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印度素食者在利福平/异烟肼治疗期间肝混合功能氧化酶的诱导作用

Hepatic mixed function oxidase induction during rifampicin/isoniazid therapy in Indian vegetarians.

作者信息

Perry W, Jenkins M V

出版信息

Int J Clin Pharmacol Ther Toxicol. 1986 Jul;24(7):344-8.

PMID:3733284
Abstract

To determine the effect of rifampicin therapy on hepatic oxidase activity in animal protein deficient patients antipyrine and quinine t 1/2 and 6B-hydroxycortisol (6B-OHF) excretion was studied in 8 Indian vegetarians during treatment for tuberculosis. In 4 patients at the start of treatment rifampicin/streptomycin caused a steady decline in by time antipyrine t 1/2 which was complete in 3 weeks, in one patient introduction of isoniazid produced a temporary reversal. After 4 months rifampicin/isoniazid 6B-OHF excretion was increased 2 to 10 fold in all patients although one followed serially showed a marked fall when isoniazid was begun. Decline in antipyrine t 1/2 persisted in 4 patients at the end of 18 months therapy and in one of these concurrent quinine t 1/2 confirmed partial isoniazid reversal of this decline. Rifampicin-mediated mixed function oxidase induction appeared similar to that reported for non-vegetarians and largely persists with combination therapy throughout treatment. Isoniazid can act as a competitive inhibitor of hepatic oxidase activity in some patients.

摘要

为了确定利福平治疗对动物蛋白缺乏患者肝脏氧化酶活性的影响,我们对8名印度素食肺结核患者在治疗期间的安替比林和奎宁半衰期以及6β - 羟基皮质醇(6β - OHF)排泄情况进行了研究。4名患者在治疗开始时,利福平/链霉素使安替比林半衰期随时间稳步下降,3周内完成,1名患者引入异烟肼后出现暂时逆转。4个月后,所有患者的利福平/异烟肼使6β - OHF排泄增加2至10倍,尽管1名患者在开始使用异烟肼后连续检测显示显著下降。18个月治疗结束时,4名患者的安替比林半衰期持续下降,其中1名患者同时检测的奎宁半衰期证实异烟肼部分逆转了这种下降。利福平介导的混合功能氧化酶诱导作用似乎与非素食者报道的相似,并且在整个联合治疗过程中基本持续存在。在一些患者中,异烟肼可作为肝脏氧化酶活性的竞争性抑制剂。

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