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Chinese Journal of Clinical Pharmacology and Therapeutics ›› 2009, Vol. 14 ›› Issue (12): 1321-1328.

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Hepatic UDP-glucuronosyltransferases in liver injury

JIANG Shan, HAO Hai-ping, WANG Guang-ji   

  1. Key Laboratory of Drug Metabolism and Pharmacokinetics, China Pharmaceutical University, Nanjing 210009,Jiangsu, China
  • Received:2009-10-12 Revised:2009-11-13 Published:2020-10-20

Abstract: Liver is the most important metabolic organ in human, including the vast majority of metabolic enzymes involving phase Ⅰ and phase Ⅱ and playing an important role on detoxification of many endogenous and exogenous substances.UDP-glucuronosyltransferases (UGT)is the most important phase Ⅱ metabolic enzyme that catalize glucuronidation in human, as compared with the CYP450 enzymes, study of UGTs lags behind, especially, the state of UGTs in liver injury is still poorly understood.This review summarizes latest studies of the UGTs in gene, protein structure and function, distribution in liver and relationship with the liver disease, then we discuss the effects of several common liver injury on hepatic UGT and glucuronidation.It will provide more reliable reference in durg metabolism in liver injury and guide the clinical rational use of drugs.

Key words: liver, UDP-glucuronosyltransferases, phase Ⅱ metabolism;, liver injury

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