Cargando…

Hypothesis on Skeletal Muscle Aging: Mitochondrial Adenine Nucleotide Translocator Decreases Reactive Oxygen Species Production While Preserving Coupling Efficiency

Mitochondrial membrane potential is the major regulator of mitochondrial functions, including coupling efficiency and production of reactive oxygen species (ROS). Both functions are crucial for cell bioenergetics. We previously presented evidences for a specific modulation of adenine nucleotide tran...

Descripción completa

Detalles Bibliográficos
Autores principales: Diolez, Philippe, Bourdel-Marchasson, Isabelle, Calmettes, Guillaume, Pasdois, Philippe, Detaille, Dominique, Rouland, Richard, Gouspillou, Gilles
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4679911/
https://www.ncbi.nlm.nih.gov/pubmed/26733871
http://dx.doi.org/10.3389/fphys.2015.00369
_version_ 1782405607556382720
author Diolez, Philippe
Bourdel-Marchasson, Isabelle
Calmettes, Guillaume
Pasdois, Philippe
Detaille, Dominique
Rouland, Richard
Gouspillou, Gilles
author_facet Diolez, Philippe
Bourdel-Marchasson, Isabelle
Calmettes, Guillaume
Pasdois, Philippe
Detaille, Dominique
Rouland, Richard
Gouspillou, Gilles
author_sort Diolez, Philippe
collection PubMed
description Mitochondrial membrane potential is the major regulator of mitochondrial functions, including coupling efficiency and production of reactive oxygen species (ROS). Both functions are crucial for cell bioenergetics. We previously presented evidences for a specific modulation of adenine nucleotide translocase (ANT) appearing during aging that results in a decrease in membrane potential - and therefore ROS production—but surprisingly increases coupling efficiency under conditions of low ATP turnover. Careful study of the bioenergetic parameters (oxidation and phosphorylation rates, membrane potential) of isolated mitochondria from skeletal muscles (gastrocnemius) of aged and young rats revealed a remodeling at the level of the phosphorylation system, in the absence of alteration of the inner mitochondrial membrane (uncoupling) or respiratory chain complexes regulation. We further observed a decrease in mitochondrial affinity for ADP in aged isolated mitochondria, and higher sensitivity of ANT to its specific inhibitor atractyloside. This age-induced modification of ANT results in an increase in the ADP concentration required to sustain the same ATP turnover as compared to young muscle, and therefore in a lower membrane potential under phosphorylating—in vivo—conditions. Thus, for equivalent ATP turnover (cellular ATP demand), coupling efficiency is even higher in aged muscle mitochondria, due to the down-regulation of inner membrane proton leak caused by the decrease in membrane potential. In the framework of the radical theory of aging, these modifications in ANT function may be the result of oxidative damage caused by intra mitochondrial ROS and may appear like a virtuous circle where ROS induce a mechanism that reduces their production, without causing uncoupling, and even leading in improved efficiency. Because of the importance of ROS as therapeutic targets, this new mechanism deserves further studies.
format Online
Article
Text
id pubmed-4679911
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-46799112016-01-05 Hypothesis on Skeletal Muscle Aging: Mitochondrial Adenine Nucleotide Translocator Decreases Reactive Oxygen Species Production While Preserving Coupling Efficiency Diolez, Philippe Bourdel-Marchasson, Isabelle Calmettes, Guillaume Pasdois, Philippe Detaille, Dominique Rouland, Richard Gouspillou, Gilles Front Physiol Physiology Mitochondrial membrane potential is the major regulator of mitochondrial functions, including coupling efficiency and production of reactive oxygen species (ROS). Both functions are crucial for cell bioenergetics. We previously presented evidences for a specific modulation of adenine nucleotide translocase (ANT) appearing during aging that results in a decrease in membrane potential - and therefore ROS production—but surprisingly increases coupling efficiency under conditions of low ATP turnover. Careful study of the bioenergetic parameters (oxidation and phosphorylation rates, membrane potential) of isolated mitochondria from skeletal muscles (gastrocnemius) of aged and young rats revealed a remodeling at the level of the phosphorylation system, in the absence of alteration of the inner mitochondrial membrane (uncoupling) or respiratory chain complexes regulation. We further observed a decrease in mitochondrial affinity for ADP in aged isolated mitochondria, and higher sensitivity of ANT to its specific inhibitor atractyloside. This age-induced modification of ANT results in an increase in the ADP concentration required to sustain the same ATP turnover as compared to young muscle, and therefore in a lower membrane potential under phosphorylating—in vivo—conditions. Thus, for equivalent ATP turnover (cellular ATP demand), coupling efficiency is even higher in aged muscle mitochondria, due to the down-regulation of inner membrane proton leak caused by the decrease in membrane potential. In the framework of the radical theory of aging, these modifications in ANT function may be the result of oxidative damage caused by intra mitochondrial ROS and may appear like a virtuous circle where ROS induce a mechanism that reduces their production, without causing uncoupling, and even leading in improved efficiency. Because of the importance of ROS as therapeutic targets, this new mechanism deserves further studies. Frontiers Media S.A. 2015-12-16 /pmc/articles/PMC4679911/ /pubmed/26733871 http://dx.doi.org/10.3389/fphys.2015.00369 Text en Copyright © 2015 Diolez, Bourdel-Marchasson, Calmettes, Pasdois, Detaille, Rouland and Gouspillou. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Diolez, Philippe
Bourdel-Marchasson, Isabelle
Calmettes, Guillaume
Pasdois, Philippe
Detaille, Dominique
Rouland, Richard
Gouspillou, Gilles
Hypothesis on Skeletal Muscle Aging: Mitochondrial Adenine Nucleotide Translocator Decreases Reactive Oxygen Species Production While Preserving Coupling Efficiency
title Hypothesis on Skeletal Muscle Aging: Mitochondrial Adenine Nucleotide Translocator Decreases Reactive Oxygen Species Production While Preserving Coupling Efficiency
title_full Hypothesis on Skeletal Muscle Aging: Mitochondrial Adenine Nucleotide Translocator Decreases Reactive Oxygen Species Production While Preserving Coupling Efficiency
title_fullStr Hypothesis on Skeletal Muscle Aging: Mitochondrial Adenine Nucleotide Translocator Decreases Reactive Oxygen Species Production While Preserving Coupling Efficiency
title_full_unstemmed Hypothesis on Skeletal Muscle Aging: Mitochondrial Adenine Nucleotide Translocator Decreases Reactive Oxygen Species Production While Preserving Coupling Efficiency
title_short Hypothesis on Skeletal Muscle Aging: Mitochondrial Adenine Nucleotide Translocator Decreases Reactive Oxygen Species Production While Preserving Coupling Efficiency
title_sort hypothesis on skeletal muscle aging: mitochondrial adenine nucleotide translocator decreases reactive oxygen species production while preserving coupling efficiency
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4679911/
https://www.ncbi.nlm.nih.gov/pubmed/26733871
http://dx.doi.org/10.3389/fphys.2015.00369
work_keys_str_mv AT diolezphilippe hypothesisonskeletalmuscleagingmitochondrialadeninenucleotidetranslocatordecreasesreactiveoxygenspeciesproductionwhilepreservingcouplingefficiency
AT bourdelmarchassonisabelle hypothesisonskeletalmuscleagingmitochondrialadeninenucleotidetranslocatordecreasesreactiveoxygenspeciesproductionwhilepreservingcouplingefficiency
AT calmettesguillaume hypothesisonskeletalmuscleagingmitochondrialadeninenucleotidetranslocatordecreasesreactiveoxygenspeciesproductionwhilepreservingcouplingefficiency
AT pasdoisphilippe hypothesisonskeletalmuscleagingmitochondrialadeninenucleotidetranslocatordecreasesreactiveoxygenspeciesproductionwhilepreservingcouplingefficiency
AT detailledominique hypothesisonskeletalmuscleagingmitochondrialadeninenucleotidetranslocatordecreasesreactiveoxygenspeciesproductionwhilepreservingcouplingefficiency
AT roulandrichard hypothesisonskeletalmuscleagingmitochondrialadeninenucleotidetranslocatordecreasesreactiveoxygenspeciesproductionwhilepreservingcouplingefficiency
AT gouspillougilles hypothesisonskeletalmuscleagingmitochondrialadeninenucleotidetranslocatordecreasesreactiveoxygenspeciesproductionwhilepreservingcouplingefficiency