Pohl R J, Philpot R M, Fouts J R
Drug Metab Dispos. 1976 Sep-Oct;4(5):442-50.
A microsomal fraction, prepared from mouse skin, catalyzed the hydroxylation of benzpyrene and aniline and the deethylation of 7-ethoxycoumarin. Contamination of the preparation by cytochrome oxidase and cytochrome P-420 was determined by spectral analysis. The enzyme activities studied in mouse skin (Swiss-Webster CD-1) did not respond to topical application of 3-MC. Twenty-four hours after topical application of TCDD to mice, microsomes from skin had 50% greater benzpyrene hydroxylase and 7-ethoxycoumarin deethylase activity, and 4- to 8-fold greater activity of these enzymes was seen after 72 hr. Increases in cytochrome P-450 content of skin microsomes could be demonstrated 24 and 72 hr after topical TCDD treatment of mice. Cholate treatment (solubilization) of skin microsomes, followed by centrifugation, removed the contaminating cytochrome oxidase. Quantitative and qualitative analyses of cytochrome P-450 difference spectra were made from the solubilized preparations.
从小鼠皮肤制备的微粒体部分催化了苯并芘和苯胺的羟基化以及7-乙氧基香豆素的脱乙基反应。通过光谱分析确定了该制剂中细胞色素氧化酶和细胞色素P-420的污染情况。在小鼠皮肤(瑞士-韦伯斯特CD-1)中研究的酶活性对局部应用3-甲基胆蒽没有反应。给小鼠局部应用2,3,7,8-四氯二苯并对二恶英24小时后,皮肤微粒体中的苯并芘羟化酶和7-乙氧基香豆素脱乙基酶活性增加了50%,72小时后这些酶的活性增加了4至8倍。在给小鼠局部应用2,3,7,8-四氯二苯并对二恶英24小时和72小时后,可以证明皮肤微粒体中细胞色素P-450含量增加。用胆酸盐处理(增溶)皮肤微粒体,然后离心,去除了污染的细胞色素氧化酶。对增溶制剂进行了细胞色素P-450差光谱的定量和定性分析。