
pmid: 16020522
Mechanisms responsible for limitation of exercise capacity in lung transplant recipients (LR) and benefits gained by exercise training were studied. Mitochondrial respiration parameters, energy transfer, and cell structure were assessed in vastus lateralis biopsies using the permeabilized fiber technique with histochemical and morphometric measurements. Twelve male controls (C) and 12 LR performed exercise training over 12 wk. Before exercise training, there were strong correlations between exercise capacity (maximal O2 consumption and endurance time at 70% maximal power output) and cellular events, as assessed by percentage of type I fibers and apparent Km for exogenous ADP. Anticalcineurins were not involved in LR exercise limitation, since there were no differences in maximal mitochondrial rate of respiration before exercise training and no abnormalities in respiratory chain complexes compared with C. Training resulted in a significant increase in physiological parameters both at the cellular (apparent Km for exogenous ADP and stimulating effect of creatine) and integrated (maximal O2 consumption, power output at ventilatory threshold, maximal power output, and endurance time at 70% maximal power output) levels in LR and C. After the training period, improvements in maximal O2 consumption and in maximal mitochondrial rate of respiration were noted, as well as changes in endurance time and percentage of type I fibers. Because there were no changes in diameters and fiber types, baseline alteration of apparent Km for exogenous ADP and its improvement after training might be related to changes within the intracellular energetic units. After the training period, intracellular energetic units exhibited a higher control of mitochondrial respiration by creatine linked to a more efficient functional coupling adenine nucleotide translocase-mitochondrial creatine kinase, resulting in better exercise performances in C and LR.
Adult, Male, MESH: Exercise Tolerance, Physiological, [SDV.BBM]Life Sciences [q-bio]/Biochemistry, Physical Exertion, Creatine Kinase, Mitochondrial Form, 610, MESH: Physical Exertion, MESH: Adaptation, Oxygen Consumption, [SDV.BBM] Life Sciences [q-bio]/Biochemistry, Molecular Biology, Humans, ATP Translocases, MESH: Oxygen Consumption, Muscle, Skeletal, Molecular Biology, Creatine Kinase, Exercise, Aged, MESH: Aged, MESH: Middle Aged, MESH: Creatine Kinase, MESH: Humans, Exercise Tolerance, MESH: Muscle, MESH: Adult, MESH: Mitochondrial ADP, Skeletal, Middle Aged, Adaptation, Physiological, MESH: Male, Isoenzymes, MESH: Exercise, MESH: Isoenzymes, MESH: Lung Transplantation, Mitochondrial Form, Mitochondrial ADP, ATP Translocases, Lung Transplantation
Adult, Male, MESH: Exercise Tolerance, Physiological, [SDV.BBM]Life Sciences [q-bio]/Biochemistry, Physical Exertion, Creatine Kinase, Mitochondrial Form, 610, MESH: Physical Exertion, MESH: Adaptation, Oxygen Consumption, [SDV.BBM] Life Sciences [q-bio]/Biochemistry, Molecular Biology, Humans, ATP Translocases, MESH: Oxygen Consumption, Muscle, Skeletal, Molecular Biology, Creatine Kinase, Exercise, Aged, MESH: Aged, MESH: Middle Aged, MESH: Creatine Kinase, MESH: Humans, Exercise Tolerance, MESH: Muscle, MESH: Adult, MESH: Mitochondrial ADP, Skeletal, Middle Aged, Adaptation, Physiological, MESH: Male, Isoenzymes, MESH: Exercise, MESH: Isoenzymes, MESH: Lung Transplantation, Mitochondrial Form, Mitochondrial ADP, ATP Translocases, Lung Transplantation
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