Characteristics of aldehyde dehydrogenase 2 (Aldh2) knockout mice

ALDH2 乙醛 醛脱氢酶 基因剔除小鼠 乙醇 化学 致癌物 毒性 乙醇代谢 生物化学 药理学 生物 基因 有机化学
作者
Hsu-Sheng Yu,Tsunehiro Oyama,Toyohi Isse,Kyoko Kitakawa,Masanori Ogawa,Thi-Thu-Phuong Pham,Toshihiro Kawamoto
出处
期刊:Toxicology Mechanisms and Methods [Informa]
卷期号:19 (9): 535-540 被引量:31
标识
DOI:10.3109/15376510903401708
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 overview 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.
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