obtain more conclusive evidence. For example, while it has been found in clinical studies that many nuclei are activated after acupuncture, the conduction paths of the neural circuits require confirmation by systematic basic research. In addition, the compatibility of acupoints, dose-effect relationships, time windows of intervention, and other parameters, require in-depth investigation to promote a greater clinical application of acupuncture in the treatment of ischemic stroke.
Figure 2. Schematic representation showing the modulation of neuroplasticity by acupuncture after ischemic stroke by the promotion of functional compensation and structural plasticity. The data of acupoint selection and mechanism are derived from the mechanistic studies by using human and rodents. PC6, Neiguan; GV26, Shuigou; GV24, Shenting; GV20, Baihui; GB7, Qubin; GB20, Fengchi; GV14, Dazhui; LI11, Quchi; LI10, Shousanli; TE5, Waiguan; LI4, Hegu; GB33, Xiyangguan; GB34, Yanglingquan; ST36, Zusanli; ST37, Shangjuxu; GB39, Xuanzhong; LR3, Taichong; KI3, Taixi; SP6, Sanyinjiao; SP10, Xuehai; EX-UE9, Baxie; NSCs, neural stem cells; NGF, nerve growth factor; BDNF, brain-derived neurotrophic factor; GAP-43, growth associated protein-43; SYN, synaptophysin; NR1, N-methyl-d-aspartate receptor subtype 1; TRPV1, transient receptor potential vanilloid subtype 1; PSD-95, postsynaptic density-95; LTP, long-term potentiation.
Author Contributions
ZX and YaG: conceptualization. SQ and ZZ: methodology, data collection, and manuscript writing. YZ and JL: data collection and analysis. YGo and WF: preparation of the figures and the graphical abstract. YoG, YiG, JQ, ZX, and YaG: review and editing. All authors contributed to the article and approved the submitted version.
Funding
This study was financially supported by the National Natural Science Foundation of China (NSFC) No. 82004464, 81904295, and 81873369; The Natural Science Foundation of Tianjin No. 20JCQNJC00920.
Conflict of Interest
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.
Publisher’s Note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
References
Allen, N. J., and Eroglu, C. (2017). Cell biology of astrocyte-synapse interactions. Neuron 96, 697–708. doi: 10.1016/j.neuron.2017.09.056
Brouns, R., and De Deyn, P. P. (2009). The complexity of neurobiological processes in acute ischemic stroke. Clin. Neurol. Neurosurg. 111, 483–495. doi: 10.1016/j.clineuro.2009.04.001
Butovsky, O., Ziv, Y., Schwartz, A., Landa, G., Talpalar, A. E., Pluchino, S., et al. (2006). Microglia activated by IL-4 or IFN-gamma differentially induce neurogenesis and oligodendrogenesis from adult stem/progenitor cells. Mol. Cell. Neurosci. 31, 149–160. doi: 10.1016/j.mcn.2005.10.006
Carey, L., Walsh, A., Adikari, A., Goodin, P., Alahakoon, D., Silva, D. De., et al. (2019). Finding the intersection of neuroplasticity, stroke recovery and learning: scope and contributions to stroke rehabilitation. Neural Plast. 2019:5232374. doi: 10.1155/2019/5232374
Carmichael, S. T., Archibeque, I., Luke, L., Nolan, T., Momiy, J., Li, S., et al. (2005). Growth-associated gene expression after stroke: evidence for a growth-promoting region in peri-infarct cortex. Exp. Neurol. 193, 291–311. doi: 10.1016/j.expneurol.2005.01.004
Carmichael, S. T., Kathirvelu, B., Schweppe, C. A., and Nie, E. H. (2017). Molecular, cellular and functional events in axonal sprouting after stroke. Exp. Neurol. 287, 384–394. doi: 10.1016/j.expneurol.2016.02.007
Cassidy, J. M., and Cramer, S. C. (2017). Spontaneous and therapeutic-induced mechanisms of functional recovery after stroke. Transl. Stroke Res. 8, 33–46. doi: 10.1007/s12975-016-0467-5
Chang, J., Yao, X., Zou, H., Wang, L., Lu, Y., Zhang, Q., et al. (2016). BDNF/PI3K/Akt and Nogo-A/RhoA/ROCK signaling pathways contribute to neurorestorative effect of Houshiheisan against cerebral ischemia injury in rats. J. Ethnopharmacol. 194, 1032–1042. doi: 10.1016/j.jep.2016.11.005
Chavez, L. M., Huang, S. S., MacDonald, I., Lin, J. G., Lee, Y. C., Chen, Y. H., et al. (2017). Mechanisms of acupuncture therapy in ischemic stroke rehabilitation: a literature review of basic studies. Int. J. Mol. Sci. 194:18. doi: 10.3390/ijms18112270
