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AMP decreases the efficiency of skeletal-muscle mitochondria.
Cadenas, S; Buckingham, J A; St-Pierre, J; Dickinson, K; Jones, R B; Brand, M D.
Affiliation
  • Cadenas S; Department of Biochemistry, University of Cambridge, Tennis Court Road, Cambridge CB2 1QW, UK. sc@mrc-dunn.ca.ac.uk
Biochem J ; 351 Pt 2: 307-11, 2000 Oct 15.
Article in En | MEDLINE | ID: mdl-11023814
ABSTRACT
Mitochondrial proton leak in rat muscle is responsible for approx. 15% of the standard metabolic rate, so its modulation could be important in regulating metabolic efficiency. We report in the present paper that physiological concentrations of AMP (K(0.5)=80 microM) increase the resting respiration rate and double the proton conductance of rat skeletal-muscle mitochondria. This effect is specific for AMP. AMP also doubles proton conductance in skeletal-muscle mitochondria from an ectotherm (the frog Rana temporaria), suggesting that AMP activation is not primarily for thermogenesis. AMP activation in rat muscle mitochondria is unchanged when uncoupling protein-3 is doubled by starvation, indicating that this protein is not involved in the AMP effect. AMP activation is, however, abolished by inhibitors and substrates of the adenine nucleotide translocase (ANT), suggesting that this carrier (possibly the ANT1 isoform) mediates AMP activation. AMP activation of ANT could be important for physiological regulation of metabolic rate.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Atractyloside / Adenosine Monophosphate / Muscle, Skeletal / Mitochondria Limits: Animals Language: En Journal: Biochem J Year: 2000 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Atractyloside / Adenosine Monophosphate / Muscle, Skeletal / Mitochondria Limits: Animals Language: En Journal: Biochem J Year: 2000 Document type: Article