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Benomyl, Aldehyde Dehydrogenase, DOPAL, and the Catecholaldehyde Hypothesis for the Pathogenesis of Parkinson’s Disease

[Image: see text] 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 f...

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Autores principales: Casida, John E., Ford, Breanna, Jinsmaa, Yunden, Sullivan, Patti, Cooney, Adele, Goldstein, David S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2014
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4137984/
https://www.ncbi.nlm.nih.gov/pubmed/25045800
http://dx.doi.org/10.1021/tx5002223
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author Casida, John E.
Ford, Breanna
Jinsmaa, Yunden
Sullivan, Patti
Cooney, Adele
Goldstein, David S.
author_facet Casida, John E.
Ford, Breanna
Jinsmaa, Yunden
Sullivan, Patti
Cooney, Adele
Goldstein, David S.
author_sort Casida, John E.
collection PubMed
description [Image: see text] 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.
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spelling pubmed-41379842015-07-21 Benomyl, Aldehyde Dehydrogenase, DOPAL, and the Catecholaldehyde Hypothesis for the Pathogenesis of Parkinson’s Disease Casida, John E. Ford, Breanna Jinsmaa, Yunden Sullivan, Patti Cooney, Adele Goldstein, David S. Chem Res Toxicol [Image: see text] 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. American Chemical Society 2014-07-21 2014-08-18 /pmc/articles/PMC4137984/ /pubmed/25045800 http://dx.doi.org/10.1021/tx5002223 Text en Copyright © 2014 American Chemical Society Terms of Use (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html)
spellingShingle Casida, John E.
Ford, Breanna
Jinsmaa, Yunden
Sullivan, Patti
Cooney, Adele
Goldstein, David S.
Benomyl, Aldehyde Dehydrogenase, DOPAL, and the Catecholaldehyde Hypothesis for the Pathogenesis of Parkinson’s Disease
title Benomyl, Aldehyde Dehydrogenase, DOPAL, and the Catecholaldehyde Hypothesis for the Pathogenesis of Parkinson’s Disease
title_full Benomyl, Aldehyde Dehydrogenase, DOPAL, and the Catecholaldehyde Hypothesis for the Pathogenesis of Parkinson’s Disease
title_fullStr Benomyl, Aldehyde Dehydrogenase, DOPAL, and the Catecholaldehyde Hypothesis for the Pathogenesis of Parkinson’s Disease
title_full_unstemmed Benomyl, Aldehyde Dehydrogenase, DOPAL, and the Catecholaldehyde Hypothesis for the Pathogenesis of Parkinson’s Disease
title_short Benomyl, Aldehyde Dehydrogenase, DOPAL, and the Catecholaldehyde Hypothesis for the Pathogenesis of Parkinson’s Disease
title_sort benomyl, aldehyde dehydrogenase, dopal, and the catecholaldehyde hypothesis for the pathogenesis of parkinson’s disease
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4137984/
https://www.ncbi.nlm.nih.gov/pubmed/25045800
http://dx.doi.org/10.1021/tx5002223
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