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脑内嘌呤能信号转导导论。

Introduction to Purinergic Signalling in the Brain.

机构信息

Autonomic Neuroscience Centre, University College Medical School, Royal Free Campus, Rowland Hill Street, NW3 2PF, London, UK.

出版信息

Adv Exp Med Biol. 2020;1202:1-12. doi: 10.1007/978-3-030-30651-9_1.

Abstract

ATP is a cotransmitter with glutamate, noradrenaline, GABA, acetylcholine and dopamine in the brain. There is a widespread presence of both adenosine (P1) and P2 nucleotide receptors in the brain on both neurons and glial cells. Adenosine receptors play a major role in presynaptic neuromodulation, while P2X ionotropic receptors are involved in fast synaptic transmission and synaptic plasticity. P2Y G protein-coupled receptors are largely involved in presynaptic activities, as well as mediating long-term (trophic) signalling in cell proliferation, differentiation and death during development and regeneration. Both P1 and P2 receptors participate in neuron-glial interactions. Purinergic signalling is involved in control of cerebral vascular tone and remodelling and has been implicated in learning and memory, locomotor and feeding behaviour and sleep. There is increasing interest in the involvement of purinergic signalling in the pathophysiology of the CNS, including trauma, ischaemia, epilepsy, neurodegenerative diseases, neuropsychiatric and mood disorders, and cancer, including gliomas.

摘要

三磷酸腺苷(ATP)是大脑中谷氨酸、去甲肾上腺素、γ-氨基丁酸、乙酰胆碱和多巴胺的共递质。在大脑中,神经元和神经胶质细胞上广泛存在腺苷(P1)和 P2 核苷酸受体。腺苷受体在突触前神经调制中起主要作用,而 P2X 离子型受体则参与快速突触传递和突触可塑性。P2Y G 蛋白偶联受体主要参与突触前活动,并在发育和再生过程中参与细胞增殖、分化和死亡的长期(营养)信号转导。P1 和 P2 受体都参与神经元-神经胶质相互作用。嘌呤能信号参与控制脑血管张力和重塑,并与学习和记忆、运动和摄食行为以及睡眠有关。嘌呤能信号在中枢神经系统的病理生理学中的作用越来越受到关注,包括创伤、缺血、癫痫、神经退行性疾病、神经精神和情绪障碍以及癌症,包括神经胶质瘤。

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