Chen, B., Tao, J., Lin, Y., Lin, R., Liu, W., Chen, L., et al. (2015). Electro-acupuncture exerts beneficial effects against cerebral ischemia and promotes the proliferation of neural progenitor cells in the cortical peri-infarct area through the Wnt/β-catenin signaling pathway. Int. J. Mol. Med. 36, 1215–1222 doi: 10.3892/ijmm.2015.2334
Chen, J., Huang, Y., Lai, X., Tang, C., Yang, J., Chen, H., et al. (2013). Acupuncture at Waiguan (TE5) influences activation/deactivation of functional brain areas in ischemic stroke patients and healthy people: a functional MRI study. Neural Regen. Res. 8, 226–232. doi: 10.3969/j.issn.1673-5374.2013.03.004
Chen, J., Wang, J., Huang, Y., Lai, X., Tang, C., Yang, J., et al. (2014). Modulatory effect of acupuncture at Waiguan (TE5) on the functional connectivity of the central nervous system of patients with ischemic stroke in the left basal ganglia. PloS One 9:e96777. doi: 10.1371/journal.pone.0096777
Chen, L., Fang, J., Ma, R., Froym, R., Gu, X., Li, J., et al. (2014). Acupuncture for acute stroke: study protocol for a multicenter, randomized, controlled trial. Trials 15:214. doi: 10.1186/1745-6215-15-214
Chen, S. Q., Cai, D. C., Chen, J. X., Yang, H., and Liu, L. S. (2020). Altered brain regional homogeneity following contralateral acupuncture at quchi (LI 11) and zusanli (ST 36) in ischemic stroke patients with left hemiplegia: an fMRI study. Chin. J. Integr. Med. 26, 20–25. doi: 10.1007/s11655-019-3079-6
Chen, S., Wang, H., Xu, H., Zhang, Y., and Sun, H. (2020). Electroacupuncture promotes axonal regrowth by attenuating the myelin-associated inhibitors-induced RhoA/ROCK pathway in cerebral ischemia/reperfusion rats. Brain Res. 1748:147075. doi: 10.1016/j.brainres.2020.147075
Cheng, C. Y., Lin, J. G., Tang, N. Y., Kao, S. T., and Hsieh, C. L. (2014). Electroacupuncture-like stimulation at the Baihui (GV20) and Dazhui (GV14) acupoints protects rats against subacute-phase cerebral ischemia-reperfusion injuries by reducing S100B-mediated neurotoxicity. PLoS One 9:e91426. doi: 10.1371/journal.pone.0091426
Cramer, S. C. (2008). Repairing the human brain after stroke. II. Restorative therapies. Ann. Neurol. 63, 549–560. doi: 10.1002/ana.21412
Dąbrowski, J., Czajka, A., Zielińska-Turek, J., Jaroszyński, J., Furtak-Niczyporuk, M., Mela, A., et al. (2019). Brain functional reserve in the context of neuroplasticity after stroke. Neural Plast. 63:9708905. doi: 10.1155/2019/9708905
Darian-Smith, C. (2009). Synaptic plasticity, neurogenesis and functional recovery after spinal cord injury. Neuroscientist 15, 149–165. doi: 10.1177/1073858408331372
Deng, B., Bai, F., Zhou, H., Zhou, D., Ma, Z., Xiong, L., et al. (2016). Electroacupuncture enhances rehabilitation through miR-181b targeting PirB after ischemic stroke. Sci. Rep. 6:38997. doi: 10.1038/srep38997
Ekdahl, C. T., Kokaia, Z., and Lindvall, O. (2009). Brain inflammation and adult neurogenesis: the dual role of microglia. Neuroscience 158, 1021–1029. doi: 10.1016/j.neuroscience.2008.06.052
Fang, Z., Ning, J., Xiong, C., and Shulin, Y. (2012). Effects of electroacupuncture at head points on the function of cerebral motor areas in stroke patients: a pet study. Evid. Based Complement. Alternat. Med. 2012:902413. doi: 10.1155/2012/902413
Felling, R. J., and Song, H. (2015). Epigenetic mechanisms of neuroplasticity and the implications for stroke recovery. Exp. Neurol. 268, 37–45. doi: 10.1016/j.expneurol.2014.09.017
Fouda, A. Y., Alhusban, A., Ishrat, T., Pillai, B., Eldahshan, W., Waller, J. L., et al. (2017). Brain-derived neurotrophic factor knockdown blocks the angiogenic and protective effects of angiotensin modulation after experimental stroke. Mol. Neurobiol. 54, 661–670. doi: 10.1007/s12035-015-9675-3
Gibon, J., and Barker, P. A. (2017). Neurotrophins and proneurotrophins: focus on synaptic activity and plasticity in the brain. Neuroscientist 23, 587–604. doi: 10.1177/1073858417697037
Go, A. S., Mozaffarian, D., Roger, V. L., Benjamin, E. J., Berry, J. D., Blaha, M. J., et al. (2014). Heart disease and stroke statistics–2014 update: a report from the american heart association. Circulation 129, e28–e292. doi: 10.1161/01.cir.0000441139.02102.80
He, X. K., Sun, Q. Q., Liu, H. H., Guo, X. Y., Chen, C., Chen, L. D., et al. (2019). Timing of acupuncture during LTP-like plasticity induced by paired-associative stimulation. Behav. Neurol. 2019:9278270. doi: 10.1155/2019/9278270
