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冠状小静脉内皮细胞的氧化损伤会耗尽细胞内谷胱甘肽并诱导热休克蛋白70信使核糖核酸的产生。

Oxidative injury of coronary venular endothelial cells depletes intracellular glutathione and induces HSP 70 mRNA.

作者信息

Aucoin M M, Barhoumi R, Kochevar D T, Granger H J, Burghardt R C

机构信息

Department of Veterinary Anatomy and Public Health, Texas A & M University, College Station 77843, USA.

出版信息

Am J Physiol. 1995 Apr;268(4 Pt 2):H1651-8. doi: 10.1152/ajpheart.1995.268.4.H1651.

Abstract

Vascular endothelium is one of the first tissues exposed to reactive oxygen species produced during myocardial ischemia-reperfusion. Bovine coronary venular endothelial cells (CVEC) were evaluated for intracellular glutathione (GSH) levels and heat shock protein 70 (HSP 70) mRNA and protein during in vitro oxidative stress. CVEC were incubated with 0.01875 U/ml xanthine oxidase (XO) and 0.5 mM hypoxanthine (HX) for 30 min and then allowed to recover for 0, 1, 2, or 3 h. Relative GSH levels were determined by evaluation of monochlorobimane fluorescence. GSH fluorescence was significantly lower in CVEC treated with XO+HX for 30 min than in controls. GSH fluorescence was also decreased in heat-shocked CVEC. After oxidative stress, GSH levels were higher than in controls at 1 h, but by 2 or 3 h after treatment, GSH fluorescence fell below control values. HSP 70 mRNA was induced in CVEC by a 30-min treatment with XO+HX exposure. These data suggest that CVEC respond to oxidative stress by reducing intracellular GSH levels and inducing HSP 70 mRNA, although significant increases in HSP 70 protein were not detected at the time points tested.

摘要

血管内皮是心肌缺血再灌注期间最早接触活性氧的组织之一。在体外氧化应激期间,对牛冠状动脉小静脉内皮细胞(CVEC)的细胞内谷胱甘肽(GSH)水平、热休克蛋白70(HSP 70)mRNA和蛋白进行了评估。将CVEC与0.01875 U/ml黄嘌呤氧化酶(XO)和0.5 mM次黄嘌呤(HX)孵育30分钟,然后使其恢复0、1、2或3小时。通过评估单氯双氢杨梅素荧光来测定相对GSH水平。用XO+HX处理30分钟的CVEC中的GSH荧光显著低于对照组。热休克的CVEC中的GSH荧光也降低。氧化应激后,1小时时GSH水平高于对照组,但处理后2或3小时,GSH荧光降至对照值以下。用XO+HX处理30分钟可诱导CVEC中HSP 70 mRNA。这些数据表明,CVEC通过降低细胞内GSH水平和诱导HSP 70 mRNA来应对氧化应激,尽管在所测试的时间点未检测到HSP 70蛋白的显著增加。

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