Regional Changes in Capillary Supply in Skeletal Muscle of Interval-Sprint and Low-Intensity, Endurance-Trained Rats

References

• Adair T H, Gay W J, Montani J. Growth regulation of the vascular system: evidence for a metabolic hypothesis. Am J Physiol 1990; 259: R393–R404
   PubMed Web of Science ®Google Scholar
• Andersen P, Henriksson J. Capillary supply of the quadriceps femoris muscle of man: adaptive response to exercise. J Physiol 1977; 270: 677–690
   PubMed Web of Science ®Google Scholar
• Ariano M A, Armstrong R B, Edgerton V R. Hindlimb muscle fiber populations of five mammals. J Histol Cytol 1973; 21: 51–55
   PubMed Web of Science ®Google Scholar
• Armstrong R B, Laughlin M H. Blood flow within and among rat muscles as a function of time during high speed treadmill exercise. J Physiol 1983; 344: 189–208
   Google Scholar
• Armstrong R B, Laughlin M H. Exercise blood flow patterns within and among rat muscles after training. Am J Physiol 1984; 246: H59–H68
   PubMed Web of Science ®Google Scholar
• Armstrong R B, Marum P, Saubert C W, IV, Seeherman H J, Taylor C R. Muscle fiber activity as a function of speed and gait. J Appl Physiol Respir 1977; 43: 672–677
   PubMed Web of Science ®Google Scholar
• Armstrong R B, Phelps R O. Muscle fiber type composition of the rat hindlimb. Am J Anat 1984; 171: 259–272
   PubMedGoogle Scholar
• Armstrong R B, Saubert C W, IV, Sembrowich W L, Shepherd R E, Gollnick P D. Glycogen depletion in rat skeletal muscle fibers at different intensities and durations of exercise. Pflugers Arch 1974; 352: 243–256
   PubMed Web of Science ®Google Scholar
• Baldwin K M, Cooke D A, Cheadle W G. Time course adaptations in cardiac and skeletal muscle to different running programs. J Appl Physiol: Respiral Environ Exercise Physiol 1977; 42: 267–276
   PubMed Web of Science ®Google Scholar
• Banchero N, Gimenes M, Aquin L, Florentz M. Effects of exercise on capillarity and enzymatic activity of rat skeletal muscle. Bull Eur Physiopathol Respir 1979; 15: 203–216
   Google Scholar
• Carrow R E, Brown R E, van Huss W D. Fiber sizes and capillary to fiber ratios in skeletal muscle of exercised rats. Anat Rec 1967; 159: 33–40
   PubMedGoogle Scholar
• Dudley G A., Abraham W M, Terjung R J. Influence of exercise intensity and duration on biochemical adaptations in skeletal muscle. J Appl Physiol: Respirat Environ Exercise Physiol 1982; 53: 844–850
   PubMed Web of Science ®Google Scholar
• Hudlicka O. What makes blood vessels grow?. J Appl Physiol 1991; 444: 1–24
   Google Scholar
• Ingjer F. Effects of endurance training on muscle fiber ATPase activity, capillary supply and mitochondrial content in man. J Physiol 1979; 294: 419–432
   PubMed Web of Science ®Google Scholar
• Klausen K, Andersen L, Pelle I. Adaptive changes in work capacity, skeletal muscle capillarization and enzyme levels during training and detraining. Acta Physiol Scand 1981; 113: 9–16
   PubMedGoogle Scholar
• Lash J, Bohlen H G. Functional adaptations of rat skeletal muscle arterioles to aerobic exercise training. J Appl Physiol 1992; 72: 2052–2062
   PubMed Web of Science ®Google Scholar
• Laughlin M H, Armstrong R B. Muscular blood flow distribution patterns as a function of running speed in rats. Am J Physiol 1982; 243: H296–H306
   PubMedGoogle Scholar
• Laughlin M H, Korthuis R J, Sexton W L, Armstrong R B. Regional muscle blood flow capacity and exercise hyperemia in high-intensity trained rats. J Appl Physiol 1988; 64: 2420–2427
   PubMed Web of Science ®Google Scholar
• Laughlin M H, Ripperger J. Vascular transport capacity of hindlimb muscles of exercise-trained rats. J Appl Physiol 1987; 62: 438–443
   PubMed Web of Science ®Google Scholar
• Laughlin M H, Tomanek R J. Myocardial capillarity and maximal capillary diffusion capacity in exercise-trained dogs. J Appl Physiol 1987; 63: 1481–1486
