1 |
Chen, P. S., Peng, G. S., Li, G., Yang, S., Wu, X., Wang, C. C., Wilson, B., Lu, R. B., Gean, P. W., Chuang, D. M. and Hong, J. S. 2006. Valproate protects dopaminergic neurons in midbrain neuron/glia cultures by stimulating the release of neurotrophic factors from astrocytes. Mol. Psychiatry 11, 1116-1125.
DOI
|
2 |
Clemmons, D. R. 2009. Role of IGF-I in skeletal muscle mass maintenance. Trends Endocrinol. Metab. 20, 349-356.
DOI
|
3 |
Clow, C. and Jasmin, B. J. 2010. Brain-derived neurotrophic factor regulates satellite cell differentiation and skeletal muscle regeneration. Mol. Biol. Cell. 21, 2182-2190.
DOI
|
4 |
Cohen, T. J., Barrientos, T., Hartman, Z. C., Garvey, S. M., Cox, G. A. and Yao, T. P. 2009. The deacetylase HDAC4 controls myocyte enhancing factor-2-dependent structural gene expression in response to neural activity. FASEB. J. 23, 99-106.
DOI
|
5 |
Colombo, E., Bedogni, F., Lorenzetti, I., Landsberger, N., Previtali, S. C. and Farina, C. 2013. Autocrine and immune cell-derived BDNF in human skeletal muscle: implications for myogenesis and tissue regeneration. J. Pathol. 231, 190-198.
DOI
|
6 |
Cotman, C. W. and Berchtold, N. C. 2002. Exercise: a behavioral intervention to enhance brain health and plasticity. Trends Neurosci. 25, 295-301.
DOI
|
7 |
Cotman, C. W., Berchtold, N. C. and Christie, L. A. 2007. Exercise builds brain health: key roles of growth factor cascades and inflammation. Trends Neurosci. 30, 464-472.
DOI
|
8 |
Dey, B. R., Furlanetto, R. W. and Nissley, P. 2000. Suppressor of cytokine signaling (SOCS)-3 protein interacts with the insulin-like growth factor-I receptor. Biochem. Biophys. Res. Commun. 278, 38-43.
DOI
|
9 |
Fu, X., Zhao, J. X., Liang, J., Zhu, M. J., Foretz, M., Viollet, B. and Du, M. 2013. AMP-activated protein kinase mediates myogenin expression and myogenesis via histone deacetylase 5. Am. J. Physiol. 305, C887-895.
DOI
|
10 |
Galvin, C. D., Hardiman, O. and Nolan, C. M. 2003. IGF-I receptor mediates differentiation of primary cultures of mouse skeletal myoblasts. Mol. Cell. Endocrinol. 200, 19-29.
DOI
|
11 |
Glass, D. J. 2003. Signalling pathways that mediate skeletal muscle hypertrophy and atrophy. Nat. Cell. Biol. 5, 87-90.
DOI
|
12 |
McKinsey, T. A., Zhang, C. L. and Olson, E. N. 2001. Control of muscle development by dueling HATs and HDACs. Curr. Opin. Genet. Dev. 11, 497-504.
DOI
|
13 |
Griesbeck, O., Parsadanian, A. S., Sendtner, M. and Thoenen, H. 1995. Expression of neurotrophins in skeletal muscle: quantitative comparison and significance for motoneuron survival and maintenance of function. J. Neurosci. Res. 42, 21-33.
DOI
|
14 |
Iezzi, S., Cossu, G., Nervi, C., Sartorelli, V. and Puri, P. L. 2002. Stage-specific modulation of skeletal myogenesis by inhibitors of nuclear deacetylases. Proc. Natl. Acad. Sci. USA 99, 7757-7762.
DOI
|
15 |
Koppel, I. and Timmusk, T. 2013. Differential regulation of BDNF expression in cortical neurons by class-selective histone deacetylase inhibitors. Neuropharmacology 75, 106-115.
DOI
|
16 |
Mitsiades, C. S., Mitsiades, N. S., McMullan, C. J., Poulaki, V., Shringarpure, R., Hideshima, T., Akiyama, M., Chauhan, D., Munshi, N., Gu, X., Bailey, C., Joseph, M., Libermann, T. A., Richon, V. M., Marks, P. A. and Anderson, K. C. 2004. Transcriptional signature of histone deacetylase inhibition in multiple myeloma: biological and clinical implications. Proc. Natl. Acad. Sci. USA 101, 540-545.
