AMPA受体弥散捕获机制作为神经退行性和神经精神疾病的早期治疗靶点。

IF 10.8 1区 医学 Q1 NEUROSCIENCES
Daniel Choquet, Patricio Opazo, Hongyu Zhang
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引用次数: 0

摘要

在过去的二十年中,人们越来越认识到AMPA受体(AMPARs)的表面扩散及其在突触中的扩散捕获的生理重要性和病理意义。AMPAR表面扩散需要这些受体在质膜内的热动力随机布朗横向运动,促进突触和突触外室之间的动态交换。这一过程还通过与突触锚定槽的短暂结合,使ampar在突触上的活动依赖的扩散捕获和积累成为可能。最近的研究强调了ampar通过扩散捕获在基本神经过程中的关键作用,如长期增强(LTP)早期阶段的发展、情境恐惧记忆、记忆巩固和感觉输入诱导的皮层重映射。此外,研究强调,AMPAR弥散捕获的调节在各种神经疾病模型中发生改变,包括亨廷顿病(HD)、阿尔茨海默病(AD)和压力相关疾病(如抑郁症)。值得注意的是,旨在纠正AMPAR弥散捕获缺陷的药理学干预已证明在这些不同疾病模型中恢复突触数量、LTP和记忆功能有效,尽管它们的致病机制不同。这篇综述提供了当前对AMPAR扩散捕获失调的分子机制的见解,强调了它作为多种病理信号通路的会聚点的作用。我们提出,靶向AMPAR弥漫性捕获代表了一种有希望的早期治疗策略,可以减轻一系列脑部疾病(包括但不限于HD, AD和压力相关疾病)中的突触可塑性和记忆缺陷。这种方法强调了这些神经退行性疾病和神经精神疾病复杂性中的综合治疗目标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
AMPA receptor diffusional trapping machinery as an early therapeutic target in neurodegenerative and neuropsychiatric disorders.

Over the past two decades, there has been a growing recognition of the physiological importance and pathological implications surrounding the surface diffusion of AMPA receptors (AMPARs) and their diffusional trapping at synapses. AMPAR surface diffusion entails the thermally powered random Brownian lateral movement of these receptors within the plasma membrane, facilitating dynamic exchanges between synaptic and extrasynaptic compartments. This process also enables the activity-dependent diffusional trapping and accumulation of AMPARs at synapses through transient binding to synaptic anchoring slots. Recent research highlights the critical role of synaptic recruitment of AMPARs via diffusional trapping in fundamental neural processes such as the development of the early phases of long-term potentiation (LTP), contextual fear memory, memory consolidation, and sensory input-induced cortical remapping. Furthermore, studies underscore that regulation of AMPAR diffusional trapping is altered across various neurological disease models, including Huntington's disease (HD), Alzheimer's disease (AD), and stress-related disorders like depression. Notably, pharmacological interventions aimed at correcting deficits in AMPAR diffusional trapping have demonstrated efficacy in restoring synapse numbers, LTP, and memory functions in these diverse disease models, despite their distinct pathogenic mechanisms. This review provides current insights into the molecular mechanisms underlying the dysregulation of AMPAR diffusional trapping, emphasizing its role as a converging point for multiple pathological signaling pathways. We propose that targeting AMPAR diffusional trapping represents a promising early therapeutic strategy to mitigate synaptic plasticity and memory deficits in a spectrum of brain disorders, encompassing but not limited to HD, AD, and stress-related conditions. This approach underscores an integrated therapeutic target amidst the complexity of these neurodegenerative and neuropsychiatric diseases.

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来源期刊
Translational Neurodegeneration
Translational Neurodegeneration Neuroscience-Cognitive Neuroscience
CiteScore
19.50
自引率
0.80%
发文量
44
审稿时长
10 weeks
期刊介绍: Translational Neurodegeneration, an open-access, peer-reviewed journal, addresses all aspects of neurodegenerative diseases. It serves as a prominent platform for research, therapeutics, and education, fostering discussions and insights across basic, translational, and clinical research domains. Covering Parkinson's disease, Alzheimer's disease, and other neurodegenerative conditions, it welcomes contributions on epidemiology, pathogenesis, diagnosis, prevention, drug development, rehabilitation, and drug delivery. Scientists, clinicians, and physician-scientists are encouraged to share their work in this specialized journal tailored to their fields.
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