应激下的神经可塑性不良:对前额皮质神经元和突触变化的见解。

IF 4.3 2区 医学 Q1 NEUROSCIENCES
Molecular Neurobiology Pub Date : 2025-11-01 Epub Date: 2025-06-23 DOI:10.1007/s12035-025-05152-5
Bingyu Ren, Quan Yuan, Shuhan Cha, Sinyi Liu, Jifeng Zhang, Guoqing Guo
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引用次数: 0

摘要

慢性压力可导致大脑的神经可塑性变化,而前额叶皮层(PFC)由于其在执行功能和情绪调节中的作用而成为脆弱的关键部位。大量证据证实,慢性应激在多个尺度上引起神经可塑性的变化,包括功能重组、神经元内在兴奋性、结构和突触可塑性。这些改变在PFC的谷氨酸能锥体神经元中尤为突出,包括突触减弱、树突回缩、脊柱丢失和长期增强功能受损。关于锥体神经元兴奋性的矛盾发现——从亢奋到低活动——突出了应力诱导可塑性的复杂性和动态性。连接这些改变的一种被提出的机制是兴奋性毒性,其特征是谷氨酸信号过度,星形细胞清除受损和钙超载,最终导致突触功能障碍和结构变性。此外,抑制性中间神经元和神经胶质细胞也可能在形成和调节应激反应中发挥重要作用。这篇综述整合了神经可塑性水平的研究结果,以提供对慢性应激如何重塑pfc的全面理解。我们进一步讨论了将稳态可塑性作为一种补偿机制的治疗潜力,并提出了未来的方向,以阐明应激相关疾病中神经可塑性不良的时间动力学、电路特异性和分子调节。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Maladaptive Neuroplasticity Under Stress: Insights into Neuronal and Synaptic Changes in the Prefrontal Cortex.

Chronic stress can lead to maladaptive neuroplastic changes in the brain, with the prefrontal cortex (PFC) being a critical site of vulnerability due to its role in executive function and emotional regulation. Extensive evidence has confirmed that chronic stress induces neuroplasticity changes at multiple scales, including functional reorganization, intrinsic neuronal excitability, and structural and synaptic plasticity. These alterations are particularly prominent in glutamatergic pyramidal neurons of the PFC and involve synaptic weakening, dendritic retraction, spine loss, and impaired long-term potentiation. The paradoxical findings regarding pyramidal neuron excitability-ranging from hyper- to hypoactivity-highlight the complex and dynamic nature of stress-induced plasticity. One proposed mechanism linking these alterations is excitotoxicity, characterized by excessive glutamate signaling, impaired astrocytic clearance, and calcium overload, ultimately leading to synaptic dysfunction and structural degeneration. Additionally, inhibitory interneurons and glial cells might also play essential roles in shaping and modulating the stress response. This review integrates findings across neuroplasticity levels to provide a comprehensive understanding of how chronic stress reshapes the PFC. We further discuss the therapeutic potential of targeting homeostatic plasticity as a compensatory mechanism and propose future directions to clarify temporal dynamics, circuit specificity, and molecular regulators underlying maladaptive neuroplasticity in stress-related disorders.

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来源期刊
Molecular Neurobiology
Molecular Neurobiology 医学-神经科学
CiteScore
9.00
自引率
2.00%
发文量
480
审稿时长
1 months
期刊介绍: Molecular Neurobiology is an exciting journal for neuroscientists needing to stay in close touch with progress at the forefront of molecular brain research today. It is an especially important periodical for graduate students and "postdocs," specifically designed to synthesize and critically assess research trends for all neuroscientists hoping to stay active at the cutting edge of this dramatically developing area. This journal has proven to be crucial in departmental libraries, serving as essential reading for every committed neuroscientist who is striving to keep abreast of all rapid developments in a forefront field. Most recent significant advances in experimental and clinical neuroscience have been occurring at the molecular level. Until now, there has been no journal devoted to looking closely at this fragmented literature in a critical, coherent fashion. Each submission is thoroughly analyzed by scientists and clinicians internationally renowned for their special competence in the areas treated.
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