The human intestinal cytochrome P450 "pie"

被引:637
作者
Paine, MF
Hart, HL
Ludington, SS
Haining, RL
Rettie, AE
Zeldin, DC
机构
[1] Univ N Carolina, Gen Clin Res Ctr, Chapel Hill, NC USA
[2] Univ N Carolina, Div Pharmacotherapy & Expt Therapeut, Chapel Hill, NC USA
[3] W Virginia Univ, Dept Basic Pharmaceut Sci, Morgantown, WV 26506 USA
[4] Univ Washington, Dept Med Chem, Seattle, WA 98195 USA
[5] NIEHS, Div Intramural Res, Res Triangle Pk, NC 27709 USA
关键词
D O I
10.1124/dmd.105.008672
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Cytochromes P450 (P450s) 3A, 2C, and 1A2 constitute the major "pieces" of the human liver P450 "pie" and account, on average, for 40, 25, and 18%, respectively, of total immunoquantified P450s (J Pharmacol Exp Ther 270: 414 - 423, 1994). The P450 profile in the human small intestine has not been fully characterized. Therefore, microsomes prepared from mucosal scrapings from the duodenal/ jejunal portion of 31 human donor small intestines were analyzed by Western blot using selective P450 antibodies. P450s 3A4, 2C9, 2C19, and 2J2 were detected in all individuals and ranged from 8.8 to 150, 2.9 to 27, < 0.6 to 3.9, and < 0.2 to 3.1 pmol/mg, respectively. CYP2D6 was detected in 29 individuals and ranged from < 0.2 to 1.4 pmol/mg. CYP3A5 was detected readily in 11 individuals, with a range ( average) of 4.9 to 25 ( 16) pmol/mg that represented from 3 to 50% of total CYP3A (CYP3A4 + CYP3A5) content. CYP1A1 was detected readily in three individuals, with a range ( average) of 3.6 to 7.7 (5.6) pmol/mg. P450s 1A2, 2A6, 2B6, 2C8, and 2E1 were not or only faintly detected. As anticipated, average CYP3A content ( 50 pmol/mg) was the highest. Excluding CYP1A1, the remaining enzymes had the following rank order: 2C9 > 2C19 > 2J2 > 2D6 (8.4, 1.1, 0.9, and 0.5 pmol/mg, respectively). Analysis of a pooled preparation of the 31 donor specimens substantiated these results. In summary, as in the liver, large interindividual variation exists in the expression levels of individual P450s. On average, CYP3A and CYP2C9 represents the major pieces of the intestinal P450 pie, accounting for 80 and 15%, respectively, of total immunoquantified P450s.
引用
收藏
页码:880 / 886
页数:7
相关论文
共 40 条
[1]  
DEWAZIERS I, 1990, J PHARMACOL EXP THER, V253, P387
[2]   Effects of a chargrilled meat diet on expression of CYP3A, CYP1A, and P-glycoprotein levels in healthy volunteers [J].
Fontana, RJ ;
Lown, KS ;
Paine, MF ;
Fortlage, L ;
Santella, RM ;
Felton, JS ;
Knize, MG ;
Greenberg, A ;
Watkins, PB .
GASTROENTEROLOGY, 1999, 117 (01) :89-98
[3]   Allelic variants of human cytochrome P450 2C9: Baculovirus-mediated expression, purification, structural characterization, substrate stereoselectivity, and prochiral selectivity of the wild-type and I359L mutant forms [J].
Haining, RL ;
Hunter, AP ;
Veronese, ME ;
Trager, WF ;
Rettie, AE .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1996, 333 (02) :447-458
[4]   Involvement of CYP2J2 and CYP4F12 in the metabolism of ebastine in human intestinal Microsomes [J].
Hashizume, T ;
Imaoka, S ;
Mise, M ;
Terauchi, Y ;
Fujii, T ;
Miyazaki, H ;
Kamataki, T ;
Funae, Y .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2002, 300 (01) :298-304
[5]   CYP2C subfamily, primarily CYP2C9, catalyses the enantioselective demethylation of the endocrine disruptor pesticide methoxychlor in human liver microsomes: use of inhibitory monoclonal antibodies in P450 identification [J].
Hu, Y ;
Krausz, K ;
Gelboin, HV ;
Kupfer, D .
XENOBIOTICA, 2004, 34 (02) :117-132
[6]   The small intestine as a xenobiotic-metabolizing organ [J].
Kaminsky, LS ;
Zhang, QY .
DRUG METABOLISM AND DISPOSITION, 2003, 31 (12) :1520-1525
[7]   Cloning of CYP2J2 gene and identification of functional polymorphisms [J].
King, LM ;
Ma, JX ;
Srettabunjong, S ;
Graves, J ;
Bradbury, JA ;
Li, LP ;
Spiecker, M ;
Liao, JK ;
Mohrenweiser, H ;
Zeldin, DC .
MOLECULAR PHARMACOLOGY, 2002, 61 (04) :840-852
[8]  
Klose TS, 1999, J BIOCHEM MOL TOXIC, V13, P289, DOI 10.1002/(SICI)1099-0461(1999)13:6<289::AID-JBT1>3.0.CO
[9]  
2-N
[10]   1ST-PASS METABOLISM OF CYCLOSPORINE BY THE GUT [J].
KOLARS, JC ;
AWNI, WM ;
MERION, RM ;
WATKINS, PB .
LANCET, 1991, 338 (8781) :1488-1490