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Potentially toxic elements in the brains of people with multiple sclerosis.
Pamphlett, Roger; Buckland, Michael E; Bishop, David P.
Afiliación
  • Pamphlett R; Discipline of Pathology, Sydney Medical School, Brain and Mind Centre, The University of Sydney, Sydney, NSW, Australia. roger.pamphlett@sydney.edu.au.
  • Buckland ME; Department of Neuropathology, Royal Prince Alfred Hospital, Sydney, NSW, Australia. roger.pamphlett@sydney.edu.au.
  • Bishop DP; Hyphenated Mass Spectrometry Laboratory, School of Mathematical and Physical Sciences, University of Technology Sydney, Sydney, NSW, Australia. roger.pamphlett@sydney.edu.au.
Sci Rep ; 13(1): 655, 2023 01 12.
Article en En | MEDLINE | ID: mdl-36635465
ABSTRACT
Potentially toxic elements such as lead and aluminium have been proposed to play a role in the pathogenesis of multiple sclerosis (MS), since their neurotoxic mechanisms mimic many of the pathogenetic processes in MS. We therefore examined the distribution of several potentially toxic elements in the autopsied brains of people with and without MS, using two methods of elemental bio-imaging. Toxicants detected in the locus ceruleus were used as indicators of past exposures. Autometallography of paraffin sections from multiple brain regions of 21 MS patients and 109 controls detected inorganic mercury, silver, or bismuth in many locus ceruleus neurons of both groups, and in widespread blood vessels, oligodendrocytes, astrocytes, and neurons of four MS patients and one control. Laser ablation-inductively coupled plasma-mass spectrometry imaging of pons paraffin sections from all MS patients and 12 controls showed that combinations of iron, silver, lead, aluminium, mercury, nickel, and bismuth were present more often in the locus ceruleus of MS patients and were located predominantly in white matter tracts. Based on these results, we propose that metal toxicants in locus ceruleus neurons weaken the blood-brain barrier, enabling multiple interacting toxicants to pass through blood vessels and enter astrocytes and oligodendroglia, leading to demyelination.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Mercurio / Esclerosis Múltiple Tipo de estudio: Risk_factors_studies Límite: Humans Idioma: En Revista: Sci Rep Año: 2023 Tipo del documento: Article País de afiliación: Australia

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Mercurio / Esclerosis Múltiple Tipo de estudio: Risk_factors_studies Límite: Humans Idioma: En Revista: Sci Rep Año: 2023 Tipo del documento: Article País de afiliación: Australia