新型肝保护剂研究中肝药物损伤的实验模拟。

Q4 Medicine
Antibiotiki i Khimioterapiya Pub Date : 2016-01-01
O V Mozhokina, N A Elistratova, L P Mikhaylova, O V Makarova
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引用次数: 0

摘要

结核病患者的有效化疗可能伴随着抗结核药物的肝保护反应。反应的频率和性质取决于药物及其在患者体内代谢的基因型和表型特征,在选择肝保护剂时应考虑这些因素。对不同乙酰化表型的大鼠进行了抗结核储备药物诱导肝损伤的实验。临床生化和形态学指标分析揭示了慢速乙酰化者和快速乙酰化者在肝损伤模拟中存在的细胞溶解机制的差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Experimental Simulation of the Liver Drug Injury for Investigation of New Hepatoprotectors.

Efficient chemotherapy of tuberculosis patients could-be complicated by hepatoprotective responses to antituberculosis drugs. The frequency and nature of the response depend on the drug and the genotypical and phenotypical characteristics of its metabolism in the patients, that should be considered while choosing the hepatoprotector. The liver injury was induced by the reserve antituberculosis drugs in experiments on rats with various acetylation phenotypes. Analysis of the clinicobiochemical and morphological indices revealed differences in the liver injury simulation: prevalence of the cytolytic mechanism in slow acetylators 'vs. the rapid ones.

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来源期刊
Antibiotiki i Khimioterapiya
Antibiotiki i Khimioterapiya Medicine-Infectious Diseases
CiteScore
0.80
自引率
0.00%
发文量
46
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