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Endocrine and metabolic regulation of muscle growth and body composition in cattle*

Published online by Cambridge University Press:  01 July 2010

J. F. Hocquette
J. F. Hocquette*
Affiliation:
INRA, UR 1213, Unité de Recherches sur les Herbivores (URH), Theix, F-63122 Saint-Genès Champanelle, France
*
†E-mail: [email protected]
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Abstract

Muscle metabolism (in interaction with other organs and tissues, including adipose tissue) plays an important role in the control of growth and body composition. Muscle ontogenesis has been described in different genotypes of cattle for myofibres, connective tissue and intramuscular depots. The ontogenesis or the action of putatively important factors controlling muscle development (IGF-II expression, IGF receptors, growth hormone (GH) receptor, myostatin, basic fibroblast growth factor, transforming growth factor-β1, insulin and thyroid hormones) has also been studied on bovine foetal muscle samples and satellite cells. The glucose/insulin axis has been specifically studied in both the bovine adipose tissue and heart. Clearly, cattle, like sheep, are mature species at birth based on their muscle characteristics compared to other mammalian or farm animal species. The different myoblast generations have been well characterised in cattle, including the second generation which is liable to be affected by foetal undernutrition at least in sheep. Interesting genotypes, for example, double-muscled genotype, have been characterised by an altered metabolic and endocrine status associated with a reduced fat mass, specific muscle traits and different foetal characteristics. Finally, the recent development of genomics in cattle has allowed the identification of novel genes controlling muscle development during foetal and postnatal life. Generally, a high muscle growth potential is associated with a reduced fat mass and a switch of muscle fibres towards the glycolytic type. The possibility and the practical consequences of manipulating muscle growth and, hence, body composition by nutritional and hormonal factors are discussed for bovines based on our current biological knowledge.

Keywords

musclenutrientshormonesadipose tissuebovines
Type
EAAP-ASAS-ADSA Growth and Development Symposium 2008
Information
animal , Volume 4 , Issue 11 , November 2010 , pp. 1797 - 1809
Copyright
Copyright © The Animal Consortium 2010

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Footnotes

*

Lecture presented at the ‘EAAP-ASAS-ADSA Growth and Development Symposium’ during the 60th Annual Meeting of the European Association for Animal production, Barcelona 2009, Session 10.

References

Aguiari, P, Leo, S, Zavan, B, Vindigni, V, Rimessi, A, Bianchi, K, Franzin, C, Cortivo, R, Rossato, M, Vettor, R, Abatangelo, G, Pozzan, T, Pinton, P, Rizzuto, R 2008. High glucose induces adipogenic differentiation of muscle-derived stem cells. Proceedings of the National Academy of Sciences of the United States of America 105, 1226–1231.CrossRefGoogle ScholarPubMed
Albertí, P, Panea, B, Sañudo, C, Olleta, JL, Ripoll, G, Ertbjerg, P, Christensen, M, Gigli, S, Failla, S, Concetti, S, Hocquette, JF, Jailler, R, Rudel, S, Renand, G, Nute, GR, Richardson, I, Williams, JL 2008. Live weight, body size and carcass characteristics of young bulls of fifteen European breeds. Livestock Science 114, 19–30.CrossRefGoogle Scholar
