Glucuronidation of trans-3′-hydroxycotinine by UGT2B17 and UGT2B10

被引:27
作者
Chen, Gang [1 ]
Giambrone, Nino E. [2 ]
Lazarus, Philip [1 ,2 ]
机构
[1] Penn State Univ, Coll Med, Dept Publ Hlth Sci, Hershey, PA USA
[2] Penn State Univ, Coll Med, Dept Pharmacol, Hershey, PA USA
基金
美国国家卫生研究院;
关键词
human liver microsomes; liquid chromatography-mass spectrometry; nicotine; tobacco; trans-3 '-hydroxycotinine; UGT2B10; UGT2B17; HUMAN LIVER; N-GLUCURONIDATION; DELETION POLYMORPHISM; O-GLUCURONIDATION; GENE DELETION; NICOTINE; COTININE; PHENOTYPE; CYTOCHROME-P450; IDENTIFICATION;
D O I
10.1097/FPC.0b013e32834ff3a5
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Objectives Trans-3'-Hydroxycotinine (3HC) and its glucuronide are major nicotine metabolites excreted in the urine of smokers and other tobacco users. Although several members of the UDP-glucuronosyltransferase (UGT) family of enzymes were previously shown to be active in catalyzing the formation of 3HC and its glucuronide, a comprehensive screening of all known human UGT1A and 2B enzymes for glucuronidation activity against 3HC was not previously performed. Methods In the present study, human liver microsomes (HLM), eight UGT1A and six UGT2B enzymes were screened for activity against 3HC. Results UGT2B17 exhibited the highest O-glucuronidation activity, exhibiting a four-fold lower (P<0.005) K-M (8.3 mmol/l) compared with that observed for UGTs 1A9 (35 mmol/l) or 2B7 (31 mmol/l) and a K-M smaller compared with that observed for human liver microsomes (HLM; 26 mmol/l). The K-M for 3HC-O-Gluc formation was 3.1-fold lower (P<0.0005) in HLM from male participants exhibiting the wild-type genotype UGT2B17 (*1/*1) compared with that in HLM from participants homozygous for the UGT2B17 deletion genotype [UGT2B17 (*2/*2)]. Both UGTs 2B10 and 1A4 exhibited 3HC-N-Gluc formation activity, with UGT2B10 exhibiting a four-fold lower (P<0.05) K-M (13 mmol/l) compared with that observed for UGT1A4 (57 mmol/l) and, which was similar to the K-M observed in HLM (14 mmol/l). There was 91 (P<0.0001) and 39% (P<0.001) decreases in the 3HC-N-Gluc formation activities in HLM from participants with the UGT2B10 (*2/*2) and UGT2B10 (*1/*2) genotypes, respectively, compared with that of HLM from participants with the wild-type UGT2B10 (*1/*1) genotype. Conclusion These results suggest that UGT2B17 and UGT2B10 play key roles in the glucuronidation of 3HC in the human liver and that functional polymorphisms in UGT2B17 and UGT2B10 are associated with significantly reduced glucuronidation activities against 3HC. Pharmacogenetics and Genomics 22: 183-190 (C) 2012 Wolters Kluwer Health vertical bar Lippincott Williams & Wilkins.
引用
收藏
页码:183 / 190
页数:8
相关论文
共 30 条
[1]  
BENOWITZ NL, 1994, J PHARMACOL EXP THER, V268, P296
[2]  
Byrd G D, 2000, Drug Metabol Drug Interact, V16, P281
[3]   DIRECT DETERMINATION OF COTININE-N-GLUCURONIDE IN URINE USING THERMOSPRAY LIQUID-CHROMATOGRAPHY MASS-SPECTROMETRY [J].
BYRD, GD ;
UHRIG, MS ;
DEBETHIZY, JD ;
CALDWELL, WS ;
CROOKS, PA ;
RAVARD, A ;
RIGGS, RM .
BIOLOGICAL MASS SPECTROMETRY, 1994, 23 (02) :103-107
[4]   CHARACTERIZATION OF THE GLUCURONIDE CONJUGATE OF COTININE - A PREVIOUSLY UNIDENTIFIED MAJOR METABOLITE OF NICOTINE IN SMOKERS URINE [J].
CALDWELL, WS ;
GREENE, JM ;
BYRD, GD ;
CHANG, KM ;
UHRIG, MS ;
DEBETHIZY, JD ;
CROOKS, PA ;
BHATTI, BS ;
RIGGS, RM .
CHEMICAL RESEARCH IN TOXICOLOGY, 1992, 5 (02) :280-285
[5]   Glucuronidation of tobacco-specific nitrosamines by UGT2B10 [J].
Chen, Gang ;
Dellinger, Ryan W. ;
Sun, Dongxiao ;
Spratt, Thomas E. ;
Lazarus, Philip .
DRUG METABOLISM AND DISPOSITION, 2008, 36 (05) :824-830
[6]   Identification of a prevalent functional missense polymorphism in the UGT2B10 gene and its association with UGT2B10 inactivation against tobacco-specific nitrosarnines [J].
Chen, Gang ;
Dellinger, Ryan W. ;
Gallagher, Carla J. ;
Sun, Dongxiao ;
Lazarus, Philip .
PHARMACOGENETICS AND GENOMICS, 2008, 18 (03) :181-191
[7]   Glucuronidation of nicotine and cotinine by UGT2B10:: Loss of function by the UGT2B10 codon 67 (Asp&gt;Tyr) polymorphism [J].
Chen, Gang ;
Blevins-Primeau, Andrea S. ;
Dellinger, Ryan W. ;
Muscat, Joshua E. ;
Lazarus, Philip .
CANCER RESEARCH, 2007, 67 (19) :9024-9029
[8]   Glucuronidation Genotypes and Nicotine Metabolic Phenotypes: Importance of Functional UGT2B10 and UGT2B17 Polymorphisms [J].
Chen, Gang ;
Giambrone, Nino E., Jr. ;
Dluzen, Douglas F. ;
Muscat, Joshua E. ;
Berg, Arthur ;
Gallagher, Carla J. ;
Lazarus, Philip .
CANCER RESEARCH, 2010, 70 (19) :7543-7552
[9]   A GENERAL ASSAY FOR UDPGLUCURONOSYLTRANSFERASE ACTIVITY USING POLAR AMINO-CYANO STATIONARY PHASE HPLC AND UDP[U-C-14]GLUCURONIC ACID [J].
COUGHTRIE, MWH ;
BURCHELL, B ;
BEND, JR .
ANALYTICAL BIOCHEMISTRY, 1986, 159 (01) :198-205
[10]   Importance of UDP-glucuronosyltransferase 1A10 (UGT1A10) in the detoxification of polycyclic aromatic hydrocarbons:: Decreased glucuronidative activity of the UGT1A10139LYS isoform [J].
Dellinger, Ryan W. ;
Fang, Jia-Long ;
Chen, Gang ;
Weinberg, Rebecca ;
Lazarus, Philip .
DRUG METABOLISM AND DISPOSITION, 2006, 34 (06) :943-949