Trevisi Lucia, Bova Sergio, Cargnelli Gabriella, Ceolotto Giulio, Luciani Sisto
Department of Pharmacology and Anaesthesiology, University of Padua, Largo E. Meneghetti 2, 35131, Padua, Italy.
Biochem Pharmacol. 2002 Aug 1;64(3):425-31. doi: 10.1016/s0006-2952(02)01066-3.
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.
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。