Alford, AR, Cafe, LM, Greenwood, PL, Griffith, GR 2007. The economic effects of early-life nutritional constraints in crossbred cattle bred on the NSW North Coast. Economic Research Report no. 33. NSW Department of Primary Industries, Armidale, NSW, Australia.Google Scholar
Artaza, JN, Bhasin, S, Magee, TR, Reisz-Porszasz, S, Shen, R, Groome, NP, Fareez, MM, Gonzalez-Cadavid, NF 2005. Myostatin inhibits myogenesis and promotes adipogenesis in C3H 10T(1/2) mesenchymal multipotent cells. Endocrinology 146, 3547–3557.CrossRefGoogle ScholarPubMed
Bailey, AJ, Enser, MB, Dransfield, D, Restall, DJ, Avery, NC 1982. Muscle and adipose tissue from normal and double muscled cattle: collagen types, muscle fibre diameter, fat cell size and fatty acid composition and organoleptic properties. In Muscle hypertrophy of genetic origin and its use to improve beef production (ed. JWB King and F Ménissier), pp. 178–203. Martinus Nijhoff, The Hague, The Netherlands.CrossRefGoogle Scholar
Bernard, C, Cassar-Malek, I, Renand, G, Hocquette, JF 2009. Changes in muscle gene expression related to metabolism according to growth potential in young bulls. Meat Science 82, 205–212.CrossRefGoogle ScholarPubMed
Berg, RA 1992. Nutritional aspects of collagen metabolism. Annual Review of Nutrition 12, 369–390.CrossRefGoogle ScholarPubMed
Blum, JW, Hammon, H 1999. Endocrine and metabolic aspects in milk–fed calves. Domestic Animal Endocrinology 17, 219–230.CrossRefGoogle ScholarPubMed
Boge, A, Sauerwein, H, Meyer, HHD 1995. IGF-I and insulin receptors in bovine skeletal muscle: comparisons of different developmental ages, two different genotypes and various individual muscles. Experimental and Clinical Endocrinology & Diabetes 103, 99–104.CrossRefGoogle ScholarPubMed
Boirie, Y, Dangin, M, Gachon, P, Vasson, MP, Maubois, JL, Beaufrere, B 1997. Slow and fast dietary proteins differently modulate postprandial protein accretion. Proceedings of the National Academy of Sciences of the United States of America 94, 14930–14935.CrossRefGoogle ScholarPubMed
Bonnet, M, Leroux, C, Faulconnier, Y, Hocquette, JF, Bocquier, F, Martin, P, Chilliard, Y 2000. Lipoprotein lipase activity and mRNA are up regulated by refeeding in adipose tissue and cardiac muscle of sheep. Journal of Nutrition 130, 749–756.CrossRefGoogle ScholarPubMed
Bonnet, M, Faulconnier, Y, Hocquette, JF, Bocquier, F, Leroux, C, Martin, P, Chilliard, Y 2004. Nutritional status induces divergent variations of GLUT4 protein content, but not lipoprotein lipase activity, between adipose tissues and muscles in adult cattle. British Journal of Nutrition 92, 617–625.CrossRefGoogle Scholar
Bonnet, M, Faulconnier, Y, Fléchet, J, Hocquette, JF, Leroux, C, Langin, D, Martin, P, Chilliard, Y 1998. Messenger RNAs encoding lipoprotein lipase, fatty acid synthase and hormone-sensitive lipase in the adipose tissue of underfed-refed ewes and cows. Reproduction Nutrition Development 38, 297–307.CrossRefGoogle ScholarPubMed
Bouhraoua, L, Barnola, I, Jadhao, SB, Durand, D, Bauchart, D, Hocquette, JF 2001. Influence de l’apport de l’huile de tournesol ou de lin sur le métabolisme musculaire chez le bouvillon en croissance. Congrès commun AFERO, AFN et SNDLF «Nutrition & Obésité 2001», 29–30 November 2001, Paris, France, poster 86.Google Scholar
Brandstetter, AM, Pfaffl, MW, Hocquette, JF, Gerrard, DE, Picard, B, Geay, Y, Sauerwein, H 2000. Effects of muscle type, castration, age and compensatory growth rate on androgen receptor mRNA expression in bovine skeletal muscle. Journal of Animal Science 78, 629–637.CrossRefGoogle ScholarPubMed
