Literature DB >> 16998828

Of bears, frogs, meat, mice and men: complexity of factors affecting skeletal muscle mass and fat.

Thea Shavlakadze1, Miranda Grounds.   

Abstract

Extreme loss of skeletal muscle mass (atrophy) occurs in human muscles that are not used. In striking contrast, skeletal muscles do not rapidly waste away in hibernating mammals such as bears, or aestivating frogs, subjected to many months of inactivity and starvation. What factors regulate skeletal muscle mass and what mechanisms protect against muscle atrophy in some species? Severe atrophy also occurs with ageing and there is much clinical interest in reducing such loss of muscle mass and strength (sarcopenia). In the meat industry, a key aim is optimizing the control of skeletal muscle growth and meat quality. The impaired response of muscle to insulin resulting in diabetes, that is a consequence of the metabolic impact of increasing obesity and fat deposition in humans, is also of increasing clinical concern. Intensive research in these fields, combined with mouse models, is reviewed with respect to the molecular control of muscle growth (myogenesis) and atrophy/hypertrophy and fat deposition (adipogenesis) in skeletal muscle, with a focus on IGF-1/insulin signaling. (c) 2006 Wiley Periodicals, Inc.

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Year:  2006        PMID: 16998828     DOI: 10.1002/bies.20479

Source DB:  PubMed          Journal:  Bioessays        ISSN: 0265-9247            Impact factor:   4.345


  24 in total

1.  Deletion of connexin43 in osteoblasts/osteocytes leads to impaired muscle formation in mice.

Authors:  Hua Shen; Susan Grimston; Roberto Civitelli; Stavros Thomopoulos
Journal:  J Bone Miner Res       Date:  2015-04       Impact factor: 6.741

2.  Expression of myocyte enhancer factor-2 and downstream genes in ground squirrel skeletal muscle during hibernation.

Authors:  Shannon N Tessier; Kenneth B Storey
Journal:  Mol Cell Biochem       Date:  2010-07-09       Impact factor: 3.396

3.  Enhanced survival of skeletal muscle myoblasts in response to overexpression of cold shock protein RBM3.

Authors:  Amy L Ferry; Peter W Vanderklish; Esther E Dupont-Versteegden
Journal:  Am J Physiol Cell Physiol       Date:  2011-05-18       Impact factor: 4.249

Review 4.  Murine models of atrophy, cachexia, and sarcopenia in skeletal muscle.

Authors:  Mark Romanick; Ladora V Thompson; Holly M Brown-Borg
Journal:  Biochim Biophys Acta       Date:  2013-03-20

5.  Platelet function in brown bear (Ursus arctos) compared to man.

Authors:  Ole Fröbert; Kjeld Christensen; Asa Fahlman; Sven Brunberg; Johan Josefsson; Eva Särndahl; Jon E Swenson; Jon M Arnemo
Journal:  Thromb J       Date:  2010-06-02

Review 6.  Regulation of muscle mass by growth hormone and IGF-I.

Authors:  C P Velloso
Journal:  Br J Pharmacol       Date:  2008-06       Impact factor: 8.739

7.  Cachexia and aging: an update based on the Fourth International Cachexia Meeting.

Authors:  J E Morley; S D Anker; W J Evans
Journal:  J Nutr Health Aging       Date:  2009-01       Impact factor: 4.075

8.  Identification of cold-shock protein RBM3 as a possible regulator of skeletal muscle size through expression profiling.

Authors:  Esther E Dupont-Versteegden; Radhakrishnan Nagarajan; Marjorie L Beggs; Edward D Bearden; Pippa M Simpson; Charlotte A Peterson
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2008-08-27       Impact factor: 3.619

Review 9.  Reproduction Symposium: developmental programming of reproductive and metabolic health.

Authors:  V Padmanabhan; A Veiga-Lopez
Journal:  J Anim Sci       Date:  2014-08       Impact factor: 3.159

10.  Increased skeletal muscle volume in women with familial partial lipodystrophy, Dunnigan variety.

Authors:  Hongzhao Ji; Paul Weatherall; Beverley Adams-Huet; Abhimanyu Garg
Journal:  J Clin Endocrinol Metab       Date:  2013-06-19       Impact factor: 5.958

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