期刊论文详细信息
Journal of Animal Science and Biotechnology
Restricted nutrient intake does not alter serum-mediated measures of implant response in cell culture
Barry J Bradford2  Laman K Mamedova2  Daniel U Thomson1  Tiffany L Lee1  Christopher D Reinhardt2 
[1] Department of Clinical Sciences, A-111 Mosier Hall, Kansas State University, Manhattan, KS 66506, USA;Department of Animal Sciences and Industry, 232 Weber Hall, Kansas State University, Manhattan, KS 66506, USA
关键词: Satellite cells;    Nutrient restriction;    Myosin heavy chain;    Muscle;    Implant;    Beef cattle;   
Others  :  804948
DOI  :  10.1186/2049-1891-4-45
 received in 2013-05-31, accepted in 2013-10-22,  发布年份 2013
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【 摘 要 】

Background

During nutritional stress, reduced intake may reduce the efficacy of anabolic implants. This study was conducted to evaluate basic cellular responses to a growth promotant implant at two intake levels.

Methods

Sixteen crossbred steers (293 ± 19.3 kg) were used to evaluate the impact of anabolic implants in either an adequate or a restricted nutritional state. Steers were trained to individual Calan gates, and then randomly assigned to 1 of 4 treatments in a 2 × 2 factorial arrangement. Treatments consisted of: presence or absence of an anabolic growth implant (Revalor-XS, 200 mg TBA and 40 mg estradiol; IMPLANT or CONTROL) and a moderate energy, pelleted, starting cattle diet fed at either 2.0 × or 1.0 × maintenance energy (NEM) requirements (HIGH or LOW). Serum (d 0, 14, and 28) was used for application to bovine muscle satellite cells. After treatment with the serum (20% of total media) from the trial cattle, the satellite cells were incubated for 72 h. Protein abundance of myosin heavy chain (MHC), phosphorylated extracellular signal-related kinase (phospho-ERK), and phosphorylated mammalian target of rapamycin (phospho-mTOR) were analyzed to determine the effects of implant, intake, and their interaction (applied via the serum).

Results

Intake had no effect on MHC (P = 0.85) but IMPLANT increased (P < 0.01) MHC abundance vs. CONTROL. Implant status, intake status, and the interaction had no effect on the abundance of phospho-ERK (P ≥ 0.23). Implanting increased phospho-mTOR (P < 0.01) but there was no effect (P ≥ 0.51) of intake or intake × implant.

Conclusions

The nearly complete lack of interaction between implant and nutritional status indicates that the signaling molecules measured herein respond to implants and nutritional status independently. Furthermore, results suggest that the muscle hypertrophic effects of anabolic implants may not be mediated by circulating IGF-1.