Hickmott, P. W., and Ethell, I. M. (2006). Dendritic plasticity in the adult neocortex. Neuroscientist 12, 16–28. doi: 10.1177/1073858405282417
Hinman, J. D. (2014). The back and forth of axonal injury and repair after stroke. Curr. Opin. Neurol. 27, 615–623. doi: 10.1097/WCO.0000000000000149
Hong, J., Wu, G., Zou, Y., Tao, J., and Chen, L. (2013). Electroacupuncture promotes neurological functional recovery via the retinoic acid signaling pathway in rats following cerebral ischemia-reperfusion injury. Int. J. Mol. Med. 31, 225–231. doi: 10.3892/ijmm.2012.1166
Huang, J., You, X., Liu, W., Song, C., Lin, X., Zhang, X., et al. (2017). Electroacupuncture ameliorating post-stroke cognitive impairments via inhibition of peri-infarct astroglial and microglial/macrophage P2 purinoceptors-mediated neuroinflammation and hyperplasia. BMC Complement. Altern. Med. 17:480. doi: 10.1186/s12906-017-1974-y
Huang, Y., Chen, J. Q., Lai, X. S., Tang, C. Z., Yang, J. J., Chen, H., et al. (2013). Lateralisation of cerebral response to active acupuncture in patients with unilateral ischaemic stroke: an fMRI study. Acupunct. Med. 31, 290–296. doi: 10.1136/acupmed-2012-010299
Huang, Y., Tang, C., Wang, S., Lu, Y., Shen, W., Yang, J., et al. (2012). Acupuncture regulates the glucose metabolism in cerebral functional regions in chronic stage ischemic stroke patients–a PET-CT cerebral functional imaging study. BMC Neurosci. 13:75. doi: 10.1186/1471-2202-13-75
Hung, C. Y., Wu, X. Y., Chung, V. C., Tang, E. C., Wu, J. C., Lau, A. Y., et al. (2019). Overview of systematic reviews with meta-analyses on acupuncture in post-stroke cognitive impairment and depression management. Integr. Med. Res. 8, 145–159. doi: 10.1016/j.imr.2019.05.001
Jiang, S., Chen, W., Zhang, Y., Chen, A., Dai, Q., Lin, S., et al. (2016). Acupuncture induces the proliferation and differentiation of endogenous neural stem cells in rats with traumatic brain injury. Evid. Based Complement. Alternat. Med. 2016:2047412. doi: 10.1155/2016/2047412
Jiang, Y., Wei, N., Zhu, J., Lu, T., Chen, Z., Xu, G., et al. (2010). Effects of brain-derived neurotrophic factor on local inflammation in experimental stroke of rat. Mediators Inflamm. 2016:372423. doi: 10.1155/2010/372423
Kalaria, R. N., Akinyemi, R., and Ihara, M. (2016). Stroke injury, cognitive impairment and vascular dementia. Biochim. Biophys. Acta 1862, 915–925. doi: 10.1016/j.bbadis.2016.01.015
Keefe, K. M., Sheikh, I. S., and Smith, G. M. (2017). Targeting neurotrophins to specific populations of neurons: NGF, BDNF and NT-3 and their relevance for treatment of spinal cord injury. Int. J. Mol. Sci. 18:915. doi: 10.3390/ijms18030548
Kim, E., Owen, B., Holmes, W. R., and Grover, L. M. (2012). Decreased afferent excitability contributes to synaptic depression during high-frequency stimulation in hippocampal area CA1. J. Neurophysiol. 108, 1965–1976. doi: 10.1152/jn.00276.2011
Kim, J. H., Choi, K. H., Jang, Y. J., Kim, H. N., Bae, S. S., Choi, B. T., et al. (2013). Electroacupuncture preconditioning reduces cerebral ischemic injury via BDNF and SDF-1α in mice. BMC Complement. Altern. Med. 13:22. doi: 10.1186/1472-6882-13-22
Kim, M. W., Chung, Y. C., Jung, H. C., Park, M.-S., Han, Y.-M., Chung, Y.-A., et al. (2012). Electroacupuncture enhances motor recovery performance with brain-derived neurotrophic factor expression in rats with cerebral infarction. Acupunct. Med. 30, 222–226. doi: 10.1136/acupmed-2011-010126
Kim, Y. R., Ahn, S. M., Pak, M. E., Lee, H. J., Jung, D. H., Shin, Y. I., et al. (2018). Potential benefits of mesenchymal stem cells and electroacupuncture on the trophic factors associated with neurogenesis in mice with ischemic stroke. Sci. Rep. 8:2044. doi: 10.1038/s41598-018-20481-3
Kim, Y. R., Kim, H. N., Ahn, S. M., Choi, Y. H., Shin, H. K., Choi, B. T., et al. (2014). Electroacupuncture promotes post-stroke functional recovery via enhancing endogenous neurogenesis in mouse focal cerebral ischemia. PloS One 9:e90000. doi: 10.1371/journal.pone.0090000
Kwon, S. E., and Chapman, E. R. (2011). Synaptophysin regulates the kinetics of synaptic vesicle endocytosis in central neurons. Neuron 70, 847–854. doi: 10.1016/j.neuron.2011.04.001
