Cardioprotective effect of water and ethanol extract of Salvia miltiorrhiza in an experimental model of myocardial infarction |
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Authors: | Zhou Ru He Li-Fen Li Yong-Jie Shen Yi Chao Ruo-Bing Du Jun-Rong |
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Affiliation: | Department of Pharmacology and Biopharmaceutics, Key Laboratory of Drug Targeting and Drug Delivery Systems Ministry of Education, West China School of Pharmacy, Sichuan University, Chengdu 610041, China |
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Abstract: |
Ethnopharmacological relevanceSalvia miltiorrhiza has long been used in the traditional Chinese formulations for the treatment of heart ischemic diseases.Aim of the studyWe investigated the cardioprotective effect of purified Salvia miltiorrhiza extract (SME) in an experimental model of acute myocardial infarction.Materials and methodsFollowing induction of acute myocardial infarction in rats by adminstration of isoproterenol, hemodynamic and electrocardiographic parameters were monitored and recorded continuously, cardiac enzymes and parameters of oxidative stress were measured, and histopathological examination of heart tissue was performed. Experiments were performed in rats treated with SME or vehicle, as well as in those treated with Fufang Danshen Tablet (FDT) as a positive control which has previously been shown to prevent myocardial ischemia.ResultsIsoproterenol-treated rats showed reductions in left ventricular systolic pressure as well as in maximum and minimum rate of developed left ventricular pressure, together with an increase in left ventricular end-diastolic pressure. They also demonstrated ST-segment elevation, together with increases in serum levels of lactate dehydrogenase, glutamic oxalacetic transaminase, creatine kinase and malondialdehyde, as well as decreases in serum activities of glutathione peroxidase and superoxide dismutase. Oral administration of SME (29.76 or 59.52 mg/kg) blunted all of the hemodynamic and biochemical changes induced by isoproterenol, as did FDT (1210 mg/kg). The protective effect of SME on isoproterenol-induced myocardial damage was further confirmed by histopathological examination.ConclusionsOur results suggest that SME affords protection against isoproterenol-induced myocardial infarction. |
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Keywords: | SME, Salvia miltiorrhiza extract FDT, Fufang Danshen Tablet MI, myocardial infarction ISO, isoproterenol LVSP, left ventricular systolic pressure LV dp/dtmax, maximum rate of developed left ventricular pressure LV dp/dtmin, minimum rate of developed left ventricular pressure LVEDP, left ventricular end-diastolic pressure MABP, mean arterial blood pressure LDH, lactate dehydrogenase GOT, glutamic oxalacetic transaminase CK, creatine kinase MDA, malondialdehyde GPx, glutathione peroxidase SOD, superoxide dismutase PAl, protocatechuic aldehyde PA, protocatechuic acid CA, caffeic acid DSS, danshensu RA, rosmarinic acid LsA, lithospermic acid SalA, salvianolic acid A SalB, salvianolic acid B ip, intraperitoneal injection H2O2, hydrogen peroxide |
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