【 授权许可】

   
2013 Reinhardt et al.; licensee BioMed Central Ltd.

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【 参考文献 】
  • [1]Duckett SK, Andrae JG: Implant strategies in an integrated beef production system. J Anim Sci 2001, 79(E. Suppl):E110-E117.
  • [2]Hutcheson DP, Cole NA: Management of transit-stress syndrome in cattle: nutritional and environmental effects. J Anim Sci 1986, 62:555-560.
  • [3]Cole NA, Delaney DD, Cummins JM, Hutcheson DP: Nitrogen metabolism of calves inoculated with bovine adenovirus-3 or with infectious bovine rhinotracheitis virus. Am J Vet Res 1986, 47:1160-1164.
  • [4]Munson RD, Thomson DU, Reinhardt CD: Effects of delayed steroid implanting on health, performance, and carcass quality in high health risk, auction market-sourced feedlot steers. J Anim Sci 2012, 90:4037-4041.
  • [5]Johnson BJ, Halstead JN, White ME, Hathaway MR, DiConstanzo A, Dayton WR: Activation state of muscle satellite cells isolated from steers implanted with a combined trenbolone acetate and estradiol implant. J Anim Sci 1998, 76:2779-2786.
  • [6]Kamanga-Sollo E, White ME, Hathaway MR, Chung KY, Johnson WR, Dayton WR: Roles of IGF-I and the estrogen, androgen and IGF-I receptors in estradiol-17β- and trenbolone acetate-stimulated proliferation of cultured bovine satellite cells. Domest Anim Endocrinol 2008, 35:88-97.
  • [7]Lewis MI, Bodine SC, Kamangar N, Xu X, Da X, Fournier M: Effect of severe short-term malnutrition on diaphragm muscle signal transduction pathways influencing protein turnover. J Appl Physiol 2006, 100:1799-1806.
  • [8]Howell J, Manning M: mTOR couples cellular nutrient sensing to organismal metabolic homeostasis. Trends Endocrinol Metab 2011, 22:94-102.
  • [9]NRC: Nutrient requirements of beef cattle. 7th rev. ed. Washington, D.C: Natl. Acad. Press; 1996.
  • [10]NRC: Nutrient requirements of beef cattle. 6th rev. ed. Washington, D.C: Natl. Acad. Press; 1984.
  • [11]Loomis RJ, Marshall LA, Johnston PV: Sera fatty acid effects on cultured rat splenocytes. J Nutr 1983, 113:1292-1298.
  • [12]Jewell DE, Drewry MM, Martin RJ, Hausman GJ: Effect of sera from control and overfed rats on preadipocyte growth in culture. J Nutr 1988, 118:803-808.
  • [13]Reecy JM, Williams JE, Kerley MS, MacDonald RS, Thornton WH Jr, Wallace LM: Abomasal casein infusion enhances the mitogenic activity of serum from protein-restricted steers. J Nutr 1994, 124:67-77.
  • [14]Krebs A, Wallaschofski H, Spilcke Liss E, Kohlmann T, Brabant G, Völzke H, Nauck M: Five commercially available insulin-like growth factor I (IGF-I) assays in comparison to the former Nichols Advantage IGF-I in a growth hormone treated population. Clin Chem Lab Med 2008, 46:1776-1783.
  • [15]Bradford MM: A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 1976, 72:248-254.
  • [16]Elsasser TH, Rumsey TS, Hammond AC: Influence of diet on basal and growth hormone-stimulated plasma concentrations of IGF-1 in beef cattle. J Anim Sci 1989, 67:128-141.
  • [17]Hayden JM, Williams JE, Collier RJ: Plasma growth hormone, insulin-like growth factor, insulin, and thyroid hormone association with body protein and fat accretion in steers undergoing compensatory gain after dietary energy restriction. J Anim Sci 1993, 71:3327-3338.
  • [18]Bryant TC, Engle TE, Galyean ML, Wagner JJ, Tatum JD, Anthony RV, Laudert SB: Effects of ractopamine and trenbolone acetate implants with or without estradiol on growth performance, carcass characteristics, adipogenic enzyme activity, and blood metabolites in feedlot steers and heifers. J Anim Sci 2010, 88:4102-4119.
