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Characterization of a rat model of moderate liver dysfunction based on alpha-naphthylisothiocyanate-induced cholestasis

机译:基于α-萘硫代噻噻烷酸甲酯诱导的胆汁淤积的中度肝功能障碍大鼠模型的表征

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摘要

Plasma amino acid level changes occur in mild, moderate and severe stages of liver injury in human patients. In animal models, however, data are mainly restricted to severe liver injury models in rats. Here we present the characterization of a rat model of moderate liver dysfunction secondary to alpha-napthylisothiocyanate (ANIT)-induced cholestasis. Rats treated with 30 mg/kg/day ANIT for 3 weeks exhibited a time-dependent increase in plasma alanine aminotransferase (ALT), aspartate aminotransferase (AST) and bilirubin levels and a decrease in albumin concentration. According to a liver dysfunction evaluation based on the human Child-Pugh-Score, animals developed a moderate liver dysfunction in the first two weeks of ANIT treatment, while only a mild dysfunction was observed at the end of week 3 despite ongoing ANIT administration. Univariate analysis of branched-chain amino acid plasma levels indicated that reduced levels of branched chain amino acids were associated with the ANIT treatment. These data may set the stage for further research of amino acid disturbances and requirements in non-severe cholestasis.
机译:血浆氨基酸水平变化发生在人类患者肝损伤中的轻度,中度和严重阶段。然而,在动物模型中,数据主要仅限于大鼠的严重肝损伤模型。在这里,我们介绍了中等肝功能障碍的大鼠模型对α-萘二硫氰酸盐(Anit)诱导的胆汁淤积酶。用30mg / kg /天anit处理的大鼠3周,表现出血浆丙氨酸氨基转移酶(ALT),天冬氨酸氨基转移酶(AST)和胆红素水平的时间依赖性增加,并且白蛋白浓度降低。根据基于人类儿童-PUGH评分的肝功能障碍评估,动物在ANIT治疗的前两周发育了中度肝功能障碍,而尽管持续的ANIT管理,但在第3周结束时只观察到轻度功能障碍。分支链氨基酸血浆水平的单变量分析表明,降低的支链氨基酸水平与ANIT治疗有关。这些数据可以设定阶段,以进一步研究氨基酸干扰和在非严重胆汁淤积中的要求。

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