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乙醇给药后体外肝微粒体药物代谢的增强

Enhancement of hepatic microsomal drug metabolism in vitro following ethanol administration.

作者信息

Ioannides C, Lake B G, Parke D V

出版信息

Xenobiotica. 1975 Nov;5(11):665-76. doi: 10.3109/00498257509056136.

Abstract
  1. Administration of ethanol intraperitoneally at low dosages (10-25 mg/kg) to rats stimulates hepatic microsomal mixed-function oxidase activity in vitro. 2. Pretreatment with ethanol administered orally has no effect on in vivo drug metabolism as measured by pentobarbitone plasma half-life and has no effect on the excretion of ascorbic acid. Ethanol administration does not enhance its own binding to cytochrome P-450. 3. These observations suggest that the administration of ethanol, at moderate dosage, does not give rise to induction of hepatic cytochrome P-450. 4. Unwashed hepatic microsomes are contaminated with alcohol dehydrogenase, but pretreatment with ethanol does not increase microsomal generation of NADH. 5. Pretreatment with ethanol has no stimulatory effect on NADH-NADP+ transhydrogenation. 6. The stimulation of hepatic drug metabolism in vitro following administration of ethanol is not due to increased cytochrome P-450 nor to increased NADPH, per se, but appears to result from an increase in the activity of NADPH-cytochrome c reductase.
摘要
  1. 给大鼠腹腔注射低剂量(10 - 25毫克/千克)乙醇,可在体外刺激肝微粒体混合功能氧化酶活性。2. 通过戊巴比妥血浆半衰期测定,口服乙醇预处理对体内药物代谢无影响,对维生素C排泄也无影响。乙醇给药不会增强其自身与细胞色素P - 450的结合。3. 这些观察结果表明,中等剂量乙醇给药不会引起肝细胞色素P - 450的诱导。4. 未洗涤的肝微粒体被乙醇脱氢酶污染,但乙醇预处理不会增加微粒体NADH的生成。5. 乙醇预处理对NADH - NADP⁺转氢作用无刺激作用。6. 乙醇给药后体外肝药物代谢的刺激并非由于细胞色素P - 450增加,也非由于NADPH本身增加,而是似乎源于NADPH - 细胞色素c还原酶活性的增加。

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