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Abstract
Highlight:
- AKT or protein kinase B increase protein synthesis and control the degradation of proteins.
- Satellite cells was provided remarkable ability to regenerate skeletal muscle.
- Stimulation of protein synthesis is effective therapy to maintain muscle mass, prevent muscle wasting to reduce risk sarcopenia and improve quality of life in the elderly.
Abstract:
Muscles have an important role as a regulator of glucose and triglyceride metabolism. Some researches show the correlation between skeletal muscle mass and metabolic diseases, such as diabetes. Skeletal muscle mass decrease occurs due to chronic illness or physiological process of aging, thus increasing the risk of metabolic diseases as well as motion difficulty in the elderly. Skeletal muscle mass depends on balanced protein synthesis and degradation, controlled through a variety of signal transduction pathways including the AKT. AKT or protein kinase B increases protein synthesis through the mTOR and GSK3β and controls the degradation of proteins through FoxO transcription factors. Another factor that has an alleged role in the regulation of skeletal muscle is the satellite cells which provide remarkable ability to regenerate skeletal muscle. A comprehensive understanding of the biomolecular mechanism of muscle mass regulation is important to develop effective treatment or prevention of muscle atrophy in many cases, either caused by pathological conditions, such as chronic diseases, or the process of aging.
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References
- Almeida, CF, Fernandes SA, Junior AR, et al (2016). Muscle satellite cells: Exploring the basic biology to rule them. Stem Cells Int. 2016, 1–14.
- Andrade GM, da Silveira JC, Perrini C, et al (2017). The role of the PI3K-Akt signaling pathway in the developmental competence of bovine oocytes. PLoS One 12, 1–15.
- Bazgir B, Fathi R, Valojerdi MR, et al (2017). Satellite cells contribution to exercise mediated muscle hypertrophy and repair. Cell J. 18, 473–484.
- Blaauw B, Canato M, Agatea L, et al (2009). Inducible activation of Akt increases skeletal muscle mass and force without satellite cell activation. FASEB J 23, 3896–3905.
- Cai X, Zhu C, Xu Y, et al (2016). Alpha-ketoglutarate promotes skeletal muscle hypertrophy and protein synthesis through Akt/mTOR signaling pathways. Sci. Rep. 6, 2–12.
- Collins KH, Herzog W, MacDonald GZ, et al (2018). Obesity, metabolic syndrome, and musculoskeletal disease: Common inflammatory pathways suggest a central role for loss of muscle integrity. Front Physiol. 9, 1–25.
- Dong YLR, Thomas SS, Dong YWXH, et al (2013). Interactions between p-Akt and Smad3 in injured muscles initiate myogenesis or fibrogenesis. Am J Physiol Endocrinol Metab 305, 367–375.
- Egerman MA, Glass DJ (2014). Signaling pathways controlling skeletal muscle mass. Crit. Rev. Biochem. Mol. Biol. 49, 59–68.
- Endo T (2015). Molecular mechanisms of skeletal muscle development, regeneration, and osteogenic conversion. Bone 80, 2–13.
- Favier FB, Benoit H, Freyssenet D (2008). Cellular and molecular events controlling skeletal muscle mass in response to altered use. Pflugers Arch 456, 587–600.
- Frontera WR, Ochala J (2015). Skeletal muscle: A brief review of structure and function. Calcif Tissue Int 96, 183–195.
- Gomes MJ, Martinez PF, Pagan LU, et al (2017). Skeletal muscle aging: influence of oxidative stress and physical exercise. Oncotarget 8, 20428–20440.
- Hauersley S, Vissing J, Krag TO (2014). Muscle atrophy reversed by growth factor activation of satellite cells in a mouse muscle atrophy model. PLoS One 9, 1–12.
- Hemmings BA, Restuccia DF (2012). PI3K-PKB/Akt pathway. Cold Spring Harb. Perspect. Biol. 4, 1–3.
- Hong, S., Chang, Y., Jung, H.-S., Yun, K.E., Shin, H., Ryu, S., 2017. Relative muscle mass and the risk of incident type 2 diabetes: A cohort study. PLoS One 12, 1–13.
- Lee MJ, Kim EH, Bae SJ, et al (2019). Protective role of skeletal muscle mass against progression from metabolically healthy to unhealthy phenotype. Clin Endocrinol 90, 102–113.
- Lee SY, Go GY, Vuong TA, et al (2018). Black ginseng activates Akt signaling, thereby enhancing myoblast differentiation and myotube growth. J Ginseng Res 42, 116–121.
- Moriya N, Miyazaki M (2018). Akt1 deficiency diminishes skeletal muscle hypertrophy by reducing satellite cell proliferation. Am J Physiol Regul Integr Comp Physiol 314, 741–751.
