Difference between revisions of "Ludzki 2014 Thesis"
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|journal=Thesis University of Guelph | |journal=Thesis University of Guelph | ||
|abstract=A hallmark of improved metabolic control is a reduced free ADP requirement for | |abstract=A hallmark of improved metabolic control is a reduced free ADP requirement for | ||
a given workload (increased ADP sensitivity). In contrast to in vivo data, | a given workload (increased ADP sensitivity). In contrast to ''in vivo'' data, | ||
in situ assessments suggest that mitochondrial ADP sensitivity is decreased following exercise training, implying external regulat ion that is not recapitulated in situ. One previously unexplored regulator is palmitoyl-CoA (P- | in situ assessments suggest that mitochondrial ADP sensitivity is decreased following exercise training, implying external regulat ion that is not recapitulated in situ. One previously unexplored regulator is palmitoyl-CoA (P- | ||
CoA), alipid metabolism intermediate that inhibits the mitochondrial ADP transport protein adenine nucleotide transferase (ANT). This thesis: 1) established reduced mitochondrial ADP sensitivity following exercise training | CoA), alipid metabolism intermediate that inhibits the mitochondrial ADP transport protein adenine nucleotide transferase (ANT). This thesis: 1) established reduced mitochondrial ADP sensitivity following exercise training | ||
in middle aged males using permeabilized muscle fibre bundles (PmFB), 2) determined a methodology to evaluate ADP kinetics in PmFB in the presence of P | in middle aged males using permeabilized muscle fibre bundles (PmFB), 2) determined a methodology to evaluate ADP kinetics in PmFB in the presence of P | ||
-CoA, and 3) found increased mitochondrial ADP sensitivity in the presence of P | -CoA, and 3) found increased mitochondrial ADP sensitivity in the presence of P | ||
-CoA following training. These data suggest that P- CoA is a key regulator of oxidative phosphorylation and direct future exploration of mitochondrial function towards the control of ADP transport via ANT and the effects of exercise on the P-CoA-ANT interaction | -CoA following training. These data suggest that P- CoA is a key regulator of oxidative phosphorylation and direct future exploration of mitochondrial function towards the control of ADP transport via ANT and the effects of exercise on the P-CoA-ANT interaction. | ||
|mipnetlab= | |mipnetlab=CA Guelph Holloway GP | ||
}} | }} | ||
{{Labeling | {{Labeling | ||
Revision as of 16:38, 9 March 2015
| Ludzki AC (2014) Palmitoyl-CoA inhibition of mitochondrial ADP sensitivity is attenuated by exercise training in human skeletal muscle. Thesis University of Guelph, 1-86. |
» Thesis
Ludzki AC (2014) Thesis University of Guelph
Abstract: A hallmark of improved metabolic control is a reduced free ADP requirement for a given workload (increased ADP sensitivity). In contrast to in vivo data, in situ assessments suggest that mitochondrial ADP sensitivity is decreased following exercise training, implying external regulat ion that is not recapitulated in situ. One previously unexplored regulator is palmitoyl-CoA (P- CoA), alipid metabolism intermediate that inhibits the mitochondrial ADP transport protein adenine nucleotide transferase (ANT). This thesis: 1) established reduced mitochondrial ADP sensitivity following exercise training in middle aged males using permeabilized muscle fibre bundles (PmFB), 2) determined a methodology to evaluate ADP kinetics in PmFB in the presence of P -CoA, and 3) found increased mitochondrial ADP sensitivity in the presence of P -CoA following training. These data suggest that P- CoA is a key regulator of oxidative phosphorylation and direct future exploration of mitochondrial function towards the control of ADP transport via ANT and the effects of exercise on the P-CoA-ANT interaction.
• O2k-Network Lab: CA Guelph Holloway GP
Labels: MiParea: Respiration, Exercise physiology;nutrition;life style
Organism: Human, Mouse
Tissue;cell: Skeletal muscle
Preparation: Permeabilized tissue
Coupling state: LEAK, OXPHOS
HRR: Oxygraph-2k
Labels
