Recovery metabolism of skipjack tuna ( Katsuwonus pelamis ) white muscle : rapid and parallel changes in lactate and phosphocreatine after exercise

Lactate. glycogen, and high-energy phosphate levels were measured in serial biopsies from Nna white muscle during recovery from 15 min of enforced swimming. Exercise caused glycogen and phosphocreatine levels to decrease sharply and lactate concentration to increase markedly (up to 150 pmol ' gl ) . Lactate was cleared from white muscle in less than 90 min. at rates comparable to those seen in mammals (about 1.3 pmol ' g' ' min-'). and this was accompanied by nearly stoichiometric increases in white muscle glycogen (2 lactate : 1 glucosyl unit). The plasma lactate concentration remained elevated (35-40 mM) until lactate clearance from white muscle was completed. whereas the level of plasma glucose was constant (I2 16 mM) for the entire 3-h recovery period. The exercise routine caused mimmal changes in white muscle purine nucleotides apart from a slight, but significant, increase in IMP content. Transient changes in ATP appear to have resulted from Short-term intense swimming activity noted during anesthetization. Unlike other teleosts. lactate clearance in NM paralleled creatine rephosphorylation during recovery from exercise. We suggest that the postexercise adjustment of intracellular pH is responsible for this relationship. Lactate was seemingly metabolized within the white muscle mass. as indicated by in situ conservation of lactate carbon apparent from stiochiometric increases in white muscle glycogen levels. This p r o m is discussed in view of low estimates of lactate utilization rates by other tissues and contrasted with expected high rates of wholebody lactate turnover during recovery. J. Z00l. 70: 1230-1239.

[1]  W. H. Neill,et al.  Respiration rates and low-oxygen tolerance limits in skipjack tuna , 2013 .

[2]  P. W. Hochachka,et al.  Mitochondrial metabolism of cardiac and skeletal muscles from a fast (Katsuwonus pelamis) and a slow (Cyprinus carpio) fish , 1992 .

[3]  R. Boutilier,et al.  WHITE MUSCLE INTRACELLULAR ACID-BASE AND LACTATE STATUS FOLLOWING EXHAUSTIVE EXERCISE: A COMPARISON BETWEEN FRESHWATER- AND SEA WATER- ADAPTED RAINBOW TROUT , 1991 .

[4]  T. Gleeson,et al.  Lactate: a substrate for reptilian muscle gluconeogenesis following exhaustive exercise , 1990, Journal of Comparative Physiology B.

[5]  G. Brooks,et al.  Lactate and pyruvate transport is dominated by a pH gradient-sensitive carrier in rat skeletal muscle sarcolemmal vesicles. , 1990, Archives of biochemistry and biophysics.

[6]  L. Spriet,et al.  EFFECT OF SPRINT TRAINING ON SWIM PERFORMANCE AND WHITE MUSCLE METABOLISM DURING EXERCISE AND RECOVERY IN RAINBOW TROUT (SALMO GAIRDNERI) , 1990 .

[7]  G. Thillart,et al.  Functional coupling of glycolysis and phosphocreatine utilization in anoxic fish muscle. , 1990 .

[8]  W. Ellington,et al.  Effects of extracellular pH and D‐lactate efflux on regulation of intracellular pH during isotonic contractions in a molluscan muscle: A 31p‐nuclear magnetic resonance study , 1989 .

[9]  F. Wibrand,et al.  Lactate transport in isolated mouse muscles studied with a tracer technique--kinetics, stereospecificity, pH dependency and maximal capacity. , 1989, Acta physiologica Scandinavica.

[10]  P. W. Hochachka,et al.  The purine nucleotide cycle as two temporally separated metabolic units: a study on trout muscle. , 1988, Metabolism: clinical and experimental.

[11]  R. Connett,et al.  Analysis of metabolic control: new insights using scaled creatine kinase model. , 1988, The American journal of physiology.

[12]  J. L. Johnson,et al.  Gluconeogenic pathway in liver and muscle glycogen synthesis after exercise. , 1988, Journal of applied physiology.

[13]  D. Mcdonald,et al.  In vivo lactate kinetics at rest and during recovery from exhaustive exercise in coho salmon (Oncorhynchus kisutch) and starry flounder (Platichthys stellatus). , 1988, The Journal of experimental biology.

[14]  C. Wood,et al.  Tissue intracellular acid-base status and the fate of lactate after exhaustive exercise in the rainbow trout. , 1986, The Journal of experimental biology.

[15]  G. Brooks,et al.  Lactate extraction during net lactate release in legs of humans during exercise. , 1986, Journal of applied physiology.

[16]  C. Daxboeck,et al.  Enzymes of energy metabolism and gluconeogenesis in the Pacific blue marlin, Makaira nigricans , 1986 .

[17]  P. Lutz,et al.  Relationships between aerobic and anaerobic energy production in turtle brain in situ. , 1984, The American journal of physiology.

[18]  C. Wood,et al.  Factors Affecting Lactate and Proton Efflux from Pre-exercised, Isolated-perfused Rainbow Trout Trunks , 1983 .

[19]  G. Somero,et al.  Buffering capacity of vertebrate muscle: Correlations with potentials for anaerobic function , 1981, Journal of comparative physiology.

[20]  R. Meyer,et al.  Differences in ammonia and adenylate metabolism in contracting fast and slow muscle. , 1979, The American journal of physiology.

[21]  L. Hermansen,et al.  Lactate disappearance and glycogen synthesis in human muscle after maximal exercise. , 1977, The American journal of physiology.