The role of mitochondrial function and cellular bioenergetics in ageing and disease.

TitleThe role of mitochondrial function and cellular bioenergetics in ageing and disease.
Publication TypeJournal Article
Year of Publication2013
AuthorsBrand MD, Orr AL, Perevoshchikova IV, Quinlan CL
JournalBr J Dermatol
Volume169 Suppl 2
Pagination1-8
Date Published2013 Jul
ISSN1365-2133
KeywordsAdenosine Triphosphate, Aging, Calcium, Energy Metabolism, Humans, Hydrogen Peroxide, Mitochondria, Mitochondrial Diseases, Superoxides
Abstract

Mitochondria constitute an important topic of biomedical enquiry (one paper in every 154 indexed in PubMed since 1998 is retrieved by the keyword 'mitochondria') because of widespread recognition of their importance in cell physiology and pathology. Mitochondrial dysfunction is widely implicated in ageing and in the diseases of ageing, through dysfunction in adenosine triphosphate (ATP) synthesis, Ca(2+) homeostasis, central metabolic pathways or radical production. Nonetheless, the mechanisms and regulation of superoxide and hydrogen peroxide formation by mitochondria remain poorly described. Measurement of the capacities of different sites of superoxide and hydrogen peroxide production in isolated skeletal muscle mitochondria show that the maximum capacities of sites in complexes I, II and III and in several associated redox enzymes greatly exceed the native rates observed in the absence of respiratory chain inhibitors. In vitro, the native rates and the relative importance of different sites both depend on the substrate being oxidized, with sites IQ, IIF, GPDH, IF and IIIQo each being important with particular substrates. The techniques involved in measuring rates from each site should become applicable to cell cultures and in vivo in the future.

DOI10.1111/bjd.12208
Alternate JournalBr. J. Dermatol.
PubMed ID23786614
PubMed Central IDPMC4321783
Grant ListPL1 AG032118 / AG / NIA NIH HHS / United States
P01 AG025901 / AG / NIA NIH HHS / United States
TL1 AG032116 / AG / NIA NIH HHS / United States
AND TL1 AG032116 / AG / NIA NIH HHS / United States
R01 AG033542 / AG / NIA NIH HHS / United States