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dc.contributor.author Salin K
dc.contributor.author Villasevil EM
dc.contributor.author Anderson GJ
dc.contributor.author Auer SK
dc.contributor.author Selman C
dc.contributor.author Hartley RC
dc.contributor.author Mullen W
dc.contributor.author Chinopoulos, Christos
dc.contributor.author Metcalfe NB
dc.date.accessioned 2019-03-28T08:25:39Z
dc.date.available 2019-03-28T08:25:39Z
dc.date.issued 2018
dc.identifier 85047664339
dc.identifier.citation journalVolume=32;journalIssueNumber=9;journalTitle=FUNCTIONAL ECOLOGY;pagerange=2149-2157;journalAbbreviatedTitle=FUNCT ECOL;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/6673
dc.identifier.uri doi:10.1111/1365-2435.13125
dc.description.abstract Many animals experience periods of food shortage in their natural environment. It has been hypothesised that the metabolic responses of animals to naturally-occurring periods of food deprivation may have long-term negative impacts on their subsequent life-history. In particular, reductions in energy requirements in response to fasting may help preserve limited resources but potentially come at a cost of increased oxidative stress. However, little is known about this trade-off since studies of energy metabolism are generally conducted separately from those of oxidative stress. Using a novel approach that combines measurements of mitochondrial function with in vivo levels of hydrogen peroxide (H2O2) in brown trout (Salmo trutta), we show here that fasting induces energy savings in a highly metabolically active organ (the liver) but at the cost of a significant increase in H2O2, an important form of reactive oxygen species (ROS). After a 2-week period of fasting, brown trout reduced their whole-liver mitochondrial respiratory capacities (state 3, state 4 and cytochrome c oxidase activity), mainly due to reductions in liver size (and hence the total mitochondrial content). This was compensated for at the level of the mitochondrion, with an increase in state 3 respiration combined with a decrease in state 4 respiration, suggesting a selective increase in the capacity to produce ATP without a concomitant increase in energy dissipated through proton leakage. However, the reduction in total hepatic metabolic capacity in fasted fish was associated with an almost two-fold increase in in vivo mitochondrial H2O2 levels (as measured by the MitoB probe). The resulting increase in mitochondrial ROS, and hence potential risk of oxidative damage, provides mechanistic insight into the trade-off between the short-term energetic benefits of reducing metabolism in response to fasting and the potential long-term costs to subsequent life-history traits. © 2018 British Ecological Society.
dc.format.extent 2149-2157
dc.relation.ispartof urn:issn:0269-8463
dc.title Decreased mitochondrial metabolic requirements in fasting animals carry an oxidative cost
dc.type Journal Article
dc.date.updated 2019-01-22T12:08:53Z
dc.language.rfc3066 en
dc.rights.holder NULL
dc.identifier.mtmt 3382133
dc.contributor.department SE/AOK/I/Orvosi Biokémiai Intézet
dc.contributor.institution Semmelweis Egyetem


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