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Hydrogen Sulfide Improves the Endothelial Dysfunction in Renovascular Hypertensive Rats

机译:硫化氢改善肾血管性高血压大鼠的内皮功能障碍

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As a novel gasotransmitter, hydrogen sulfide (H2S) has vasodilating and antihypertensive effects in cardiovascular system. Thus, we hypothesized that H2S might have beneficial effects on thoracic endothelial function in two-kidney one-clip (2K1C) rats, a model of renovascular hypertension. Sodium hydrosulfide (NaHS, 56 mu mol/kg/day) was administrated intra-peritoneally from the third day after the 2K1C operation. Along with the development of hypertension, the systolic blood pressure (SBP) was measured before the operation and each week thereafter. The oxidative stress was determined by measurement of malondialdehyde (MDA) concentration, superoxide dismutase (SOD) activity and protein expression of oxidative stress-related proteins (AT(1)R, NADPH oxidase subunits). Acetylcholine (ACh)-induced vasorelaxation and angiotensin II (Ang II)-induced vasocontraction were performed on isolated thoracic aorta. The SBP was significantly increased from the first week after operation, and was lowered by NaHS. NaHS supplementation ameliorated endothelial dysfunction. The protein expression of oxidative stress-related proteins were downregulated, while SOD activity upregulated. In conclusion, improvement of endothelial function is involved in the antihypertensive mechanism of H2S. The protective effect of H2S is attributable to suppression of vascular oxidative stress that involves inhibition of Ang II-AT(1)R action, downregulation of oxidases, as well as upregulation of antioxidant enzyme.
机译:硫化氢(H2S)作为一种新型的气体递质,在心血管系统中具有血管舒张和降压作用。因此,我们假设H2S可能对两肾一夹(2K1C)大鼠(一种肾血管性高血压的模型)的胸腔内皮功能有有益作用。从2K1C手术后的第三天开始腹膜内施用氢硫化钠(NaHS,56μmol / kg /天)。随着高血压的发展,在手术前和手术后的每周测量收缩压(SBP)。通过测量丙二醛(MDA)浓度,超氧化物歧化酶(SOD)活性和氧化应激相关蛋白(AT(1)R,NADPH氧化酶亚基)的蛋白表达来确定氧化应激。对孤立的胸主动脉进行乙酰胆碱(ACh)诱导的血管舒张和血管紧张素II(Ang II)诱导的血管收缩。从术后第一周开始,SBP显着升高,而NaHS降低了SBP。 NaHS补充改善了内皮功能障碍。氧化应激相关蛋白的蛋白表达下调,而SOD活性上调。总之,内皮功能的改善与H2S的降压机制有关。 H2S的保护作用可归因于血管氧化应激的抑制,其中包括抑制Ang II-AT(1)R的作用,氧化酶的下调以及抗氧化酶的上调。

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