Carta Acesso aberto Revisado por pares

Mitochondrial dysfunction in amyotrophic lateral sclerosis also affects skeletal muscle

2006; Wiley; Volume: 34; Issue: 2 Linguagem: Inglês

10.1002/mus.20566

ISSN

1097-4598

Autores

Luc Dupuis, José‐Luis González de Aguilar, Andoni Echaniz‐Laguna, Jean‐Philippe Loeffler,

Tópico(s)

Muscle Physiology and Disorders

Resumo

Muscle & NerveVolume 34, Issue 2 p. 253-254 Letters to the Editor Mitochondrial dysfunction in amyotrophic lateral sclerosis also affects skeletal muscle Luc Dupuis PhD, Luc Dupuis PhD Laboratoire de Signalisations Moléculaires et Neurodégénérescence INSERM U-692, Univerité Louis Pasteur, Faculté de Médecine, 11 rue Humann, 67085 Strasbourg, FranceSearch for more papers by this authorJose-Luis Gonzalez de Aguilar PhD, Jose-Luis Gonzalez de Aguilar PhD Laboratoire de Signalisations Moléculaires et Neurodégénérescence INSERM U-692, Univerité Louis Pasteur, Faculté de Médecine, 11 rue Humann, 67085 Strasbourg, FranceSearch for more papers by this authorAndoni Echaniz-Laguna MD, Andoni Echaniz-Laguna MD Laboratoire de Signalisations Moléculaires et Neurodégénérescence INSERM U-692, Univerité Louis Pasteur, Faculté de Médecine, 11 rue Humann, 67085 Strasbourg, FranceSearch for more papers by this authorJean-Philippe Loeffler PhD, Jean-Philippe Loeffler PhD Laboratoire de Signalisations Moléculaires et Neurodégénérescence INSERM U-692, Univerité Louis Pasteur, Faculté de Médecine, 11 rue Humann, 67085 Strasbourg, FranceSearch for more papers by this author Luc Dupuis PhD, Luc Dupuis PhD Laboratoire de Signalisations Moléculaires et Neurodégénérescence INSERM U-692, Univerité Louis Pasteur, Faculté de Médecine, 11 rue Humann, 67085 Strasbourg, FranceSearch for more papers by this authorJose-Luis Gonzalez de Aguilar PhD, Jose-Luis Gonzalez de Aguilar PhD Laboratoire de Signalisations Moléculaires et Neurodégénérescence INSERM U-692, Univerité Louis Pasteur, Faculté de Médecine, 11 rue Humann, 67085 Strasbourg, FranceSearch for more papers by this authorAndoni Echaniz-Laguna MD, Andoni Echaniz-Laguna MD Laboratoire de Signalisations Moléculaires et Neurodégénérescence INSERM U-692, Univerité Louis Pasteur, Faculté de Médecine, 11 rue Humann, 67085 Strasbourg, FranceSearch for more papers by this authorJean-Philippe Loeffler PhD, Jean-Philippe Loeffler PhD Laboratoire de Signalisations Moléculaires et Neurodégénérescence INSERM U-692, Univerité Louis Pasteur, Faculté de Médecine, 11 rue Humann, 67085 Strasbourg, FranceSearch for more papers by this author First published: 26 April 2006 https://doi.org/10.1002/mus.20566Citations: 10Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat No abstract is available for this article. References 1 Clement AM, Nguyen MD, Roberts EA, Garcia ML, Boillee S, Rule M, et al. Wild-type nonneuronal cells extend survival of SOD1 mutant motor neurons in ALS mice. Science 2003; 302: 113–117. 2 Derave W, Van Den Bosch L, Lemmens G, Eijnde BO, Robberecht W, Hespel P. Skeletal muscle properties in a transgenic mouse model for amyotrophic lateral sclerosis: effects of creatine treatment. Neurobiol Dis 2003; 13: 264–272. 3 Desport JC, Preux PM, Magy L, Boirie Y, Vallat JM, Beaufrere B, et al. Factors correlated with hypermetabolism in patients with amyotrophic lateral sclerosis. Am J Clin Nutr 2001; 74: 328–334. 4 Dobrowolny G, Giacinti C, Pelosi L, Nicoletti C, Winn N, Barberi L, et al. Muscle expression of a local Igf-1 isoform protects motor neurons in an ALS mouse model. J Cell Biol 2005; 168: 193–199. 5 Dupuis L, di Scala F, Rene F, de Tapia M, Oudart H, Pradat PF, et al. Up-regulation of mitochondrial uncoupling protein 3 reveals an early muscular metabolic defect in amyotrophic lateral sclerosis. FASEB J 2003; 17: 2091–2093. 6 Dupuis L, Oudart H, Rene F, Gonzalez de Aguilar JL, Loeffler JP. Evidence for defective energy homeostasis in amyotrophic lateral sclerosis: benefit of a high-energy diet in a transgenic mouse model. Proc Natl Acad Sci U S A 2004; 101: 11159–11164. 7 Echaniz-Laguna A, Zoll J, Ponsot E, N'guessan B, Tranchant C, Loeffler JP, et al. Muscular mitochondrial function in amyotrophic lateral sclerosis is progressively altered as the disease develops: a temporal study in man. Exp Neurol 2006; 198: 25–30. 8 Echaniz-Laguna A, Zoll J, Ribera F, Tranchant C, Warter JM, Lonsdorfer J, et al. Mitochondrial respiratory chain function in skeletal muscle of ALS patients. Ann Neurol 2002; 52: 623–627. 9 Fischer LR, Culver DG, Tennant P, Davis AA, Wang M, Castellano-Sanchez A, et al. Amyotrophic lateral sclerosis is a distal axonopathy: evidence in mice and man. Exp Neurol 2004; 185: 232–240. 10 Gong YH, Parsadanian AS, Andreeva A, Snider WD, Elliott JL. Restricted expression of G86R Cu/Zn superoxide dismutase in astrocytes results in astrocytosis but does not cause motoneuron degeneration. J Neurosci 2000; 20: 660–665. 11 Hervias I, Beal MF, Manfredi G. Mitochondrial dysfunction and amyotrophic lateral sclerosis. Muscle Nerve 2006; 33: 598–608. 12 Kirkinezos IG, Hernandez D, Bradley WG, Moraes CT. Regular exercise is beneficial to a mouse model of amyotrophic lateral sclerosis. Ann Neurol 2003; 53: 804–807. 13 Krasnianski A, Deschauer M, Neudecker S, Gellerich FN, Muller T, Schoser BG et al. Mitochondrial changes in skeletal muscle in amyotrophic lateral sclerosis and other neurogenic atrophies. Brain 2005; 128: 1870–1876. 14 Leclerc N, Ribera F, Zoll J, Warter JM, Poindron P, Lampert E et al. Selective changes in mitochondria respiratory properties in oxidative or glycolytic muscle fibers isolated from G93AhumanSOD1 transgenic mice. Neuromuscul Disord 2001; 11: 722–727. 15 Pramatarova A, Laganiere J, Roussel J, Brisebois K, Rouleau GA. Neuron-specific expression of mutant superoxide dismutase 1 in transgenic mice does not lead to motor impairment. J Neurosci 2001; 21: 3369–3374. 16 Vielhaber S, Kunz D, Winkler K, Wiedemann FR, Kirches E, Feistner H, et al. Mitochondrial DNA abnormalities in skeletal muscle of patients with sporadic amyotrophic lateral sclerosis. Brain 2000; 123: 1339–1348. Citing Literature Volume34, Issue2August 2006Pages 253-254 ReferencesRelatedInformation

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