PHYSICAL ACTIVITY AND COGNITIVE FUNCTIONS: ROLE OF THE BRAIN-DERIVED NEUROTROPHIC FACTOR (BDNF)

Rosaria Arcone, Mariorosario Masullo

Abstract


The skeletal muscle is considered an endocrine organ as it secretes various myokines. The myokines are produced during skeletal muscle contraction and exert autocrine, paracrine, and endocrine effects even on different organs and tissues. Up to now, many myokines have been described, including the brain-derived neurotrophic factor (BDNF), interleukin-6 (IL-6), irisin, leukemia inhibitory factor (LIF), and insulin-like growth factor1 (IGF-1) are the most relevant also for brain functions. In particular, it is well known that BDNF ameliorates cognitive functions via neuronal differentiation and plasticity in the hippocampal region. Therefore, myokines represent key molecules in the cross-talk between skeletal muscle and brain.


Keywords


Scienze motorie

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References


Agrawal, R., Noble, E., Tyagi, E., Zhuang, Y., Ying, Z., & Gomez-Pinilla, F. (2015). Flavonoid derivative 7,8-DHF attenuates TBI pathology via TrkB activation. Biochimica et biophysica acta, 1852(5), 862–872. https://doi.org/10.1016/j.bbadis.2015.01.018

Arcone, R., Palma, M., Pagliara, V., Graziani, G., Masullo, M., & Nardone, G. (2016). Green tea polyphenols affect invasiveness of human gastric MKN-28 cells by inhibition of LPS or TNF-α induced Matrix Metalloproteinase-9/2. Biochimie open, 3, 56–63. https://doi.org/10.1016/j.biopen.2016.10.002

Bortoluzzi, S., Scannapieco, P., Cestaro, A., Danieli, G. A., & Schiaffino, S. (2006). Computational reconstruction of the human skeletal muscle secretome. Proteins, 62(3), 776–792. https://doi.org/10.1002/prot.20803

Chang, Y. K., Labban, J. D., Gapin, J. I., & Etnier, J. L. (2012). The effects of acute exercise on cognitive performance: a meta-analysis. Brain research, 1453, 87–101. https://doi.org/10.1016/j.brainres.2012.02.068

Chen, W., Wang, L., You, W., & Shan, T. (2021). Myokines mediate the cross talk between skeletal muscle and other organs. Journal of cellular physiology, 236(4), 2393–2412. https://doi.org/10.1002/jcp.30033

Chieffi, S., Messina, G., Villano, I., Messina, A., Valenzano, A., Moscatelli, F., Salerno, M., Sullo, A., Avola, R., Monda, V., Cibelli, G., & Monda, M. (2017). Neuroprotective Effects of Physical Activity: Evidence from Human and Animal Studies. Frontiers in neurology, 8, 188. https://doi.org/10.3389/fneur.2017.00188

Colucci-D'Amato, L., Speranza, L., & Volpicelli, F. (2020). Neurotrophic Factor BDNF, Physiological Functions and Therapeutic Potential in Depression, Neurodegeneration and Brain Cancer. International journal of molecular sciences, 21(20), 7777. https://doi.org/10.3390/ijms21207777

Fuss, J., Steinle, J., Bindila, L., Auer, M. K., Kirchherr, H., Lutz, B., & Gass, P. (2015). A runner's high depends on cannabinoid receptors in mice. Proceedings of the National Academy of Sciences of the United States of America, 112(42), 13105–13108. https://doi.org/10.1073/pnas.1514996112

Görgens, S. W., Eckardt, K., Jensen, J., Drevon, C. A., & Eckel, J. (2015). Exercise and Regulation of Adipokine and Myokine Production. Progress in molecular biology and translational science, 135, 313–336. https://doi.org/10.1016/bs.pmbts.2015.07.002

Leal, G., Comprido, D., & Duarte, C. B. (2014). BDNF-induced local protein synthesis and synaptic plasticity. Neuropharmacology, 76 Pt C, 639–656. https://doi.org/10.1016/j.neuropharm.2013.04.005

Lee, J. H., & Jun, H. S. (2019). Role of Myokines in Regulating Skeletal Muscle Mass and Function. Frontiers in physiology, 10, 42. https://doi.org/10.3389/fphys.2019.00042

