Demyelination in psychiatric and neurological disorders: Mechanisms, clinical impact, and novel therapeutic strategies

IF 7.5 1区 医学 Q1 BEHAVIORAL SCIENCES
Rumi Murayama , Yi Cai , Hiroyuki Nakamura , Kenji Hashimoto
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引用次数: 0

Abstract

Demyelination, defined as the loss of myelin sheaths around neuronal axons, is increasingly recognized as a key factor in a broad range of psychiatric and neurological disorders, including schizophrenia, major depressive disorder, bipolar disorder, post-traumatic stress disorder, autism spectrum disorder, substance use disorders, Alzheimer’s disease, Parkinson’s disease, and multiple sclerosis. This review investigates the core mechanisms driving demyelination, its clinical impact, and emerging therapeutic strategies aimed at maintaining or restoring myelin integrity. Disruption of myelin impairs crucial neural communication pathways, resulting in cognitive, motor, and behavioral deficits that substantially reduce quality of life and create significant economic and social challenges. Key contributors to demyelination include genetic predisposition, environmental triggers, immune dysregulation, neuroinflammation, and alterations in the gut–brain axis mediated by the vagus nerve. Promising therapies include sphingosine 1-phosphate receptor modulators and muscarinic acetylcholine receptor antagonists, both of which diminish immune-related myelin damage and may enhance neuroprotection. In addition, the novel antidepressant arketamine appears to boost myelination through transforming growth factor-β1 signaling pathways. Approaches targeting the gut–brain axis, such as noninvasive transcutaneous auricular vagus nerve stimulation and fecal microbiota transplantation, may also help reduce inflammation and support myelin repair. Future research should center on clarifying the precise molecular mechanisms of demyelination, developing targeted therapies, and leveraging advanced neuroimaging for earlier detection and personalized treatment. By combining immunomodulatory and neuroprotective strategies, there is potential to significantly improve outcomes for individuals affected by demyelinating psychiatric and neurological disorders.
精神和神经疾病的脱髓鞘:机制、临床影响和新的治疗策略。
脱髓鞘,被定义为神经元轴突周围髓鞘的丢失,越来越被认为是广泛的精神和神经疾病的一个关键因素,包括精神分裂症、重度抑郁症、双相情感障碍、创伤后应激障碍、自闭症谱系障碍、物质使用障碍、阿尔茨海默病、帕金森病和多发性硬化症。本文综述了驱动脱髓鞘的核心机制,其临床影响,以及旨在维持或恢复髓鞘完整性的新兴治疗策略。髓磷脂的破坏损害了关键的神经通信通路,导致认知、运动和行为缺陷,大大降低了生活质量,并造成了重大的经济和社会挑战。脱髓鞘的主要原因包括遗传易感性、环境诱因、免疫失调、神经炎症和迷走神经介导的肠-脑轴改变。有希望的治疗方法包括鞘氨醇1-磷酸受体调节剂和毒蕈碱乙酰胆碱受体拮抗剂,两者都可以减少免疫相关的髓磷脂损伤,并可能增强神经保护。此外,新型抗抑郁药阿克他命似乎通过转化生长因子-β1信号通路促进髓鞘形成。针对肠-脑轴的方法,如无创经皮耳迷走神经刺激和粪便微生物群移植,也可能有助于减少炎症和支持髓鞘修复。未来的研究应集中在明确脱髓鞘的精确分子机制,开发靶向治疗,并利用先进的神经影像学进行早期发现和个性化治疗。通过结合免疫调节和神经保护策略,有可能显著改善脱髓鞘精神和神经疾病患者的预后。
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
CiteScore
14.20
自引率
3.70%
发文量
466
审稿时长
6 months
期刊介绍: The official journal of the International Behavioral Neuroscience Society publishes original and significant review articles that explore the intersection between neuroscience and the study of psychological processes and behavior. The journal also welcomes articles that primarily focus on psychological processes and behavior, as long as they have relevance to one or more areas of neuroscience.
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