Li, A. H., Zhang, J. M., and Xie, Y. K. (2004). Human acupuncture points mapped in rats are associated with excitable muscle/skin-nerve complexes with enriched nerve endings. Brain Res. 1012, 154–159. doi: 10.1016/j.brainres.2004.04.009
Li, X., and Wang, Q. (2013). Acupuncture therapy for stroke patients. Int. Rev. Neurobiol. 111, 159–179. doi: 10.1016/B978-0-12-411545-3.00008-0
Li, Y., Wang, Y., Zhang, H., Wu, P., and Huang, W. (2015). The effect of acupuncture on the motor function and white matter microstructure in ischemic stroke patients. Evid. Based Complement. Alternat. Med. 2015:164792. doi: 10.1155/2015/164792
Li, Z., Yang, M., Lin, Y., Liang, S., Liu, W., Chen, B., et al. (2021). Electroacupuncture promotes motor function and functional connectivity in rats with ischemic stroke: an animal resting-state functional magnetic resonance imaging study. Acupunct. Med. 39, 146–155. doi: 10.1177/0964528420920297
Liang, S., Lin, Y., Lin, B., Li, J., Liu, W., Chen, L., et al. (2017). Resting-state functional magnetic resonance imaging analysis of brain functional activity in rats with ischemic stroke treated by electro-acupuncture. J. Stroke Cerebrovasc. Dis. 26, 1953–1959. doi: 10.1016/j.jstrokecerebrovasdis.2017.06.018
Liao, S. L., Lin, Y. W., and Hsieh, C. L. (2017). Neuronal regeneration after electroacupuncture treatment in ischemia-reperfusion-injured cerebral infarction rats. Biomed Res. Int. 2017:3178014. doi: 10.1155/2017/3178014
Lillard, A. S., and Erisir, A. (2011). Old dogs learning new tricks: neuroplasticity beyond the juvenile period. Dev. Rev. 31, 207–239. doi: 10.1016/j.dr.2011.07.008
Lin, R., Wu, Y., Tao, J., Chen, B., Chen, J., Zhao, C., et al. (2016). Electroacupuncture improves cognitive function through Rho GTPases and enhances dendritic spine plasticity in rats with cerebral ischemia-reperfusion. Mol. Med. Rep. 13, 2655–2660. doi: 10.3892/mmr.2016.4870
Lin, Y. W., and Hsieh, C. L. (2010). Electroacupuncture at Baihui acupoint (GV20) reverses behavior deficit and long-term potentiation through N-methyl-d-aspartate and transient receptor potential vanilloid subtype 1 receptors in middle cerebral artery occlusion rats. J. Integr. Neurosci. 9, 269–282. doi: 10.1142/s0219635210002433
Liu, A. J., Li, J. H., Li, H. Q., Fu, D.-L., Lu, L., Bian, Z.-X., et al. (2015). Electroacupuncture for acute ischemic stroke: a meta-analysis of randomized controlled trials. Am. J. Chin. Med. 43, 1541–1566. doi: 10.1142/S0192415X15500883
Liu, F., Li, Z. M., Jiang, Y. J., and Chen, L. D. (2014). A meta-analysis of acupuncture use in the treatment of cognitive impairment after stroke. J. Altern. Complement. Med. 20, 535–544. doi: 10.1089/acm.2013.0364
Liu, H., Chen, L., Zhang, G., Jiang, Y., Qu, S., Liu, S., et al. (2020). Scalp Acupuncture enhances the functional connectivity of visual and cognitive-motor function network of patients with acute ischemic stroke. Evid. Based Complement. Alternat. Med. 2020:8836794. doi: 10.1155/2020/8836794
Liu, S. J., Zheng, S. S., Dan, Q. Q., Liu, J., and Wang, T. H. (2014). Effects of Governor Vessel electroacupuncture on the systematic expressions of NTFs in spinal cord transected rats. Neuropeptides 48, 239–247. doi: 10.1016/j.npep.2014.04.004
Liu, W., Wu, J., Huang, J., Zhuo, P., Lin, Y., Wang, L., et al. (2017). Electroacupuncture regulates hippocampal synaptic plasticity via miR-134-Mediated LIMK1 function in rats with ischemic stroke. Neural Plast. 2017:9545646. doi: 10.1155/2017/9545646
Luo, D., Fan, X., Ma, C., Fan, T., Wang, X., Chang, N., et al. (2014). A study on the effect of neurogenesis and regulation of GSK3β/PP2A expression in acupuncture treatment of neural functional damage caused by focal ischemia in MCAO rats. Evid. Based Complement. Alternat. Med. 2014:962343. doi: 10.1155/2014/962343
Magnusson, J. P., Göritz, C., Tatarishvili, J., Dias, D. O., Smith, E. M., Lindvall, O., et al. (2014). A latent neurogenic program in astrocytes regulated by Notch signaling in the mouse. Science (New York, NY) 346, 237–241. doi: 10.1126/science.346.6206.237
Mang, C. S., Campbell, K. L., Ross, C. J., and Boyd, L. A. (2013). Promoting neuroplasticity for motor rehabilitation after stroke: considering the effects of aerobic exercise and genetic variation on brain-derived neurotrophic factor. Phys. Ther. 93, 1707–1716. doi: 10.2522/ptj.20130053
