Chemogenetic modulation in stroke recovery: A promising stroke therapy Approach.

IF 7.6 1区 医学 Q1 CLINICAL NEUROLOGY
Xinyuan Yu, Zhihong Jian, Lihong Dang, Xu Zhang, Peibang He, Xiaoxing Xiong, Yanping Feng, Ata Ur Rehman
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引用次数: 0

Abstract

Stroke remains a leading cause of long-term disability and mortality worldwide, necessitating novel therapeutic strategies to enhance recovery. Traditional rehabilitation approaches, including physical therapy and pharmacological interventions, often provide limited functional improvement. Neuromodulation has emerged as a promising strategy to promote post-stroke recovery by enhancing neuroplasticity and functional reorganization. Among various neuromodulatory techniques, chemogenetics, particularly Designer Receptors Exclusively Activated by Designer Drugs (DREADDs), offers precise, cell-type-specific, and temporally controlled modulation of neuronal and glial activity. This review explores the mechanisms and therapeutic potential of chemogenetic modulation in stroke recovery. Preclinical studies have demonstrated that activation of excitatory DREADDs (hM3Dq) in neurons located within the peri-infarct area or contralateral M1 has been shown to enhance neuroplasticity, facilitate axonal sprouting, and lead to improved behavioral recovery following stroke. Conversely, stimulation of inhibitory DREADDs (hM4Di) suppresses stroke-induced excitotoxicity, mitigates peri-infarct spreading depolarizations (PIDs), and modulates neuroinflammatory responses. By targeting specific neuronal and glial populations, chemogenetics enables phase-specific interventions-early inhibition to minimize damage during the acute phase and late excitation to promote plasticity during the recovery phase. Despite its advantages over traditional neuromodulation techniques, such as optogenetics and deep brain stimulation, several challenges remain before chemogenetics can be translated into clinical applications. These include optimizing viral vector delivery, improving ligand specificity, minimizing off-target effects, and ensuring long-term receptor stability. Furthermore, integrating chemogenetics with existing stroke rehabilitation strategies, including brain-computer interfaces and physical therapy, may enhance functional recovery by facilitating adaptive neuroplasticity. Future research should focus on refining chemogenetic tools to enable clinical application. By offering a highly selective, reversible, and minimally invasive approach, chemogenetics holds great potential for revolutionizing post-stroke therapy and advancing personalized neuromodulation strategies.

脑卒中恢复中的化学发生调节:一种有前途的脑卒中治疗方法。
中风仍然是世界范围内长期残疾和死亡的主要原因,需要新的治疗策略来增强康复。传统的康复方法,包括物理治疗和药物干预,往往提供有限的功能改善。神经调节已成为一种很有前途的策略,通过增强神经可塑性和功能重组来促进脑卒中后的恢复。在各种神经调节技术中,化学遗传学,特别是由设计药物独家激活的设计受体(DREADDs),提供了精确的、细胞类型特异性的、暂时控制的神经元和神经胶质活性调节。本文综述了化学发生调节在脑卒中康复中的作用机制和治疗潜力。临床前研究表明,位于梗死周围区域或对侧M1神经元的兴奋性DREADDs (hM3Dq)的激活已被证明可以增强神经可塑性,促进轴突生长,并导致中风后行为恢复的改善。相反,刺激抑制性脏脏蛋白(hM4Di)可抑制脑卒中引起的兴奋性毒性,减轻梗死周围扩散性去极化(PIDs),并调节神经炎症反应。通过针对特定的神经元和神经胶质群体,化学遗传学实现了阶段特异性干预——早期抑制以减少急性期的损伤,晚期兴奋以促进恢复期的可塑性。尽管化学遗传学比传统的神经调节技术(如光遗传学和深部脑刺激)有优势,但在化学遗传学转化为临床应用之前,仍存在一些挑战。这些包括优化病毒载体传递,提高配体特异性,最大限度地减少脱靶效应,并确保受体的长期稳定性。此外,将化学遗传学与现有的中风康复策略(包括脑机接口和物理治疗)相结合,可能通过促进适应性神经可塑性来增强功能恢复。未来的研究应集中在改进化学发生工具,使临床应用。通过提供高选择性、可逆性和微创性的方法,化学遗传学在彻底改变中风后治疗和推进个性化神经调节策略方面具有巨大的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Brain Stimulation
Brain Stimulation 医学-临床神经学
CiteScore
13.10
自引率
9.10%
发文量
256
审稿时长
72 days
期刊介绍: Brain Stimulation publishes on the entire field of brain stimulation, including noninvasive and invasive techniques and technologies that alter brain function through the use of electrical, magnetic, radiowave, or focally targeted pharmacologic stimulation. Brain Stimulation aims to be the premier journal for publication of original research in the field of neuromodulation. The journal includes: a) Original articles; b) Short Communications; c) Invited and original reviews; d) Technology and methodological perspectives (reviews of new devices, description of new methods, etc.); and e) Letters to the Editor. Special issues of the journal will be considered based on scientific merit.
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