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肠神经系统中的配体门控离子通道。

Ligand-gated ion channels in the enteric nervous system.

作者信息

Galligan J J

机构信息

Department of Pharmacology and Toxicology and the Neuroscience Program, Michigan State University, East Lansing 48824, USA.

出版信息

Neurogastroenterol Motil. 2002 Dec;14(6):611-23. doi: 10.1046/j.1365-2982.2002.00363.x.

Abstract

There are many cell surface receptors expressed by neurones in the enteric nervous system (ENS). These receptors respond to synaptically released neurotransmitters, circulating hormones and locally released substances. Cell surface receptors are also targets for many therapeutically used drugs. This review will focus on ligand-gated ion channels, i.e. receptors in which the ligand binding site and the ion channel are parts of a single multimeric receptor. Ligand-gated ion channels expressed by enteric nerves are: nicotinic acetylcholine receptors (nAChRs), P2X receptors, 5-hydroxytryptamine3 (5-HT3) receptors, gamma-aminobutyric acid (GABAA) receptors, N-methyl-d-aspartate (NMDA) receptors,alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptors and glycine receptors. P2X, 5-HT3 and nAChRs participate in fast synaptic transmission in S-type neurones in the ENS. Fast synaptic transmission occurs in some AH-type neurones, and AH neurones express all the ligand-gated ion channels listed above. Ligand-gated ion channels may be localized at extra-synaptic sites in some AH neurones and these extra-synaptic receptors may be useful targets for drugs that can be used to treat disorders of gastrointestinal function.

摘要

肠神经系统(ENS)中的神经元表达多种细胞表面受体。这些受体对突触释放的神经递质、循环激素和局部释放的物质作出反应。细胞表面受体也是许多治疗用药物的作用靶点。本综述将聚焦于配体门控离子通道,即配体结合位点和离子通道是单个多聚体受体一部分的受体。肠神经表达的配体门控离子通道有:烟碱型乙酰胆碱受体(nAChRs)、P2X受体、5-羟色胺3(5-HT3)受体、γ-氨基丁酸(GABAA)受体、N-甲基-D-天冬氨酸(NMDA)受体、α-氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA)受体和甘氨酸受体。P2X、5-HT3和nAChRs参与肠神经系统中S型神经元的快速突触传递。快速突触传递发生在一些AH型神经元中,并且AH神经元表达上述所有配体门控离子通道。在一些AH神经元中,配体门控离子通道可能定位于突触外位点,这些突触外受体可能是可用于治疗胃肠功能紊乱药物的有用靶点。

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