  • [19]Johnson BJ, Hathaway MR, Anderson PT, Meiske JC, Dayton WR: Stimulation of circulating insulin-like growth factor I (IGF-I) and insulin-like growth factor binding proteins (IGFBP) due to administration of a combined trenbolone acetate and estradiol implant in feedlot cattle. J Anim Sci 1996, 74:372-379.
  • [20]Reinhardt CD: Metabolic indices for growth: Endocrine profile of steers on different nutritional and growth regulation regimes. College Station, TX: Texas A&M University; 1991. [Master’s thesis]
  • [21]Anderson SM, Shah N, Evans WS, Patrie JT, Bowers CY, Veldhuis JD: Short-term estradiol supplementation augments growth hormone (GH) secretory responsiveness to dose-varying GH-releasing peptide infusions in healthy postmenopausal women. J Clin Endocrinol Metab 2001, 86:551-560.
  • [22]Baxa TJ, Hutcheson JP, Miller MF, Brooks JC, Nichols WT, Streeter MN, Yates DA, Johnson BJ: Additive effects of a steroidal implant and zilpaterol hydrochloride on feedlot performance, carcass characteristics, and skeletal muscle messenger ribonucleic acid abundance in finishing steers. J Anim Sci 2010, 88:330-337.
  • [23]Baxa TJ: Effect of zilpaterol hydrochloride and steroid implantation on yearling steer feedlot performance, carcass characteristics, and skeletal muscle gene expression. Manhattan, KS: Kansas State University; 2004. [Master’s Thesis]
  • [24]Chung KY, Baxa TJ, Parr SL, Luqué LD, Johnson BJ: Administration of estradiol, trenbolone acetate, and trenbolone acetate/estradiol implants alters adipogenic and myogenic gene expression in bovine skeletal muscle. J Anim Sci 2012, 90:1421-1427.
  • [25]Gonzalez JM, Carter JN, Johnson DD, Ouellette SE, Johnson SE: Effect of ractopamine-hydrochloride and trenbolone acetate on longissimus muscle fiber area, diameter, and satellite cell numbers in cull beef cows. J Anim Sci 2007, 85:1893-1901.
  • [26]Kellermeier JD, Tittor AW, Brooks JC, Galyean ML, Yates DA, Hutcheson JP, Nichols WT, Streeter MN, Johnson BJ, Miller MF: Effects of zilpaterol hydrochloride with or without an estrogen-trenbolone acetate terminal implant on carcass traits, retail cutout, tenderness, and muscle fiber diameter in finishing steers. J Anim Sci 2009, 87:3702-3711.
  • [27]Johnson BJ, Reinhardt CD: Growth promotants for beef production: Anabolic steroids: Performance responses and Mode of action. In Current Veterinary Therapy: Food Animal Practice 5th Volume. Edited by Anderson DE, Rings DM. St. Louis, MO: Saunders/Elsevier, Inc; 2009:643-651.
  • [28]Hwang SL, Jeong YT, Li X, Kim YD, Yue L, Chang YC, Lee IK, Chang HW: Inhibitory cross-talk between the AMPK and ERK pathways mediates endoplasmic reticulum stress-induced insulin resistance in skeletal muscle. Br J Pharmacol 2013. doi:10.1111/bph.12124. [Epub ahead of print]
  • [29]Peng Y, Zheng Y, Zhang Y, Zhao J, Chang F, Lu T, Zhang R, Li Q, Hu X, Li N: Different effects of omega-3 fatty acids on the cell cycle in C2C12 myoblast proliferation. Mol Cell Biochem 2012, 367:165-173.
  • [30]Fuentes EN, Bjornsson BT, Valdes JA, Einarsdottir IE, Lorca B, Alvarez M, Molina A: IGF-I/PI3K/AkT and IGF-I/MAPK/ERK pathways in vivo in skeletal muscle are regulated by nutrition and contribute to somatic growth in the fine flounder. Am J Physiol 2011, 300:R1532-R1542.
  • [31]Corradetti MN, Guan KL: Upstream of the mammalian target of rapamycin: do all roads pass through mTOR? Oncogene 2006, 25:6347-6360.
  • [32]Yang X, Yang C, Farberman A, Rideout TC, de Lange CFM, France J, Fan MZ: The mammalian target of rapamycin-signaling pathway in regulating metabolism and growth. J Anim Sci 2008, 86:E36-E50.
  • [33]Sorbassov DD, Ali SM, Sabatini DM: Growing roles for the mTOR pathway. Curr Opin Cell Biol 2005, 17:596-603.
