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
[21]   First-pass metabolism of midazolam by the human intestine [J].
Paine, MF ;
Shen, DD ;
Kunze, KL ;
Perkins, JD ;
Marsh, CL ;
McVicar, JP ;
Barr, DM ;
Gillies, BS ;
Thummel, KE .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 1996, 60 (01) :14-24
[22]   Do men and women differ in proximal small intestinal CYP3A or P-glycoprotein expression? [J].
Paine, MF ;
Ludington, SS ;
Chen, ML ;
Stewart, PW ;
Huang, SM ;
Watkins, PB .
DRUG METABOLISM AND DISPOSITION, 2005, 33 (03) :426-433
[23]  
Paine MF, 1999, DRUG METAB DISPOS, V27, P360
[24]  
Paine MF, 1997, J PHARMACOL EXP THER, V283, P1552
[25]  
Prueksaritanont T, 1996, DRUG METAB DISPOS, V24, P634
[26]   CLONING AND EXPRESSION OF COMPLEMENTARY DNAS FOR MULTIPLE MEMBERS OF THE HUMAN CYTOCHROME-P450IIC SUBFAMILY [J].
ROMKES, M ;
FALETTO, MB ;
BLAISDELL, JA ;
RAUCY, JL ;
GOLDSTEIN, JA .
BIOCHEMISTRY, 1991, 30 (13) :3247-3255
[27]  
Sambrook J, 1989, MOL CLONING LAB MANU
[28]   P450 subfamily CYP2J and their role in the bioactivation of arachidonic acid in extrahepatic tissues [J].
Scarborough, PE ;
Ma, JX ;
Qu, W ;
Zeldin, DC .
DRUG METABOLISM REVIEWS, 1999, 31 (01) :205-234
[29]   Clinical pharmacokinetics of fluvastatin [J].
Scripture, CD ;
Pieper, JA .
CLINICAL PHARMACOKINETICS, 2001, 40 (04) :263-281
[30]  
SHIMADA T, 1994, J PHARMACOL EXP THER, V270, P414