ACETALDEHYDE METABOLISM IN DIFFERENT ALDEHYDE DEHYDROGENASE-2 GENOTYPES

被引:223
作者
ENOMOTO, N [1 ]
TAKASE, S [1 ]
YASUHARA, M [1 ]
TAKADA, A [1 ]
机构
[1] KANAZAWA MED UNIV,DEPT INTERNAL MED,DIV GASTROENTEROL,KAHOKU,ISHIKAWA 92002,JAPAN
关键词
ALDEHYDE DEHYDROGENASE; GENOTYPES; ALDH2; ACETALDEHYDE METABOLISM;
D O I
10.1111/j.1530-0277.1991.tb00532.x
中图分类号
R194 [卫生标准、卫生检查、医药管理];
学科分类号
摘要
In order to clarify the relationships between acetaldehyde (Ac-CHO) metabolism and low K(m) (mitochondrial) aldehyde dehydrogenase (ALDH2) genotypes, hepatic ALDH2 activity was determined and serial changes of blood Ac-CHO levels after ethanol administration were analyzed in the individuals homozygous for the normal ALDH2 genes, heterozygous for the normal and mutant ALDH2 genes, and homozygous for the mutant ALDH2 genes. Genomic DNA was extracted from white blood cells and genotyping of ALDH2 was performed using the polymerase chain reaction technique and slot blot hybridization with synthesized oligonucleotide probes specific to the normal and mutant ALDH2 genes. ALDH2 activity was not detectable in the liver in two cases of the mutant homozygote. In four out of eight cases of the heterozygote, hepatic ALDH2 activity was measurable, although the activity was lower compared with that in the normal homozygote. Blood ethanol levels after alcohol administration were not different among the three different ALDH2 genotypes. Blood Ac-CHO levels after drinking of alcohol were significantly higher in the heterozygotes and the mutant homozygotes than in the normal homozygotes. The levels after a moderate amount of ethanol (0.8 g/kg of body weight) in a case of the mutant homozygote were not different from those of the heterozygotes. However, the levels after a small amount of ethanol (0.1 g/kg of body weight) were significantly higher in the mutant homozygotes than in the heterozygotes. These results indicate that hepatic ALDH2 activity is lacking completely, and metabolism of Ac-CHO in the liver is severely impaired in the homozygotes of the mutant ALDH2 genes. On the other hand, the lack of hepatic ALDH2 activity is partial, and impairment of hepatic Ac-CHO metabolism is mild, in the heterozygotes of the ALDH2 genes. Clear differences of blood Ac-CHO levels after a small amount of ethanol suggest that blood Ac-CHO levels after a small amount of ethanol are good markers for the evaluation of ALDH2 genotypes.
引用
收藏
页码:141 / 144
页数:4
相关论文
共 17 条
  • [1] GENOTYPES FOR ALDEHYDE DEHYDROGENASE-DEFICIENCY AND ALCOHOL SENSITIVITY - THE INACTIVE ALDH22 ALLELE IS DOMINANT
    CRABB, DW
    EDENBERG, HJ
    BOSRON, WF
    LI, TK
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1989, 83 (01) : 314 - 316
  • [2] ENOMOTO N, 1990, ALCOHOL METAB LIVER, V9, P27
  • [3] 2 ALDEHYDE DEHYDROGENASES FROM HUMAN LIVER - ISOLATION VIA AFFINITY CHROMATOGRAPHY AND CHARACTERIZATION OF ISOZYMES
    GREENFIELD, NJ
    PIETRUSZKO, R
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA, 1977, 483 (01) : 35 - 45
  • [4] ELECTROPHORETIC AND BIOCHEMICAL-STUDIES OF HUMAN ALDEHYDE DEHYDROGENASE ISOZYMES IN VARIOUS TISSUES
    HARADA, S
    AGARWAL, DP
    GOEDDE, HW
    [J]. LIFE SCIENCES, 1980, 26 (21) : 1773 - 1780
  • [5] HARADA S, 1981, LANCET, V2, P982
  • [6] HARADA S, 1980, AM J HUM GENET, V32, P8
  • [7] CORRELATION BETWEEN HUMAN-ERYTHROCYTE ALDEHYDE DEHYDROGENASE-ACTIVITY AND SENSITIVITY TO ALCOHOL
    INOUE, K
    FUKUNAGA, M
    YAMASAWA, K
    [J]. PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1980, 13 (02) : 295 - 297
  • [8] A SIMPLE SALTING OUT PROCEDURE FOR EXTRACTING DNA FROM HUMAN NUCLEATED CELLS
    MILLER, SA
    DYKES, DD
    POLESKY, HF
    [J]. NUCLEIC ACIDS RESEARCH, 1988, 16 (03) : 1215 - 1215
  • [9] ALCOHOL SENSITIVITY RELATED TO POLYMORPHISM OF ALCOHOL-METABOLIZING ENZYMES IN JAPANESE
    MIZOI, Y
    TATSUNO, Y
    ADACHI, J
    KOGAME, M
    FUKUNAGA, T
    FUJIWARA, S
    HISHIDA, S
    IJIRI, I
    [J]. PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1983, 18 : 127 - 133
  • [10] PRIMER-DIRECTED ENZYMATIC AMPLIFICATION OF DNA WITH A THERMOSTABLE DNA-POLYMERASE
    SAIKI, RK
    GELFAND, DH
    STOFFEL, S
    SCHARF, SJ
    HIGUCHI, R
    HORN, GT
    MULLIS, KB
    ERLICH, HA
    [J]. SCIENCE, 1988, 239 (4839) : 487 - 491