Byrne, KA, Wang, YH, Lehnert, SA, Harper, GS, McWilliam, SM, Bruce, HL, Reverter, A 2005. Gene expression profiling of muscle tissue in Brahman steers during nutritional restriction. Journal of Animal Science 83, 1–12.CrossRefGoogle ScholarPubMed
Cassar-Malek, I, Langlois, N, Picard, B, Geay, Y 1999. Regulation of bovine satellite cell proliferation and differentiation by insulin and triiodothyronine. Domestic Animal Endocrinology 17, 373–388.CrossRefGoogle ScholarPubMed
Cassar-Malek, I, Kahl, S, Jurie, C, Picard, B 2001. Influence of feeding level during post-weaning growth on circulating concentration of thyroid hormones and extrathyroidal 5’-deiodination in steers. Journal of Animal Science 79, 2679–2687.CrossRefGoogle Scholar
Cassar-Malek, I, Passelaigue, F, Bernard, C, Léger, J, Hocquette, JF 2007a. Target genes of myostatin loss-of-function in muscles of late bovine fetuses. BMC Genomics 8, 63.CrossRefGoogle ScholarPubMed
Cassar-Malek, I, Picard, B, Kahl, S, Hocquette, JF 2007b. Relationships between thyroid status, tissue oxidative metabolism, and muscle differentiation in bovine fetuses. Domestic Animal Endocrinology 33, 91–106.CrossRefGoogle ScholarPubMed
Cassar-Malek, I, Jurie, C, Bernard, C, Barnola, I, Micol, D, Hocquette, JF 2009. Pasture-feeding of charolais steers influences skeletal muscle metabolism and gene expression. Journal of Physiology Pharmacology 60 (suppl. 2), 83–90.Google ScholarPubMed
Cassar-Malek, I, Hocquette, JF, Jurie, C, Listrat, A, Jailler, R, Bauchart, D, Briand, Y, Picard, B 2004. Muscle-specific metabolic, histochemical and biochemical responses to a nutritionally induced discontinuous growth path. Animal Science 79, 49–59.CrossRefGoogle Scholar
Chelh, I, Meunier, B, Picard, B, Reecy, MJ, Chevalier, C, Hocquette, JF, Cassar-Malek, I 2009. Molecular profiles of quadriceps muscle in myostatin-null mice reveal P13K and apoptotic pathways as myostatin targets. BMC Genomics 10, 196.CrossRefGoogle Scholar
Cortright, RN, Muoio, DM, Dohm, L 1997. Skeletal muscle lipid metabolism: a frontier for new insights into fuel homoeostasis (review). Journal of Nutritional Biochemistry 8, 228–245.CrossRefGoogle Scholar
Deveaux, V, Cassar-Malek, I, Picard, B 2001. Comparison of contractile characteristics of muscle from Holstein and double-muscled Belgian-Blue foetuses. Comparative Biochemistry and Physiology Part A 131, 21–29.CrossRefGoogle ScholarPubMed
Dietze, D, Koenen, M, Rohrig, K, Horikoshi, H, Hauner, H, Eckel, J 2002. Impairment of insulin signaling in human skeletal muscle cells by co-culture with human adipocytes. Diabetes 51, 2369–2376.CrossRefGoogle ScholarPubMed
Dodson, MV, Jiang, ZH, Chen, J, Hausman, GJ, Guan, LL, Novakofski, J, Thompson, DP, Lorenzen, CL, Fernyhough, ME, Mir, PS, Reecy, JM 2010. Allied industry approaches to alter intramuscular fat content and composition in beef animals. Journal of Food Science 75, R1–R8.CrossRefGoogle ScholarPubMed
Dwyer, CM, Stickland, NC 1991. Sources of variation in myofibre number within and between litters of pigs. Animal Production 52, 527–533.Google Scholar
Duris, MP, Renand, G, Picard, B 1999. Genetic variability of foetal bovine myoblasts in primary culture. Histochemical Journal 31, 753–760.CrossRefGoogle ScholarPubMed
Etherton, TD 2009. ASAS Centennial Paper: animal growth and development research: historical perspectives. Journal of Animal Science 87, 3060–3064.CrossRefGoogle ScholarPubMed
Gagnière, H, Picard, B, Jurie, C, Geay, Y 1999. Comparison of foetal metabolic differentiation in three cattle muscles. Reproduction Nutrition Development 39, 105–112.CrossRefGoogle ScholarPubMed
