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Amelioration of thioacetamide-induced liver toxicity in Wistar rats by rutin

机译:芦丁可改善硫代乙酰胺诱导的Wistar大鼠肝脏毒性

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This study was designed to evaluate the effect of rutin on hepatotoxicity induced by thioacetamide (TAA) in rats. Four groups of male Wistar rats consisting of six rats each were used: Group I: control group; Group II: rats receiving single injection of 300?mg?kg ? 1?body weight of TAA intraperitoneally; Group III: rats administered rutin (10?mg?kg ? 1?body weight) dissolved in saline orally for 2?weeks; and Group IV: rats administered rutin (10?mg?kg ? 1?body weight) dissolved in saline orally for 2?weeks followed by TAA injection last day of second week. All groups were sacrificed after 24?h of treatment and hepatic toxicity was analyzed with respect to liver toxicity markers, liver DNA fragmentation, and histology of liver tissue. Administration of TAA in Wistar rats resulted in significant increase of hepatic markers, DNA fragmentation in the hepatocytes, and changes in histology. Pretreatment of rats with rutin before 2?weeks of TAA assault resulted in the complete reversal of TAA-mediated hepatic toxicity (P P
机译:本研究旨在评估芦丁对硫代乙酰胺(TAA)诱导的大鼠肝毒性的影响。使用四组雄性Wistar大鼠,每组六只大鼠。第二组:大鼠单次注射300?mg?kg ?腹膜内TAA的体重为1 ;第三组:大鼠口服溶于生理盐水中的芦丁(10?mg?kg ?1 ?体重)2周。第四组:给大鼠口服溶于生理盐水中的芦丁(10?mg?kg ?1 ?体重)2周,然后在第二周的最后一天注射TAA。治疗24小时后将所有组处死,并就肝毒性标志物,肝DNA片段化和肝组织的组织学分析肝毒性。在Wistar大鼠中施用TAA导致肝标记物显着增加,肝细胞DNA片段化以及组织学改变。在TAA攻击2周前对芦丁进行预处理可完全逆转TAA介导的肝毒性(P P

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