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首页> 外文期刊>Canadian Journal of Physiology and Pharmacology >Aldose reductase inhibitors zopolrestat and ferulic acid alleviate hypertension associated with diabetes: Effect on vascular reactivity
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Aldose reductase inhibitors zopolrestat and ferulic acid alleviate hypertension associated with diabetes: Effect on vascular reactivity

机译:醛糖还原酶抑制剂佐泊司他和阿魏酸缓解与糖尿病有关的高血压:对血管反应性的影响

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This study investigated the effect of aldose reductase (AR) inhibitors on hypertension in diabetes. Diabetes was induced with streptozotocin, while AR inhibitors zopolrestat and ferulic acid were administered at 2 weeks after streptozotocin treatment and for 6 weeks afterwards. Then, blood pressure (BP) and serum level of glucose were determined. Concentration-response curves for phenylephrine (PE), KCl, and acetylcholine (ACh) were obtained in isolated aorta. In addition, ACh-induced NO and reactive oxygen species (ROS) generation in aorta and histopathology were examined. Compared with the control animals, diabetes increased diastolic and systolic BP. AR inhibitors reduced diastolic BP elevation without affecting the developed hyperglycaemia. Diabetes increased the contractile response of aorta to KCl, and decreased the relaxation response to Ach, while administering AR inhibitors prevented an impaired response to ACh. Incubation of aorta isolated from diabetic animals with AR inhibitors did not affect the impaired relaxation response to ACh. In addition, AR inhibitors negated the impaired Ach-stimulated NO generation seen in aorta isolated from diabetic animals. Furthermore, diabetes was accompanied with marked infiltration of leukocytes in aortic adventitia, endothelial cell pyknosis, and increased ROS formation. AR inhibitors reduced leukocyte infiltration and inhibited endothelial pyknosis and ROS formation. In conclusion, AR inhibitors negate diabetes-evoked hypertension via ameliorating impaired endothelial relaxation and NO production.
机译:这项研究调查了醛糖还原酶(AR)抑制剂对糖尿病高血压的影响。链脲佐菌素可诱发糖尿病,而链脲佐菌素治疗后2周和此后6周,则给予AR抑制剂zopolrestat和阿魏酸。然后,测定血压(BP)和血清葡萄糖水平。在分离的主动脉中获得去氧肾上腺素(PE),氯化钾和乙酰胆碱(ACh)的浓度-响应曲线。此外,检查了ACh诱导的主动脉NO和活性氧(ROS)的生成以及组织病理学。与对照组动物相比,糖尿病增加了舒张压和收缩压。 AR抑制剂可降低舒张压BP升高,而不会影响已发展的高血糖症。糖尿病可增加主动脉对KCl的收缩反应,并降低对Ach的舒张反应,而给予AR抑制剂可防止对ACh的反应减弱。从糖尿病动物中分离出的主动脉与AR抑制剂一起孵育不会影响对ACh的松弛反应。此外,AR抑制剂消除了从糖尿病动物分离的主动脉中Ach刺激的NO生成受损的现象。此外,糖尿病伴有主动脉外膜的白细胞显着浸润,内皮细胞固缩,以及ROS形成增加。 AR抑制剂可减少白细胞浸润并抑制内皮细胞的py缩和ROS的形成。总之,AR抑制剂通过改善受损的内皮舒张功能和NO产生来消除糖尿病诱发的高血压。

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