Leibrock, J., Lottspeich, F., Hohn, A., Hofer, M., Hengerer, B., Masiakowski, P., Thoenen, H., & Barde, Y. A. (1989). Molecular cloning and expression of brain-derived neurotrophic factor. Nature, 341(6238), 149–152. https://doi.org/10.1038/341149a0

Mackay, C. P., Kuys, S. S., & Brauer, S. G. (2017). The Effect of Aerobic Exercise on Brain-Derived Neurotrophic Factor in People with Neurological Disorders: A Systematic Review and Meta-Analysis. Neural plasticity, 2017, 4716197. https://doi.org/10.1155/2017/4716197

Mandolesi, L., Polverino, A., Montuori, S., Foti, F., Ferraioli, G., Sorrentino, P., & Sorrentino, G. (2018). Effects of Physical Exercise on Cognitive Functioning and Wellbeing: Biological and Psychological Benefits. Frontiers in psychology, 9, 509. https://doi.org/10.3389/fpsyg.2018.00509

Miranda, M., Morici, J. F., Zanoni, M. B., & Bekinschtein, P. (2019). Brain-Derived Neurotrophic Factor: A Key Molecule for Memory in the Healthy and the Pathological Brain. Frontiers in cellular neuroscience, 13, 363. https://doi.org/10.3389/fncel.2019.00363

Miyamoto, T., Hashimoto, S., Yanamoto, H., Ikawa, M., Nakano, Y., Sekiyama, T., Kou, K., Kashiwamura, S. I., Takeda, C., & Fujioka, H. (2018). Response of brain-derived neurotrophic factor to combining cognitive and physical exercise. European journal of sport science, 18(8), 1119–1127. https://doi.org/10.1080/17461391.2018.1470676

Nasso, R., Pagliara, V., D'Angelo, S., Rullo, R., Masullo, M., & Arcone, R. (2021). Annurca Apple Polyphenol Extract Affects Acetyl- Cholinesterase and Mono-Amine Oxidase In Vitro Enzyme Activity. Pharmaceuticals (Basel, Switzerland), 14(1), 62. https://doi.org/10.3390/ph14010062

Pagliara, V., Nasso, R., Di Donato, P., Finore, I., Poli, A., Masullo, M., & Arcone, R. (2019). Lemon Peel Polyphenol Extract Reduces Interleukin-6-Induced Cell Migration, Invasiveness, and Matrix Metalloproteinase-9/2 Expression in Human Gastric Adenocarcinoma MKN-28 and AGS Cell Lines. Biomolecules, 9(12), 833. https://doi.org/10.3390/biom9120833

Pagliara, V., Parafati, M., Adornetto, A., White, M.C., Masullo, M., Grimaldi, M. & Arcone, R. (2018). Dibutyryl cAMP- or Interleukin-6-induced astrocytic differentiation enhances mannose binding lectin (MBL)-associated serine protease (MASP)-1/3 expression in C6 glioma cells. Archives of Biochemistry and Biophysics, 653, 39-49. https://doi.org/10.1016/j.abb.2018.06.016

Pedersen, B. K., & Febbraio, M. A. (2012). Muscles, exercise and obesity: skeletal muscle as a secretory organ. Nature reviews. Endocrinology, 8(8), 457–465. https://doi.org/10.1038/nrendo.2012.49

Pedersen B. K. (2019). Physical activity and muscle-brain crosstalk. Nature reviews. Endocrinology, 15(7), 383–392. https://doi.org/10.1038/s41574-019-0174-x

Pietrelli, A., Matković, L., Vacotto, M., Lopez-Costa, J. J., Basso, N., & Brusco, A. (2018). Aerobic exercise upregulates the BDNF-Serotonin systems and improves the cognitive function in rats. Neurobiology of learning and memory, 155, 528–542. https://doi.org/10.1016/j.nlm.2018.05.007

Sasi, M., Vignoli, B., Canossa, M., & Blum, R. (2017). Neurobiology of local and intercellular BDNF signaling. Pflugers Archiv : European journal of physiology, 469(5-6), 593–610. https://doi.org/10.1007/s00424-017-1964-4




DOI: https://doi.org/10.32043/gsd.v6i1.529

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