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- W2016667458 abstract "Endothelial nitric oxide synthase (eNOS) produces nitric oxide (NO), which is involved in various physiological functions of the cardiovascular system. eNOS is activated by dephosphorylation at Thr495 and phosphorylation at Ser1177. Inhibition of Rho-kinase, an effector of the small GTPase RhoA, leads to activation of Akt/PKB, which phosphorylates eNOS at Ser1177 and thereby promotes NO production. However, little is known about the effects of Rho-kinase on phosphorylation of Thr495. We here found that the constitutively active form of Rho-kinase phosphorylated eNOS at Thr495 in vitro. Expression of the constitutively active form of RhoA or Rho-kinase increased this phosphorylation in COS-7 cells. Addition of thrombin to cultured human umbilical vein endothelial cells induced phosphorylation of eNOS at Thr495. Treatment with Y27632, a Rho-kinase inhibitor, suppressed thrombin-induced phosphorylation at Thr495. These results indicate that Rho-kinase can directly phosphorylate eNOS at Thr495 to suppress NO production in endothelium." @default.
- W2016667458 created "2016-06-24" @default.
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- W2016667458 date "2006-01-01" @default.
- W2016667458 modified "2023-09-27" @default.
- W2016667458 title "Tu-P7:168 Endothelial function in patients with significant coronary artery stenosis: Interrelation with coronary stenosis index, lipid and insulin level" @default.
- W2016667458 doi "https://doi.org/10.1016/s1567-5688(06)80874-3" @default.
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