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内皮素-1通过细胞外信号调节激酶途径激活大鼠血管平滑肌中的胞质磷脂酶A2诱导花生四烯酸释放。

Endothelin-1-induced arachidonic acid release by cytosolic phospholipase A2 activation in rat vascular smooth muscle via extracellular signal-regulated kinases pathway.

作者信息

Trevisi Lucia, Bova Sergio, Cargnelli Gabriella, Ceolotto Giulio, Luciani Sisto

机构信息

Department of Pharmacology and Anaesthesiology, University of Padua, Largo E. Meneghetti 2, 35131, Padua, Italy.

出版信息

Biochem Pharmacol. 2002 Aug 1;64(3):425-31. doi: 10.1016/s0006-2952(02)01066-3.

Abstract

The present study investigates whether endothelin-1 (ET-1), like noradrenaline (NA), stimulates the release of arachidonic acid (AA) via cytosolic phospholipase A2 (cPLA2) in rat tail artery. In tail artery segments labelled with [3H]AA, ET-1-induced AA release in a concentration-dependent manner with an EC50 of 1.3 nM. The effect of ET-1 was inhibited by bosentan and was insensitive to BQ788, suggesting the involvement of ETA receptor. The stimulation of AA release induced by ET-1 was prevented by arachydonyl trifluoromethyl ketone (AACOCF3), a selective inhibitor of cPLA2 and not by RHC80267, a diacylglycerol lipase inhibitor. Furthermore, PD98059, inhibitor of mitogen-activated protein kinase kinase (MEK) cascade and calphostin C, a protein kinase C (PKC) inhibitor, prevented the stimulation of AA release induced by ET-1 and NA. Immunoblotting of the cytosolic fraction of rat tail arteries stimulated with ET-1 or NA showed an increase in extracellular signal-regulated kinases (ERKs) phosphorylation and this effect was abolished by calphostin C treatment. These findings show that in rat tail artery ET-1 and NA induce a sequential activation of protein kinase C and extracellular signal-regulated kinases that results in stimulation of AA release via cPLA2 activation. This may represent a general pathway by which G-proteins coupled receptors stimulate AA release and its metabolites in vascular smooth muscle.

摘要

本研究调查了内皮素 -1(ET -1)是否与去甲肾上腺素(NA)一样,通过胞质磷脂酶A2(cPLA2)刺激大鼠尾动脉中花生四烯酸(AA)的释放。在用[3H]AA标记的尾动脉段中,ET -1以浓度依赖的方式诱导AA释放,EC50为1.3 nM。波生坦抑制了ET -1的作用,且其对BQ788不敏感,提示ETA受体参与其中。ET -1诱导的AA释放刺激被cPLA2的选择性抑制剂花生四烯酰三氟甲基酮(AACOCF3)所阻断,而二酰甘油脂肪酶抑制剂RHC80267则无此作用。此外,丝裂原活化蛋白激酶激酶(MEK)级联反应的抑制剂PD98059和蛋白激酶C(PKC)抑制剂钙泊三醇C,均能阻断ET -1和NA诱导的AA释放刺激。用ET -1或NA刺激的大鼠尾动脉胞质部分的免疫印迹显示,细胞外信号调节激酶(ERKs)磷酸化增加,而钙泊三醇C处理可消除这种作用。这些发现表明,在大鼠尾动脉中,ET -1和NA诱导蛋白激酶C和细胞外信号调节激酶的顺序激活,进而通过cPLA2激活刺激AA释放。这可能代表了一种普遍途径,通过该途径G蛋白偶联受体刺激血管平滑肌中AA的释放及其代谢产物的生成。

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