Skeletal muscle adaptations to testosterone and resistance training in men with COPD.

We recently reported increased leg lean mass and strength in men with chronic obstructive pulmonary disease (COPD) receiving 10 wk of testosterone (T) and leg resistance training (R) (Casaburi R, Bhasin S, Cosentino L, Porszasz J, Somfay A, Lewis M, Fournier M, Storer T. Am J Respir Crit Care Med 170: 870-878, 2004). The present study evaluates the role of muscle IGF and related factors as potential mechanisms for our findings, using quadriceps muscle biopsies from the same cohort. Patient groups were 1) weekly placebo (P) injections + no R; 2) P and R; 3) weekly injections of T + no R; and 4) T + R (TR). Muscle fibers were classified histochemically, and their cross-sectional areas (CSAs) and fiber density (number of fibers per unit area) were determined. Gene transcripts were determined by real-time PCR and protein expression by RIA. While no significant changes in fiber CSAs were noted across groups, increased trends were observed after 10 wk, and significant decrements in muscle fiber density were noted in all treated groups. A global increase in all myosin heavy chain (MyHC) mRNA isoforms was observed in TR patients. Muscle IGF-IEa and IGF-IEc mRNAs were significantly increased with TR group. Muscle IGF-I protein was increased in all intervention groups (greatest in TR). While TR IGF-II mRNA was increased, protein levels were unaltered. IGF binding protein-4 mRNA was increased with TR. Myogenin mRNA was increased in both T groups, while MyoD and myostatin were unchanged. Muscle atrophy F-box mRNA tended to increase with TR. Our data suggest that the combined interventions produced an enhanced local anabolic milieu driven in large part by the muscle IGF system, despite potentially negative biochemical influences present in COPD patients.

[1]  A. Narva,et al.  The National Kidney Disease Education Program and other related efforts in the United States , 2008, Scandinavian journal of clinical and laboratory investigation. Supplementum.

[2]  P. Schjerling,et al.  Suppression of testosterone does not blunt mRNA expression of myoD, myogenin, IGF, myostatin or androgen receptor post strength training in humans , 2007, The Journal of physiology.

[3]  A. Russell,et al.  Akt signalling through GSK‐3β, mTOR and Foxo1 is involved in human skeletal muscle hypertrophy and atrophy , 2006, The Journal of physiology.

[4]  David J. Kosek,et al.  Efficacy of myonuclear addition may explain differential myofiber growth among resistance-trained young and older men and women. , 2006, American journal of physiology. Endocrinology and metabolism.

[5]  David J. Kosek,et al.  Efficacy of 3 days/wk resistance training on myofiber hypertrophy and myogenic mechanisms in young vs. older adults. , 2006, Journal of applied physiology.

[6]  G. Goldspink Mechanical signals, IGF-I gene splicing, and muscle adaptation. , 2005, Physiology.

[7]  M. Tobin,et al.  Hypogonadism in men with chronic obstructive pulmonary disease: prevalence and quality of life. , 2005, American journal of respiratory and critical care medicine.

[8]  R. Casaburi,et al.  Effects of testosterone and resistance training in men with chronic obstructive pulmonary disease. , 2004, American journal of respiratory and critical care medicine.

[9]  Wei Zheng,et al.  Androgen receptor in human skeletal muscle and cultured muscle satellite cells: up-regulation by androgen treatment. , 2004, The Journal of clinical endocrinology and metabolism.

[10]  M. Kjaer,et al.  The effect of recombinant human growth hormone and resistance training on IGF‐I mRNA expression in the muscles of elderly men , 2004, The Journal of physiology.

[11]  W. Mitch,et al.  Activation of caspase-3 is an initial step triggering accelerated muscle proteolysis in catabolic conditions. , 2004, The Journal of clinical investigation.

[12]  W. Reid,et al.  Respiratory muscle injury in animal models and humans , 2004, Molecular and Cellular Biochemistry.

[13]  H. Pilegaard,et al.  Resistance exercise alters MRF and IGF-I mRNA content in human skeletal muscle. , 2003, Journal of applied physiology.

[14]  A. Hoeflich,et al.  IGF-binding protein-4: biochemical characteristics and functional consequences. , 2003, The Journal of endocrinology.

[15]  B. Cercek,et al.  Insulin-like growth factor I prevents corticosteroid-induced diaphragm muscle atrophy in emphysematous hamsters. , 2003, American journal of physiology. Regulatory, integrative and comparative physiology.

[16]  S. Roth,et al.  Testosterone-induced muscle hypertrophy is associated with an increase in satellite cell number in healthy, young men. , 2003, American journal of physiology. Endocrinology and metabolism.

[17]  E. Metter,et al.  Myostatin Gene Expression is Reduced in Humans with Heavy-Resistance Strength Training: A Brief Communication , 2003, Experimental biology and medicine.

