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Benomyl, aldehyde dehydrogenase, DOPAL, and the catecholaldehyde hypothesis for the pathogenesis of Parkinson's disease.

Abstract
The dopamine metabolite 3,4-dihydroxyphenylacetaldehyde (DOPAL) is detoxified mainly by aldehyde dehydrogenase (ALDH). We find that the fungicide benomyl potently and rapidly inhibits ALDH and builds up DOPAL in vivo in mouse striatum and in vitro in PC12 cells and human cultured fibroblasts and glial cells. The in vivo results resemble those noted previously with knockouts of the genes encoding ALDH1A1 and 2, a mouse model of aging-related Parkinson's disease (PD). Exposure to pesticides that inhibit ALDH may therefore increase PD risk via DOPAL buildup. This study lends support to the "catecholaldehyde hypothesis" that the autotoxic dopamine metabolite DOPAL plays a pathogenic role in PD.
AuthorsJohn E Casida, Breanna Ford, Yunden Jinsmaa, Patti Sullivan, Adele Cooney, David S Goldstein
JournalChemical research in toxicology (Chem Res Toxicol) Vol. 27 Issue 8 Pg. 1359-61 (Aug 18 2014) ISSN: 1520-5010 [Electronic] United States
PMID25045800 (Publication Type: Journal Article, Research Support, N.I.H., Intramural, Research Support, Non-U.S. Gov't)
Chemical References
  • Aldehydes
  • Antifungal Agents
  • Enzyme Inhibitors
  • 3,4-Dihydroxyphenylacetic Acid
  • 3,4-dihydroxyphenylacetaldehyde
  • Aldehyde Dehydrogenase
  • 4-hydroxy-2-nonenal
  • Benomyl
Topics
  • 3,4-Dihydroxyphenylacetic Acid (analogs & derivatives, chemistry, metabolism)
  • Aldehyde Dehydrogenase (antagonists & inhibitors, genetics, metabolism)
  • Aldehydes (chemistry, toxicity)
  • Animals
  • Antifungal Agents (chemistry, metabolism, toxicity)
  • Benomyl (chemistry, metabolism, toxicity)
  • Cell Line
  • Enzyme Inhibitors (chemistry, metabolism)
  • Humans
  • Lipid Peroxidation (drug effects)
  • Mice
  • PC12 Cells
  • Parkinson Disease (etiology)
  • Rats

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