Gallou-Kabani, C, Vigé, A, Gross, MS, Junien, C 2007. Nutri-epigenomics: lifelong remodelling of our epigenomes by nutritional and metabolic factors and beyond. Clinical Chemistry and Laboratory Medicine 45, 321–327.CrossRefGoogle ScholarPubMed
Gayraud-Morel, B, Chretien, F, Flamant, P, Gomes, D, Zammit, PS, Tajbakhsh, S 2007. A role for the myogenic determination gene Myf5 in adult regenerative myogenesis. Developmental Biology 312, 13–28 (Erratum 317, 705–706).CrossRefGoogle ScholarPubMed
Geay, Y, Bauchart, D, Hocquette, JF, Culioli, J 2001. Effect of nutritional factors on biochemical, structural and metabolic characteristics of muscles in ruminants, consequences on dietetic value and sensorial qualities of meat. Reproduction Nutrition Development 41, 1–26 (Erratum 41, 377).CrossRefGoogle ScholarPubMed
Gill, M, Smith, P, Wilkinson, JM 2010. Mitigating climate change: the role of domestic livestock. Animal 4, 323–333.CrossRefGoogle ScholarPubMed
Greenwood, PL, Cafe, LM 2007. Prenatal and pre-weaning growth and nutrition of cattle: long-term consequences for beef production. Animal 1, 1283–1296.CrossRefGoogle ScholarPubMed
Grobet, L, Poncelet, D, Royo, LJ, Brouwers, B, Pirottin, D, Michaux, C, Ménissier, F, Zanotti, M, Dunner, S, Georges, M 1998. Molecular definition of an allelic series of mutations disrupting the myostatin function and causing double-muscling in cattle. Mammalian Genome 9, 210–213.CrossRefGoogle ScholarPubMed
Guilloteau, P, Zabielski, R, Hammon, HM, Metges, CC 2009. Adverse effects of nutritional programming during prenatal and early postnatal life, some aspects of regulation and potential prevention and treatments. Journal of Physiology and Pharmacology 60 (suppl. 3), 17–35.Google ScholarPubMed
Hirai, S, Matsumoto, H, Hino, N, Kawachi, H, Matsui, T, Yano, H 2007. Myostatin inhibits differentiation of bovine preadipocyte. Domestic Animal Endocrinology 32, 1–14.CrossRefGoogle ScholarPubMed
Hishikawa, D, Hong, YH, Roh, SG, Miyahara, H, Nishimura, Y, Tomimatsu, A, Tsuzuki, H, Gotoh, C, Kuno, M, Choi, KC, Lee, HG, Cho, KK, Hidari, H, Sasaki, S 2005. Identification of genes expressed differentially in subcutaneous and visceral fat of cattle, pig, and mouse. Physiological Genomics 21, 343–350.CrossRefGoogle Scholar
Hocquette, JF, Abe, H 2000. Facilitative glucose transporters in livestock species. Reproduction Nutrition Development 40, 517–533.CrossRefGoogle ScholarPubMed
Hocquette, JF, Piot, C, Picard, B 2000. Metabolic differentiation of bovine cardiac and skeletal muscles during fœtal development. International Congress of Myology, 27–31 March 2000, Nice, France, abstract no. 47, p. 185 (poster).Google Scholar
Hocquette, JF, Graulet, B, Vermorel, M, Bauchart, D 2001a. Weaning affects lipoprotein lipase activity and gene expression only in adipose tissues and in masseter but not in other muscles of the calf. British Journal of Nutrition 86, 433–441.CrossRefGoogle Scholar
Hocquette, JF, Ortigues-Marty, I, Vermorel, M 2001b. Manipulation of tissue energy metabolism in meat-producing ruminants (review). Asian-Australasian Journal of Animal Sciences 14, 720–732.CrossRefGoogle Scholar
Hocquette, JF, Jurie, C, Bonnet, M, Pethick, DW 2005. Bovine intramuscular adipose tissue has a higher potential for fatty acid synthesis from glucose than subcutaneous adipose tissue. Book of Abstracts of the 56th Annual Meeting of the European Association for Animal production, 5–8 June 2005, Uppsala, Sweden, p. 248.Google Scholar
Hocquette, JF, Cassar-Malek, I, Scalbert, A, Guillou, F 2009. Contribution of genomics to the understanding of physiological functions. Journal of Physiology and Pharmacology 60 (suppl. 3), 5–16.Google Scholar
