Cyclosporine administration decreases liver vitamin A stores in normal and vitamin A-deficient rats.

Drug-nutrient interactions Pub Date : 1987-01-01
V Azaïs, F Rachman, S Gros, G Pascal, O Amédée-Manesme
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Abstract

Thirty-four Wistar rats were fed a marginal or normal vitamin A diet and received daily for 14 days an intragastric intubation of oil supplemented with 0, 20, or 60 mg X kg-1 of cyclosporine A. The hepatic content and concentration of vitamin A were significantly decreased by cyclosporine treatment, whereas no modification occurred in kidney or serum vitamin A levels. No induction of hepatic cytochrome P-450 was observed in treated animals. These results suggest that cyclosporine interferes with vitamin A stores; thus, vitamin A supplementation may be useful in patients receiving cyclosporine therapy. Drug-metabolizing enzymes, which are cytochrome P-450 dependent, did not seem to be involved in the hepatic vitamin A decrease observed.

环孢素可降低正常和维生素A缺乏大鼠肝脏中维生素A的储存。
34只Wistar大鼠饲喂少量维生素a或正常维生素a饮食,并每天接受添加0、20或60 mg X kg-1环孢素a的油的灌胃,持续14天。环孢素处理显著降低了肝脏维生素a的含量和浓度,而肾脏和血清维生素a水平未发生改变。未观察到肝细胞色素P-450的诱导作用。这些结果表明环孢素干扰维生素A的储存;因此,补充维生素A可能对接受环孢素治疗的患者有用。依赖于细胞色素P-450的药物代谢酶似乎与肝脏维生素A的减少无关。
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