Manni, L., Albanesi, M., Guaragna, M., Barbaro Paparo, S., and Aloe, L. (2010). Neurotrophins and acupuncture. Auton. Neurosci. 157, 9–17. doi: 10.1016/j.autneu.2010.03.020
Manni, L., Florenzano, F., and Aloe, L. (2011). Electroacupuncture counteracts the development of thermal hyperalgesia and the alteration of nerve growth factor and sensory neuromodulators induced by streptozotocin in adult rats. Diabetologia 54, 1900–1908. doi: 10.1007/s00125-011-2117-5
Martino, G., Pluchino, S., Bonfanti, L., and Schwartz, M. (2011). Brain regeneration in physiology and pathology: the immune signature driving therapeutic plasticity of neural stem cells. Physiol. Rev. 91, 1281–1304. doi: 10.1152/physrev.00032.2010
Matsuzaki, M., Honkura, N., Ellis-Davies, G. C., and Kasai, H. (2004). Structural basis of long-term potentiation in single dendritic spines. Nature 429, 761–766. doi: 10.1038/nature02617
Merson, T. D., and Bourne, J. A. (2014). Endogenous neurogenesis following ischaemic brain injury: insights for therapeutic strategies. Int. J. Biochem. Cell Biol. 56, 4–19. doi: 10.1016/j.biocel.2014.08.003
Mishra, S., Kelly, K. K., Rumian, N. L., and Siegenthaler, J. A. (2018). Retinoic acid is required for neural stem and progenitor cell proliferation in the adult hippocampus. Stem Cell Rep. 10, 1705–1720. doi: 10.1016/j.stemcr.2018.04.024
Morrison, H. W., and Filosa, J. A. (2013). A quantitative spatiotemporal analysis of microglia morphology during ischemic stroke and reperfusion. J. Neuroinflammation 10:4. doi: 10.1186/1742-2094-10-4
Mundy, W. R., Robinette, B., Radio, N. M., and Freudenrich, T. M. (2008). Protein biomarkers associated with growth and synaptogenesis in a cell culture model of neuronal development. Toxicology 249, 220–229. doi: 10.1016/j.tox.2008.05.012
Murphy, T. H. (2015). Two-photon imaging of neuronal structural plasticity in mice during and after ischemia. Cold Spring Harb. Protoc. 2015, 548–557. doi: 10.1101/pdb.prot087486
Murphy, T. H., and Corbett, D. (2009). Plasticity during stroke recovery: from synapse to behaviour. Nat. Rev. Neurosci. 10, 861–872. doi: 10.1038/nrn2735
Nakajima, K., Yamamoto, S., Kohsaka, S., and Kurihara, T. (2008). Neuronal stimulation leading to upregulation of glutamate transporter-1 (GLT-1) in rat microglia in vitro. Neurosci. Lett. 436, 331–334. doi: 10.1016/j.neulet.2008.03.058
Neumann, J., Gunzer, M., Gutzeit, H. O., Ullrich, O., Reymann, K. G., Dinkel, K., et al. (2006). Microglia provide neuroprotection after ischemia. FASEB J. 20, 714–716. doi: 10.1096/fj.05-4882fje
Neves, G., Cooke, S. F., and Bliss, T. V. (2008). Synaptic plasticity, memory and the hippocampus: a neural network approach to causality. Nat. Rev. Neurosci. 9, 65–75. doi: 10.1038/nrn2303
Park, K., Heo, H., Han, M. E., Choi, K., Yi, J. H., Kang, S. J., et al. (2015). Learning-induced synaptic potentiation in implanted neural precursor cell-derived neurons. Sci. Rep. 5:17796. doi: 10.1038/srep17796
Pekna, M., Pekny, M., and Nilsson, M. (2012). Modulation of neural plasticity as a basis for stroke rehabilitation. Stroke 43, 2819–2828. doi: 10.1161/STROKEAHA.112.654228
Pocock, J. M., and Kettenmann, H. (2007). Neurotransmitter receptors on microglia. Trends Neurosci. 30, 527–535. doi: 10.1016/j.tins.2007.07.007
Qing, P., Chai, T. Q., Ding, H. M., Zhao, C. H., and Hu, J. (2016). Effect of electroacupuncture combined with rehabilitation training on neurological function and expression of neuronal growth associated protein 43 and synaptophysin in rats with focal cerebral ischemia/reperfusion injury. Zhen Ci Yan Jiu 41, 314–320. doi: 10.13702/j.1000-0607.2016.04.006
Rathore, S. S., Hinn, A. R., Cooper, L. S., Tyroler, H. A., and Rosamond, W. D. (2002). Characterization of incident stroke signs and symptoms: findings from the atherosclerosis risk in communities study. Stroke 33, 2718–2721. doi: 10.1161/01.str.0000035286.87503.31
Sandvig, I., Augestad, I. L., Håberg, A. K., and Sandvig, A. (2018). Neuroplasticity in stroke recovery. The role of microglia in engaging and modifying synapses and networks. Eur. J. Neurosci. 47, 1414–1428. doi: 10.1111/ejn.13959
Schacher, S., and Hu, J. Y. (2014). The less things change, the more they are different: contributions of long-term synaptic plasticity and homeostasis to memory. Learn Mem. 21, 128–134. doi: 10.1101/lm.027326.112