  • [34]Nave BT, Ouwens M, Withers DJ, Alessi DR, Shepherd PR: Mammalian target of rapamycin is a direct target for protein kinase B: identification of a convergence point for opposing effects of insulin and amino-acid deficiency on protein translation. Biochem J 1999, 344(Pt 2):427-431.
  • [35]Soliman GA, Acosta-Jaquez HA, Dunlop EA, Ekim B, Maj NE, Tee AR, Fingar DC: mTOR Ser-2481 autophosphorylation monitors mTORC-specific catalytic activity and clarifies rapamycin mechanism of action. J Biol Chem 2010, 285:7866-7879.
  • [36]Du M, Zhu MJ, Means WJ, Hess BW, Ford SP: Nutrient restriction differentially modulates the mammalian target of rapamycin signaling and the ubiquitin-proteasome system in skeletal muscle of cows and their fetuses. J Anim Sci 2005, 83:117-123.
  • [37]Vestergaard M, Purup S, Frystyk J, Løvendahl P, Sørensen MT, Riis PM, Flint DJ, Sejrsen K: Effects of growth hormone and feeding level on endocrine measurements, hormone receptors, muscle growth and performance of prepubertal heifers. J Anim Sci 2003, 81:2189-2198.
  • [38]Pampusch MS, Johnson BJ, White ME, Hathaway MR, Dunn JD, Waylan AT, Dayton WR: Time course of changes in growth factor mRNA levels in muscle of steroid-implanted and non-implanted steers. J Anim Sci 2003, 81:2733-2740.
  • [39]Pampusch MS, White ME, Hathaway MR, Baxa TJ, Chung KY, Parr SL, Johnson BJ, Weber WJ, Dayton WR: Effects of implants of trenbolone acetate, estradiol, or both, on muscle insulin-like growth factor-I, insulin-like growth factor-I receptor, estrogen receptor-a, and androgen receptor messenger ribonucleic acid levels in feedlot steers. J Anim Sci 2008, 86:3418-3423.
  • [40]Kamanga-Sollo E, White ME, Hathaway MR, Weber WJ, Dayton WR: Effect of Estradiol-17 beta on protein synthesis and degradation rates in fused bovine satellite cell cultures. Domest Anim Endocrinol 2010, 39:54-62.
  • [41]Kamanga-Sollo E, White ME, Hathaway MR, Weber WJ, Dayton WR: Effect of trenbolone acetate on protein synthesis and degradation rates in fused bovine satellite cell cultures. Domest Anim Endocrinol 2011, 40:60-66.
  • [42]Kamanga-Sollo E, Pampusch MS, Xi G, White ME, Hathaway MR, Dayton WR: IGF-I mRNA levels in bovine satellite cell cultures: effects of fusion and anabolic steroid treatment. J Cell Physiol 2004, 201:181-189.
  • [43]Joubert Y, Tobin C: Testosterone Treatment Results in Quiescent Satellite Cells Being Activated and Recruited into Cell Cycle in Rat Levator Ani Muscle. Devel Biol 1995, 169(1):286-294.
  • [44]Breier BH, Gluckman PD, Bass JJ: Influence of nutritional status and oeshadiol-17B on plasma growth hormone, insulin-like growth factors-I and -II and the response to exogenous growth hormone in young steers. J Endocrinol 1988, 118:243.
  • [45]Hayden JM, Bergen WG, Merkel RA: Skeletal muscle protein metabolism and serum growth hormone, insulin, and cortisol concentrations in growing steers implanted with estradiol-17 beta, trenbolone acetate, or estradiol-17 beta plus trenbolone acetate. J Anim Sci 1992, 70:2109-2019.
  • [46]Hongerholt DD, Crooker BA, Wheaton JE, Carlson KM, Jorgenson DM: Effects of a growth hormone-releasing factor analogue and an estradiol-trenbolone acetate implant on somatotropin, insulin-like growth factor I, and metabolite profiles in growing Hereford steers. J Anim Sci 1992, 70:1439-1448.
  • [47]Milewicz T, Krzysiek J, Sztefko K, Radowicki S, Krzyczkowska-Sendrakowska M: 17 beta-estradiol regulation of human growth hormone (hGH), insulin-like growth factor-I (IGF-I) and insulin-like growth factor binding protein-3 (IGFBP-3) axis in hypoestrogenic, hypergonadotropic women. Endokrynol Pol 2005, 56:876-882.