Hocquette, JF, Ortigues-Marty, I, Pethick, DW, Herpin, P, Fernandez, X 1998. Nutritional and hormonal regulation of energy metabolism in skeletal muscles of meat-producing animals. Livestock Production Science 56, 115–143.CrossRefGoogle Scholar
Hocquette, JF, Bas, P, Bauchart, D, Vermorel, M, Geay, Y 1999. Fat partitioning and biochemical characteristics of fatty tissues in relation to plasma metabolites and hormones in normal and double-muscled young growing bulls. Comparative Biochemistry and Physiology Part A 122, 127–138 (Erratum 123, 311–312).CrossRefGoogle ScholarPubMed
Hocquette, JF, Sauerwein, H, Higashiyama, Y, Picard, B, Abe, H 2006. Prenatal developmental changes in glucose transporters, intermediary metabolism and hormonal receptors related to the IGF/insulin-glucose axis in the heart and adipose tissue of bovines. Reproduction Nutrition Development 46, 257–272.CrossRefGoogle Scholar
Hocquette, JF, Lehnert, S, Barendse, W, Cassar-Malek, I, Picard, B 2007a. Recent advances in cattle functional genomics and their application to beef quality. Animal 1, 159–173.CrossRefGoogle ScholarPubMed
Hocquette, JF, Jurie, C, Picard, B, Albertí, P, Panea, B, Christensen, M, Failla, S, Gigli, S, Levéziel, H, Olleta, JL, Sañudo, C, Ertbjerg, P, Nute, GR, Williams, JL 2007b. Metabolic and contractile characteristics of Longissimus thoracis muscle of young bulls from 15 European breeds in relationship with body composition. In Proceeding of the 2nd International Symposium on Energy and Protein Metabolism and Nutrition, 9–13 September 2007, Vichy, France (ed. I. Ortigues-Marty), EAAP publication no. 124, pp. 111–114. Wageningen Academic Publishers, Wageningen, The Netherlands.Google Scholar
Hocquette, JF, Tesseraud, S, Cassar-Malek, I, Chilliard, Y, Ortigues-Marty, I 2007c. Responses to nutrients in farm animals: implications for production and quality. Animal 1, 1297–1313.CrossRefGoogle ScholarPubMed
Hocquette, JF, Castiglia-Delavaud, C, Graulet, B, Ferré, P, Picard, B, Vermorel, M 1997. Weaning marginally affects glucose transporter (GLUT4) expression in muscles and adipose tissues in the calf. British Journal of Nutrition 78, 251–271.CrossRefGoogle ScholarPubMed
Hocquette, JF, Gondret, F, Baéza, E, Médale, F, Jurie, C, Pethick, DW 2010. Intramuscular fat content in meat-producing animals: development, genetic and nutritional control, identification of putative markers. Animal 4, 303–319.CrossRefGoogle ScholarPubMed
Izumiya, Y, Hopkins, T, Morris, C, Sato, K, Zeng, L, Viereck, J, Hamilton, JA, Ouchi, N, LeBrasseur, NK, Walsh, K 2008. Fast/glycolytic muscle fiber growth reduces fat mass and improves metabolic parameters in obese mice. Cell Metabolism 7, 159–172.CrossRefGoogle ScholarPubMed
Jadhao, SB, Chilliard, Y, Faulconnier, Y, Picard, B, Hocquette, JF 2001. Metabolic differentiation of bovine adipose tissue during the fetal life. FASEB Journal 15, A70 (abstract).Google Scholar
Jensen, RB, Chellakooty, M, Vielwerth, S, Vaag, A, Larsen, T, Greisen, G, Skakkebaek, NE, Scheike, T, Juul, A 2003. Intrauterine growth retardation and consequences for endocrine and cardiovascular diseases in adult life: does insulin-like growth factor-I play a role? Hormone Research 60 (suppl. 3), 136–148.CrossRefGoogle ScholarPubMed
Jones, RH, Ozanne, SE 2009. Fetal programming of glucose-insulin metabolism. Molecular and cellular Endocrinology 297, 4–9.CrossRefGoogle ScholarPubMed
Jurie, C, Ortigues-Marty, I, Picard, B, Micol, D, Hocquette, JF 2006. The separate effects of the nature of diet and grazing mobility on metabolic potential of muscles from Charolais steers. Livestock Science 104, 182–192.CrossRefGoogle Scholar