Sha, R., Han, X., Zheng, C., Peng, J., Wang, L., Chen, L., et al. (2019). The effects of electroacupuncture in a rat model of cerebral ischemia-reperfusion injury following middle cerebral artery occlusion involves MicroRNA-223 and the PTEN signaling pathway. Med. Sci. Monit. 25, 10077–10088. doi: 10.12659/MSM.919611
Shao, T. Y., Ding, M. R., Ye, Z. X., Qian, M. X., Zhou, X., Jin, Z. Q., et al. (2021). Governor vessel acupuncture for acute ischemic stroke: a systematic review and meta-analysis. Ann. Palliat. Med. 10, 7236–7246. doi: 10.21037/apm-21-691
Shih, C. C., Liao, C. C., Sun, M. F., Su, Y.-C., Wen, C.-P., Morisky, D. E., et al. (2015). A retrospective cohort study comparing stroke recurrence rate in ischemic stroke patients with and without acupuncture treatment. Medicine (Baltimore) 94:e1572. doi: 10.1097/MD.0000000000001572
Silver, J., and Miller, J. H. (2004). Regeneration beyond the glial scar. Nat. Rev. Neurosci. 5, 146–156. doi: 10.1038/nrn1326
Sims, N. R., and Yew, W. P. (2017). Reactive astrogliosis in stroke: contributions of astrocytes to recovery of neurological function. Neurochem. Int. 107, 88–103. doi: 10.1016/j.neuint.2016.12.016
Song, M., Martinowich, K., and Lee, F. S. (2017). BDNF at the synapse: why location matters. Mol. Psychiatry 22, 1370–1375. doi: 10.1038/mp.2017.144
Stewart, M. R., and Dringenberg, H. C. (2016). Potential role of synaptic activity to inhibit LTD induction in rat visual cortex. Neural Plast. 2016:1401935. doi: 10.1155/2016/1401935
Stogsdill, J. A., and Eroglu, C. (2017). The interplay between neurons and glia in synapse development and plasticity. Curr. Opin. Neurobiol. 42, 1–8. doi: 10.1016/j.conb.2016.09.016
Sun, Y., Xue, S. A., and Zuo, Z. (2012). Acupuncture therapy on apoplectic aphasia rehabilitation. J. Tradit. Chin. Med. 32, 314–321. doi: 10.1016/s0254-6272(13)60031-x
Tan, F., Wang, J., Liu, J. X., Wang, C., Li, M., Gu, Y., et al. (2018). Electroacupuncture stimulates the proliferation and differentiation of endogenous neural stem cells in a rat model of ischemic stroke. Exp. Ther. Med. 16, 4943–4950. doi: 10.3892/etm.2018.6848
Tao, J., Xue, X. H., Chen, L. D., Yang, S. L., Jiang, M., Gao, Y. L., et al. (2010). Electroacupuncture improves neurological deficits and enhances proliferation and differentiation of endogenous nerve stem cells in rats with focal cerebral ischemia. Neurol. Res. 32, 198–204. doi: 10.1179/174313209X414506
Tao, J., Zheng, Y., Liu, W., Yang, S., Huang, J., Xue, X., et al. (2016). Electro-acupuncture at LI11 and ST36 acupoints exerts neuroprotective effects via reactive astrocyte proliferation after ischemia and reperfusion injury in rats. Brain Res. Bull. 120, 14–24. doi: 10.1016/j.brainresbull.2015.10.011
Tejeda, G. S., Esteban-Ortega, G. M., San Antonio, E., Vidaurre, Ó. G., and Díaz-Guerra, M. (2019). Prevention of excitotoxicity-induced processing of BDNF receptor TrkB-FL leads to stroke neuroprotection. EMBO Mol. Med. 11:e9950. doi: 10.15252/emmm.201809950
Wake, H., Moorhouse, A. J., Jinno, S., Kohsaka, S., and Nabekura, J. (2009). Resting microglia directly monitor the functional state of synapses in vivo and determine the fate of ischemic terminals. J. Neurosci. 29, 3974–3980. doi: 10.1523/JNEUROSCI.4363-08.2009
Wang, J., Pei, J., Khiati, D., Fu, Q., Cui, X., Song, Y., et al. (2017). Acupuncture treatment on the motor area of the scalp for motor dysfunction in patients with ischemic stroke: study protocol for a randomized controlled trial. Trials 18:287. doi: 10.1186/s13063-017-2000-x
Wang, K., Zhang, R., He, F., Lin, L.-B., Xiang, X.-H., Ping, X.-J., et al. (2012). Electroacupuncture frequency-related transcriptional response in rat arcuate nucleus revealed region-distinctive changes in response to low- and high-frequency electroacupuncture. J. Neurosci. Res. 90, 1464–1473. doi: 10.1002/jnr.23028
Wen, T., Zhang, X., Liang, S., Li, Z., Xing, X., Liu, W., et al. (2018). Electroacupuncture ameliorates cognitive impairment and spontaneous low-frequency brain activity in rats with ischemic stroke. J. Stroke Cerebrovasc. Dis. 27, 2596–2605. doi: 10.1016/j.jstrokecerebrovasdis.2018.05.021
World Health Organization (2002). Acupuncture: Review and Analysis of Reports on Controlled Clinical Trials. Geneva: World Health Organization.