  • [48]Dawson-Hughes B, Stern D, Goldman J, Reichlin S: Regulation of growth hormone and somatomedin-C secretion in postmenopausal women: effect of physiological estrogen replacement. J Clin Endocrinol Metab. 1986, 63:424-432.
  • [49]Scanlan N, Skinner DC: Estradiol modulation of growth hormone secretion in the ewe: No growth hormone-releasing hormone neurons and few somatotropes express estradiol receptor α. Biol Reprod 2002, 66:1267-1273.
  • [50]Sotiropoulos A, Ohanna M, Kedzia C, Menon RK, Kopchick JJ, Kelly PA, Pende M: Growth hormone promotes skeletal muscle cell fusion independent of insulin-like growth factor 1 up-regulation. Proc Natl Acad Sci U S A 2006, 103:7315-7320.
  • [51]Ge X, Yu J, Jiang H: Growth hormone stimulates protein synthesis in bovine skeletal muscle cells without altering insulin-like growth factor-I mRNA expression. J Anim Sci 2012, 90:1126-1133.
  • [52]Allen RE, Sheehan SM, Taylor RG, Kendall TL, Rice GM: Hepatocyte growth factor activates quiescent skeletal muscle satellite cells in vitro. J Cell Physiol 1995, 165:307-312.
  • [53]Tatsumi R, Anderson JE, Nevoret CJ, Halevy O, Allen RE: HGF/SF is present in normal adult skeletal muscle and is capable of activating satellite cells. Devel Biol 1998, 194:114-128.
  • [54]Sheehan SM, Tatsumi R, Temm-Grove CJ, Allen RE: HGF is an autocrine growth factor for skeletal muscle satellite cells in vitro. Muscle Nerve 2000, 23:239-245.
  • [55]Gospodarowicz D, Moran J, Braun D, Birdwell C: Clonal growth of bovine vascular endothelial cells: fibroblast growth factor as a survival agent. Proc Natl Acad Sci U S A 1976, 73:4120-4124.
  • [56]Rusnati M, Dell’Era P, Urbinati C, Tanghetti E, Massardi ML, Nagamine Y, Monti E, Presta M: A distinct basic fibroblast growth factor (FGF-2)/FGF receptor interaction distinguishes urokinase-type plasminogen activator induction from mitogenicity in endothelial cells. Mol Biol Cell 1996, 7:369-381.
  • [57]Taylor KM, Chen C, Gray CA, Bazer FW, Spencer TE: Expression of messenger ribonucleic acids for fibroblast growth factors 7 and 10, hepatocyte growth factor, and insulin-like growth factors and their receptors in the neonatal ovine uterus. Biol Reprod 2001, 64:1236-1246.
  • [58]Coleman KD, Wright JA, Ghosh M, Wira CR, Fahey JV: Estradiol modulation of hepatocyte growth factor by stromal fibroblasts in the female reproductive tract. Fertil Steril 2009, 92:1107-1109.
  • [59]Coleman KD, Ghosh M, Crist SG, Wright JA, Rossoll RM, Wira CR, Fahey JV: Modulation of hepatocyte growth factor secretion in human female reproductive tract stromal fibroblasts by poly (I:C) and estradiol. Am J Reprod Immunol 2012, 67:44-53.
  • [60]Frey RS, Johnson BJ, Hathaway MR, White ME, Dayton WR: Growth factor responsiveness of primary satellite cell cultures from steers implanted with trenbolone acetate and estradiol-17b. Basic Appl Myol 1995, 5:71-79.
  • [61]Wing LY, Chuang PC, Wu MH, Chen HM, Tsai SJ: Expression and mitogenic effect of fibroblast growth factor-9 in human endometriotic implant is regulated by aberrant production of estrogen. J Clin Endocrinol Metab 2003, 88:5547-5554.
  • [62]White ME, Johnson BJ, Hathaway MR, Dayton WR: Growth factor messenger RNA levels in muscle and liver of steroid-implanted and nonimplanted steers. J Anim Sci 2003, 81:965-972.
  • [63]Wu Y, Bauman WA, Blitzer RD, Cardozo C: Testosterone-induced hypertrophy of L6 myoblasts is dependent upon Erk and mTOR. Biochem Biophys Res Commun 2010, 400:679-683.
  • [64]Jones NC, Fedorov YV, Rosenthal RS, Olwin BB: ERK1/2 is required for myoblast proliferation but is dispensable for muscle gene expression and cell fusion. J Cell Physiol 2001, 186:104-115.
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