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

Antibiotiki Pub Date : 1984-06-01
T A Bogush, S M Sitdikova
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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.

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肝单加氧酶与卡米霉素和红霉素的药效学研究。
研究了卡米霉素对肝脏单羟化酶活性的影响。研究指出,每公斤2、3和4毫克剂量的抗生素对己烯醛治疗的小鼠的睡眠时间没有影响。这意味着它不会改变酶系统的活性。5和10 mg/kg剂量的卡米霉素对肝脏单羟基酶的诱导和抑制不影响毒性作用。红霉素和阿霉素对肝单羟化酶的诱导毒性降低,对肝单羟化酶的抑制毒性增加。像阿霉素一样,红霉素降低了这个酶系统的活性。与对照组相比,5 mg/kg剂量的红霉素延长了己烯醛睡眠的持续时间几乎1.5-2倍。讨论了肝单羟基酶参与四环素类抗生素代谢转化的可能性。
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