Jurie, C, Picard, B, Heyman, Y, Cassar-Malek, I, Chavatte-Palmer, P, Richard, C, Hocquette, JF 2009. Comparison of cloned and non-cloned Holstein heifers in muscle contractile and metabolic characteristics. Animal 3, 244–250.CrossRefGoogle ScholarPubMed
Jurie, C, Cassar-Malek, I, Bonnet, M, Leroux, C, Bauchart, D, Boulesteix, P, Pethick, DW, Hocquette, JF 2007. Adipocyte fatty acid-binding protein and mitochondrial enzyme activities in muscles as relevant indicators of marbling in cattle. Journal of Animal Science 85, 2660–2669.CrossRefGoogle ScholarPubMed
Kajimura, S, Seale, P, Kubota, K, Lunsford, E, Frangioni, JV, Gygi, SP, Spiegelman, BM 2009. Initiation of myoblast to brown fat switch by a PRDM16-C/EBP-beta transcriptional complex. Nature 460, 1154–1158.CrossRefGoogle ScholarPubMed
Karunaratne, JF, Ashton, CJ, Stickland, NC 2005. Fetal programming of fat and collagen in porcine skeletal muscles. Journal of Anatomy 207, 763–768.CrossRefGoogle ScholarPubMed
Kokta, TA, Dodson, MV, Gertler, A, Hill, RA 2004. Intercellular signalling between adipose tissue and muscle tissue (review). Domestic Animal Endocrinology 27, 303–331.CrossRefGoogle Scholar
Krause, MP, Liu, Y, Vu, V, Chan, L, Xu, A, Riddell, MC, Sweeney, G, Hawke, TJ 2008. Adiponectin is expressed by skeletal muscle fibers and influences muscle phenotype and function. American Journal of Physiology – Cell Physiology 295, C203–C212.CrossRefGoogle ScholarPubMed
Lehnert, SA, Byrne, KA, Reverter, A, Nattrass, GS, Greenwood, PL, Wang, YH, Hudson, NJ, Harper, GS 2006. Gene expression profiling of bovine skeletal muscle in response to and during recovery from chronic and severe undernutrition. Journal of Animal Science 84, 3239–3250.CrossRefGoogle ScholarPubMed
Listrat, A, Belair, L, Picard, B, Boulle, N, Geay, Y, Djiane, J, Jammes, H 1999a. Insulin-like growth factor II (IGF-II) mRNA expression during skeletal muscle development of double-muscled and normal bovine foetuses. Reproduction Nutrition Development 39, 113–124.CrossRefGoogle ScholarPubMed
Listrat, A, Jammes, H, Djiane, J, Geay, Y, Robelin, J 1999b. Characterisation and location of insulin-like-growth factor (IGF) receptors and in the foetal bovine Semitendinosus muscle. Reproduction Nutrition Development 39, 467–479.CrossRefGoogle ScholarPubMed
Listrat, A, Rakadjiyski, N, Jurie, C, Picard, B, Touraille, C, Geay, Y 1999c. Effect of the type of diet on muscle characteristics and meat palatability of growing Salers bulls. Meat Science 53, 115–124.CrossRefGoogle ScholarPubMed
Listrat, A, Lethias, C, Hocquette, JF, Renand, G, Ménissier, F, Geay, Y, Picard, B 2000. Age-related changes and location of types I, III, XII and XIV collagen during development of skeletal muscles from genetically different animals. Histochemical Journal 32, 349–356.CrossRefGoogle ScholarPubMed
Listrat, A, Picard, B, Jailler, R, Collignon, H, Peccatte, JR, Micol, D, Geay, Y, Dozias, D 2001. Grass valorisation and muscular characteristics of blonde d’Aquitaine steers. Animal Research 50, 105–118.CrossRefGoogle Scholar
Markham, TCW, Latorre, RM, Lawlor, PG, Ashton, CJ, McNamara, LB, Natter, R, Rowlerson, A, Stickland, NC 2009. Developmental programming of skeletal muscle phenotype/metabolism. Animal 3, 1001–1012.CrossRefGoogle ScholarPubMed
Oldham, JM, Osepchook, CC, Jeanplong, F, Falconer, SJ, Matthews, KG, Conaglen, JV, Gerrard, DF, Smith, HK, Wilkins, RJ, Bass, JJ, McMahon, CD 2009. The decrease in mature myostatin protein in male skeletal muscle is developmentally regulated by growth hormone. Journal of Physiology 587, 669–677.CrossRefGoogle ScholarPubMed
