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菱叶梵天花提取物对异丙肾上腺素诱导的大鼠心肌坏死的心脏保护作用。

Cardioprotective effect of Sida rhomboidea. Roxb extract against isoproterenol induced myocardial necrosis in rats.

作者信息

Thounaojam Menaka C, Jadeja Ravirajsinh N, Karn Sanjay S, Shah Jigar D, Patel Dipak K, Salunke Sunita P, Padate Geeta S, Devkar Ranjitsinh V, Ramachandran A V

机构信息

Division of Phytotherapeutics and Metabolic Endocrinology, Department of Zoology, Faculty of Science, The M.S. University of Baroda, Vadodara 390002, India.

出版信息

Exp Toxicol Pathol. 2011 May;63(4):351-6. doi: 10.1016/j.etp.2010.02.010. Epub 2010 Mar 19.

Abstract

The present study investigates cardioprotective effect of Sida rhomboidea. Roxb (SR) extract on heart weight, plasma lipid profile, plasma marker enzymes, lipid peroxidation, endogenous enzymatic and non-enzymatic antioxidants and membrane bound ATPases against isoproterenol (IP) induced myocardial necrosis (MN) in rats. Rats treated with IP (85 mg/kg, s.c.) recorded significant (p<0.05) increment in heart weight, plasma lipid profile, plasma marker enzymes of cardiac damage, cardiac lipid peroxidation (LPO) and activity levels of Ca(+2) ATPase whereas there was significant (p<0.05) decrease in plasma HDL, cardiac endogenous enzymatic and non-enzymatic antioxidants, Na(+)-K(+) ATPase and Mg(+2) ATPase. Pre-treatment with SR extract (400 mg/kg per day, p.o.) for 30 consecutive days followed by IP injections on days 29th and 30th, showed significant (p<0.05) decrease in heart weight, plasma lipid profile, plasma marker enzymes of cardiac damage, cardiac lipid peroxidation, Ca(+2) ATPase and significant increase in plasma HDL, cardiac endogenous enzymatic and non-enzymatic antioxidants, Na(+)-K(+) ATPase and Mg(+2) ATPase compared to IP treated group. Hence, this study is the first scientific report on cardioprotective effect of SR against IP induced MN in rats.

摘要

本研究调查了菱叶马松子提取物对大鼠心脏重量、血脂谱、血浆标志物酶、脂质过氧化、内源性酶促和非酶促抗氧化剂以及膜结合ATP酶的心脏保护作用,该作用针对异丙肾上腺素(IP)诱导的大鼠心肌坏死(MN)。用IP(85mg/kg,皮下注射)处理的大鼠心脏重量、血脂谱、心脏损伤的血浆标志物酶、心脏脂质过氧化(LPO)以及Ca(+2)ATP酶活性水平显著(p<0.05)增加,而血浆高密度脂蛋白、心脏内源性酶促和非酶促抗氧化剂、Na(+)-K(+)ATP酶和Mg(+2)ATP酶显著(p<0.05)降低。连续30天每天口服SR提取物(400mg/kg)预处理,然后在第29天和第30天注射IP,与IP处理组相比,心脏重量、血脂谱、心脏损伤的血浆标志物酶、心脏脂质过氧化、Ca(+2)ATP酶显著(p<0.05)降低,血浆高密度脂蛋白、心脏内源性酶促和非酶促抗氧化剂、Na(+)-K(+)ATP酶和Mg(+2)ATP酶显著增加。因此,本研究是关于SR对IP诱导的大鼠MN的心脏保护作用的第一份科学报告。

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