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吸烟或奥美拉唑对人十二指肠黏膜活检组织中细胞色素P4501A的诱导作用与尿苷二磷酸葡萄糖醛酸基转移酶的比较

Induction of cytochrome P4501A by smoking or omeprazole in comparison with UDP-glucuronosyltransferase in biopsies of human duodenal mucosa.

作者信息

Buchthal J, Grund K E, Buchmann A, Schrenk D, Beaune P, Bock K W

机构信息

Institute of Toxicology, University of Tübingen, Germany.

出版信息

Eur J Clin Pharmacol. 1995;47(5):431-5. doi: 10.1007/BF00196857.

Abstract

Drug-metabolizing enzymes were investigated in duodenal biopsy specimens. Cytochrome P4501A (CYP1A) activity was determined by measuring 7-ethoxyresorufin O-deethylase (EROD) activity in biopsies from 20 smokers (3-30 cigarettes per day), 21 nonsmokers, and 10 nonsmokers receiving omeprazole treatment (20-60 mg/day for at least 1 week). Omeprazole is known to act as a polycyclic aromatic hydrocarbon (PAH)-type inducer in humans. EROD activity was found to be significantly induced in smokers and omeprazole-treated patients, with medians of 2.1 and 1.1 pmol.min-1.mg protein-1, respectively, compared with 0.5 pmol.min-1.mg protein-1 in nonsmokers. Immunoblot analysis substantiated that EROD activity was correlated with CYP1A protein. In contrast, UDP-glucuronosyltransferase (UGT) activity towards 4-methylumbelliferone (an overlapping substrate of several constitutive and inducible UGTs) was not significantly affected. The results demonstrate CYP1A induction by omeprazole and by constituents of cigarette smoke in the human duodenum and support the utility of duodenal biopsies to monitor CYP1A induction by PAH-type inducers.

摘要

在十二指肠活检标本中对药物代谢酶进行了研究。通过测量20名吸烟者(每天3 - 30支香烟)、21名不吸烟者以及10名接受奥美拉唑治疗(每天20 - 60毫克,至少1周)的不吸烟者活检组织中的7 - 乙氧基异吩恶唑酮O - 脱乙基酶(EROD)活性,来确定细胞色素P4501A(CYP1A)的活性。已知奥美拉唑在人体内作为多环芳烃(PAH)型诱导剂起作用。发现吸烟者和接受奥美拉唑治疗的患者中EROD活性显著诱导,中位数分别为2.1和1.1皮摩尔·分钟⁻¹·毫克蛋白⁻¹,而不吸烟者为0.5皮摩尔·分钟⁻¹·毫克蛋白⁻¹。免疫印迹分析证实EROD活性与CYP1A蛋白相关。相比之下,针对4 - 甲基伞形酮(几种组成型和诱导型尿苷二磷酸葡萄糖醛酸基转移酶的重叠底物)的尿苷二磷酸葡萄糖醛酸基转移酶(UGT)活性没有受到显著影响。结果表明奥美拉唑和香烟烟雾成分可诱导人十二指肠中的CYP1A,并支持十二指肠活检用于监测PAH型诱导剂对CYP1A诱导作用的实用性。

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