Increased acetyl group availability enhances contractile function of canine skeletal muscle during ischemia.
about
New insights concerning the role of carnitine in the regulation of fuel metabolism in skeletal muscleMetabolic adaptations to repeated periods of contraction with reduced blood flow in canine skeletal muscle.Oxygen uptake on-kinetics in dog gastrocnemius in situ following activation of pyruvate dehydrogenase by dichloroacetateThe effects of increasing exercise intensity on muscle fuel utilisation in humansRoles of the creatine kinase system and myoglobin in maintaining energetic state in the working heart.Muscle oxygen uptake in humans at onset of and during intense exercise.Fat burners: nutrition supplements that increase fat metabolism.Variability in training-induced skeletal muscle adaptation.Metabolic inertia in contracting skeletal muscle: a novel approach for pharmacological intervention in peripheral vascular diseaseCarnitine Acetyltransferase Mitigates Metabolic Inertia and Muscle Fatigue during ExerciseSubstrate availability limits human skeletal muscle oxidative ATP regeneration at the onset of ischemic exercise.Exercise: Kinetic considerations for gas exchange.The intramuscular contribution to the slow oxygen uptake kinetics during exercise in chronic heart failure is related to the severity of the condition.Effects of acetate infusion and hyperoxia on muscle substrate phosphorylation after onset of moderate exercise.Dynamic asymmetry of phosphocreatine concentration and O(2) uptake between the on- and off-transients of moderate- and high-intensity exercise in humans.The acetyl group deficit at the onset of contraction in ischaemic canine skeletal muscle.Bicarbonate-induced alkalosis augments cellular acetyl group availability and isometric force during the rest-to-work transition in canine skeletal muscle.Carbohydrate ingestion reduces skeletal muscle acetylcarnitine availability but has no effect on substrate phosphorylation at the onset of exercise in man.Dichloroacetate accelerates the fall in intracellular PO2 at onset of contractions in Xenopus single muscle fibers.Effects of dichloroacetate on VO2 and intramuscular 31P metabolite kinetics during high-intensity exercise in humans.Acetyl-CoA provision and the acetyl group deficit at the onset of contraction in ischemic canine skeletal muscle.Acetyl group availability influences phosphocreatine degradation even during intense muscle contraction.Regulation of pyruvate dehydrogenase activity and citric acid cycle intermediates during high cardiac power generation.Muscle pyruvate availability can limit the flux, but not activation, of the pyruvate dehydrogenase complex during submaximal exercise in humans.Prior heavy exercise eliminates VO2 slow component and reduces efficiency during submaximal exercise in humans.On-off asymmetries in oxygen consumption kinetics of single Xenopus laevis skeletal muscle fibres suggest higher-order control.No effect of glutamine supplementation and hyperoxia on oxidative metabolism and performance during high-intensity exercise.Bioenergetics of contracting skeletal muscle after partial reduction of blood flow.Linear relation between time constant of oxygen uptake kinetics, total creatine, and mitochondrial content in vitro.No acetyl group deficit is evident at the onset of exercise at 90% of maximal oxygen uptake in humans.Pharmacological activation of the pyruvate dehydrogenase complex reduces statin-mediated upregulation of FOXO gene targets and protects against statin myopathy in rodents.A raised metabolic rate slows pulmonary O2uptake kinetics on transition to moderate-intensity exercise in humans independently of work rate
P2860
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P2860
Increased acetyl group availability enhances contractile function of canine skeletal muscle during ischemia.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on February 1996
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Increased acetyl group availab ...... eletal muscle during ischemia.
@en
Increased acetyl group availab ...... eletal muscle during ischemia.
@nl
type
label
Increased acetyl group availab ...... eletal muscle during ischemia.
@en
Increased acetyl group availab ...... eletal muscle during ischemia.
@nl
prefLabel
Increased acetyl group availab ...... eletal muscle during ischemia.
@en
Increased acetyl group availab ...... eletal muscle during ischemia.
@nl
P2860
P50
P356
P1476
Increased acetyl group availab ...... keletal muscle during ischemia
@en
P2093
S M Poucher
P2860
P304
P356
10.1172/JCI118490
P407
P577
1996-02-01T00:00:00Z