Characteristics of aldehyde dehydrogenase 2 (Aldh2) knockout mice

被引:26
|
作者
Yu, Hsu-Sheng [1 ]
Oyama, Tsunehiro [1 ]
Isse, Toyohi [2 ]
Kitakawa, Kyoko [3 ]
Ogawa, Masanori [4 ]
Pham, Thi-Thu-Phuong [1 ]
Kawamoto, Toshihiro [1 ]
机构
[1] Univ Occupat & Environm Hlth, Dept Environm Hlth, Yahatanishi Ku, Kitakyushu, Fukuoka 8078555, Japan
[2] Univ Occupat & Environm Hlth, Sect Postgrad Guidance, Sch Med, Yahatanishi Ku, Kitakyushu, Fukuoka 8078555, Japan
[3] Hamamatsu Univ Sch Med, Dept Biochem, Shizuoka, Japan
[4] Jichi Med Univ, Hlth Care Sect, Shimotsuke, Tochigi 3290498, Japan
关键词
Acetaldehyde; ALDH2; DNA adducts; ethanol; knockout mice; GENE TARGETING MOUSE; NITRATE TOLERANCE; ORGANIC NITRATES; ALCOHOL METABOLISM; ETHANOL TREATMENT; OXIDATIVE STRESS; COVALENT BINDING; CROSS-TOLERANCE; ACETALDEHYDE; BIOACTIVATION;
D O I
10.3109/15376510903401708
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Acetaldehyde is an intermediate of ethanol oxidation. It covalently binds to DNA, and is known as a carcinogen. Aldehyde dehydrogenase 2 (ALDH2) is an important enzyme that oxidizes acetaldehyde. Approximately 45% of Chinese and Japanese individuals have the inactive ALDH2 genotypes (ALDH2* 2/*2 and ALDH2* 1/*2), and Aldh2 knockout mice appear to be a valid animal model for humans with inactive ALDH2. This review gives an over view of published studies on Aldh2 knockout mice, which were treated with ethanol or acetaldehyde. According to these studies, it was found that Aldh2 -/- mice (Aldh2 knockout mice) are more susceptible to ethanol and acetaldehyde-induced toxicity than Aldh2 +/+ mice (wild type mice). When mice were fed with ethanol, the mortality was increased. When they were exposed to atmospheres containing acetaldehyde, the Aldh2 -/- mice showed more severe toxic symptoms, like weight loss and higher blood acetaldehyde levels, as compared with the Aldh2 +/+ mice. Thus, ethanol and acetaldehyde treatment affects Aldh2 knockout mice more than wild type mice. Based on these findings, it is suggested that ethanol consumption and acetaldehyde inhalation are inferred to pose a higher risk to ALDH2-inactive humans. These results also support that ALDH2-deficient humans who habitually consume alcohol have a higher rate of cancer than humans with functional ALDH2.
引用
收藏
页码:535 / 540
页数:6
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