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细胞色素P-450作为大鼠药物代谢性别差异的一个决定因素。

Cytochrome P-450 as a determinant of sex difference of drug metabolism in the rat.

作者信息

Kato R, Kamataki T

出版信息

Xenobiotica. 1982 Nov;12(11):787-800. doi: 10.3109/00498258209038950.

Abstract
  1. Recent advances in the studies of sex-related differences of drug metabolism in the rat are described. Experiments with novel substrates have provided new insights into the sex differences of drug metabolism. 2. One of each form of cytochrome P-450, P-450-male and P-450-female, from liver microsomes of male and female rats, respectively, were purified to electrophoretic homogeneity. 3. These forms of cytochrome P-450 are distinguishable from each other in their catalytic, physical and immunochemical properties. 4. The use of antibodies to the two forms of cytochrome P-450 shows that P-450-male and P-450-female, present in rat-liver microsomes, are dependent on sex hormones. 5. In addition, evidence for the involvement of multiple forms of cytochrome P-450 in the occurrence of the sex difference has been presented.
摘要
  1. 本文描述了大鼠药物代谢性别差异研究的最新进展。使用新型底物的实验为药物代谢的性别差异提供了新的见解。2. 分别从雄性和雌性大鼠的肝脏微粒体中纯化出细胞色素P-450的每种形式,即P-450-雄性和P-450-雌性,使其达到电泳纯。3. 这些细胞色素P-450形式在催化、物理和免疫化学性质上彼此不同。4. 使用针对两种细胞色素P-450形式的抗体表明,大鼠肝脏微粒体中的P-450-雄性和P-450-雌性依赖于性激素。5. 此外,还提出了多种细胞色素P-450形式参与性别差异发生的证据。

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