Wu, J., Lin, B., Liu, W., Huang, J., Shang, G., Lin, Y., et al. (2017). Roles of electro-acupuncture in glucose metabolism as assessed by 18F-FDG/PET imaging and AMPKα phosphorylation in rats with ischemic stroke. Int. J. Mol. Med. 40, 875–882. doi: 10.3892/ijmm.2017.3057
Wu, P., Zeng, F., Yin, C., Xiong, Y., Bai, Y., Wang, D., et al. (2017). Effect of acupuncture plus conventional treatment on brain activity in ischemic stroke patients: a regional homogeneity analysis. J. Tradit. Chin. Med. 37, 650–658.
Wu, P., Zhou, Y. M., Liao, C. X., Tang, Y. Z., Li, Y. X., Qiu, L. H., et al. (2018). Structural changes induced by acupuncture in the recovering brain after ischemic stroke. Evid. Based Complement. Alternat. Med. 2018:5179689. doi: 10.1155/2018/5179689
Xia, W. G., Zheng, C. J., Zhang, X., and Wang, J. (2017). Effects of nourishing liver and kidney acupuncture therapy on expression of brain derived neurotrophic factor and synaptophysin after cerebral ischemia reperfusion in rats. J. Huazhong Univ. Sci. Technol. Med. Sci. 37, 271–278. doi: 10.1007/s11596-017-1727-7
Xiao, L. Y., Wang, X. R., Yang, Y., Yang, J.-W., Cao, Y., Ma, S.-M., et al. (2018). Applications of acupuncture therapy in modulating plasticity of central nervous system. Neuromodulation 21, 762–776. doi: 10.1111/ner.12724
Xiao, X., Lin, Q., Lo, W. L., Mao, Y.-R., Shi, X.-C., Cates, R. S., et al. (2017). Cerebral reorganization in subacute stroke survivors after virtual reality-based training: a preliminary study. Behav. Neurol. 2017:6261479. doi: 10.1155/2017/6261479
Xie, G., Song, C., Lin, X., Yang, M., Fan, X., Liu, W., et al. (2019). Electroacupuncture regulates hippocampal synaptic plasticity via inhibiting janus-activated kinase 2/signal transducer and activator of transcription 3 signaling in cerebral ischemic rats. J. Stroke Cerebrovasc. Dis. 28, 792–799. doi: 10.1016/j.jstrokecerebrovasdis.2018.11.025
Xu, L., Yan, X. Z., Li, Z. Y., Cao, X. F., and Wang, M. (2017). Effect of xingnao kaiqiao zhenfa (acupuncture technique for restoring consciousness) combined with rehabilitation training on nerve repair and expression of growth-associated protein-43 of peri-ischemic cortex in ischemic stroke rats. Zhen Ci Yan Jiu 42, 223–228. doi: 10.13702/j.1000-0607.2017.03.006
Yamashita, T., Ninomiya, M., Hernández Acosta, P., García-Verdugo, J. M., Sunabori, T., Sakaguchi, M., et al. (2006). Subventricular zone-derived neuroblasts migrate and differentiate into mature neurons in the post-stroke adult striatum. J. Neurosci. 26, 6627–6636. doi: 10.1523/JNEUROSCI.0149-06.2006
Yang, A., Wu, H. M., Tang, J. L., Xu, L., Yang, M., Liu, G. J., et al. (2016). Acupuncture for stroke rehabilitation. Cochrane Database Syst. Rev. 8:CD004131. doi: 10.1002/14651858.CD004131.pub3
Yang, Y., Eisner, I., Chen, S., Wang, S., Zhang, F., Wang, L., et al. (2017). Neuroplasticity changes on human motor cortex induced by acupuncture therapy: a preliminary study. Neural Plast. 2017:4716792. doi: 10.1155/2017/4716792
Ye, Y., Li, H., Yang, J. W., Wang, X. R., Shi, G. X., Yan, C. Q., et al. (2017). Acupuncture attenuated vascular dementia-induced hippocampal long-term potentiation impairments via activation of d1/d5 receptors. Stroke 48, 1044–1051. doi: 10.1161/STROKEAHA.116.014696
Yi, W., Xu, N. G., and Wang, G. B. (2006). Experimental study on effects of electro-acupuncture in improving synaptic plasticity in focal cerebral ischemia rats. Zhongguo Zhong Xi Yi Jie He Za Zhi 26, 710–714.
