Skeletal muscle enlargement in response to increased mechanical loading appears to include the proliferation and differentiation of satellite cells via myogenic processes which are similar to, but distinct from, the type of growth seen during both early development and maturation. Findings to date suggest that insulin like growth factor-1 (IGF-1), acting in an autocrine/paracrine mode, serves as a primary mediator of these myogenic mechanisms which support the hypertrophy process in mature skeletal muscle fibers. Potential mechanisms by which IGF-1 modulates the process of myogenic cell proliferation, differentiation, and fusion have been delineated using in vitro approaches. The premise is presented that relatively little is known with regard to whether the processes identified in vitro also occur in skeletal muscle in vivo under conditions in which myofibers undergo compensatory hypertrophy due to chronic increases in loading. The proposed objective of this proposal is to test the hypothesis that IGF-1 mediates muscle hypertrophy by promoting myogenic processes in vivo. The proposed experiments will employ rodent models that target individual skeletal muscles. The treatments will include the delivery of growth factors and / or inhibitory agents either alone or in conjunction with resistance training of the target muscle. Analyses will include morphological, biochemical, molecular, microscopic and electron microscopic measures of cellular proliferation, differentiation and fusion as well as quantification of hypertrophy responses including measurements of muscle function. The proposed experiments will elucidate the role of the IGF-1 signaling system in the hypertrophy process.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Research Project (R01)
Project #
5R01AR045594-03
Application #
6375161
Study Section
Respiratory and Applied Physiology Study Section (RAP)
Program Officer
Lymn, Richard W
Project Start
1999-09-01
Project End
2004-08-31
Budget Start
2001-09-01
Budget End
2002-08-31
Support Year
3
Fiscal Year
2001
Total Cost
$215,901
Indirect Cost
Name
University of California Irvine
Department
Physiology
Type
Schools of Medicine
DUNS #
161202122
City
Irvine
State
CA
Country
United States
Zip Code
92697
Mozaffar, Tahseen; Haddad, Fadia; Zeng, Ming et al. (2007) Molecular and cellular defects of skeletal muscle in an animal model of acute quadriplegic myopathy. Muscle Nerve 35:55-65
Haddad, Fadia; Adams, Gregory R (2006) Aging-sensitive cellular and molecular mechanisms associated with skeletal muscle hypertrophy. J Appl Physiol 100:1188-203
Adams, Gregory R; Vaziri, Nosratola D (2006) Skeletal muscle dysfunction in chronic renal failure: effects of exercise. Am J Physiol Renal Physiol 290:F753-61
Adams, Gregory R; Zhan, Chang-De; Haddad, Fadia et al. (2005) Voluntary exercise during chronic renal failure in rats. Med Sci Sports Exerc 37:557-62
Bickel, C Scott; Slade, Jill; Mahoney, Ed et al. (2005) Time course of molecular responses of human skeletal muscle to acute bouts of resistance exercise. J Appl Physiol 98:482-8
Haddad, F; Zaldivar, F; Cooper, D M et al. (2005) IL-6-induced skeletal muscle atrophy. J Appl Physiol 98:911-7
Adams, Gregory R; Cheng, Daniel C; Haddad, Fadia et al. (2004) Skeletal muscle hypertrophy in response to isometric, lengthening, and shortening training bouts of equivalent duration. J Appl Physiol 96:1613-8
Haddad, Fadia; Adams, Gregory R (2004) Inhibition of MAP/ERK kinase prevents IGF-I-induced hypertrophy in rat muscles. J Appl Physiol 96:203-10
Bamman, Marcas M; Hill, Vernishia J; Adams, Gregory R et al. (2003) Gender differences in resistance-training-induced myofiber hypertrophy among older adults. J Gerontol A Biol Sci Med Sci 58:108-16
Adams, Gregory R; Caiozzo, Vincent J; Baldwin, Kenneth M (2003) Skeletal muscle unweighting: spaceflight and ground-based models. J Appl Physiol 95:2185-201

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