| Literature DB >> 29991444 |
Ester López-Gallardo1, Sonia Emperador2, Carmen Hernández-Ainsa3, Julio Montoya4, M Pilar Bayona-Bafaluy5, Eduardo Ruiz-Pesini6.
Abstract
Mitochondrial DNA mutations in genes encoding respiratory complex I polypeptides can cause Leber hereditary optic neuropathy. Toxics affecting oxidative phosphorylation system can also cause mitochondrial optic neuropathy. Some complex I inhibitors found in edible plants might differentially interact with these pathologic mutations and modify their penetrance. To analyze this interaction, we have compared the effect of rotenone, capsaicin and rolliniastatin-1 on cybrids harboring the most frequent Leber hereditary optic neuropathy mutations and found that m.3460G > A mutation increases rotenone resistance but capsaicin and rolliniastatin-1 susceptibility. Thus, to explain the pathogenicity of mitochondrial diseases due to mitochondrial DNA mutations, their potential interactions with environment factors will have to be considered.Entities:
Keywords: Gene-environment interaction; Leber hereditary optic neuropathy; Mitochondrial DNA; Respiratory complex I; Xenobiotic
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Year: 2018 PMID: 29991444 DOI: 10.1016/j.fct.2018.07.014
Source DB: PubMed Journal: Food Chem Toxicol ISSN: 0278-6915 Impact factor: 6.023