- Musarò A (2014). The basis of muscle regeneration. Adv. Biol. 2014, 1–16.
- Sambasivan R, Yao R, Kissenpfennig A, et al (2011). Pax7-expressing satellite cells are indispensable for adult skeletal muscle regeneration. Development 138, 3647–3656.
- Santos SDL, Garcia-Perez V, Hernández-Reséndiz S, et al (2017). ‘(-)-Epicatechin induces physiological cardiac growth by activation of the PI3K/Akt pathway in mice. Mol Nutr Food Res 61, 1–32.
- Yoon MS (2017). mTOR as a key regulator in maintaining skeletal muscle mass. Front. Physiol 8, 1–9.
References
Almeida, CF, Fernandes SA, Junior AR, et al (2016). Muscle satellite cells: Exploring the basic biology to rule them. Stem Cells Int. 2016, 1–14.
Andrade GM, da Silveira JC, Perrini C, et al (2017). The role of the PI3K-Akt signaling pathway in the developmental competence of bovine oocytes. PLoS One 12, 1–15.
Bazgir B, Fathi R, Valojerdi MR, et al (2017). Satellite cells contribution to exercise mediated muscle hypertrophy and repair. Cell J. 18, 473–484.
Blaauw B, Canato M, Agatea L, et al (2009). Inducible activation of Akt increases skeletal muscle mass and force without satellite cell activation. FASEB J 23, 3896–3905.
Cai X, Zhu C, Xu Y, et al (2016). Alpha-ketoglutarate promotes skeletal muscle hypertrophy and protein synthesis through Akt/mTOR signaling pathways. Sci. Rep. 6, 2–12.
Collins KH, Herzog W, MacDonald GZ, et al (2018). Obesity, metabolic syndrome, and musculoskeletal disease: Common inflammatory pathways suggest a central role for loss of muscle integrity. Front Physiol. 9, 1–25.
Dong YLR, Thomas SS, Dong YWXH, et al (2013). Interactions between p-Akt and Smad3 in injured muscles initiate myogenesis or fibrogenesis. Am J Physiol Endocrinol Metab 305, 367–375.
Egerman MA, Glass DJ (2014). Signaling pathways controlling skeletal muscle mass. Crit. Rev. Biochem. Mol. Biol. 49, 59–68.
Endo T (2015). Molecular mechanisms of skeletal muscle development, regeneration, and osteogenic conversion. Bone 80, 2–13.
Favier FB, Benoit H, Freyssenet D (2008). Cellular and molecular events controlling skeletal muscle mass in response to altered use. Pflugers Arch 456, 587–600.
Frontera WR, Ochala J (2015). Skeletal muscle: A brief review of structure and function. Calcif Tissue Int 96, 183–195.
Gomes MJ, Martinez PF, Pagan LU, et al (2017). Skeletal muscle aging: influence of oxidative stress and physical exercise. Oncotarget 8, 20428–20440.
Hauersley S, Vissing J, Krag TO (2014). Muscle atrophy reversed by growth factor activation of satellite cells in a mouse muscle atrophy model. PLoS One 9, 1–12.
Hemmings BA, Restuccia DF (2012). PI3K-PKB/Akt pathway. Cold Spring Harb. Perspect. Biol. 4, 1–3.
Hong, S., Chang, Y., Jung, H.-S., Yun, K.E., Shin, H., Ryu, S., 2017. Relative muscle mass and the risk of incident type 2 diabetes: A cohort study. PLoS One 12, 1–13.
Lee MJ, Kim EH, Bae SJ, et al (2019). Protective role of skeletal muscle mass against progression from metabolically healthy to unhealthy phenotype. Clin Endocrinol 90, 102–113.
Lee SY, Go GY, Vuong TA, et al (2018). Black ginseng activates Akt signaling, thereby enhancing myoblast differentiation and myotube growth. J Ginseng Res 42, 116–121.
Moriya N, Miyazaki M (2018). Akt1 deficiency diminishes skeletal muscle hypertrophy by reducing satellite cell proliferation. Am J Physiol Regul Integr Comp Physiol 314, 741–751.
Musarò A (2014). The basis of muscle regeneration. Adv. Biol. 2014, 1–16.
Sambasivan R, Yao R, Kissenpfennig A, et al (2011). Pax7-expressing satellite cells are indispensable for adult skeletal muscle regeneration. Development 138, 3647–3656.
Santos SDL, Garcia-Perez V, Hernández-Reséndiz S, et al (2017). ‘(-)-Epicatechin induces physiological cardiac growth by activation of the PI3K/Akt pathway in mice. Mol Nutr Food Res 61, 1–32.
Yoon MS (2017). mTOR as a key regulator in maintaining skeletal muscle mass. Front. Physiol 8, 1–9.