6533b7dafe1ef96bd126e1cc

RESEARCH PRODUCT

Control of glycolysis in vertebrate skeletal muscle during exercise

G. WegenerU. Krause

subject

Malemedicine.medical_specialtyPhysiologyPhosphofructokinase-1Physical ExertionRana temporariaBiologychemistry.chemical_compoundGlycogen phosphorylasePhysiology (medical)Internal medicinemedicineAnimalsGlycolysisHexosephosphatesExercise physiologyMuscle SkeletalGlycogenSkeletal muscleHindlimbEnzyme Activationmedicine.anatomical_structureEndocrinologychemistryBiochemistryAnaerobic glycolysisGlycolysisAnaerobic exerciseGlycogenPhosphofructokinase

description

The gastrocnemius muscle of the frog (Rana temporaria) has a high capacity for anaerobic glycolysis from glycogen. Glycolytic metabolites and effectors of phosphofructokinase, particularly the hexose bisphosphates, were followed in muscle during exercise (swimming between 5 s and 5 min), recovery (rest for up to 2 h after 5 min of swimming), and repeated exercise (swimming for up to 60 s after 2 h of recovery). Glycogen phosphorylase and phosphofructokinase were swiftly activated with exercise. The hexose bisphosphates followed markedly different time courses. Fructose 1,6-bisphosphate was transiently increased in both exercise and repeated exercise. This appears to be an effect rather than a cause of phosphofructokinase activation. Glucose 1,6-biphosphate was accumulated only while phosphofructokinase was active and was unchanged at other times. Fructose 2,6-biphosphate showed a 10-fold transient increase on exercise in rested frogs, almost disappeared from the muscle during recovery, and did not change during repeated exercise. Fructose 2,6-biphosphate is a potent activator of phosphofructokinase in vitro under near physiological assay conditions, and it may serve this function also in vivo during exercise. Glucose 1,6-biphosphate could be an activator of phosphofructokinase in repeated exercise when fructose 2,6-biphosphate is not available.

https://doi.org/10.1152/ajpregu.1996.270.4.r821