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Lead as an environmental toxicant in models of synucleinopathies

datacite.subject.fosCiências Médicas::Ciências da Saúde
datacite.subject.sdg03:Saúde de Qualidade
dc.contributor.authorShvachiy, Liana
dc.contributor.authorAmaro-Leal, Ângela
dc.contributor.authorMachado, Filipa
dc.contributor.authorRocha, Isabel
dc.contributor.authorGeraldes, Vera
dc.contributor.authorOuteiro, Tiago F.
dc.date.accessioned2026-05-13T10:44:52Z
dc.date.available2026-05-13T10:44:52Z
dc.date.issued2025-06
dc.description.abstractLead, a toxic heavy metal, is prevalent in various industrial applications, contributing to environmental contamination and significant health concerns. Lead affects various body systems, especially the brain, causing long-lasting cognitive and behavioral changes. While most studies have focused on continuous lead exposure, intermittent exposure, such as that caused by migration or relocations, has received less attention. Importantly, lead exposure intensifies the severity of Parkinson's disease (PD) and dementia with Lewy bodies, diseases involving the accumulation of alpha-synuclein (aSyn) in the brain and in the gut. Although the precise mechanisms underlying these observations remain unclear, oxidative stress and mitochondrial dysfunction likely play a role. Here, we investigated how two different profiles of lead exposure - continuous and intermittent - affect models of synucleinopathies. We found that lead exposure enhances the formation of aSyn inclusions, resulting in an increase in both their number and size in cell models. In addition, we found that animals injected with aSyn pre-formed fibrils display serine 129-phosphorylated aSyn inclusions and a reduction in astrocytes in the substantia nigra. These animals also display neuronal damage and alterations in locomotor activity, exploration behavior, anxiety, memory impairments and hypertension. Our results suggest a mechanistic link between environmental lead exposure and the onset and progression of diseases associated with aSyn pathology. Understanding the molecular and cellular interactions between lead and aSyn is crucial for shaping public health policies and may provide novel insight into strategies for mitigating the impact of environmental toxins on neurodegenerative processes involved in Parkinson's disease and related synucleinopathies.eng
dc.identifier.citationShvachiy, L., Amaro-Leal, Â., Machado, F., Rocha, I., Geraldes, V., & Outeiro, T. F. (2025). Lead as an environmental toxicant in models of synucleinopathies. Chemosphere, 380, 144477. https://doi.org/10.1016/j.chemosphere.2025.144477
dc.identifier.doi10.1016/j.chemosphere.2025.144477
dc.identifier.issn1879-1298
dc.identifier.urihttp://hdl.handle.net/10400.26/63100
dc.language.isoeng
dc.peerreviewedyes
dc.publisherElsevier
dc.relation.hasversionhttps://doi.org/10.1016/j.chemosphere.2025.144477
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectAlpha-synuclein
dc.subjectParkinson's disease
dc.subjectSynucleinopathies
dc.subjectLead
dc.subjectHeavy-metal exposure
dc.subjectEnvironmental factor
dc.titleLead as an environmental toxicant in models of synucleinopathieseng
dc.typecontribution to journal
dspace.entity.typePublication
oaire.citation.startPage144477
oaire.citation.titleChemosphere
oaire.citation.volume380
oaire.versionhttp://purl.org/coar/version/c_970fb48d4fbd8a85

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