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Effect of Shenmai injection on preventing the development of nitroglycerin-induced tolerance in rats

机译:参麦注射液对大鼠硝酸甘油耐受性发展的预防作用

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摘要

Long-term nitroglycerin (NTG) therapy causes tolerance to its effects attributing to increased oxidative stress and endothelial dysfunction. Shenmai injection (SMI), which is clinically used to treat cardiovascular diseases, consists of two herbal medicines, Ginseng Rubra and Ophiopogonjaponicas, and is reported to have antioxidant effects. The present study was designed to investigate the potential preventive effects of Shenmai injection on development of nitroglycerin-induced tolerance. The present study involves both in vivo and in vitro experiments to investigate nitroglycerin-induced tolerance. We examined the effect of Shenmai injection on the cardiovascular oxidative stress by measuring the serum levels of malondialdehyde (MDA) and superoxide dismutase (SOD). Endothelial dysfunction was determined by an endothelium-dependent vasorelaxation method in aortic rings and NOS activity. Inhibition of the cGMP/cGK-I signalling pathway was determined from released serum levels of cGMP and the protein expression levels of sGC, cGK-I, PDE1A and P-VASP by western blot. Here, we showed that SMI ameliorated the decrease in AV Peak Vel, the attenuation in the vasodilation response to nitroglycerin and endothelial dysfunction. SMI also reduced the cardiovascular oxidative stress by reducing the release of MDA and increasing the activity of SOD. Shenmai injection further ameliorated inhibition of the cGMP/cGK-I signalling pathway triggered by nitroglycerin-induced tolerance through up-regulating the protein expression of sGC, cGK-I, and P-VASP and down- regulating the proteins expression of PDE1A. In vitro studies showed that Shenmai injection could recover the attenuated vasodilation response to nitroglycerin following incubation (of aortic rings) with nitroglycerin via activating the enzymes of sGC and cGK-I. Therefore, we conclude that Shenmai injection could prevent NTG nitroglycerin-induced tolerance at least in part by decreasing the cardiovascular oxidative stress, meliorating the endothelial dysfunction and ameliorating the inhibition of the cGMP/cGK-I signalling pathway. These findings indicate the potential of Shenmai injection (SMI) as a promising medicine for preventing the development of nitroglycerin-induced tolerance.
机译:长期使用硝酸甘油(NTG)治疗可导致其耐受性增加,这归因于氧化应激增加和内皮功能障碍。参麦注射液(SMI)在临床上用于治疗心血管疾病,由人参Rubra和Ophiopogonjaponicas两种草药组成,据报道具有抗氧化作用。本研究旨在探讨参麦注射液对硝化甘油诱导的耐受性发展的潜在预防作用。本研究涉及体内和体外实验,以研究硝酸甘油诱导的耐受性。我们通过测量血清丙二醛(MDA)和超氧化物歧化酶(SOD)的水平检查了参麦注射液对心血管氧化应激的影响。内皮功能障碍是通过内皮依赖性血管舒张方法测定主动脉环和NOS活性的。通过western印迹从释放的血清cGMP水平和sGC,cGK-1,PDE1A和P-VASP的蛋白表达水平确定对cGMP / cGK-1信号通路的抑制。在这里,我们表明SMI改善了AV Peak Vel的降低,对硝酸甘油的血管舒张反应和内皮功能障碍的减弱。 SMI还通过减少MDA的释放和增加SOD的活性来降低心血管氧化应激。参麦注射液通过上调sGC,cGK-1和P-VASP的蛋白表达并下调PDE1A的蛋白表达,进一步减轻了由硝酸甘油诱导的耐受性触发的cGMP / cGK-1信号通路的抑制。体外研究表明,参麦注射液可以通过激活sGC和cGK-I的酶,使(主动脉环)与硝酸甘油孵育后恢复对硝酸甘油的减弱的血管舒张反应。因此,我们得出结论,参麦注射液可以至少部分通过降低心血管氧化应激,改善内皮功能障碍和改善对cGMP / cGK-1信号通路的抑制来预防NTG硝酸甘油诱导的耐受性。这些发现表明,参麦注射液(SMI)作为预防硝化甘油诱导的耐受性发展的有前途的药物的潜力。

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