Literature DB >> 7568058

Daidzin suppresses ethanol consumption by Syrian golden hamsters without blocking acetaldehyde metabolism.

W M Keung1, O Lazo, L Kunze, B L Vallee.   

Abstract

Daidzin is a potent, selective, and reversible inhibitor of human mitochondrial aldehyde dehydrogenase (ALDH) that suppresses free-choice ethanol intake by Syrian golden hamsters. Other ALDH inhibitors, such as disulfiram (Antabuse) and calcium citrate carbimide (Temposil), have also been shown to suppress ethanol intake of laboratory animals and are thought to act by inhibiting the metabolism of acetaldehyde produced from ingested ethanol. To determine whether or not daidzin inhibits acetaldehyde metabolism in vivo, plasma acetaldehyde in daidzin-treated hamsters was measured after the administration of a test dose of ethanol. Daidzin treatment (150 mg/kg per day i.p. for 6 days) significantly suppresses (> 70%) hamster ethanol intake but does not affect overall acetaldehyde metabolism. In contrast, after administration of the same ethanol dose, plasma acetaldehyde concentration in disulfiram-treated hamsters reaches 0.9 mM, 70 times higher than that of the control. In vitro, daidzin suppresses hamster liver mitochondria-catalyzed acetaldehyde oxidation very potently with an IC50 value of 0.4 microM, which is substantially lower than the daidzin concentration (70 microM) found in the liver mitochondria of daidzin-treated hamsters. These results indicate that (i) the action of daidzin differs from that proposed for the classic, broad-acting ALDH inhibitors (e.g., disulfiram), and (ii) the daidzin-sensitive mitochondrial ALDH is not the one and only enzyme that is essential for acetaldehyde metabolism in golden hamsters.

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Year:  1995        PMID: 7568058      PMCID: PMC41093          DOI: 10.1073/pnas.92.19.8990

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  18 in total

1.  Estimation of blood acetaldehyde during ethanol metabolism: a sensitive HPLC/fluorescence microassay with negligible artifactual interference.

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2.  Possible protective role against alcoholism for aldehyde dehydrogenase isozyme deficiency in Japan.

Authors:  S Harada; D P Agarwal; H W Goedde; S Tagaki; B Ishikawa
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3.  Aldehyde dehydrogenase deficiency as cause of facial flushing reaction to alcohol in Japanese.

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4.  The oxidation of acetaldehyde by isolated mitochondria from various organs of the rat and hepatocellular carcinoma.

Authors:  A I Cederbaum; E Rubin
Journal:  Arch Biochem Biophys       Date:  1977-02       Impact factor: 4.013

5.  Disulfiram treatment of alcoholism. A Veterans Administration cooperative study.

Authors:  R K Fuller; L Branchey; D R Brightwell; R M Derman; C D Emrick; F L Iber; K E James; R B Lacoursiere; K K Lee; I Lowenstam
Journal:  JAMA       Date:  1986-09-19       Impact factor: 56.272

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Authors:  C J Eriksson
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Authors:  C J Eriksson
Journal:  Biochem Pharmacol       Date:  1973-09-15       Impact factor: 5.858

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Authors:  G W Svanas; H Weiner
Journal:  Arch Biochem Biophys       Date:  1985-01       Impact factor: 4.013

10.  Suppression of alcohol drinking with brain aldehyde dehydrogenase inhibition.

Authors:  J D Sinclair; K O Lindros
Journal:  Pharmacol Biochem Behav       Date:  1981-03       Impact factor: 3.533

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  13 in total

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4.  Dark Hydrazone Fluorescence Labeling Agents Enable Imaging of Cellular Aldehydic Load.

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Authors:  W M Keung; B L Vallee
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6.  Daidzin inhibits mitochondrial aldehyde dehydrogenase and suppresses ethanol intake of Syrian golden hamsters.

Authors:  W M Keung; A A Klyosov; B L Vallee
Journal:  Proc Natl Acad Sci U S A       Date:  1997-03-04       Impact factor: 11.205

Review 7.  Aldehyde dehydrogenase inhibitors: a comprehensive review of the pharmacology, mechanism of action, substrate specificity, and clinical application.

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8.  Kudzu extract treatment does not increase the intoxicating effects of acute alcohol in human volunteers.

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10.  Suppression of heavy drinking and alcohol seeking by a selective ALDH-2 inhibitor.

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Journal:  Alcohol Clin Exp Res       Date:  2009-08-10       Impact factor: 3.455

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