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[肝脏单加氧酶与洋红霉素和柔红霉素的药效学]

[Liver mono-oxygenases and the pharmacodynamics of carminomycin and rubomycin].

作者信息

Bogush T A, Sitdikova S M

出版信息

Antibiotiki. 1984 Jun;29(6):446-50.

PMID:6476808
Abstract

The effect of carminomycin on the activity of liver monohydroxygenases was estimated. It mas noted that in doses of 2, 3 and 4 mg/kg the antibiotic had no effect on the sleep duration in mice treated with hexenal. This meant that it did not change the activity of the enzymatic system. Induction and inhibition of liver monohydroxygenases did not influence the toxic effect of carminomycin used in doses of 5 and 10 mg/kg. It was also shown that the toxicity of both rubomycin and adriamycin decreased on induction and increased on inhibition of liver monohydroxygenases. Like adriamycin rubomycin lowered the activity of this enzymatic system. Administration of rubomycin in a dose of 5 mg/kg prolonged the duration of the hexenal sleep almost 1.5-2 times as compared to the control. The possible participation of liver monohydroxygenases in metabolic transformations of the antracycline antibiotics is discussed.

摘要

评估了卡米诺霉素对肝脏单加氧酶活性的影响。注意到,在2、3和4毫克/千克的剂量下,该抗生素对用己烯醛处理的小鼠的睡眠时间没有影响。这意味着它没有改变酶系统的活性。肝脏单加氧酶的诱导和抑制并不影响5和10毫克/千克剂量的卡米诺霉素的毒性作用。还表明,柔红霉素和阿霉素的毒性在肝脏单加氧酶诱导时降低,在抑制时增加。与阿霉素一样,柔红霉素降低了该酶系统的活性。与对照组相比,以5毫克/千克的剂量施用柔红霉素使己烯醛睡眠时间延长了近1.5至2倍。讨论了肝脏单加氧酶可能参与蒽环类抗生素的代谢转化。

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