咪康唑对小鼠细胞免疫反应和肝脏药物代谢的影响。

J Descotes, P André, R Tedone, J C Evreux
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引用次数: 1

摘要

发现咪康唑对成年瑞士小鼠的细胞免疫反应和肝脏药物代谢均有双相影响。事实上,经腹腔注射2.5或12.5 mg/kg/ 2次,咪康唑可降低绵羊红细胞延迟型超敏反应(DTH)和肝脏药物代谢(通过巴比妥酸盐睡眠时间测定)。相比之下,在相同剂量水平下,咪康唑在给药5天后可增强DTH和肝脏药物代谢。初级体液反应和胶体碳清除不受影响。尽管潜在的机制仍有待完全阐明,但这些发现清楚地表明,细胞免疫反应的调节与肝脏药物代谢酶的活性之间存在密切关系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Miconazole influence on both cellular immune response and hepatic drug metabolism in mice.

Miconazole was found to exert a biphasic influence on both cellular immune response and hepatic drug metabolism in adult Swiss mice. Indeed, at the dose of 2.5 or 12.5 mg/kg/twice daily via intraperitoneal route, miconazole depressed delayed-type hypersensitivity (DTH) to sheep red blood cells and hepatic drug metabolism as determined from barbiturate sleeping time, following one-day treatment. By contrast, at the same dose level, miconazole enhanced DTH and hepatic drug metabolism after a five-day administration schedule. Primary humoral response and colloidal carbon clearance were not affected. Although the underlying mechanism remains to be fully elucidated, these findings clearly suggest a close relation between modulation of the cellular immune response and activity of liver drug metabolizing enzymes.

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