DOI
|
17 |
Miura, P., Amirouche, A., Clow, C., Belanger, G. and Jasmin, B. J. 2012. Brain-derived neurotrophic factor expression is repressed during myogenic differentiation by miR-206. J. Neurochem. 120, 230-238.
DOI
|
18 |
Ntanasis-Stathopoulos, J., Tzanninis, J. G., Philippou, A. and Koutsilieris, M. 2013. Epigenetic regulation on gene expression induced by physical exercise. J. Musculoskelet. Neuronal. Interact. 13, 133-146.
|
19 |
Mousavi, K. and Jasmin, B. J. 2006. BDNF is expressed in skeletal muscle satellite cells and inhibits myogenic differentiation. J. Neurosci. 26, 5739-5749.
DOI
|
20 |
Mousavi, K., Parry, D. J. and Jasmin, B. J. 2004. BDNF rescues myosin heavy chain IIB muscle fibers after neonatal nerve injury. Am. J. Physiol. 287, C22-29.
DOI
|
21 |
Pandorf, C. E., Haddad, F., Wright, C., Bodell, P. W. and Baldwin, K. M. 2009. Differential epigenetic modifications of histones at the myosin heavy chain genes in fast and slow skeletal muscle fibers and in response to muscle unloading. Am. J. Physiol. 297, C6-16.
DOI
|
22 |
Park, H. and Poo, M. M. 2013. Neurotrophin regulation of neural circuit development and function. Nat. Rev. Neurosci. 14, 7-23.
DOI
|
23 |
Pedersen, B. K. and Febbraio, M. A. 2008. Muscle as an endocrine organ: focus on muscle-derived interleukin-6. Physiol. Rev. 88, 1379-1406.
DOI
|
24 |
Pedersen, B. K. 2009. Muscle as an endocrine organ: IL-6 and other myokines. J. Appl. Physiol. 107, 1006-1014.
DOI
|
25 |
Pedersen, B. K. and Febbraio, M. A. 2012. Muscles, exercise and obesity: skeletal muscle as a secretory organ. Nat. Rev. Endocrinol. 8, 457-465.
DOI
|
26 |
Sacheck, J. M., Ohtsuka, A., McLary, S. C. and Goldberg, A. L. 2004. IGF-I stimulates muscle growth by suppressing protein breakdown and expression of atrophy-related ubiquitin ligases, atrogin-1 and MuRF1. Am. J. Physiol. 287, E591-601.
|
27 |
Bharathy, N., Ling, B. M. and Taneja, R. 2013. Epigenetic regulation of skeletal muscle development and differentiation. Subcell. Biochem. 61, 139-150.
|
28 |
Wrann, C. D., White, J. P., Salogiannnis, J., Laznik-Bogoslavski, D., Wu, J., Ma, D., Lin, J. D., Greenberg, M. E. and Spiegelman, B. M. 2013. Exercise induces hippocampal BDNF through a PGC- /FNDC5 pathway. Cell. Metab. 18, 649-659.
DOI
|
29 |
Adams, G. R. 2002. Autocrine/paracrine IGF-I and skeletal muscle adaptation. J. Appl. Physiol. 93, 1159-1167.
DOI
|
30 |
Anderson, B. C., Christiansen, S. P., Grandt, S., Grange, R. W. and McLoon, L. K. 2006. Increased extraocular muscle strength with direct injection of insulin-like growth factor-I. Invest. Ophthalmol. Vis. Sci. 47, 2461-2467.
DOI
|
31 |
Zwetsloot, K. A., Laye, M. J. and Booth, F. W. 2009. Novel epigenetic regulation of skeletal muscle myosin heavy chain genes. Focus on "Differential epigenetic modifications of histones at the myosin heavy chain genes in fast and slow skeletal muscle fibers and in response to muscle unloading". Am. J. Physiol. 297, C1-3.
DOI
|
32 |
Xu, B. 2013. BDNF (I)rising from exercise. Cell. Metab. 18, 612-614.
DOI
|