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Artemisinin attenuates doxorubicin induced cardiotoxicity and hepatotoxicity in rats

机译:青蒿素衰减多柔比星诱导的大鼠心脏毒性和肝毒性

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摘要

We investigated the effects of artemisinin on doxorubicin (Dox) induced heart and liver pathology in rats. We divided 49 male rats into seven groups: group 1 was the untreated control. Dox was administered intraperitoneally to groups 2, 3 and 4 on day 1. Artemisinin was administered by gavage to groups 3 and 6 at a dose of 7 mg/kg, and to groups 4 and 7 at a dose of 35 mg/kg for 14 days. Group 5 was given only 0.9% NaCl orally for 14 days. At the end of the study, heart and liver samples were collected for histopathology and immunohistochemistry. Hyperemia and slight hemorrhages were observed in both livers and hearts of rats treated with Dox only. Significant increases in caspase-3, TNF-alpha, iNOS and NF-kappa B expression were observed in the myocardial cells and hepatocytes of group 2. Significant reductions in caspase-3, TNF-alpha, iNOS and NF-kappa B expression were observed in groups 3 and 4 following artemisinin treatment compared to group 2. Artemisinin may exert protective effects against Dox induced cardiotoxicity and hepatotoxicity in rats.
机译:我们调查了青蒿素对多柔比星(DOX)诱导的大鼠心脏和肝病理学的影响。我们将49只雄性大鼠分为七组:第1组是未经处理的控制。在第1天腹膜内施用Dox。在第1天中给予第2,3和4组。用饲料以7mg / kg的剂量给予组3和6,并以35mg / kg的剂量为4和7的剂量给予Artemisinin。天。第5组仅给口服0.9%的NaCl 14天。在研究结束时,收集心脏和肝脏样品用于组织病理学和免疫组化。在用DOX治疗的大鼠的肝脏和心脏中观察到充血和轻微的出血。在M心肌细胞和肝细胞中观察到Caspase-3,TNF-α,InOS和NF-Kappa B表达的显着增加。观察到Caspase-3,TNF-α,InOS和NF-Kappa B表达的显着降低在阿尔脲素治疗后的第3组和第4组中,与第2组相比。青蒿素可能对DOX诱导的大鼠诱导的心脏毒性和肝毒性发挥保护作用。

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