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Research Article

Effect of chronic AICAR treatment on muscle fiber composition and enzyme activity in skeletal muscle of rats

ORCID Icon, ORCID Icon, , , , , & ORCID Icon show all
Pages 89-96 | Received 13 Mar 2020, Accepted 08 Feb 2021, Published online: 26 Feb 2021

References

  • Avelar NC, Simão AP, Tossige-Gomes R, Neves CD, Mezencio B, Szmuchrowski L, Coimbra CC, Lacerda AC. 2011. Oxygen consumption and heart rate during repeated squatting exercises with or without whole-body vibration in the elderly. J Strength Condition Res. 25(12):3495–3500. doi:10.1519/JSC.0b013e3182176664.
  • Brooke MH, Kaise KK. 1970. Three “myosin adenosine triphosphatase” systems: the nature of their pH lability and sulfhydryl dependence. J Histochem Cytochem. 18(9):670–672.
  • Cantó C, Auwerx J. 2010. AMP-activated protein kinase and its downstream transcriptional pathways. Cell Mol Life Sci. 67(20):3407–3423. doi:10.1007/s00018-010-0454-z.
  • Chen X, Gang Jia YG, Liu G, Zhao H, Huang Z. 2018. Arginine promotes skeletal muscle fiber type transformation from fast-twitch to slow-twitch via Sirt1/AMPK pathway. J Nutr Biochem. 61:155–162.
  • Choi YM, Hwang S, Lee K. 2016. Comparison of muscle fiber and meat quality characteristics in different Japanese quail lines. Asian-Australas J Anim Sci. 29:1331–1337. doi:10.5713/ajas.16.0329.
  • Conjard A, Peuker H, Pette D. 1998. Energy state and myosin heavy chain isoforms in single fibres of normal and transforming rabbit muscles. Pflügers Archiv Eur J Physiol. 436(6):962–969. doi:10.1007/s004240050730.
  • Czubryt MP, McAnally J, Fishman GI, Olson EN. 2003. Regulation of peroxisome proliferator-activated receptor γ coactivator 1α (PGC-1α) and mitochondrial function by MEF2 and HDAC5. Proc Natl Acad Sci USA. 100(4):1711–1716.
  • Green HJ, Düsterhöft S, Dux L, Pette D. 1992. Metabolite patterns related to exhaustion, recovery and transformation of chronically stimulated rabbit fast-twitch muscle. Pflügers Archiv Eur J Physiol. 420(3-4):359–366. doi:10.1007/BF00374471.
  • Haihong Z, Ming RJ, Young LH, Marc P, James M, Birnbaum MJ, Shulman GI. 2002. AMP kinase is required for mitochondrial biogenesis in skeletal muscle in response to chronic energy deprivation. Proc Natl Acad Sci USA. 99(25):15983–15987.
  • Han Y, Wang Q, Song P, Zhu Y, Zou MH, Xu A. 2010. Redox regulation of the AMP-activated protein kinase. Plos One. 5(11):e15420.
  • Handschin C, Chin S, Li P, Liu F, Maratos-Flier E, LeBrasseur NK, Yan Z, Spiegelman BM. 2007b. Skeletal muscle fiber-type switching, exercise intolerance, and myopathy in PGC-1α muscle-specific knock-out animals. J Biol Chem. 282(41):30014–30021.
  • Handschin C, Choi CS, Chin S, Kim S, Kawamori D, Kurpad AJ, Neubauer N, Hu J, Mootha VK, Kim Y-B, et al. 2007a. Abnormal glucose homeostasis in skeletal muscle-specific PGC-1alpha knockout mice reveals skeletal muscle-pancreatic beta cell crosstalk. J Clin Invest. 117(11):3463–3474.
  • Handschin C, Spiegelman BM. 2006. Peroxisome proliferator-activated receptor γ coactivator 1 coactivators, energy homeostasis, and metabolism. Endocr Rev. 27(7):728–735. doi:10.1210/er.2006-0037.
  • Hardie DG, Carling D, Carlson M. 1998. The AMP-activated/SNF1 protein kinase subfamily: metabolic sensors of the eukaryotic cell? Annu Rev Biochem. 67(1):821–855.
  • Hardie DG, Sakamoto K. 2006. AMPK: a key sensor of fuel and energy status in skeletal muscle. Physiology. 21(1):48–60. doi:10.1152/physiol.00044.2005.
  • Hatakeyama H, Kanzaki M. 2013. Regulatory mode shift of Tbc1d1 is required for acquisition of insulin-responsive GLUT4-trafficking activity. Mol Biol Cell. 24(6):809–817. doi:10.1091/mbc.e12-10-0725.
  • He X, Duan Y, Yao K, Li F, Hou Y, Wu G, Yin Y. 2015. β-Hydroxy-β-methylbutyrate, mitochondrial biogenesis, and skeletal muscle health. Amino Acids. 48(3):653–664.
  • Herbison GJ, Jaweed MM, Ditunno JF. 1982. Muscle fiber types. Arch Phys Med Rehabil. 63(5):227–230.
  • Hoh JF. 1992. Muscle fiber types and function. Curr Opin Rheumatol. 4(6):801–808.