Zhang, J., Malik, A., Choi, H. B., Ko, R. W., Dissing-Olesen, L., MacVicar, B. A., et al. (2014). Microglial CR3 activation triggers long-term synaptic depression in the hippocampus via NADPH oxidase. Neuron 82, 195–207. doi: 10.1016/j.neuron.2014.01.043
Zhang, Q., Li, J., Huang, S., Yang, M., Liang, S., Liu, W., et al. (2021). Functional connectivity of the retrosplenial cortex in rats with ischemic stroke is improved by electroacupuncture. Acupunct. Med. 39, 200–207. doi: 10.1177/0964528420921190
Zhang, S., Jin, T., Wang, L., Liu, W., Zhang, Y., Zheng, Y., et al. (2020). Electro-acupuncture promotes the differentiation of endogenous neural stem cells via exosomal microRNA 146b after ischemic stroke. Front. Cell. Neurosci. 14:223. doi: 10.3389/fncel.2020.00223
Zhang, Y., Zhang, Z. L., Wang, X., and Xinjv, L. I. (2018). Exploration on the characteristics of meridian points in the treatment of Spasticity paralysis after stroke with acupuncture and moxibustion based on the data mining technology. Nei Mongol J. Tradit. Chin. Med. 33:940. doi: 10.16040/j.cnki.cn15-1101.2018.02.044
Zhao, J., Sui, M., Lü, X., Jin, D., Zhuang, Z., and Yan, T. (2015). Electroacupuncture promotes neural stem cell proliferation and neurogenesis in the dentate gyrus of rats following stroke via upregulation of Notch1 expression. Mol. Med. Rep. 12, 6911–6917. doi: 10.3892/mmr.2015.4279
Zhao, J., Xu, H., Tian, Y., Hu, M., and Xiao, H. (2013). Effect of electroacupuncture on brain-derived neurotrophic factor mRNA expression in mouse hippocampus following cerebral ischemia-reperfusion injury. J. Tradit. Chin. Med. 33, 253–257. doi: 10.1016/s0254-6272(13)60135-1
Zhao, X., Bai, F., Zhang, E., Zhou, D., Jiang, T., Zhou, H., et al. (2018). Electroacupuncture improves neurobehavioral function through targeting of SOX2-mediated axonal regeneration by MicroRNA-132 after ischemic stroke. Front. Mol. Neurosci. 11:471. doi: 10.3389/fnmol.2018.00471
Zhao, Z. Q. (2008). Neural mechanism underlying acupuncture analgesia. Prog. Neurobiol. 85, 355–375. doi: 10.1016/j.pneurobio.2008.05.004
Zhou, F., Guo, J., Cheng, J., Wu, G., and Xia, Y. (2013). Effect of electroacupuncture on rat ischemic brain injury: importance of stimulation duration. Evid. Based Complement. Alternat. Med. 2013:878521. doi: 10.1155/2013/878521
Zhou, Y. C., Wu, X. G., and Xiao, Y. C. (2011). Effects of electroacupuncture at Zusanli (ST 36) and Neiguan (PC 6) on expression of GAP-43 in cerebral infarction rats. Zhongguo Zhen Jiu 31, 55–59. doi: 10.13703/j.0255-2930.2011.01.016
Keywords: acupuncture, ischemic stroke, neuroplasticity, neurogenesis, axon regeneration, synapse, neurotrophic factors, glia
Citation: Qin S, Zhang Z, Zhao Y, Liu J, Qiu J, Gong Y, Fan W, Guo Y, Guo Y, Xu Z and Guo Y (2022) The impact of acupuncture on neuroplasticity after ischemic stroke: a literature review and perspectives. Front. Cell. Neurosci. 16:817732. doi: 10.3389/fncel.2022.817732
Received: 18 November 2021; Accepted: 24 October 2022;
Published: 10 November 2022.
Edited by:
Binlong Zhang, Guang’anmen Hospital, China Academy of Chinese Medical Sciences, ChinaReviewed by:
Elizabeth Hernández-Echeagaray, National Autonomous University of Mexico, MexicoAbdelrahman Fouda, University of Arkansas for Medical Sciences, United States
Copyright © 2022 Qin, Zhang, Zhao, Liu, Qiu, Gong, Fan, Guo, Guo, Xu and Guo. 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) and the copyright owner(s) 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: Zhifang Xu, eHV6aGlmYW5nbXNuQGhvdG1haWwuY29t; Yang Guo, Z3VvZ3VvX2d1b3lhbmdAaG90bWFpbC5jb20=
† These authors have contributed equally to this work and share first authorship
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