Pharmacokinetic and pharmacodynamic basis for overcoming acetaldehyde-induced adverse reaction in Asian alcoholics, heterozygous for the variant ALDH2*2 gene allele

被引:64
作者
Chen, Yi-Chyan [2 ]
Peng, Giia-Sheun [3 ]
Tsao, Tien-Ping [4 ]
Wang, Ming-Fang
Lu, Ru-Band [5 ]
Yin, Shih-Jiun [1 ]
机构
[1] Natl Def Med Ctr, Dept Biochem, Sect 6, Taipei 11453, Taiwan
[2] Triserv Gen Hosp, Dept Psychiat, Taipei, Taiwan
[3] Triserv Gen Hosp, Dept Neurol, Taipei, Taiwan
[4] Triserv Gen Hosp, Dept Internal Med, Taipei, Taiwan
[5] Natl Cheng Kung Univ, Coll Med, Dept Psychiat, Tainan 70101, Taiwan
关键词
acetaldehydism; alcoholism; alcohol sensitivity; aldehyde dehydrogenase-2; Asian alcoholics; blood ethanol/acetaldehyde/acetate; cardiovascular response; genetic polymorphism; partial protection; subjective sensation; ALDEHYDE DEHYDROGENASE GENOTYPES; BLOOD-ACETALDEHYDE; DRINKING BEHAVIOR; ETHANOL-METABOLISM; ACETATE; POLYMORPHISMS; INVOLVEMENT; PROTECTION; CHINESE; ELIMINATION;
D O I
10.1097/FPC.0b013e32832ecf2e
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 It has been well documented that although homozygosity of the variant aldehyde dehydrogenese-2 (ALDH2) gene allele, ALDH2*2, in Asians almost fully protects against alcoholism, the heterozygosity only affords a partial protection to varying degrees. The partial protection against alcoholism has been ascribed to the faster elimination of acetaldehyde by residual hepatic ALDH2 activity and the lower accumulation in circulation in nonalcoholic heterozygotes. The physiological basis for overcoming the protection in ALDH2*1/*2 alcoholics, however, remains unclear. Methods To address this question, we recruited a total of 27 Han Chinese alcohol-dependent men, matched by age and body mass index, controlled for normal liver and cardiovascular functions, from a population base of 221 alcoholics. The participants were divided into ALDH2*1/*1 homozygotes (n = 13) and ALDH2*1/*2 heterozygotes (n=14). After a moderate dose of ethanol (0.5 g/kg body weight), blood ethanol/acetaldehyde/acetate concentrations, cardiac and extracranial/intracranial arterial hemodynamic parameters, as well as self-rated subjective sensations, were measured for 130 min. Results ALDH2*1/*2 alcoholics exhibited significantly higher blood acetaldehyde levels as well as prominent cardiovascular effects and the subjective perceptions, compared with the ALDH2*1/*1 alcoholics. Comparable profiles of blood acetaldehyde were found between heterozygotic alcoholics and the previously reported nonalcoholic heterozygotes intaking the same dose of ethanol. ALDH2*1/*2 alcoholics revealed, however, significantly lower intensities in both physiologic and psychologic responses than did the nonalcoholic heterozygotes. Conclusion These results indicate that acetaldehyde, rather than ethanol or acetate, is primarily responsible for the observed alcohol sensitivity reactions in heterozygotic alcoholics and suggest that physiological tolerance and/or innate low sensitivity may play a crucial role in overcoming the deterring response. A potential pharmacogenetic classification of acetaldehydism and alcoholism for alcoholics carrying the different ALDH2 genotypes is proposed. Pharmacogenetics and Genomics 19:588-599. (C) 2009 Wolters Kluwer Health | Lippincott Williams & Wilkins.
引用
收藏
页码:588 / 599
页数:12
相关论文
共 51 条
[1]   COMPARATIVE-STUDY ON ETHANOL ELIMINATION AND BLOOD-ACETALDEHYDE BETWEEN ALCOHOLICS AND CONTROL SUBJECTS [J].
ADACHI, J ;
MIZOI, Y ;
FUKUNAGA, T ;
OGAWA, Y ;
IMAMICHI, H .
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 1989, 13 (05) :601-604
[2]  
BRIEN JF, 1979, CLIN PHARMACOL THER, V25, P454
[3]   Interaction between the functional polymorphisms of the alcohol-metabolism genes in protection against alcoholism [J].
Chen, CC ;
Lu, RB ;
Chen, YC ;
Wang, MF ;
Chang, YC ;
Li, TK ;
Yin, SJ .
AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 65 (03) :795-807
[4]   Alcohol metabolism and cardiovascular response in an alcoholic patient homozygous for the ALDH2*2 variant gene allele [J].
Chen, YC ;
Lu, RB ;
Peng, GS ;
Wang, MF ;
Wang, HK ;
Ko, HC ;
Chang, YC ;
Lu, JJ ;
Li, TK ;
Yin, SJ .
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 1999, 23 (12) :1853-1860
[5]   Polymorphism of ethanol-metabolism genes and alcoholism: Correlation of allelic variations with the pharmacokinetic and pharmacodynamic consequences [J].
Chen, Yi-Chyan ;
Peng, Giia-Sheun ;
Wang, Ming-Fang ;
Tsao, Tien-Ping ;
Yin, Shih-Jiun .
CHEMICO-BIOLOGICAL INTERACTIONS, 2009, 178 (1-3) :2-7
[6]   Overview of the role of alcohol dehydrogenase and aldehyde dehydrogenase and their variants in the genesis of alcohol-related pathology [J].
Crabb, DW ;
Matsumoto, M ;
Chang, D ;
You, M .
PROCEEDINGS OF THE NUTRITION SOCIETY, 2004, 63 (01) :49-63
[7]   Acetaldehyde: Deja vu du jour [J].
Deitrich, RA .
JOURNAL OF STUDIES ON ALCOHOL, 2004, 65 (05) :557-572
[8]  
DIPADOVA C, 1987, ALCOHOL CLIN EXP RES, V11, P559
[9]  
EDENBERG HJ, BIOTRANSFOR IN PRESS, V4
[10]   The role of acetaldehyde in the actions of alcohol (Update 2000) [J].
Eriksson, CJP .
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 2001, 25 (05) :15S-32S