Saito T, Itoh H, Chun T, Igaki T, Mori Y, Yamashita J, Doi K, Tanaka T, Inoue M, Masatsugu K, Fukunaga Y, Sawada N, Tojo K, Saito Y, Hosoya T, Nakao K
Department of Medicine and Clinical Science, Kyoto University Graduate School of Medicine, Japan.
J Cardiovasc Pharmacol. 1998;31 Suppl 1:S345-7. doi: 10.1097/00005344-199800001-00096.
To address endothelial function on vascular walls exposed to oxidative stress, we investigated the effect of oxidative stress on the secretion of endothelin-1 (ET-1) from cultured bovine carotid artery endothelial cells (BAECs). Concentrations of ET-1 in the media were measured by a specific radioimmunoassay and ET-1 mRNA expression was estimated by Northern blot analysis. Treatment of BAECs with 0.5-2.0 mM H2O2 for 3 h suppressed both ET-1 secretion and ET-1 mRNA expression in a dose-dependent manner compared to control. Attenuation of ET-1 mRNA expression by H2O2 was revealed to take place at the transcriptional level. The addition of NG-nitro-L-arginine-methyl ester (L-NAME) 10 microns, a specific nitric oxide synthase inhibitor, had no effect on H2O2-induced suppression of ET-1 mRNA expression. Suppression of ET secretion under oxidative stress observed in the present study is proposed to be a compensatory mechanism of endothelial cells to inhibit vasoconstriction and proliferation during oxidative stress.
为了研究氧化应激对血管壁内皮功能的影响,我们调查了氧化应激对培养的牛颈动脉内皮细胞(BAECs)分泌内皮素-1(ET-1)的作用。通过特异性放射免疫测定法测量培养基中ET-1的浓度,并通过Northern印迹分析估计ET-1 mRNA的表达。与对照相比,用0.5-2.0 mM H2O2处理BAECs 3小时以剂量依赖的方式抑制了ET-1的分泌和ET-1 mRNA的表达。H2O2对ET-1 mRNA表达的减弱作用发生在转录水平。添加10微摩尔的NG-硝基-L-精氨酸甲酯(L-NAME),一种特异性一氧化氮合酶抑制剂,对H2O2诱导的ET-1 mRNA表达抑制没有影响。本研究中观察到的氧化应激下ET分泌的抑制被认为是内皮细胞在氧化应激期间抑制血管收缩和增殖的一种补偿机制。