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[高剂量利福平对大鼠肝脏的致脂肪变性作用]

[Liver steatogenic power of high doses of rifampicin in rats].

作者信息

Truhaut R, Claude J R, Warnet J M, Jacqueson A, Piriou A

出版信息

C R Acad Hebd Seances Acad Sci D. 1978 Feb 13;286(6):493-7.

PMID:95890
Abstract

The possible induction of fatty liver by Rifampicin has been investigated by oral administration of two different doses (200 and 400 mg/kg/24 h) of this antibiotic for a period of 8 days to male and female Rats. The results obtained are more constant and more coherent in male than in female. It is the 400 mg/kg/24 h dose which is more effective, leading to an increase of lipids, triglycerides and cholesterol in the liver and a decrease of serum triglycerides. A dose-effect relationship may exist. These preliminary data lead us to believe that Rifampicin may inhibit the synthesis of the protein moiety of lipoproteins, such as alpha-Amanitin, which is also a RNA-polymerase inhibitor.

摘要

通过对雄性和雌性大鼠口服两种不同剂量(200和400毫克/千克/24小时)的这种抗生素,持续8天,研究了利福平可能诱导脂肪肝的情况。在雄性大鼠中获得的结果比雌性大鼠更稳定、更一致。400毫克/千克/24小时的剂量更有效,导致肝脏中脂质、甘油三酯和胆固醇增加,血清甘油三酯降低。可能存在剂量效应关系。这些初步数据使我们相信,利福平可能抑制脂蛋白蛋白质部分的合成,如α-鹅膏蕈碱,它也是一种RNA聚合酶抑制剂。

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