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G蛋白偶联受体在结构可塑性和认知功能调节中的作用。

Role of G Protein-Coupled Receptors in the Regulation of Structural Plasticity and Cognitive Function.

作者信息

Leung Crystal C Y, Wong Yung H

机构信息

Division of Life Science, Biotechnology Research Institute, Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong, China.

State Key Laboratory of Molecular Neuroscience, Molecular Neuroscience Center, Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong, China.

出版信息

Molecules. 2017 Jul 24;22(7):1239. doi: 10.3390/molecules22071239.

Abstract

Cognition and other higher brain functions are known to be intricately associated with the capacity of neural circuits to undergo structural reorganization. Structural remodelling of neural circuits, or structural plasticity, in the hippocampus plays a major role in learning and memory. Dynamic modifications of neuronal connectivity in the form of dendritic spine morphology alteration, as well as synapse formation and elimination, often result in the strengthening or weakening of specific neural circuits that determine synaptic plasticity. Changes in dendritic complexity and synapse number are mediated by cellular processes that are regulated by extracellular signals such as neurotransmitters and neurotrophic factors. As many neurotransmitters act on G protein-coupled receptors (GPCRs), it has become increasingly apparent that GPCRs can regulate structural plasticity through a myriad of G protein-dependent pathways and non-canonical signals. A thorough understanding of how GPCRs exert their regulatory influence on dendritic spine morphogenesis may provide new insights for treating cognitive impairment and decline in various age-related diseases. In this article, we review the evidence of GPCR-mediated regulation of structural plasticity, with a special emphasis on the involvement of common as well as distinct signalling pathways that are regulated by major neurotransmitters.

摘要

认知和其他高级脑功能与神经回路进行结构重组的能力密切相关。海马体中神经回路的结构重塑,即结构可塑性,在学习和记忆中起着重要作用。以树突棘形态改变以及突触形成和消除形式的神经元连接的动态变化,通常会导致决定突触可塑性的特定神经回路的增强或减弱。树突复杂性和突触数量的变化由细胞过程介导,这些过程受神经递质和神经营养因子等细胞外信号的调节。由于许多神经递质作用于G蛋白偶联受体(GPCR),越来越明显的是,GPCR可以通过无数G蛋白依赖性途径和非经典信号来调节结构可塑性。深入了解GPCR如何对树突棘形态发生施加调节影响,可能为治疗各种与年龄相关疾病中的认知障碍和衰退提供新的见解。在本文中,我们综述了GPCR介导的结构可塑性调节的证据,特别强调了主要神经递质调节的常见以及不同信号通路的参与。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e7b4/6152405/85c03a190370/molecules-22-01239-g001.jpg

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