Isotopic Evidence for Disrupted Copper Metabolism in Amyotrophic Lateral Sclerosis

Summary: Redox-active metals are thought to be implicated in neurodegenerative diseases including amyotrophic lateral sclerosis (ALS). To address this point, we measured the concentrations of 12 elements and, for the first time, the stable isotope compositions of copper (redox-active) and zinc (redo...

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Main Authors: Lucie Sauzéat, Emilien Bernard, Armand Perret-Liaudet, Isabelle Quadrio, Alain Vighetto, Pierre Krolak-Salmon, Emmanuel Broussolle, Pascal Leblanc, Vincent Balter
Format: Article
Language:English
Published: Elsevier 2018-08-01
Series:iScience
Online Access:http://www.sciencedirect.com/science/article/pii/S2589004218301111
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spelling doaj-43e5361b27b449fcba379df890dfe9652020-11-25T01:59:01ZengElsevieriScience2589-00422018-08-016264271Isotopic Evidence for Disrupted Copper Metabolism in Amyotrophic Lateral SclerosisLucie Sauzéat0Emilien Bernard1Armand Perret-Liaudet2Isabelle Quadrio3Alain Vighetto4Pierre Krolak-Salmon5Emmanuel Broussolle6Pascal Leblanc7Vincent Balter8Université de Lyon, ENS de Lyon, CNRS, LGL-TPE, 69007 Lyon, FranceHospices Civils de Lyon, Hôpital Neurologique Pierre Wertheimer, Centre de Ressources et de Compétence SLA de Lyon, Service de Neurologie C, Bron, FranceUniversité de Lyon, CNRS UMR5292, INSERM U1028, BioRan, Lyon, France; Hospices Civils de Lyon, Neurobiology Laboratory, Biochemistry and Molecular Biology Department, Lyon, FranceUniversité de Lyon, CNRS UMR5292, INSERM U1028, BioRan, Lyon, France; Hospices Civils de Lyon, Neurobiology Laboratory, Biochemistry and Molecular Biology Department, Lyon, FranceService Neurocognition et Neuroophtalmologie, Hôpital Neurologique, 59 Boulevard Pinel, 69677 Bron Cedex, France; Centre Mémoire Ressources Recherche de Lyon, Hospices Civils de Lyon, Hôpital des Charpennes, Villeurbanne, France; Université Lyon 1, Hospices Civils de Lyon, Centre de Recherche en Neurosciences de Lyon, équipe IMPACT, Lyon, FranceCentre Mémoire Ressources Recherche de Lyon, Hospices Civils de Lyon, Hôpital des Charpennes, Villeurbanne, FranceUniversité de Lyon, Faculté de Médecine Lyon Sud Charles Mérieux, Institut des Sciences Cognitives Marc Jeannerod, CNRS, UMR 5229, Lyon, FranceInstitut NeuroMyoGène, CNRS UMR5310, INSERM U1217, Faculté de Médecine Rockefeller, Université Claude Bernard Lyon I, 8 Avenue Rockefeller, 69373 Lyon Cedex 08, FranceUniversité de Lyon, ENS de Lyon, CNRS, LGL-TPE, 69007 Lyon, France; Corresponding authorSummary: Redox-active metals are thought to be implicated in neurodegenerative diseases including amyotrophic lateral sclerosis (ALS). To address this point, we measured the concentrations of 12 elements and, for the first time, the stable isotope compositions of copper (redox-active) and zinc (redox-inactive) in human cerebrospinal fluids of 31 patients with ALS, 11 age-matched controls (CTRL), and 14 patients with Alzheimer disease. We first show that metal concentrations weakly discriminate patients with ALS from the two other groups. We then report that zinc isotopic compositions are similar in the three groups, but that patients with ALS have significantly 65copper-enriched isotopic compositions relative to CTRL and patients with AD. This result unambiguously demonstrates that copper is implicated in ALS. We suggest that this copper isotopic signature may result from abnormal protein aggregation in the brain parenchyma, and propose that isotopic analysis is a potential tool that may help unraveling the molecular mechanisms at work in ALS. : Nuclear Medicine; Isotope Chemistry; Neuroscience; Clinical Neuroscience Subject Areas: Nuclear Medicine, Isotope Chemistry, Neuroscience, Clinical Neurosciencehttp://www.sciencedirect.com/science/article/pii/S2589004218301111
collection DOAJ
language English
format Article
sources DOAJ
author Lucie Sauzéat
Emilien Bernard
Armand Perret-Liaudet
Isabelle Quadrio
Alain Vighetto
Pierre Krolak-Salmon
Emmanuel Broussolle
Pascal Leblanc
Vincent Balter
spellingShingle Lucie Sauzéat
Emilien Bernard
Armand Perret-Liaudet
Isabelle Quadrio
Alain Vighetto
Pierre Krolak-Salmon
Emmanuel Broussolle
Pascal Leblanc
Vincent Balter
Isotopic Evidence for Disrupted Copper Metabolism in Amyotrophic Lateral Sclerosis
iScience
author_facet Lucie Sauzéat
Emilien Bernard
Armand Perret-Liaudet
Isabelle Quadrio
Alain Vighetto
Pierre Krolak-Salmon
Emmanuel Broussolle
Pascal Leblanc
Vincent Balter
author_sort Lucie Sauzéat
title Isotopic Evidence for Disrupted Copper Metabolism in Amyotrophic Lateral Sclerosis
title_short Isotopic Evidence for Disrupted Copper Metabolism in Amyotrophic Lateral Sclerosis
title_full Isotopic Evidence for Disrupted Copper Metabolism in Amyotrophic Lateral Sclerosis
title_fullStr Isotopic Evidence for Disrupted Copper Metabolism in Amyotrophic Lateral Sclerosis
title_full_unstemmed Isotopic Evidence for Disrupted Copper Metabolism in Amyotrophic Lateral Sclerosis
title_sort isotopic evidence for disrupted copper metabolism in amyotrophic lateral sclerosis
publisher Elsevier
series iScience
issn 2589-0042
publishDate 2018-08-01
description Summary: Redox-active metals are thought to be implicated in neurodegenerative diseases including amyotrophic lateral sclerosis (ALS). To address this point, we measured the concentrations of 12 elements and, for the first time, the stable isotope compositions of copper (redox-active) and zinc (redox-inactive) in human cerebrospinal fluids of 31 patients with ALS, 11 age-matched controls (CTRL), and 14 patients with Alzheimer disease. We first show that metal concentrations weakly discriminate patients with ALS from the two other groups. We then report that zinc isotopic compositions are similar in the three groups, but that patients with ALS have significantly 65copper-enriched isotopic compositions relative to CTRL and patients with AD. This result unambiguously demonstrates that copper is implicated in ALS. We suggest that this copper isotopic signature may result from abnormal protein aggregation in the brain parenchyma, and propose that isotopic analysis is a potential tool that may help unraveling the molecular mechanisms at work in ALS. : Nuclear Medicine; Isotope Chemistry; Neuroscience; Clinical Neuroscience Subject Areas: Nuclear Medicine, Isotope Chemistry, Neuroscience, Clinical Neuroscience
url http://www.sciencedirect.com/science/article/pii/S2589004218301111
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