{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["13"],"submitter":["Hernandez-Camacho JD"],"funding":["Instituto de Salud Carlos III","Ministerio de Ciencia, Innovación y Universidades","Junta de Andalucía","Association Française contre les Myopathies","European Commission","Ministerio de Educación, Cultura y Deporte","National Health Research In"],"pubmed_abstract":["ADCK2 haploinsufficiency-mediated mitochondrial coenzyme Q deficiency in skeletal muscle causes mitochondrial myopathy associated with defects in beta-oxidation of fatty acids, aged-matched metabolic reprogramming, and defective physical performance. Calorie restriction has proven to increase lifespan and delay the onset of chronic diseases associated to aging. To study the possible treatment by food deprivation, heterozygous <i>Adck2</i> knockout mice were fed under 40% calorie restriction (CR) and the phenotype was followed for 7 months. The overall glucose and fatty acids metabolism in muscle was restored in mutant mice to WT levels after CR. CR modulated the skeletal muscle metabolic profile of mutant mice, partially rescuing the profile of WT animals. The analysis of mitochondria isol"],"journal":["Frontiers in physiology"],"pagination":["898792"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC9351392"],"repository":["biostudies-literature"],"pubmed_title":["Calorie Restriction Rescues Mitochondrial Dysfunction in Adck2-Deficient Skeletal Muscle."],"pmcid":["PMC9351392"],"pubmed_authors":["Vicente-Garcia C","Hernandez-Camacho JD","Carvajal JJ","Fernandez-Ayala DJM","Navas-Enamorado I","Garcia-Villoria J","Ribes A","Lopez-Lluch G","Oliva C","Artuch R","Navas P","de Cabo R"],"additional_accession":[]},"is_claimable":false,"name":"Calorie Restriction Rescues Mitochondrial Dysfunction in Adck2-Deficient Skeletal Muscle.","description":"ADCK2 haploinsufficiency-mediated mitochondrial coenzyme Q deficiency in skeletal muscle causes mitochondrial myopathy associated with defects in beta-oxidation of fatty acids, aged-matched metabolic reprogramming, and defective physical performance. Calorie restriction has proven to increase lifespan and delay the onset of chronic diseases associated to aging. To study the possible treatment by food deprivation, heterozygous <i>Adck2</i> knockout mice were fed under 40% calorie restriction (CR) and the phenotype was followed for 7 months. The overall glucose and fatty acids metabolism in muscle was restored in mutant mice to WT levels after CR. CR modulated the skeletal muscle metabolic profile of mutant mice, partially rescuing the profile of WT animals. The analysis of mitochondria isol","dates":{"release":"2022-01-01T00:00:00Z","publication":"2022","modification":"2026-07-14T17:39:04.423Z","creation":"2025-02-19T02:27:02.7Z"},"accession":"S-EPMC9351392","cross_references":{"pubmed":["35936917"],"doi":["10.3389/fphys.2022.898792"]}}