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Skeletal Muscle Metabolism: Origin or Prognostic Factor for Amyotrophic Lateral Sclerosis (ALS) Development?
Quessada, Cyril; Bouscary, Alexandra; René, Frédérique; Valle, Cristiana; Ferri, Alberto; Ngo, Shyuan T; Loeffler, Jean-Philippe.
Afiliação
  • Quessada C; Mécanismes Centraux et Périphériques de la Neurodégénérescence, INSERM, UMR_S 1118, Centre de Recherche de Biomédecine de Strasbourg (CRBS), Université de Strasbourg, F-67000 Strasbourg, France.
  • Bouscary A; Mécanismes Centraux et Périphériques de la Neurodégénérescence, INSERM, UMR_S 1118, Centre de Recherche de Biomédecine de Strasbourg (CRBS), Université de Strasbourg, F-67000 Strasbourg, France.
  • René F; Neuro-Sys SAS, F-13120 Gardanne, France.
  • Valle C; Mécanismes Centraux et Périphériques de la Neurodégénérescence, INSERM, UMR_S 1118, Centre de Recherche de Biomédecine de Strasbourg (CRBS), Université de Strasbourg, F-67000 Strasbourg, France.
  • Ferri A; IRCCS Fondazione Santa Lucia, Institute of Translational Pharmacology, CNR, 00133 Roma, Italy.
  • Ngo ST; IRCCS Fondazione Santa Lucia, Institute of Translational Pharmacology, CNR, 00133 Roma, Italy.
  • Loeffler JP; Australian Institute for Bioengineering and Nanotechnology, The University of Queensland, Brisbane, QLD 4072, Australia.
Cells ; 10(6)2021 06 09.
Article em En | MEDLINE | ID: mdl-34207859
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease characterized by progressive and selective loss of motor neurons, amyotrophy and skeletal muscle paralysis usually leading to death due to respiratory failure. While generally considered an intrinsic motor neuron disease, data obtained in recent years, including our own, suggest that motor neuron protection is not sufficient to counter the disease. The dismantling of the neuromuscular junction is closely linked to chronic energy deficit found throughout the body. Metabolic (hypermetabolism and dyslipidemia) and mitochondrial alterations described in patients and murine models of ALS are associated with the development and progression of disease pathology and they appear long before motor neurons die. It is clear that these metabolic changes participate in the pathology of the disease. In this review, we summarize these changes seen throughout the course of the disease, and the subsequent impact of glucose-fatty acid oxidation imbalance on disease progression. We also highlight studies that show that correcting this loss of metabolic flexibility should now be considered a major goal for the treatment of ALS.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Músculo Esquelético / Esclerose Lateral Amiotrófica Tipo de estudo: Prognostic_studies Limite: Animals / Humans / Male Idioma: En Revista: Cells Ano de publicação: 2021 Tipo de documento: Article País de afiliação: França

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Músculo Esquelético / Esclerose Lateral Amiotrófica Tipo de estudo: Prognostic_studies Limite: Animals / Humans / Male Idioma: En Revista: Cells Ano de publicação: 2021 Tipo de documento: Article País de afiliação: França