   PubMedGoogle Scholar
• Ljundgqvist G, Unge G. Capillary proliferative activity in myocardium and skeletal muscle of exercised rats. J Appl Physiol 1977; 43: 306–307
   Google Scholar
• Mackie B G, Terjung R L. Influence of training on blood flow to different skeletal muscle fiber types. J Appl Physiol 1983; 55: 1072–1078
   PubMed Web of Science ®Google Scholar
• Mai J V, Edgerton V R, Barnard R J. Capillarity of red, white, and intermediate muscle fibers in trained and untrained guinea pigs. Experimentia 1970; 26: 1222–1223
   Google Scholar
• Mathieu-Costello O, Hoppeler H, Weibel E R. Capillary tortuosity in skeletal muscles of mammals depends on muscle contraction. J Appl Physiol 1989; 66: 1436–1442
   PubMed Web of Science ®Google Scholar
• Mathieu-Costello O, Potter R F, Ellis C G, Groom A C. Capillary configuration and fiber shortening in muscles of the rat hindlimb: correlation between corrosion casts and stereological measurements. Microvasc Res 1987; 36: 40–55
   Google Scholar
• McAllister R M, Terjung R L. Training-induced muscle adaptations: increased performance and oxygen consumption. J Appl Physiol 1991; 70: 1569–1574
   Google Scholar
• Peter J B, Barnard R J, Edgerton V R, Gillespie C A, Stempel K E. Metabolic profiles of three fiber types of skeletal muscle in guinea pigs and rabbits. Biochemistry 1972; 11: 2627–2633
   PubMed Web of Science ®Google Scholar
• Poole D C, Mathieu-Costello O, West J B. Capillary tortuosity in rat soleus muscle is not affected by endurance training. Am J Physiol 1989; 256: H1110–H1116
   Google Scholar
• Roca J, Agusti A GN, Alonso A, Poole D C, Viegas C, Barbera J A, Rodriguez-Roisin R, Ferrer A, Wagner P D. Effects of training on muscle O2, transport at VO2 max. J Appl Physiol 1992; 73: 1067–1076
   PubMed Web of Science ®Google Scholar
• Rowell L B. Cardiovascular adaptations to chronic physical activity and inactivity. Human Circulation. Oxford University Press, New York 1986; 257–286
   Google Scholar
• Roy R R, Hutchison D L, Pierotti D J, Hodgson J A, Edgerton V R. EMG patterns of rat ankle extensors and flexors during treadmill locomotion and swimming. J Appl Physiol 1991; 70: 2522–2529
   PubMed Web of Science ®Google Scholar
• Saltin B. Hemodynamic adaptations to exercise. Am J Cardiol 1985; 26: 42D–47D
   Google Scholar
• Saltin B, Gollnick P D. Skeletal muscle adaptability: significance for metabolism and performance. Handbook of Physiology. Skeletal Muscle. American Physiological Society, Bethesda, MD. 1983; 555–631
   Google Scholar
• Sexton W L, Korthuis R J, Laughlin M H. High-intensity exercise training increases vascular transport capacity of rat hindquarters. Am J Physiol 1988; 254: H274–H278
   Google Scholar
• Sheehan D C, Hrapchak B B. Nuclear and cytoplasmic stains. Theory and Practice of Histotechnology. Batelle Press, Columbus, OH. 1987; 144
   Google Scholar
• Smith J L, Edgerton V R, Betts B, Collates T C. EMG of slow and fast ankle extensors of cat during posture, locomotion, and jumping. J Neurophysiol 1977; 40: 503–512
   PubMed Web of Science ®Google Scholar
• Srere P A. Citrate synthase. Met Enz 1969; 13: 3–11
   Google Scholar
• Steel R GD, Torrie J H. Principles and Procedures of Statistics. McGraw-Hill, New York 1960; 161–182
   Google Scholar
• Walmsley B, Hodgson J A, Burke R E. Forces produced by medial gastrocnemius and soleus muscles during locomotion in freely moving cats. J Neurophysiol 1978; 41: 1203–1216
   PubMed Web of Science ®Google Scholar
• Wayne D W. Applied Nonparametric Statistics, 2nd ed. PWS-KENT, Boston 1990; 240–241
   Google Scholar
• Yang H T, Ogilvie R W, Terjung R L. Low-intensity training produces muscle adaptations in rats with femoral artery stenosis. J Appl Physiol 1991; 71: 1822–1829
   Google Scholar