Premium
Cytochrome P450 2E1 and 3A activities do not differ between Mexicans and European Americans *
Author(s) -
Poland Russell A.,
Lin KehMing,
Nuccio Cenci,
Wilkinson Grant R.
Publication year - 2002
Publication title -
clinical pharmacology and therapeutics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.941
H-Index - 188
eISSN - 1532-6535
pISSN - 0009-9236
DOI - 10.1067/mcp.2002.127398
Subject(s) - medicine
Objectives Population differences in the activity of various cytochrome P450 (CYP) enzymes have been demonstrated on the basis of either genetic or environmental determinants. Hispanics are a large demographic group both worldwide and within the United States; hence the possibility of differences in metabolism between one such group—Mexicans—and a European‐derived population was determined with respect to CYP2E1 and CYP3A. Methods Young healthy Mexican immigrants living in Los Angeles, Calif, who had maintained a traditional diet were compared with previously and identically studied groups of age‐, sex‐, and weight‐matched European Americans who resided in middle Tennessee and ate a “western” diet (15 men and 15 women). In one study carried out in 15 women, the disposition of chlorzoxazone after an oral dose (250 mg) was compared. In the other investigation, all of the 15 subjects were men and received intravenous [ 15 N 3 ]‐labeled midazolam (1 mg) and oral midazolam (2 mg) simultaneously to characterize the disposition of benzodiazepine in the two populations. Results Plasma concentration‐time profiles of chlorzoxazone and its 6‐hydroxy metabolite and the 0‐ to 24‐hour urinary recovery of the latter were not different between Mexicans and European Americans. This indicates that CYP2E1 activity is similar in the two populations. Similarly, no significant intergroup differences were noted in the plasma concentration‐time profiles of midazolam after either intravenous or oral administration. Accordingly, CYP3A does not appear to be different between Mexicans and European Americans. Conclusions Similarity in the metabolism of chlorzoxazone between Mexicans and European Americans suggests that the risk associated with CYP2E1‐mediated activation of procarcinogens is not different between these two populations. Likewise, the absence of any difference in the disposition of midazolam indicates that, from a pharmacokinetic standpoint, dosages of drugs metabolized by CYP3A need not be different between Mexicans and European Americans. Clinical Pharmacology & Therapeutics (2002) 72 , 288–293; doi: 10.1067/mcp.2002.127398