Sex differences in the toxicokinetics of inhaled solvent vapors in humans -: 2.: 2-propanol

被引:34
作者
Ernstgård, L [1 ]
Sjögren, B [1 ]
Warholm, M [1 ]
Johanson, G [1 ]
机构
[1] Karolinska Inst, Inst Environm Med, SE-17177 Stockholm, Sweden
关键词
human; 2-propanol; acetone; sex; toxicokinetics; genotypes;
D O I
10.1016/j.taap.2003.08.005
中图分类号
R9 [药学];
学科分类号
1007 [药学];
摘要
The aim of this study was to evaluate possible sex differences in the inhalation toxicokinetics of 2-propanol vapor. Nine women and eight men were exposed on different occasions for 2 h during light physical exercise (50 W) to 2-propanol (350 mg/m(3)) and to clean air (control exposure). The level corresponds to the Swedish occupational exposure limit. 2-Propanol and its metabolite acetone were monitored up to 24 It after exposure in exhaled air, blood, saliva, and urine by headspace gas chromatography. Body fat and lean body mass were estimated from sex-specific equations using bioelectrical impedance, body weight, height, and age. Genotypes were determined by PCR-based assays for alcohol dehydrogenase and cytochrome P450 2E1 (CYP2E1). The CYP2E1 phenotype was assessed by the 2-h plasma 6-hydroxychlorzoxazone/chlorzoxazone metabolic ratio in vivo. The toxicokinetic profile in blood was analyzed using a one-compartment population model. The following sex differences were significant at the p = 0.05 level (Student's t test). The respiratory uptake was lower and the volume of distribution smaller in females. The women had a slightly shorter half-time of 2-propanol in blood and a higher apparent total clearance when corrected for body composition. However, women reached approximately four times higher 2-propanol levels in exhaled air at 10-min postexposure and onward. Acetone in blood was markedly higher in females than in males in the control experiment and slightly higher following exposure to 2-propanol. A marked sex difference was that of a 10-fold higher in vivo blood:breath ratio in men, suggesting sex differences in the lung metabolism of 2-propanol. The most marked sex difference was that of salivary acetone, for which an approximately 100-fold increase was seen in women, but no increase in men, after exposure to 2-propanol compared to clean air. The toxicokinetic analysis revealed no significant differences in toxicokinetics between subjects of different metabolic genotypes or phenotypes. In conclusion, the study indicates several sex differences in the inhalation toxicokinetics of 2-propanol. Most of these differences are consistent with anatomical differences between women and men. However, body build can not explain the sex differences in 2-propanol levels in expired air and acetone in saliva. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:158 / 167
页数:10
相关论文
共 23 条
[1]
*ACGIH, 2000, DOC THRESH LIM VAL B
[2]
Gender differences in pharmacokinetics of alcohol [J].
Baraona, E ;
Abittan, CS ;
Dohmen, K ;
Moretti, M ;
Pozzato, G ;
Chayes, ZW ;
Schaefer, C ;
Lieber, CS .
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 2001, 25 (04) :502-507
[3]
Beal SL., 1998, NONMEM Users Guides
[4]
Genetic polymorphism of alcohol dehydrogenase in Europeans:: The ADH2*2 allele decreases the risk for alcoholism and is associated with ADH3*1 [J].
Borràs, E ;
Coutelle, C ;
Rosell, A ;
Fernández-Muixi, F ;
Broch, M ;
Crosas, B ;
Hjelmqvist, L ;
Lorenzo, A ;
Gutiérrez, C ;
Santos, M ;
Szczepanek, M ;
Heilig, M ;
Quattrocchi, P ;
Farrés, J ;
Vidal, F ;
Richart, C ;
Mach, T ;
Bogdal, J ;
Jörnvall, H ;
Seitz, HK ;
Couzigou, P ;
Parés, X .
HEPATOLOGY, 2000, 31 (04) :984-989
[5]
CATALYTIC PROPERTIES OF HUMAN-LIVER ALCOHOL-DEHYDROGENASE ISOENZYMES [J].
BOSRON, WF ;
LI, TK .
ENZYME, 1987, 37 (1-2) :19-28
[6]
Chao You-Chen, 1994, Proceedings of the National Science Council Republic of China Part B Life Sciences, V18, P101
[7]
Development of a physiologically based pharmacokinetic model of isopropanol and its metabolite acetone [J].
Clewell, HJ ;
Gentry, PR ;
Gearhart, JM ;
Covington, TR ;
Banton, MI ;
Andersen, ME .
TOXICOLOGICAL SCIENCES, 2001, 63 (02) :160-172
[8]
Recommended nomenclature for the vertebrate alcohol dehydrogenase gene family [J].
Duester, G ;
Farrés, J ;
Felder, MR ;
Holmes, RS ;
Höög, JO ;
Parés, X ;
Plapp, BV ;
Yin, SJ ;
Jörnvall, H .
BIOCHEMICAL PHARMACOLOGY, 1999, 58 (03) :389-395
[9]
Are women more sensitive than men to 2-propanol and m-xylene vapours? [J].
Ernstgård, L ;
Gullstrand, E ;
Löf, A ;
Johanson, G .
OCCUPATIONAL AND ENVIRONMENTAL MEDICINE, 2002, 59 (11) :759-767
[10]
ERNSTGARD L, 2003, TOXICOL APPL PHARM, V193