| Literature DB >> 26523761 |
Marina Villanueva Paz1, David Cotán1, Juan Garrido-Maraver1, Mario D Cordero2, Manuel Oropesa-Ávila1, Mario de La Mata1, Ana Delgado Pavón1, Isabel de Lavera1, Elizabet Alcocer-Gómez1, José A Sánchez-Alcázar1.
Abstract
INTRODUCTION: Mitochondrial diseases are a group of rare genetic diseases with complex and heterogeneous origins which manifest a great variety of phenotypes. Disruption of the oxidative phosphorylation system is the main cause of pathogenicity in mitochondrial diseases since it causes accumulation of reactive oxygen species (ROS) and ATP depletion. AREAS COVERED: Current evidences support the main protective role of autophagy and mitophagy in mitochondrial diseases and other diseases associated with mitochondrial dysfunction. EXPERT OPINION: The use of autophagy and/or mitophagy inducers may allow a novel strategy for improving mitochondrial function for both mitochondrial diseases and other diseases with altered mitochondrial metabolism. However, a deeper investigation of the molecular mechanisms behind mitophagy and mitochondrial biogenesis is needed in order to safely modulate these processes. In the coming years, we will also see an increase in awareness of mitochondrial dynamics modulation that will allow the therapeutic use of new drugs for improving mitochondrial function in a great variety of mitochondrial disorders.Entities:
Keywords: AICAR; AMPK; Parkin; ROS; autophagy; coenzyme Q10; heteroplasmy; mTOR; mitochondrial dynamics; mitophagy; rapamycin
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Year: 2015 PMID: 26523761 DOI: 10.1517/14728222.2016.1101068
Source DB: PubMed Journal: Expert Opin Ther Targets ISSN: 1472-8222 Impact factor: 6.902