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首页> 外文期刊>Acta Diabetologica >Beneficial effects of astragalus polysaccharides treatment on cardiac chymase activities and cardiomyopathy in diabetic hamsters
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Beneficial effects of astragalus polysaccharides treatment on cardiac chymase activities and cardiomyopathy in diabetic hamsters

机译:黄芪多糖治疗对糖尿病仓鼠心脏糜酶活性和心肌病的有益作用

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摘要

Over-activation of the local chymase–angiotensin II (Ang II) system has a dominant role in diabetic cardiomyopathy. Astragalus polysaccharides (APS) are used in traditional Chinese medicine to boost immunity. In this study, we investigated the effects of APS treatment on cardiac function, myocardial collagen expression, cardiac ultrastructure, cardiac matrix metalloproteinase (MMP) activity, levels of plasma glycosylated serum protein (GSP), and myocardial enzymes, and the expression of Ang II, chymase, and angiotensin-converting enzyme (ACE) in the diabetic hamster myocardium. Diabetes was induced by a single injection of streptozotocin (60 mg/kg ip). The experimental groups consisted of normal control (n = 15), diabetic (n = 15), insulin-treated diabetic (n = 15, NPH 1–2 U/day ip), and APS-treated diabetic (n = 30, APS 1–2 g/kg/day orally for 10 weeks) hamsters. Diabetic hamsters treated with insulin or APS exhibited significantly decreased blood glucose, plasma GSP, and myocardial enzymes, as well as improvements in cardiac function and cardiac ultrastructure. Compared with insulin treatment, APS treatment significantly reduced myocardial collagen (type I and III) expression and lowered cardiac MMP-2 activity, myocardial Ang II levels, myocardial chymase expression, and p-ERK1/2 kinase expression. In diabetic hamsters, myocardial ACE expression and plasma Ang II levels was not altered by insulin or APS treatment. These results indicate that treatment of diabetic hamsters with APS inhibited the local chymase–Ang II system and improved markers of diabetic cardiomyopathy.
机译:局部糜酶-血管紧张素II(Ang II)系统的过度激活在糖尿病性心肌病中起主要作用。黄芪多糖(APS)用于中药以增强免疫力。在这项研究中,我们调查了APS治疗对心脏功能,心肌胶原蛋白表达,心脏超微结构,心脏基质金属蛋白酶(MMP)活性,血浆糖基化血清蛋白(GSP)和心肌酶水平以及Ang II表达的影响,仓鼠心肌中的糜蛋白酶,糜酶和血管紧张素转换酶(ACE)。一次注射链脲佐菌素(60 mg / kg ip)可诱发糖尿病。实验组包括正常对照组(n = 15),糖尿病(n = 15),胰岛素治疗的糖尿病(n = 15,NPH 1-2 U /天ip)和APS治疗的糖尿病(n = 30,APS口服1–2 g / kg /天,持续10周)。用胰岛素或APS治疗的糖尿病仓鼠显示血糖,血浆GSP和心肌酶显着降低,并且心脏功能和心脏超微结构得到改善。与胰岛素治疗相比,APS治疗显着降低了心肌胶原(I型和III型)的表达,并降低了心脏MMP-2活性,心肌Ang II水平,心肌糜酶表达和p-ERK1 / 2激酶表达。在糖尿病仓鼠中,胰岛素或APS处理不会改变心肌ACE表达和血浆Ang II水平。这些结果表明,用APS治疗糖尿病仓鼠可抑制局部糜酶-Ang II系统并改善糖尿病性心肌病的标志物。

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