Larsen 2011 Acta Physiol (Oxf): Difference between revisions

From Bioblast
No edit summary
No edit summary
Line 1: Line 1:
{{Publication
{{Publication
|title=Larsen S, Kristensen JM, Stride N, Wojtaszewski JF, Helge JW, Dela F (2011) Skeletal muscle mitochondrial respiration in AMPKฮฑ2 kinase-dead mice. Acta Physiol (Oxf) Epub ahead of print.
|title=Larsen S, Kristensen JM, Stride N, Wojtaszewski JF, Helge JW, Dela F (2011) Skeletal muscle mitochondrial respiration in AMPKฮฑ2 kinase-dead mice. Acta Physiol (Oxf) 205: 314-320
|info=[http://www.ncbi.nlm.nih.gov/pubmed/22192354 PMID:22192354]
|info=[http://www.ncbi.nlm.nih.gov/pubmed/22192354 PMID:22192354]
|authors=Larsen S, Kristensen JM, Stride N, Wojtaszewski JF, Helge JW, Dela F
|authors=Larsen S, Kristensen JM, Stride N, Wojtaszewski JF, Helge JW, Dela F

Revision as of 16:34, 8 March 2013

Publications in the MiPMap
Larsen S, Kristensen JM, Stride N, Wojtaszewski JF, Helge JW, Dela F (2011) Skeletal muscle mitochondrial respiration in AMPKฮฑ2 kinase-dead mice. Acta Physiol (Oxf) 205: 314-320

ยป PMID:22192354

Larsen S, Kristensen JM, Stride N, Wojtaszewski JF, Helge JW, Dela F (2011) Acta Physiol (Oxf)

Abstract: AIM: To study whether the phenotypical characteristics (exercise intolerance; reduced spontaneous activity) of the AMPKฮฑ2 kinase-dead (KD) mice can be explained by a reduced mitochondrial respiratory flux rates (JO(2) ) in skeletal muscle. Secondly, the effect of the maturation process on JO(2) was studied.

METHODS: In tibialis anterior (almost exclusively type 2 fibres) muscle from young (12-17 weeks, n = 7) and mature (25-27 weeks, n = 12) KD and wild-type (WT) (12-17 weeks, n = 9; 25-27 weeks, n = 11) littermates, JO(2) was quantified in permeabilized fibres ex vivo by respirometry, using a substrate-uncoupler-inhibitor-titration (SUIT) protocol: malate, octanoyl carnitine, ADP and glutamate (GMO(3) ), + succinate (GMOS(3) ), + uncoupler (U) and inhibitor (rotenone) of complex I respiration. Citrate synthase (CS) activity was measured as an index of mitochondrial content.

RESULTS: Citrate synthase activity was highest in young WT animals and lower in KD animals compared with age-matched WT. JO(2) per mg tissue was lower (P < 0.05) in KD animals (state GMOS(3) ). No uncoupling effect was seen in any of the animals. Normalized oxygen flux (JO(2) /CS) revealed a uniform pattern across the SUIT protocol with no effect of KD. However, JO(2) /CS was higher [GMO(3) , GMOS(3) , U and rotenone (only WT)] in the mature compared with the young mice - irrespective of the genotype (P < 0.05).

CONCLUSION: Exercise intolerance and reduced activity level seen in KD mice may be explained by reduced JO(2) in the maximally coupled respiratory state. Furthermore, an enhancement of oxidative phosphorylation capacity per mitochondrion is seen with the maturation process. โ€ข Keywords: AMPKฮฑ2 kinase-dead (KD) mice; substrate-uncoupler-inhibitor-titration (SUIT) protocol

โ€ข O2k-Network Lab: DK_Copenhagen_Dela F


Labels:


Organism: Mouse  Tissue;cell: Skeletal muscle  Preparation: Permeabilized tissue  Enzyme: Complex I 


HRR: Oxygraph-2k 


Cookies help us deliver our services. By using our services, you agree to our use of cookies.