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内皮素 -1 诱发肾上腺嗜铬细胞分泌反应的动力学

Dynamics of the secretory response evoked by endothelin-1 in adrenal chromaffin cells.

作者信息

Ohara-Imaizumi M, Kumakura K

机构信息

Life Science Institute, Sophia University, Tokyo, Japan.

出版信息

J Cardiovasc Pharmacol. 1991;17 Suppl 7:S156-8. doi: 10.1097/00005344-199100177-00043.

Abstract

Recently, we have observed that endothelin-1 (ET-1) evokes the release of catecholamines (CA) from adrenal chromaffin cells. We have investigated this secretagogue action of ET-1 on cultured adrenal chromaffin cells using a real-time monitoring system. Pulsatile exposure to ET-1 evoked transient secretory responses in a dose-dependent manner, whereas repetitive stimulation produced a rapid tachyphylaxis. This secretagogue activity was dependent on extracellular Ca2+ and was blocked by 85% by 10(-5) M nifedipine. The onset of the secretory response to ET-1 was very slow, and the duration of the response was much longer than that seen with acetylcholine (ACh). These novel dynamics may well be related to the mechanism of action of ET-1 in these cells. In addition, ET-1 produced a synergistic increase in ACh-evoked release, suggesting that ET-1 may physiologically modulate ACh-evoked CA release in adrenal chromaffin cells by a mechanism involving dihydropyridine-sensitive Ca2+ channels.

摘要

最近,我们观察到内皮素-1(ET-1)可引起肾上腺嗜铬细胞释放儿茶酚胺(CA)。我们使用实时监测系统研究了ET-1对培养的肾上腺嗜铬细胞的这种促分泌作用。脉冲式暴露于ET-1以剂量依赖的方式引起瞬时分泌反应,而重复刺激则产生快速脱敏。这种促分泌活性依赖于细胞外Ca2+,并被10(-5)M硝苯地平阻断85%。对ET-1的分泌反应起始非常缓慢,且反应持续时间比乙酰胆碱(ACh)引起的反应长得多。这些新的动力学很可能与ET-1在这些细胞中的作用机制有关。此外,ET-1使ACh诱发的释放协同增加,表明ET-1可能通过涉及二氢吡啶敏感Ca2+通道的机制在生理上调节肾上腺嗜铬细胞中ACh诱发的CA释放。

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