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Glutathione Supplementation Attenuates Oxidative Stress and Improves Vascular Hyporesponsiveness in Experimental Obstructive Jaundice

机译:补充谷胱甘肽可减轻实验性阻塞性黄疸患者的氧化应激并改善其血管低反应性

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摘要

We investigated the protective effects and mechanism of glutathione (GSH) on vascular hyporesponsiveness induced by bile duct ligation (BDL) in a rat model. Seventy-two male Sprague-Dawley rats were randomly divided into four groups: a NS group, a GSH group, a BDL + NS group, and a BDL + GSH group. GSH was administrated into rats in the GSH and BDL + GSH groups by gastric gavage. An equal volume of normal saline was, respectively, given in the NS group and BDL + NS group. Blood was gathered for serological determination and thoracic aorta rings were isolated for measurement of isometric tension. Obstructive jaundice led to a significant increase in the serum total bilirubin, AST, and ALT levels. The proinflammatory cytokines levels (TNF-α and IL-1β), concentration of NO, and oxidative stress markers (MDA and 3-NT) were increased as well. All of those were reduced by the treatment of GSH. Meanwhile, contraction of aorta rings to NA and vasorelaxation to ACh or SNP in the BDL group rats were markedly decreased, while GSH administration reversed this change. Our findings suggested that GSH supplementation attenuated overexpressed ONOO(−) from the reaction of excessive NO with O2 ∙- and protected against obstructive jaundice-induced vascular hyporesponsiveness in rats.
机译:我们调查了大鼠模型中谷胱甘肽(GSH)对胆管结扎(BDL)诱导的血管低反应性的保护作用及其机制。将72只雄性Sprague-Dawley大鼠随机分为四组:NS组,GSH组,BDL + NS组和BDL + GSH组。通过胃管灌胃法将GSH和BDL + GSH组的大鼠服用GSH。 NS组和BDL + NS组分别给予等量的生理盐水。收集血液用于血清学测定,并分离胸主动脉环以测量等轴测张力。梗阻性黄疸导致血清总胆红素,AST和ALT水平显着增加。促炎细胞因子水平(TNF-α和IL-1β),NO浓度和氧化应激标志物(MDA和3-NT)也增加。所有这些通过GSH的治疗而减少。同时,BDL组大鼠的主动脉环收缩至NA和血管舒张至ACh或SNP明显减少,而GSH给药逆转了这一变化。我们的发现表明,GSH补充剂可减轻过量NO与O2 ∙-的反应,从而减轻过表达的ONOO(-),并防止梗阻性黄疸引起的大鼠血管低反应性。

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