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组胺 H1 受体激活诱发的 Ca(2+)信号可被人主动脉平滑肌细胞中前列腺素 EP2 和 EP4 受体的激活所减弱。

Ca(2+) signals evoked by histamine H1 receptors are attenuated by activation of prostaglandin EP2 and EP4 receptors in human aortic smooth muscle cells.

机构信息

Department of Pharmacology, University of Cambridge, Cambridge, UK.

出版信息

Br J Pharmacol. 2013 Aug;169(7):1624-34. doi: 10.1111/bph.12239.

Abstract

BACKGROUND AND PURPOSE

Histamine and prostaglandin E2 (PGE2 ), directly and via their effects on other cells, regulate the behaviour of vascular smooth muscle (VSM), but their effects on human VSM are incompletely resolved.

EXPERIMENTAL APPROACH

The effects of PGE2 on histamine-evoked changes in intracellular free Ca(2+) concentration ([Ca(2+) ]i ) and adenylyl cyclase activity were measured in populations of cultured human aortic smooth muscle cells (ASMCs). Selective ligands of histamine and EP receptors were used to identify the receptors that mediate the responses.

KEY RESULTS

Histamine, via H1 receptors, stimulates an increase in [Ca(2+) ]i that is entirely mediated by activation of inositol 1,4,5-trisphosphate receptors. Selective stimulation of EP2 or EP4 receptors attenuates histamine-evoked Ca(2+) signals, but the effects of PGE2 on both Ca(2+) signals and AC activity are largely mediated by EP2 receptors.

CONCLUSIONS AND IMPLICATIONS

Two important inflammatory mediators, histamine via H1 receptors and PGE2 acting largely via EP2 receptors, exert opposing effects on [Ca(2+) ]i in human ASMCs.

摘要

背景与目的

组胺和前列腺素 E2(PGE2)可直接作用于血管平滑肌(VSM)或通过对其他细胞的影响来调节 VSM 的功能,但它们对人 VSM 的作用尚未完全阐明。

实验方法

本研究采用培养的人主动脉平滑肌细胞(ASMCs)群体,检测 PGE2 对组胺诱导的细胞内游离 Ca2+浓度([Ca2+]i)变化和腺苷酸环化酶活性的影响。采用选择性的组胺和 EP 受体激动剂来鉴定介导这些反应的受体。

主要结果

组胺通过 H1 受体刺激 [Ca2+]i 的增加,该反应完全由三磷酸肌醇受体的激活介导。选择性刺激 EP2 或 EP4 受体可减弱组胺诱导的 Ca2+信号,但 PGE2 对 Ca2+信号和 AC 活性的影响主要通过 EP2 受体介导。

结论与意义

两种重要的炎症介质,通过 H1 受体的组胺和主要通过 EP2 受体发挥作用的 PGE2,对人 ASMCs 的 [Ca2+]i 产生相反的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a97a/3724117/33caa53e928c/bph0169-1624-f1.jpg

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