Orzechowski, A, Gajkowska, B, Wojewódzka, U, Cassar-Malek, I, Picard, B, Hocquette, JF 2002a. Immunohistochemical analysis of bFGF, TGF-beta 1 and catalase in rectus abdominis muscle from cattle foetuses at 180 and 260 days post-conception. Tissue and Cell 34, 416–426.CrossRefGoogle ScholarPubMed
Orzechowski, A, ̡okociejewska, M, Muras, P, Hocquette, JF 2002b. Preconditioning with millimolar concentrations of Vitamin C or N-acetylcysteine protects L6 muscle cells insulin-stimulated viability and DNA synthesis under oxidative stress. Life Sciences 71, 1793–1808.CrossRefGoogle ScholarPubMed
Pethick, DW, Harper, GS, Oddy, VH 2004. Growth, development and nutritional manipulation of marbling in cattle: a review. Australian Journal of Agricultural Research 44, 705–715.Google Scholar
Picard, B, Lefaucheur, L, Berri, C, Duclos, MJ 2002. Muscle fibre ontogenesis in farm animal species (review). Reproduction Nutrition Development 42, 415–431.CrossRefGoogle Scholar
Picard, B, Gagniere, H, Geay, Y, Hocquette, JF, Robelin, J 1995. Study of the influence of age and weaning on the contractile and metabolic characteristics of bovine muscle. Reproduction Nutrition Development 35, 71–84.CrossRefGoogle ScholarPubMed
Renand, G, Berge, P, Picard, B, Robelin, J, Geay, Y, Krauss, D, Ménissier, F 1994. Genetic parameters of beef production and meat quality traits of young Charolais bulls progeny of divergently selected sires. Proceedings of the 5th World Congress on Genetics Applied to Livestock Production 19, 446–449.Google Scholar
Rowe, JB, Choct, M, Pethick, DW 1999. Processing cereal grain for animal feeding. Australian Journal of Agricultural Research 50, 721–736.CrossRefGoogle Scholar
Schuenke, MD, Kopchick, JJ, Hikida, RS, Kraemer, WJ, Staron, RS 2008. Effects of growth hormone overexpression vs. growth hormone receptor gene disruption on mouse hindlimb muscle fiber type composition. Growth Hormone & IGF Research 18, 479–486.CrossRefGoogle ScholarPubMed
Seale, P, Bjork, B, Yang, W, Kajimura, S, Chin, S, Kuang, S, Scimè, A, Devarakonda, S, Conroe, HM, Erdjument-Bromage, H, Tempst, P, Rudnicki, MA, Beier, DR, Spiegelman, BM 2008. PRDM16 controls a brown fat/skeletal muscle switch. Nature 454, 961–967.CrossRefGoogle Scholar
Serrano, E, Pradel, P, Jailler, R, Dubroeuq, H, Bauchart, D, Hocquette, JF, Listrat, A, Agabriel, J, Micol, D 2007. Young Salers suckled bull production: effect of diet on performance, carcass and muscle characteristics and meat quality. Animal 1, 1068–1079.CrossRefGoogle ScholarPubMed
Setia, S, Sridhar, MG 2009. Changes in GH/IGF-1 axis in intrauterine growth retardation: consequences of fetal programming? Hormone and Metabolic Research 41, 791–798.CrossRefGoogle ScholarPubMed
Shibata, M, Matsumoto, K, Oe, M, Ohnishi-Kameyama, M, Ojima, K, Nakajima, I, Muroya, S, Chikuni, K 2009. Differential expression of the skeletal muscle proteome in grazed cattle. Journal of Animal Science 87, 2700–2708.CrossRefGoogle ScholarPubMed
Shin, J, Li, B, Davis, ME, Suh, Y, Lee, K 2009. Comparative analysis of fatty acid-binding protein 4 promoters: conservation of peroxisome proliferator-activated receptor binding sites. Journal of Animal Science 87, 3923–3934.CrossRefGoogle ScholarPubMed
Smith, SB, Kawachi, H, Choi, CB, Choi, CW, Wu, G, Sawyer, JE 2009. Cellular regulation of bovine intramuscular adipose tissue development and composition. Journal of Animal Science 87 (suppl. E), E72–E82.CrossRefGoogle ScholarPubMed
