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尿苷二磷酸葡萄糖醛酸转移酶与内源性物质的相互作用 被引量:5

Interaction of uridine diphosphate glucuronic acid transferase and endogenous substances
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摘要 尿苷二磷酸葡萄糖醛酸转移酶(UGT)是人体重要的II相代谢酶,代谢药物的同时也代谢许多重要的内源性物质,如胆红素、甲状腺激素、雌激素、雄激素、胆汁酸和5-羟色胺等。该酶对许多内源性物质的代谢是灭活和清除这些内源性物质的关键步骤,能够防止内源性物质累积引发的毒性反应,或及时终止内源性激素的信号防止肿瘤的发生。然而,内源性物质对UGT酶也会产生影响,特别是在一些生理病理条件下,某些内源性物质能够抑制UGT酶活性,影响其参与的代谢反应。将就内源性物质和UGT酶的相互作用做一综述,以引起人们对UGT酶和内源性物质相互作用的关注。 Uridine diphosphate glucuronic acid transferase (UGT) is an important phase II metabolism enzyme in human body, it metabolites many drugs and endogenous substances. For many endogenous substances, such as bilirubin, thyroid hormones, estrogens, et al, the UGT enzymes are the key enzymes for inactivated and remove endogenous substances. It can prevent toxic effects caused by accumulation, its termination of endogenous hormone signal can prevent the occurrence of cancer. On the other hand, endogenous substances can affect the enzymes. In some physiological and pathological conditions, some of endogenous substances can inhibit UGT enzymes, and exert an influence on UGT enzymes involved metabolism. This article will make a review on the interaction of endogenous substances and UGT enzymes.
出处 《药物评价研究》 CAS 2015年第4期421-428,共8页 Drug Evaluation Research
关键词 药物代谢 尿苷二磷酸葡萄糖醛酸转移酶 内源性物质 drug metabolism, uridine diphosphate glucuronyl transferase, endogenous substance
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  • 1Ming-rong QIAN Su ZENG.Biosynthesis of imipramine glucuronide and characterization of imipramine glucuronidation catalyzed by recombinant UGTIA4[J].Acta Pharmacologica Sinica,2006,27(5):623-628. 被引量:3
  • 2Ada Piepoli,Annamaria Gentile,Maria Rosa Valvano,Daniela Barana,Cristina Oliani,Rosa Cotugno,Michele Quitadamo,Angelo Andriulli,Francesco Perri.Lack of association between UGT1A7,UGT1A9,ARP,SPINK1 and CFTR gene polymorphisms and pancreatic cancer in Italian patients[J].World Journal of Gastroenterology,2006,12(39):6343-6348. 被引量:3
  • 3Mazur CS, Kenneke JF, Hess-Wilson JK, et al. Differences between human and rat intestinal and hepatic blsphenol A glucuronidation and the influence of alamethicin on in witro kinetic measurements [J].Drug Metab Dispos, 2010, 38(12):2232--2238.
  • 4Mano Y, Usui T, Kamimura H. Species differences in inhibition potential of nonsteroidal anti inflamma tory drugs against estradiol 3beta glucuronidation between rats, dogs, and humans[J].J Pharm Sci, 2008, 97(7): 2805-2810.
  • 5Zhou SF, Tingle MD, Kestell P, et al. Species differences in the metabolism of the antitumour agent 5,6 dimethylxanthenone 4 acetic acid in vitro :implications for prediction of metabolic interactions invivo[J].Xenobiotica, 2002, 32(2): 87- 107.
  • 6Tukey RH, Strassburg CP. Human UDP-glucuronosyltransIerases: metabolism, expression, and disease[J]. Annu Rev Pharmacol Toxicol, 2000, 40: 581-616.
  • 7Coffman BL, Rios GR, King CD, et al. Human UGT2B7 catalyzes morphine glucuronidation[J]. Drug Metah Dispos, 1997,25(1): 1-4.
  • 8Mackenzie PI, Bock KW, Burchell B, et al. No menclature update for the mammalian UDP glyco syltransferase (UGT) gene superfamily[J]. Phar maeogenet Genomics, 2005,15(10): 677-685.
  • 9Nakamura A, Nakajima M, Yamanaka H, et ah Expression of UGT1A and UGT2B mRNA in human normal tissues and various cell lines[J]. Drug Metab Dispos, 2008,36(8): 1461-1464.
  • 10Kiang TK, Ensom MH, Chang TK. UDP-glucuronosyltransferases and clinical drug-drug interactions [J]. PharmacolTher, 2005, 106(1): 97-132.

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