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Mitochondrial and performance adaptations to exercise training in mice lacking skeletal muscle LKB1.

American journal of physiology. Endocrinology and metabolism (2013-08-29)
Colby B Tanner, Steven R Madsen, David M Hallowell, Darren M J Goring, Timothy M Moore, Shalene E Hardman, Megan R Heninger, Daniel R Atwood, David M Thomson
ABSTRACT

LKB1 and its downstream targets of the AMP-activated protein kinase family are important regulators of many aspects of skeletal muscle cell function, including control of mitochondrial content and capillarity. LKB1 deficiency in skeletal and cardiac muscle (mLKB1-KO) greatly impairs exercise capacity. However, cardiac dysfunction in that genetic model prevents a clear assessment of the role of skeletal muscle LKB1 in the observed effects. Our purposes here were to determine whether skeletal muscle-specific knockout of LKB1 (skmLKB1-KO) decreases exercise capacity and mitochondrial protein content, impairs accretion of mitochondrial proteins after exercise training, and attenuates improvement in running performance after exercise training. We found that treadmill and voluntary wheel running capacity was reduced in skmLKB1-KO vs. control (CON) mice. Citrate synthase activity, succinate dehydrogenase activity, and pyruvate dehydrogenase kinase content were lower in KO vs. CON muscles. Three weeks of treadmill training resulted in significantly increased treadmill running performance in both CON and skmLKB1-KO mice. Citrate synthase activity increased significantly with training in both genotypes, but protein content and activity for components of the mitochondrial electron transport chain increased only in CON mice. Capillarity and VEGF protein was lower in skmLKB1-KO vs. CON muscles, but VEGF increased with training only in skmLKB1-KO. Three hours after an acute bout of muscle contractions, PGC-1α, cytochrome c, and VEGF gene expression all increased in CON but not skmLKB1-KO muscles. Our findings indicate that skeletal muscle LKB1 is required for accretion of some mitochondrial proteins but not for early exercise capacity improvements with exercise training.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Cytochrome c Oxidase Assay Kit, sufficient for 100 tests, soluble and membrane bound mitochondria
Sigma-Aldrich
KiCqStart® SYBR® Green qPCR ReadyMix, For Bio-Rad, Cepheid, Eppendorf, Illumina, Corbett, and Roche systems
Sigma-Aldrich
KiCqStart® SYBR® Green qPCR ReadyMix, Low ROX, for ABI and Stratagene instruments
Sigma-Aldrich
Anti-PGC-1 Antibody, Chemicon®, from rabbit
Sigma-Aldrich
KiCqStart® SYBR® Green qPCR ReadyMix, iQ, with fluorescein for Bio-Rad systems