Steelman, CA, Recknor, JC, Nettleton, D, Reecy, JM 2006. Transcriptional profiling of myostatin-knockout mice implicates Wnt signaling in postnatal skeletal muscle growth and hypertrophy. FASEB Journal 20, 580–582.CrossRefGoogle ScholarPubMed
Steinfeld, H, Gerber, P, Wassenaar, T, Castel, V, Rosales, M, de Haan, C 2006. Livestock’s long shadow: environmental issues and options. FAO, Rome, Italy.Google Scholar
Sudre, K, Cassar-Malek, I, Listrat, A, Ueda, Y, Leroux, C, Jurie, C, Auffray, C, Renand, G, Martin, P, Hocquette, JF 2005. Biochemical and transcriptomic analyses of two bovine skeletal muscles in Charolais bulls divergently selected for muscle growth. Meat Science 70, 267–277.CrossRefGoogle ScholarPubMed
Stickland, NC, Demirtas, B, Clelland, AK, Ashton, C 2000. Genetic and nutritional influence on muscle growth in farm animals. Comparative Biochemistry and Physiology 126A (suppl. 1), 141.CrossRefGoogle Scholar
Symonds, ME, Mostyn, A, Pearce, S, Budge, H, Stephenson, T 2003. Endocrine and nutritional regulation of fetal adipose tissue development. Journal of Endocrinology 179, 293–299.CrossRefGoogle ScholarPubMed
Symonds, ME, Pearce, S, Bispham, J, Gardner, DS, Stephenson, T 2004. Timing of nutrient restriction and programming of fetal adipose tissue development (review). Proceedings of the Nutrition Society 63, 397–403.CrossRefGoogle Scholar
Timmons, JA, Wennmalm, K, Larsson, O, Walden, TB, Lassmann, T, Petrovic, N, Hamilton, DL, Gimeno, RE, Wahlestedt, C, Baar, K, Nedergaard, J, Cannon, B 2007. Myogenic gene expression signature establishes that brown and white adipocytes originate from distinct cell lineages. Proceedings of the National Academy of Sciences of the United States of America 104, 4401–4406.CrossRefGoogle Scholar
Ukropec, J, Penesová, A, Skopková, M, Pura, M, Vlcek, M, Rádiková, Z, Imrich, R, Ukropcová, B, Tajtáková, M, Koska, J, Zórad, S, Belan, V, Vanuga, P, Payer, J, Eckel, J, Klimes, I, Gasperíková, D 2008a. Adipokine protein expression pattern in growth hormone deficiency predisposes to the increased fat cell size and the whole body metabolic derangements. Journal of Clinical Endocrinology and Metabolism 93, 2255–2262.CrossRefGoogle Scholar
Ukropec, J, Ukropcova, B, Kurdiova, T, Gasperikova, D, Klimes, I 2008b. Adipose tissue and skeletal muscle plasticity modulates metabolic health. Archives of Physiology and Biochemistry 114, 357–368.CrossRefGoogle ScholarPubMed
Wegner, J, Albrecht, E, Ender, K 1998. Morphological aspects of growth in subcutaneous and intramuscular adipocytes in cattle. Archiv für Tierzucht – Archives of Animal Breeding 41, 313–320.Google Scholar
Wegner, J, Albrecht, E, Fiedler, I, Teuscher, F, Papstein, HJ, Ender, K 2000. Growth-and breed-related changes of muscle fiber characteristics in cattle. Journal of Animal Science 78, 1485–1496.CrossRefGoogle ScholarPubMed
Welle, S, Burgess, K, Thornton, CA, Tawil, R 2009. Relation between extent of myostatin depletion and muscle growth in mature mice. American Journal of Physiology – Endocrinology and Metabolism 297, E935–E940.CrossRefGoogle ScholarPubMed
Wyrwoll, CS, Mark, PJ, Mori, TA, Waddell, BJ 2008. Developmental programming of adult hyperinsulinemia, increased proinflammatory cytokine production, and altered skeletal muscle expression of SLC2A4 (GLUT4) and uncoupling protein 3. Journal of Endocrinology 198, 571–579.CrossRefGoogle ScholarPubMed
Yajnik, CS, Deshmukh, US 2008. Maternal nutrition, intrauterine programming and consequential risks in the offspring. Reviews in Endocrine and Metabolic Disorders 9, 203–211.CrossRefGoogle ScholarPubMed