Abstract | BACKGROUND AND PURPOSE: EXPERIMENTAL APPROACH: We evaluated the effectiveness of some common pharmacological agents that have been utilized in the treatment of MELAS, in yeast, fibroblast and cybrid models of the disease. The yeast model harbouring the A14G mutation in the mitochondrial tRNALeu(UUR) gene, which is equivalent to the A3243G mutation in humans, was used in the initial screening. Next, the most effective drugs that were able to rescue the respiratory deficiency in MELAS yeast mutants were tested in fibroblasts and cybrid models of MELAS disease. KEY RESULTS: According to our results, supplementation with riboflavin or coenzyme Q(10) effectively reversed the respiratory defect in MELAS yeast and improved the pathologic alterations in MELAS fibroblast and cybrid cell models. CONCLUSIONS AND IMPLICATIONS: Our results indicate that cell models have great potential for screening and validating the effects of novel drug candidates for MELAS treatment and presumably also for other diseases with mitochondrial impairment.
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Authors | Juan Garrido-Maraver, Mario D Cordero, Irene Domínguez Moñino, Sheila Pereira-Arenas, Ana V Lechuga-Vieco, David Cotán, Mario De la Mata, Manuel Oropesa-Ávila, Manuel De Miguel, Juan Bautista Lorite, Eloy Rivas Infante, Manuel Alvarez-Dolado, Plácido Navas, Sandra Jackson, Silvia Francisci, José A Sánchez-Alcázar |
Journal | British journal of pharmacology
(Br J Pharmacol)
Vol. 167
Issue 6
Pg. 1311-28
(Nov 2012)
ISSN: 1476-5381 [Electronic] England |
PMID | 22747838
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | © 2012 The Authors. British Journal of Pharmacology © 2012 The British Pharmacological Society. |
Chemical References |
- RNA, Transfer, Leu
- Reactive Oxygen Species
- Ubiquinone
- coenzyme Q10
- Riboflavin
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Topics |
- Autophagy
(drug effects)
- Cell Line
- Cells, Cultured
- Drug Evaluation, Preclinical
(methods)
- Fibroblasts
(drug effects, metabolism)
- Genes, Mitochondrial
(genetics)
- Humans
- MELAS Syndrome
(drug therapy)
- Models, Biological
- Mutation
- RNA, Transfer, Leu
(genetics)
- Reactive Oxygen Species
- Riboflavin
(pharmacology)
- Saccharomyces cerevisiae
- Ubiquinone
(analogs & derivatives, pharmacology)
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