  • Holmes BF, Kurthkraczek EJ, Winder WW. 1999. Chronic activation of 5'-AMP-activated protein kinase increases GLUT-4, hexokinase, and glycogen in muscle. J Appl Physiol. 87(5):1990–1995. doi:10.1016/j.laa.2005.07.006.
  • James DE, Strube M, Muecdler M. 1989. Molecular cloning and characterization of an insulin-regulatable glucose transporter. Nature. 338(6210):83–87. doi:10.1038/338083a0.
  • Kang YK, Choi YM, Lee SH, Choe JH, Hong KC, Kim BC. 2011. Effects of myosin heavy chain isoforms on meat quality, fatty acid composition, and sensory evaluation in Berkshire pigs. Meat Sci. 89(4):384–389. doi:10.1016/j.meatsci.2011.04.019.
  • Ko JR, Seo DY, Park SH, Kwak HB, Kim M, Ko KS, Rhee BD, Han J. 2018. Aerobic exercise training decreases cereblon and increases AMPK signaling in the skeletal muscle of STZ-induced diabetic rats. Biochem Biophys Res Commun. 501(2):448–453. doi:10.1016/j.bbrc.2018.05.009.
  • Koistinen HA, Galuska D, Chibalin AV, Yang J, Zierath JR, Holman GD, Wallberg-Henriksson H. 2003. 5-amino-imidazole carboxamide riboside increases glucose transport and cell-surface GLUT4 content in skeletal muscle from subjects with type 2 diabetes. Diabetes. 52(5):1066–1072. doi:10.2337/diabetes.52.5.1066.
  • Leick L, Fentz J, Biensø RS, Knudsen JG, Jeppesen J, Kiens B, Wojtaszewski JFP, Pilegaard H. 2010. PGC-1α is required for AICAR-induced expression of GLUT4 and mitochondrial proteins in mouse skeletal muscle. Am J Physiol Endocrinol Metab. 299(3):E456.
  • Lin CC, Liang JH. 2002. Effect of antioxidants on the oxidative stability of chicken breast meat in a dispersion system. J Food Sci. 67(2):530–533.
  • Lin J, Wu H, Tarr PT, Zhang C-Y, Wu Z, Boss O, Michael LF, Puigserver P, Isotani E, Olson EN, et al. 2002. Transcriptional co-activator PGC-1 alpha drives the formation of slow-twitch muscle fibres. Nature. 418(6899):797.
  • Marette A, Richardson JM, Ramlal T, Balon TW, Vranic M, Pessin JE, Klip a. 1992. Abundance, localization, and insulin-induced translocation of glucose transporters in red and white muscle. Am J Physiol. 263(2 Pt 1):C443–C452. doi:10.0000/PMID1514590.
  • Michael LF, Wu Z, Cheatham RB, Puigserver P, Adelmant G, Lehman JJ, Kelly DP, Spiegelman BM. 2001. Restoration of insulin-sensitive glucose transporter (GLUT4) gene expression in muscle cells by the transcriptional coactivator PGC-1. Proc Natl Acad Sci USA. 98(7):3820–3825. doi:10.1073/pnas.061035098.
  • Mu J, Brozinick JT, Valladares O, Bucan M, Birnbaum MJ. 2001. A role for AMP-activated protein kinase in contraction- and hypoxia-regulated glucose transport in skeletal muscle. Mol Cell. 7(5):1085–1094. doi:10.1016/S1097-2765(01)00251-9.
  • Nakazato K, Tsutaki A. 2012. Regulatory mechanisms of muscle fiber types and their possible interactions with external nutritional stimuli. J Phys Fitness Sports Med. 1(4):655–664. doi:10.7600/jpfsm.1.655.
  • Ojuka EO, Nolte LA, Holloszy JO. 2000. Increased expression of GLUT-4 and hexokinase in rat epitrochlearis muscles exposed to AICAR in vitro. J Appl Physiol. 88(3):1072–1075. doi:10.1152/jappl.2000.88.3.1072.
  • Park S, Scheffler TL, Gunawan AM, Shi H, Zeng C, Hannon KM, Grant AL, Gerrard DE. 2009a. Chronic elevated calcium blocks AMPK-induced GLUT-4 expression in skeletal muscle. Am J Physiol Cell Physiol. 296(1):106–115. doi:10.1152/ajpcell.00114.2008.
  • Park SK, Sheffler TL, Spurlock ME, Grant AL, Gerrard DE. 2009b. Chronic activation of 5"-AMP-activated protein kinase changes myosin heavy chain expression in growing pigs. J Anim Sci. 87(10):3124–3133. doi:10.2527/jas.2009-1989.
  • Pette D, Staron RS. 1997. Mammalian skeletal muscle fiber type transitions. Int Rev Cytol. 170:143–223. doi:10.1016/S0074-7696(08)61622-8.
  • Pette D, Staron RS. 2000. Myosin isoforms, muscle fiber types, and transitions. Microsc Res Tech. 50(6):500–509. doi:10.1002/1097-0029(20000915)50:6 < 500::AID-JEMT7 > 3.3.CO;2-Z.
