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高血压血管平滑肌细胞中钙与组胺在丝裂原活化蛋白激酶表达中的相互作用。

Cross-talking between calcium and histamine in the expression of MAPKs in hypertensive vascular smooth muscle cells.

作者信息

Edwards C, Armstrong P, Goode G, Mtshali C, Williams S, Myles E L, Washington B

机构信息

Department of Biological Sciences, Tennessee State University, Nashville, Tennessee 37209, USA.

出版信息

Cell Mol Biol (Noisy-le-grand). 2007 May 15;53(4):61-6.

Abstract

Histamine (HA) is one of many neurotransmitters that have been implicated in cardiovascular functioning. Alterations in vascular smooth muscle due to the effects of histamine have been suggested. We investigated the modulatory effect of HA on mitogen activated protein kinase (MAPK) expression, specifically extracellular regulating kinase (ERK) 1 & 2 in vascular smooth muscle cells (VSMCs) from both spontaneously hypertensive (SHR) and control Wistar Kyoto (WKY) rats. Cross-talking between calcium (Ca2+) and HA during HA-induced modulatory effect on MAPK expression in SHR VSMCs was also investigated. A stimulatory increase in expression of ERK 1 & 2 was observed to be dose and time dependent with maximum expression occurring within 5 min in both SHR and WKY VSMCs. The stimulatory increase in expression is persistent for 60 min in SHR VSMCs, whereas, in WKY cells the stimulatory effect persists for only 20 min. Mepyramine, the H1 receptor antagonist, reduced the HA-induced increase in ERK 1 & 2 significantly in SHR VSMCs. A reduction in the HA stimulated increase in ERK 1 & 2 expression was observed at 20 min of exposing cells to diltiazem, the calcium channel blocker, whereas, the calcium chelator, BAPTA effect on ERK 1 & 2 expression was observed within 5 min in SHR VSMCs. The data demonstrates that cross-talking occurs between HA stimulation and Ca2+ induction during HA-induced activation of ERK 1 & 2 in VSMCs of both cell types. Although both intracellular calcium ([Ca2+]i) and extracellular Ca2+ maybe involved in the activation of ERK 1 & 2 by HA, the dependence on [Ca2+]i is more dramatic than the dependence on extracellular Ca2+ in hypertensive cells, which may contribute to the role of HA as a risk factor of hypertension in VSMCs of the aorta.

摘要

组胺(HA)是众多与心血管功能相关的神经递质之一。有研究表明,组胺的作用会导致血管平滑肌发生改变。我们研究了HA对丝裂原活化蛋白激酶(MAPK)表达的调节作用,特别是对自发性高血压大鼠(SHR)和对照Wistar Kyoto(WKY)大鼠血管平滑肌细胞(VSMC)中细胞外调节激酶(ERK)1和2的影响。同时还研究了在SHR VSMC中,HA诱导对MAPK表达的调节作用期间钙(Ca2+)与HA之间的相互作用。在SHR和WKY VSMC中均观察到ERK 1和2表达的刺激增加呈剂量和时间依赖性,最大表达在5分钟内出现。SHR VSMC中表达的刺激增加持续60分钟,而在WKY细胞中,刺激作用仅持续20分钟。H1受体拮抗剂美吡拉敏显著降低了SHR VSMC中HA诱导的ERK 1和2的增加。在将细胞暴露于钙通道阻滞剂地尔硫卓20分钟时,观察到HA刺激的ERK 1和2表达增加有所减少,而在SHR VSMC中,钙螯合剂BAPTA对ERK 1和2表达的影响在5分钟内即可观察到。数据表明,在两种细胞类型的VSMC中,HA诱导ERK 1和2激活期间,HA刺激与Ca2+诱导之间存在相互作用。尽管细胞内钙([Ca2+]i)和细胞外Ca2+可能都参与了HA对ERK 1和2的激活,但在高血压细胞中,对[Ca2+]i的依赖性比对细胞外Ca2+的依赖性更为显著,这可能有助于解释HA在主动脉VSMC中作为高血压危险因素的作用。

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