Literature DB >> 17590985

Removal of acetaldehyde from the body.

Richard A Deitrich1, Dennis Petersen, Vasilis Vasiliou.   

Abstract

The reduction of acetaldehyde back to ethanol via NAD-linked alcohol dehydrogenase is an important mechanism for keeping acetaldehyde levels low following ethanol ingestion. However, this does not remove acetaldehyde from the body, but just delays its eventual removal. Acetaldehyde is removed from the body primarily by oxidation to acetate via a number of NAD-linked aldehyde dehydrogenase (ALDH) enzymes. There are nineteen known ALDHs in humans, but only a few of them appear to be involved in acetaldehyde oxidation. There are many analogous enzymes in other organisms. Genetic polymorphisms of several ALDHs have been identified in humans that are responsible for several hereditary defects in the metabolism of normal endogenous substrates. The best known ALDH genetic polymorphism is in ALDH2 gene, which encodes a mitochondrial enzyme primarily responsible for the oxidation of the ethanol-derived acetaldehyde. This common polymorphism is known to dominantly inhibit its enzymatic activity resulting in reduced ability to clear acetaldehyde in both homozygote and heterozygote individuals. These individuals are generally protected against alcohol abuse but are susceptible to oesophageal cancer. For those enzymes that are capable of reacting with acetaldehyde, they may do so at the expense of their normal substrates, resulting in abnormal accumulation of these substrates. Examples of this are the aldehydes of the biogenic amines, dopamine, noradrenaline, adrenaline, serotonin and long chain lipid aldehydes such as nonenal. Not all of these enzymes are capable of efficient oxidation of acetaldehyde; however, it is possible that acetaldehyde may function as an inhibitor of these enzymes as well. The aldehydes whose metabolism is interfered with may also serve as inhibitors of ALDHs as well. However, this aspect of aldehyde function has not been extensively studied. A number of other mechanisms for the removal of acetaldehyde exist. For example, reaction of acetaldehyde with protein or nucleic acids is responsible for the disappearance of a small amount of acetaldehyde, but may be responsible for some pathological effects of acetaldehyde. There are a few other enzymes such as aldehyde oxidase, xanthine oxidase, cytochrome P450 oxidase and glyceraldehyde-3-phosphate dehydrogenase that are capable of oxidizing acetaldehyde. However, these enzymes account for only a small fraction of the total activity.

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Year:  2007        PMID: 17590985     DOI: 10.1002/9780470511848.ch3

Source DB:  PubMed          Journal:  Novartis Found Symp        ISSN: 1528-2511


  13 in total

1.  No acute effects of an exposure to 50 ppm acetaldehyde on the upper airways.

Authors:  A Muttray; J Gosepath; J Brieger; A Faldum; A Pribisz; O Mayer-Popken; D Jung; B Rossbach; W Mann; S Letzel
Journal:  Int Arch Occup Environ Health       Date:  2008-08-21       Impact factor: 3.015

2.  Suppression of spermatogenesis by bisdichloroacetyldiamines is mediated by inhibition of testicular retinoic acid biosynthesis.

Authors:  John K Amory; Charles H Muller; Jakob A Shimshoni; Nina Isoherranen; Jisun Paik; Jan S Moreb; David W Amory; Ryan Evanoff; Alex S Goldstein; Michael D Griswold
Journal:  J Androl       Date:  2010-08-12

3.  Ethanol suppresses ureagenesis in rat hepatocytes: role of acetaldehyde.

Authors:  Ekhson L Holmuhamedov; Christoph Czerny; Craig C Beeson; John J Lemasters
Journal:  J Biol Chem       Date:  2012-01-06       Impact factor: 5.157

4.  Ethanol, acetaldehyde, and estradiol affect growth and differentiation of rhesus monkey embryonic stem cells.

Authors:  Catherine A VandeVoort; Dana L Hill; Charles L Chaffin; Alan J Conley
Journal:  Alcohol Clin Exp Res       Date:  2011-03-25       Impact factor: 3.455

5.  An optimized method for the measurement of acetaldehyde by high-performance liquid chromatography.

Authors:  Xiangying Guan; Emanuel Rubin; Helen Anni
Journal:  Alcohol Clin Exp Res       Date:  2011-09-06       Impact factor: 3.455

6.  In vivo measurement of aldehyde dehydrogenase-2 activity in rat liver ethanol model using dynamic MRSI of hyperpolarized [1-(13) C]pyruvate.

Authors:  Sonal Josan; Tao Xu; Yi-Fen Yen; Ralph Hurd; Julio Ferreira; Che-Hong Chen; Daria Mochly-Rosen; Adolf Pfefferbaum; Dirk Mayer; Daniel Spielman
Journal:  NMR Biomed       Date:  2012-12-06       Impact factor: 4.044

Review 7.  Putative role of brain acetaldehyde in ethanol addiction.

Authors:  Xin-sheng Deng; Richard A Deitrich
Journal:  Curr Drug Abuse Rev       Date:  2008-01

8.  Acetate causes alcohol hangover headache in rats.

Authors:  Christina R Maxwell; Rebecca Jay Spangenberg; Jan B Hoek; Stephen D Silberstein; Michael L Oshinsky
Journal:  PLoS One       Date:  2010-12-31       Impact factor: 3.240

Review 9.  Effect of the allelic variants of aldehyde dehydrogenase ALDH2*2 and alcohol dehydrogenase ADH1B*2 on blood acetaldehyde concentrations.

Authors:  Giia-Sheun Peng; Shih-Jiun Yin
Journal:  Hum Genomics       Date:  2009-01       Impact factor: 4.639

10.  ALDH1 expression correlates with favorable prognosis in ovarian cancers.

Authors:  Bin Chang; Guangzhi Liu; Fengxia Xue; Daniel G Rosen; Lianchun Xiao; Xuemei Wang; Jinsong Liu
Journal:  Mod Pathol       Date:  2009-03-27       Impact factor: 7.842

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