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首页> 外文期刊>Journal of Young Pharmacists >Effect of Ethanolic Extract Fractions of Boerhaavia diffusa in Doxorubicin-induced Myocardial Toxicity in Albino Rats
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Effect of Ethanolic Extract Fractions of Boerhaavia diffusa in Doxorubicin-induced Myocardial Toxicity in Albino Rats

机译:白花蛇舌草乙醇提取物组分对阿霉素致大鼠心肌毒性的影响

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Background: Doxorubicin is a Anthracycline derivative and has proven efficacy in various malignancies. It is the most effective cytotoxic agent in current use. The clinical usefulness is limited due to its cardiac toxicity. Objectives: To study the preventive role of ethanolic extract fractions of Boerhaavia diffusa (BD) against doxorubicin (Dox) induced myocardial toxicity in albino rats. Methods: The ethanolic extract of whole plant of Boerhaavia diffusa was prepared by hot extraction method and further fractionated into Petroleum ether (PEBD), Chloroform (CLBD), Ethyl acetate (EABD) and Aqueous (AQBD) fractions by increasing in order of polarity. Cardiotoxicity was produced by cumulative administration of Dox (2.5 mg/kg, i.p. alternative day for two weeks). All four fractions (PEBD-20 mg/kg, CLBD-25 mg/kg, EABD-30 mg/kg and AQBD-25 mg/kg) and vitamin E as standard (100 mg/kg) were administered orally as pretreatment for two weeks followed by Dox on alternative days for two weeks. The general observations, biomarker enzymes like lactate dehydrogenase (LDH), Creatine kinase (CK-MB) and Troponin-I (cTnI), biochemical parameters such as aspartate aminotransferase (AST) and alanine aminotransferase (ALT) were monitored after three weeks of last dose. Myocardial toxicity was also evaluated by histopathologic studies. Results: Repeated administration of Dox-induced cardiomyopathy characterized with an increased level of biomarkers and antioxidant deficit. Pretreatment with the EABD and Vit-E significantly protected myocardium from the toxic effects of Dox by reducing the elevated level of biomarker enzymes like LDH, CK-MB, biochemical parameters such as AST and ALT, absence of cTnI and restoring of disorganized myocardial tissue to normal. Conclusion: The biomarker, biochemical and histopathological data evidently substantiate the cardioprotective effect of EABD, which could be attributed to flavanoids present in the ethyl acetate fraction.
机译:背景:阿霉素是蒽环类药物的衍生物,并已证明对多种恶性肿瘤有效。它是当前使用的最有效的细胞毒剂。由于其心脏毒性,临床上的应用受到限制。目的:研究白花蛇舌草(BD)乙醇提取物组分对阿霉素致阿霉素(Dox)心肌毒性的预防作用。方法:采用热提取法制备白花蛇舌草全株乙醇提取物,并按极性依次增加,依次分为石油醚(PEBD),氯仿(CLBD),乙酸乙酯(EABD)和水(AQBD)级分。通过累计服用Dox(2.5 mg / kg,隔日腹腔注射两周)产生心脏毒性。口服四个部分(PEBD-20 mg / kg,CLBD-25 mg / kg,EABD-30 mg / kg和AQBD-25 mg / kg)和维生素E作为标准品(100 mg / kg)进行口服治疗个星期,然后是隔天的Dox,持续两个星期。在最后三周后,对一般观察结果,诸如乳酸脱氢酶(LDH),肌酸激酶(CK-MB)和肌钙蛋白-I(cTnI)等生物标记酶,天冬氨酸转氨酶(AST)和丙氨酸转氨酶(ALT)等生化参数进行了监测。剂量。还通过组织病理学研究评估了心肌毒性。结果:重复给药Dox引起的心肌病,其特征在于生物标志物水平增加和抗氧化剂缺乏。 EABD和Vit-E预处理可通过降低生物标志物酶(如LDH,CK-MB)水平升高,生化参数(如AST和ALT),cTnI缺失以及心肌组织紊乱恢复到高水平,从而显着保护心肌免受Dox的毒性作用。正常。结论:生物标志物,生化和组织病理学数据明显证实了EABD的心脏保护作用,这可能归因于乙酸乙酯级分中存在的类黄酮。

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