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首页> 外文期刊>Carbohydrate Polymers: Scientific and Technological Aspects of Industrially Important Polysaccharides >Protective effect of a polysaccharide from Salvia miltiorrhiza on isoproterenol (ISO)-induced myocardial injury in rats
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Protective effect of a polysaccharide from Salvia miltiorrhiza on isoproterenol (ISO)-induced myocardial injury in rats

机译:丹参多糖对异丙肾上腺素(ISO)致大鼠心肌的保护作用

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In this study, we investigated the cardioprotective effect of one purified polysaccharide (SMP1) from Salvia miltiorrhiza on isoproterenol (ISO)-induced myocardial infarction (MI) in rats. ISO-treated rats showed severe myocardial damage and high lipid peroxidation level, as well as decreased endogenous myocardial antioxidant function. Pretreatment with SMP1 (100 and 400 mg/kg) for 30 days significantly increased the body weight, decreased the heart weight, attenuated the serum levels of creatine kinase (CK), creatine phospokinase-MB (CK-MB), dehydrogenase (LDH), alkaline phosphate (ALP), aspartate transaminase (AST), alanine transaminase (ALT), total cholesterol, triglyceride, and LDL-cholesterol (LDL-C), along with the increased concentration of HDL-cholesterol (HDL-C). In addition, SMP1 also enhanced myocardial superoxide dismutase (SOD), catalase (CAT), and glutathione peroxidase (GPX) activities and elevated myocardial reduced glutathione (GSH) level, along with a decrease in thiobarbituric acid reactive substances (TBARS) concentration. Collectively, our results indicated that long-term oral administration of SMP1 offered significant protection against the damage induced by ISO in rat heart through enhancement of endogenous antioxidants and antihyperlipidemic activity. (C) 2015 Elsevier Ltd. All rights reserved.
机译:在这项研究中,我们调查了丹参中的一种纯化多糖(SMP1)对异丙肾上腺素(ISO)诱导的大鼠心肌梗死(MI)的心脏保护作用。经ISO治疗的大鼠表现出严重的心肌损害和高脂质过氧化水平,以及内源性心肌抗氧化功能下降。用SMP1(100和400 mg / kg)预处理30天可显着增加体重,降低心脏重量,减弱血清肌酸激酶(CK),肌酸磷酸激酶-MB(CK-MB),脱氢酶(LDH)的水平,碱性磷酸酯(ALP),天冬氨酸转氨酶(AST),丙氨酸转氨酶(ALT),总胆固醇,甘油三酸酯和LDL-胆固醇(LDL-C),以及HDL-胆固醇(HDL-C)的浓度增加。此外,SMP1还增强了心肌超氧化物歧化酶(SOD),过氧化氢酶(CAT)和谷胱甘肽过氧化物酶(GPX)的活性,并增加了心肌还原型谷胱甘肽(GSH)的水平,同时降低了硫代巴比妥酸反应性物质(TBARS)的浓度。总体而言,我们的结果表明,长期口服SMP1可通过增强内源性抗氧化剂和降血脂活性,对大鼠心脏中的ISO损伤提供显着保护。 (C)2015 Elsevier Ltd.保留所有权利。

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