[18]  Richard W. Orrell,et al.  Expression of IGF-I splice variants in young and old human skeletal muscle after high resistance exercise.[see comment] , 2003 .

[19]  R W Orrell,et al.  Expression of IGF‐I splice variants in young and old human skeletal muscle after high resistance exercise , 2003, The Journal of physiology.

[20]  J. Patrie,et al.  Single and combined effects of growth hormone and testosterone administration on measures of body composition, physical performance, mood, sexual function, bone turnover, and muscle gene expression in healthy older men. , 2002, The Journal of clinical endocrinology and metabolism.

[21]  J. Thissen,et al.  Inhibition of muscle insulin-like growth factor I expression by tumor necrosis factor-alpha. , 2002, American journal of physiology. Endocrinology and metabolism.

[22]  N. Chavannes,et al.  Local and systemic inflammation in patients with chronic obstructive pulmonary disease: soluble tumor necrosis factor receptors are increased in sputum. , 2002, American journal of respiratory and critical care medicine.

[23]  R. Wolfe,et al.  Testosterone administration to older men improves muscle function: molecular and physiological mechanisms. , 2002, American journal of physiology. Endocrinology and metabolism.

[24]  D. Clemmons,et al.  Role of IGF-I and IGF-binding proteins within diaphragm muscle in modulating the effects of nandrolone. , 2002, American journal of physiology. Endocrinology and metabolism.

[25]  A. Goldberg,et al.  Atrogin-1, a muscle-specific F-box protein highly expressed during muscle atrophy , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[26]  F. Maltais,et al.  Peripheral muscle wasting in chronic obstructive pulmonary disease. Clinical relevance and mechanisms. , 2001, American journal of respiratory and critical care medicine.

[27]  D J Glass,et al.  Identification of Ubiquitin Ligases Required for Skeletal Muscle Atrophy , 2001, Science.

[28]  A. Ionescu,et al.  Inflammatory response and body composition in chronic obstructive pulmonary disease. , 2001, American journal of respiratory and critical care medicine.

[29]  B. Ursø,et al.  Oral creatine supplementation facilitates the rehabilitation of disuse atrophy and alters the expression of muscle myogenic factors in humans , 2001, The Journal of physiology.

[30]  E. Wouters,et al.  Systemic anti-inflammatory mediators in COPD: increase in soluble interleukin 1 receptor II during treatment of exacerbations , 2001, Thorax.

[31]  S. Lareau,et al.  Pulmonary rehabilitation , 2001, Breathe.

[32]  S. Adi,et al.  Opposing early inhibitory and late stimulatory effects of insulin‐like growth factor‐I on myogenin gene transcription , 2000, Journal of cellular biochemistry.

[33]  A. Hoeflich,et al.  Transgenic mouse models for studying the functions of insulin‐like growth factor‐binding proteins , 2000, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[34]  S Rozen,et al.  Primer3 on the WWW for general users and for biologist programmers. , 2000, Methods in molecular biology.

[35]  R. Simsolo,et al.  Effect of weight loss on muscle fiber type, fiber size, capillarity, and succinate dehydrogenase activity in humans. , 1999, The Journal of clinical endocrinology and metabolism.

[36]  A. Masuda,et al.  Anisotropic electrical conduction and reduction in dangling-bond density for polycrystalline Si films prepared by catalytic chemical vapor deposition , 1999 .

[37]  A. Musarò,et al.  Maturation of the Myogenic Program Is Induced by Postmitotic Expression of Insulin-Like Growth Factor I , 1999, Molecular and Cellular Biology.

[38]  G. Sieck,et al.  Alterations in diaphragm contractility after nandrolone administration: an analysis of potential mechanisms. , 1999, Journal of applied physiology.

[39]  J. Kehayias,et al.  Insulin-like growth factor I in skeletal muscle after weight-lifting exercise in frail elders. , 1999, The American journal of physiology.

[40]  J. Arenas,et al.  Histochemical study of the vastus lateralis muscle fibre types of athletes. , 1998, Journal of physiology and biochemistry.

[41]  Reid Wd,et al.  Respiratory muscle injury in animal models and humans , 1998 .

[42]  H. Magnussen,et al.  Testosterone levels in men with chronic obstructive pulmonary disease with or without glucocorticoid therapy. , 1998, The European respiratory journal.

[43]  E. Wouters,et al.  Peak exercise response in relation to tissue depletion in patients with chronic obstructive pulmonary disease. , 1997, The European respiratory journal.

[44]  E. Wouters,et al.  Effects of an acute exacerbation on nutritional and metabolic profile of patients with COPD. , 1997, The European respiratory journal.

[45]  F. Booth,et al.  Myogenic regulatory factors during regeneration of skeletal muscle in young, adult, and old rats. , 1997, Journal of applied physiology.

