3-morpholinosyndnonimine inhibits 5-hydroxytryptamine-induced phosphorylation of nitric oxide synthase in endothelial cells

被引:0
|
作者
Richardson, SM
Maleque, MA
Motley, ED
机构
[1] Meharry Med Coll, Dept Physiol, Nashville, TN 37208 USA
[2] Meharry Med Coll, Dept Pharmacol, Nashville, TN 37208 USA
关键词
peroxynitrite; endothelial nitric oxide synthase; bovine aortic endothelial cells; 3-morpholinosyndnonimine; 5-hydroxytryptamine;
D O I
暂无
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
5-Hydroxytryptamine (5-HT) is a vasoactive substance that is taken up by endothelial cells to activate endothelial nitrite oxide synthase (eNOS). The activation of eNOS results in the production of nitric oxide (NO), which is responsible for vasodilation of blood vessels. NO also interacts with superoxide anion (O-2(-)) to form peroxynitrite (ONOO-), a potent oxidant that has been shown to induce vascular endothelial dysfunction. We examined the ability of 3-morpholinosyndnonimine (SIN-1), an ONOO- generator, to inhibit 5-HT-induced phosphorylation of eNOS in cultured bovine aortic endothelial cells (BAECs). We observed that 5-HT phosphorylates Ser(1179) eNOS in a time- and concentration-dependent manner. Maximum phosphorylation occurred at 30 sec using a concentration of 1.0 muM 5-HT. BAECs treated with SIN-1 (1-1000 muM) for 30 min showed no significant increase in eNOS phosphorylation. However, 5-HT-induced eNOS phosphorylation was inhibited in cells treated with various concentrations of SIN-1 for 30 min and stimulated with 5-HT. These data suggest that an increase in ONOO- as a result of an increase in the production of O-2(-), may feedback to inhibit 5-HT-induced eNOS phosphorylation at Ser(1179) and therefore, contribute to endothelial dysfunction associated with cardiovascular diseases.
引用
收藏
页码:1385 / 1389
页数:5
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