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平滑肌中的兰尼碱受体

Ryanodine receptors in smooth muscle.

作者信息

Guerrero-Hernández Agustín, Gómez-Viquez Leticia, Guerrero-Serna Guadalupe, Rueda Angélica

机构信息

Departamento de Bioquímica, CINVESTAV-IPN, México D.F. 07000, México.

出版信息

Front Biosci. 2002 Jul 1;7:d1676-88. doi: 10.2741/a871.

Abstract

The sarcoplasmic reticulum (SR) of smooth muscle is endowed with two different types of Ca2+ release channels, i.e. inositol 1,4,5-trisphosphate receptors (IP3Rs) and ryanodine receptors (RyRs). In general, both release channels mobilize Ca2+ from the same internal store in smooth muscle. While the importance of IP3Rs in agonist-induced contraction is well established, the role of RyRs in excitation-contraction coupling of smooth muscle is not clear. The participation of smooth muscle RyRs in the amplification of Ca2+ transients induced by either opening of Ca2+-permeable channels or IP3-triggered Ca2+ release has been studied. The efficacy of both processes to activate RyRs by calcium-induced calcium release (CICR) is highly variable and not widely present in smooth muscle. Although RyRs in smooth muscle generate Ca2+ sparks that are similar to those observed in striated muscles, the contribution of these local Ca2+ events to depolarization-induced global rise in [Ca2+]i is rather limited. Recent data suggest that RyRs are involved in regulating the luminal [Ca2+] of SR and also in smooth muscle relaxation. This review summarizes studies that were carried out mainly in muscle strips or in freshly isolated myocytes, and that were aimed to determine the physiological role of RyRs in smooth muscle.

摘要

平滑肌的肌浆网(SR)具有两种不同类型的Ca2+释放通道,即肌醇1,4,5-三磷酸受体(IP3Rs)和兰尼碱受体(RyRs)。一般来说,这两种释放通道都从平滑肌的同一内部储存库中动员Ca2+。虽然IP3Rs在激动剂诱导的收缩中的重要性已得到充分证实,但RyRs在平滑肌兴奋-收缩偶联中的作用尚不清楚。人们已经研究了平滑肌RyRs在由Ca2+通透通道开放或IP3触发的Ca2+释放所诱导的Ca2+瞬变放大中的参与情况。这两个过程通过钙诱导钙释放(CICR)激活RyRs的效能变化很大,且在平滑肌中并不广泛存在。尽管平滑肌中的RyRs产生的Ca2+火花与在横纹肌中观察到的相似,但这些局部Ca2+事件对去极化诱导的[Ca2+]i全局升高的贡献相当有限。最近的数据表明,RyRs参与调节SR的腔内[Ca2+],也参与平滑肌舒张。这篇综述总结了主要在肌条或新鲜分离的心肌细胞中进行的研究,这些研究旨在确定RyRs在平滑肌中的生理作用。

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