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巯基试剂对大鼠肝细胞原代培养物中苯胺代谢物4-氨基苯酚及其硫酸盐和葡糖醛酸共轭物形成的影响。

Effects of sulphydryl reagents on the formation of the aniline metabolite 4-aminophenol and its sulphate and glucuronide conjugates in primary cultures of rat hepatocytes.

作者信息

Boot J H, Van Holsteijn C W, Seinen W, Blaauboer B J

机构信息

Research Institute of Toxicology (RITOX), University of Utrecht, The Netherlands.

出版信息

Xenobiotica. 1989 Nov;19(11):1267-73. doi: 10.3109/00498258909043178.

Abstract
  1. The effects of various sulphydryl-blocking reagents on aniline biotransformation and cytochrome P-450 levels were studied in cultured rat hepatocytes. 2. Exposure of aniline-metabolizing hepatocytes to p-chloro-mercuribenzoate (PCMB) or p-chloromercuribenzenesulphonic acid (PCMBS) resulted in decreased levels of cytochrome P-450, decreased glucuronidation of 4-aminophenol and increased levels of free 4-aminophenol. 3. Incubation of aniline-metabolizing hepatocytes with disulfiram resulted in decreased formation of 4-aminophenol, but this was not associated with impaired glucuronidation or cytochrome P-450 levels. 4. Exposure of aniline-metabolizing hepatocytes to mersalyl, 2,2'-dithiodipyridine (DTP), 6,6'-carboxydipyridine disulphide (CPDS) or N-ethylmaleimide did not affect the biotransformation of aniline or cytochrome P-450 levels. 5. Metyrapone prevented degradation of cytochrome P-450. Exposure of cells to SKF-525 A inhibited aniline biotransformation without altering cytochrome P-450 levels. 6. PCMB and PCMBS inhibited aniline metabolism, probably by binding to a cysteinyl-SH residue in cytochrome P-450 apoenzyme and 'active sites' of UDP-glucuronyl transferases. Disulfiram inhibited aniline biotransformation, probably indirectly by diminishing NADPH.
摘要
  1. 在培养的大鼠肝细胞中研究了各种巯基阻断剂对苯胺生物转化和细胞色素P - 450水平的影响。2. 将代谢苯胺的肝细胞暴露于对氯汞苯甲酸(PCMB)或对氯汞苯磺酸(PCMBS)会导致细胞色素P - 450水平降低、4 - 氨基酚葡萄糖醛酸化减少以及游离4 - 氨基酚水平升高。3. 用双硫仑孵育代谢苯胺的肝细胞会导致4 - 氨基酚形成减少,但这与葡萄糖醛酸化受损或细胞色素P - 450水平无关。4. 将代谢苯胺的肝细胞暴露于汞撒利、2,2'-二硫代二吡啶(DTP)、6,6'-羧基二吡啶二硫化物(CPDS)或N - 乙基马来酰亚胺不会影响苯胺的生物转化或细胞色素P - 450水平。5. 甲吡酮可防止细胞色素P - 450降解。将细胞暴露于SKF - 525 A可抑制苯胺生物转化而不改变细胞色素P - 450水平。6. PCMB和PCMBS可能通过与细胞色素P - 450脱辅基酶中的半胱氨酰 - SH残基以及UDP - 葡萄糖醛酸基转移酶的“活性位点”结合来抑制苯胺代谢。双硫仑可能通过减少NADPH间接抑制苯胺生物转化。

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