[46]  K. Westerterp,et al.  Total free living energy expenditure in patients with severe chronic obstructive pulmonary disease. , 1997, American journal of respiratory and critical care medicine.

[47]  J R Florini,et al.  Growth hormone and the insulin-like growth factor system in myogenesis. , 1996, Endocrine reviews.

[48]  C. Stewart,et al.  Growth, differentiation, and survival: multiple physiological functions for insulin-like growth factors. , 1996, Physiological reviews.

[49]  W. Parkhouse,et al.  The potential role of insulin-like growth factors in skeletal muscle regeneration. , 1996, Canadian journal of applied physiology = Revue canadienne de physiologie appliquee.

[50]  M. Decramer,et al.  Functional and histologic picture of steroid-induced myopathy in chronic obstructive pulmonary disease. , 1996, American journal of respiratory and critical care medicine.

[51]  M. Decramer,et al.  Peripheral muscle weakness contributes to exercise limitation in COPD. , 1996, American journal of respiratory and critical care medicine.

[52]  Andrew,et al.  Lack of effect of recombinant human growth hormone (GH) on muscle morphology and GH-insulin-like growth factor expression in resistance-trained elderly men. , 1996, The Journal of clinical endocrinology and metabolism.

[53]  A. Musarò,et al.  Enhanced expression of myogenic regulatory genes in aging skeletal muscle. , 1995, Experimental cell research.

[54]  R. Wolfe,et al.  Testosterone administration to elderly men increases skeletal muscle strength and protein synthesis. , 1995, The American journal of physiology.

[55]  M. Boska,et al.  Modulation of ATP production by oxygen in obstructive lung disease as assessed by 31P-MRS. , 1995, Journal of applied physiology.

[56]  E. Wouters,et al.  Nutritional depletion in relation to respiratory and peripheral skeletal muscle function in out-patients with COPD. , 1994, The European respiratory journal.

[57]  W. Gonyea,et al.  Muscle fiber splitting in stretch-enlarged avian muscle. , 1994, Medicine and science in sports and exercise.

[58]  J. Ketelslegers,et al.  Nutritional regulation of the insulin-like growth factors. , 1994, Endocrine reviews.

[59]  B. Warren Lung Biology in Health and Disease Series , 1993 .

[60]  M. Haida,et al.  31P-NMR study of skeletal muscle metabolism in patients with chronic respiratory impairment. , 1992, The American review of respiratory disease.

[61]  W. Gonyea,et al.  Morphological observations supporting muscle fiber hyperplasia following weight‐lifting exercise in cats , 1992, The Anatomical record.

[62]  R. Casaburi,et al.  Reductions in exercise lactic acidosis and ventilation as a result of exercise training in patients with obstructive lung disease. , 1991, The American review of respiratory disease.

[63]  E. Wouters,et al.  Energy balance in chronic obstructive pulmonary disease. , 1991, The American review of respiratory disease.

[64]  J. Lexell,et al.  Variability in muscle fibre areas in whole human quadriceps muscle: effects of increasing age. , 1991, Journal of anatomy.

[65]  F. Pernus,et al.  Muscle fibre types in the human vastus lateralis muscles: do symmetrical sites differ in their composition? , 1990, Anatomischer Anzeiger.

[66]  J. Lexell,et al.  Variability in muscle fibre areas in whole human quadriceps muscle. How much and why? , 1989, Acta physiologica Scandinavica.

[67]  R Scelsi,et al.  Automatic morphometric analysis of skeletal muscle fibers in the aging man , 1987, The Anatomical record.

[68]  J Lexell,et al.  Distribution of different fibre types in human skeletal muscles. 2. A study of cross-sections of whole m. vastus lateralis. , 1983, Acta physiologica Scandinavica.

[69]  G C Elder,et al.  Variability of fiber type distributions within human muscles. , 1982, Journal of applied physiology: respiratory, environmental and exercise physiology.

[70]  R. Roy,et al.  Skeletal muscle fiber splitting with weight-lifting exercise in rats. , 1980, The American journal of anatomy.

[71]  W. Gonyea,et al.  Skeletal muscle fiber splitting induced by weight-lifting exercise in cats. , 1977, Acta physiologica Scandinavica.

[72]  M. Swash,et al.  Longitudinal fibre splitting in neurogenic muscular disorders--its relation to the pathogenesis of "myopathic" change. , 1976, Brain : a journal of neurology.

[73]  M. M. Bradford A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. , 1976, Analytical biochemistry.

[74]  M. Brooke,et al.  Muscle fiber types: how many and what kind? , 1970, Archives of neurology.

[75]  L. Guth,et al.  Procedure for the histochemical demonstration of actomyosin ATPase. , 1970, Experimental neurology.

[76]  J. Bergstrom MUSCLE ELECTROLYTES IN MAN DETERMINED BY NEUTRON ACTIVATION ANALYSIS ON NEEDLE BIOPSY SPECIMENS , 1962 .