  • Puigserver P, Adelmant G, Wu Z, Fan M, Xu J, O’Malley B, Spiegelman BM. 1999. Activation of PPARgamma coactivator-1 through transcription factor docking. Science. 286:1368–1371.
  • Puigserver P, Spiegelman BM. 2003. Peroxisome proliferator-activated receptor-γ coactivator 1α (PGC-1α): transcriptional coactivator and metabolic regulator. Endocr Rev. 24(1):78–90.
  • Puigserver P, Wu Z, Park CW, Graves R, Spiegelman BM. 1998. A cold-inducible coactivator of nuclear receptors linked to adaptive thermogenesis. Cell. 92(6):829–839. doi:10.1016/S0092-8674(00)81410-5.
  • Rockl KSC, Hirshman MF, Brandauer J, Fujii N, Witters LA, Goodyear LJ. 2007. Skeletal muscle adaptation to exercise training: AMP-activated protein kinase mediates muscle fiber type shift. Diabetes. 56(8):2062–2069. doi:10.2337/db07-0255.
  • Rønnestad BR, Ellefsen S. 2011. The effects of adding different whole-body vibration frequencies to preconditioning exercise on subsequent sprint performance. J Strength Cond Res. 25(12):3306–3310. doi:10.1519/JSC.0b013e318215f298.
  • Scarpulla RC. 2002. Nuclear activators and coactivators in mammalian mitochondrial biogenesis. Biochim Biophys Acta Gene Struct Expr. 1576(1):1–14. doi:10.1016/S0167-4781(02)00343-3.
  • Schiaffino S, Reggiani C. 2011. Fiber types in mammalian skeletal muscles. Physiol Rev. 91(4):1447–1531.
  • Silva-Grigoletto MED, Hoyo MD, Sañudo B, Carrasco L, García-Manso JM. 2011. Determining the optimal whole-body vibration dose–response relationship for muscle performance. J Strength Condition Res. 25(12):3326–3333. doi:10.1519/JSC.0b013e3182163047.
  • Su R, Luo Y, Wang B, Hou Y, Zhao L, Su L, Yao D, Qian Y, Jin Y. 2019. Effects of physical exercise on meat quality characteristics of Sunit sheep. Small Ruminant Res. 173:54–58. doi:10.1016/j.smallrumres.2019.02.002.
  • Suwa M, Nakano H, Kumagai S. 2003. Effects of chronic AICAR treatment on fiber composition, enzyme activity, UCP3, and PGC-1 in rat muscles. J Appl Physiol. 95(3):960–968. doi:10.1152/japplphysiol.00349.2003.
  • Suwa M, Nakano H, Radak Z, Kumagai S. 2011. Short-term adenosine monophosphate-activated protein kinase activator 5-aminoimidazole-4-carboxamide-1-β-d-ribofuranoside treatment increases the sirtuin 1 protein expression in skeletal muscle. Metab Clin Exp. 60(3):394–403. doi:10.1016/j.metabol.2010.03.003.
  • Tanner CJ, Barakat HA, Dohm GL, Pories WJ, MacDonald KG, Cunningham PRG, Swanson MS, Houmard JA. 2002. Muscle fiber type is associated with obesity and weight loss. Am J Physiol Endocrinol Metab. 282(6):E1191–E1196. doi:10.1152/ajpendo.00416.2001.
  • Tetsuo Y, Takayoshi S, Hideaki A, Shihori T, Yoriko A. 2010. Continuous mild heat stress induces differentiation of mammalian myoblasts, shifting fiber type from fast to slow. Am J Physiol Cell Physiol. 298(1):C140–C148.
  • Thomson DM, Fick CA, Gordon SE. 2008. AMPK activation attenuates S6K1, 4E-BP1, and eEF2 signaling responses to high-frequency electrically stimulated skeletal muscle contractions. J Appl Physiol. 104(3):625–632.
  • Vladimir L, Pedro M, Matthew B, Louise B, Shiemaa K, Lunde JA, Renaud J-M, Jasmin BJ. 2011. Chronic AMPK activation evokes the slow, oxidative myogenic program and triggers beneficial adaptations in mdx mouse skeletal muscle. Hum Mol Genet. 20(17):3478–3493.
  • Wu Z, Puigserver P, Andersson U, Zhang C, Adelmant G, Mootha V, Troy A, Cinti S, Lowell B, Scarpulla RC, Spiegelman BM. 1999. Mechanisms controlling mitochondrial biogenesis and respiration through the thermogenic coactivator PGC-1. Cell. 98(1):115–124.
  • Yan Z, Okutsu M, Akhtar YN, Lira VA. 2011. Regulation of exercise-induced fiber type transformation, mitochondrial biogenesis, and angiogenesis in skeletal muscle. J Appl Physiol. 110(1):264–274. doi:10.1152/japplphysiol.00993.2010.
  • Ying F, Zhang L, Bu G, Xiong Y, Zuo B. 2016. Muscle fiber-type conversion in the transgenic pigs with overexpression of PGC1α gene in muscle. Biochem Biophys Res Commun. 480(4):669–674. doi:10.1016/j.bbrc.2016.10.113.