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胃肠道功能中的酸敏感离子通道。

Acid-sensitive ion channels in gastrointestinal function.

作者信息

Holzer Peter

机构信息

Department of Experimental and Clinical Pharmacology, University of Graz, Universitätsplatz 4, A-8010 Graz, Austria.

出版信息

Curr Opin Pharmacol. 2003 Dec;3(6):618-25. doi: 10.1016/j.coph.2003.06.008.

Abstract

Deviations from the physiological values of extracellular pH are monitored by multiple acid sensors. Acid-sensing ion channels are activated by moderate acidification, whereas transient receptor potential cation channels, notably TRPV1, are gated by severe acidosis. In contrast, ionotropic purinoceptor (P2X) ion channels, particularly P2X(2), and two-pore domain background K(+) channels, such as TASK, do not directly signal acidification but rather modulate cell membrane excitability in response to acidosis. These acid sensors, which are expressed by afferent neurons, are most relevant to the regulation of acid secretion, foregut motility and mucosal protection, as well as to gastrointestinal disturbances associated with inflammation, ischaemia and stasis.

摘要

多种酸传感器可监测细胞外pH值与生理值的偏差。酸敏感离子通道在适度酸化时被激活,而瞬时受体电位阳离子通道,尤其是TRPV1,则在严重酸中毒时被门控。相比之下,离子型嘌呤受体(P2X)离子通道,特别是P2X(2),以及双孔结构域背景钾(K+)通道,如TASK,并不直接对酸化发出信号,而是在酸中毒时调节细胞膜兴奋性。这些由传入神经元表达的酸传感器,与酸分泌、前肠运动和黏膜保护的调节最为相关,也与炎症、缺血和淤血相关的胃肠道紊乱有关。

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