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Effect of Aerobic Physical Exercise in an Animal Model of Duchenne Muscular Dystrophy.

Hoepers, A ; Alberti, A ; et al.
In: Journal of molecular neuroscience : MN, Jg. 70 (2020-10-01), Heft 10, S. 1552-1564
Online academicJournal

Titel:
Effect of Aerobic Physical Exercise in an Animal Model of Duchenne Muscular Dystrophy.
Autor/in / Beteiligte Person: Hoepers, A ; Alberti, A ; Freiberger, V ; Ventura, L ; Grigollo, LR ; Andreu, CS ; da Silva BB ; Martins, DF ; Junior, RJN ; Streck, EL ; Comim, CM
Link:
Zeitschrift: Journal of molecular neuroscience : MN, Jg. 70 (2020-10-01), Heft 10, S. 1552-1564
Veröffentlichung: Totowa, NJ : Humana Press ; <i>Original Publication</i>: Boston : Birkhäuser [i.e. Cambridge, MA : Birkhäuser Boston, c1989-, 2020
Medientyp: academicJournal
ISSN: 1559-1166 (electronic)
DOI: 10.1007/s12031-020-01565-0
Schlagwort:
  • Animals
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Inbred mdx
  • Muscle, Skeletal metabolism
  • Muscle, Skeletal physiopathology
  • Oxidative Stress
  • Exercise Therapy methods
  • Muscular Dystrophy, Duchenne therapy
  • Physical Conditioning, Animal methods
Sonstiges:
  • Nachgewiesen in: MEDLINE
  • Sprachen: English
  • Publication Type: Journal Article
  • Language: English
  • [J Mol Neurosci] 2020 Oct; Vol. 70 (10), pp. 1552-1564. <i>Date of Electronic Publication: </i>2020 Jun 08.
  • MeSH Terms: Exercise Therapy / *methods ; Muscular Dystrophy, Duchenne / *therapy ; Physical Conditioning, Animal / *methods ; Animals ; Male ; Mice ; Mice, Inbred C57BL ; Mice, Inbred mdx ; Muscle, Skeletal / metabolism ; Muscle, Skeletal / physiopathology ; Oxidative Stress
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(PMID: 10.1016/j.freeradbiomed.2007.04.00317561103) ; Kogelman B, Putker K, Hulsker M, Tanganyika-de Winter C, van der Weerd L, Aartsma-Rus A et al (2018) Voluntary exercise improves muscle function and does not exacerbate muscle and heart pathology in aged Duchenne muscular dystrophy mice. J Mol Cell Cardiol 125:29–38. https://doi.org/10.1016/j.yjmcc.2018.10.008. (PMID: 10.1016/j.yjmcc.2018.10.00830336143) ; Kostek M (2019) Precision medicine and exercise therapy in Duchenne muscular dystrophy. Sports 7(3):64. https://doi.org/10.3390/sports7030064. (PMID: 10.3390/sports70300646473733) ; Le Rumeur E (2015) Dystrophin and the two related genetic diseases, Duchenne and Becker muscular dystrophies. Bosn J Basic Med Sci 15(3):14–20. (PMID: 10.17305/bjbms.2015.636262952894594321) ; Levine A, Tenhaken R, Dixon R, Lamb C (1994) H2O2 from the oxidative burst orchestrates the plant hypersensitive disease resistance response. Cell 79:583–593. 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(PMID: 10.1016/0009-8981(94)90055-8) ; Savino W, Pinto-Mariz F, Mouly V (2018) Flow cytometry-defined CD49d expression in circulating T-lymphocytes is a biomarker for disease progression in Duchenne muscular dystrophy. In: Bernardini C (ed) Duchenne Muscular Dystrophy. Humana Press, New York, pp 219–227. (PMID: 10.1007/978-1-4939-7374-3_16) ; Shan X, Aw TY, Jones DP (1990) Glutathione-dependent protection against oxidative injury. Pharmacol Ther 47:61–71. (PMID: 10.1016/0163-7258(90)90045-42195557) ; Timpani CA, Hayes A, Rybalka E (2015) Revisiting the dystrophin-ATP connection: how half a century of research still implicates mitochondrial dysfunction in Duchenne muscular dystrophy aetiology. Med Hypotheses. ; Tuon L, Comim CM, Fraga DB, Scain G (2010) Mitochondrial respiratory chain and creatine kinase activities in the brain mdx mouse. Muscle Nerve 257–264. ; Urhausen A, Coen B, Weiler B, Kindermann W (1993) Individual anaerobic threshold and maximum lactate steady state. 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  • Contributed Indexing: Keywords: Animal; Duchenne muscular dystrophy; Muscle; Oxidative stress; Physical exercise
  • Entry Date(s): Date Created: 20200609 Date Completed: 20210629 Latest Revision: 20211116
  • Update Code: 20240513

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