Cellular and Molecular Mechanisms Mediating Methylmercury Neurotoxicity and Neuroinflammation
Main Author: | |
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Publication Date: | 2021 |
Other Authors: | , , , , , |
Format: | Article |
Language: | eng |
Source: | Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) |
Download full: | https://hdl.handle.net/10316/104748 https://doi.org/10.3390/ijms22063101 |
Summary: | Methylmercury (MeHg) toxicity is a major environmental concern. In the aquatic reservoir, MeHg bioaccumulates along the food chain until it is consumed by riverine populations. There has been much interest in the neurotoxicity of MeHg due to recent environmental disasters. Studies have also addressed the implications of long-term MeHg exposure for humans. The central nervous system is particularly susceptible to the deleterious effects of MeHg, as evidenced by clinical symptoms and histopathological changes in poisoned humans. In vitro and in vivo studies have been crucial in deciphering the molecular mechanisms underlying MeHg-induced neurotoxicity. A collection of cellular and molecular alterations including cytokine release, oxidative stress, mitochondrial dysfunction, Ca2+ and glutamate dyshomeostasis, and cell death mechanisms are important consequences of brain cells exposure to MeHg. The purpose of this review is to organize an overview of the mercury cycle and MeHg poisoning events and to summarize data from cellular, animal, and human studies focusing on MeHg effects in neurons and glial cells. This review proposes an up-to-date compendium that will serve as a starting point for further studies and a consultation reference of published studies. |
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Cellular and Molecular Mechanisms Mediating Methylmercury Neurotoxicity and Neuroinflammationmercury cycleMethylmercuryneuroinflammationneurotoxicitymicrogliaoligodendrocytesastrocytesneuronsoxidative stressMethylmercury (MeHg) toxicity is a major environmental concern. In the aquatic reservoir, MeHg bioaccumulates along the food chain until it is consumed by riverine populations. There has been much interest in the neurotoxicity of MeHg due to recent environmental disasters. Studies have also addressed the implications of long-term MeHg exposure for humans. The central nervous system is particularly susceptible to the deleterious effects of MeHg, as evidenced by clinical symptoms and histopathological changes in poisoned humans. In vitro and in vivo studies have been crucial in deciphering the molecular mechanisms underlying MeHg-induced neurotoxicity. A collection of cellular and molecular alterations including cytokine release, oxidative stress, mitochondrial dysfunction, Ca2+ and glutamate dyshomeostasis, and cell death mechanisms are important consequences of brain cells exposure to MeHg. The purpose of this review is to organize an overview of the mercury cycle and MeHg poisoning events and to summarize data from cellular, animal, and human studies focusing on MeHg effects in neurons and glial cells. This review proposes an up-to-date compendium that will serve as a starting point for further studies and a consultation reference of published studies.The authors would like to thank the funding from National Funds via FCT (Portuguese Foundation for Science and Technology) through the Strategic Project UIDB/04539/2020 and UIDP/-04539/2020 (CIBB), Pest UID/NEU/04539/2013; FCT/FUNCAP cooperative project POCTI-FEDER02/SAICT/2017/31699:MercuMemory; POCI-01-0145-FEDER-007440, CENTRO010145FEDER0000012:Healthy Aging 2020 and the Brazilian Coordination for the Improvement of Higher EducationPersonnel [CAPES] Procad [88881.068408/2014-01] and CAPES PrInt grants.MDPI AG2021-03-18info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttps://hdl.handle.net/10316/104748https://hdl.handle.net/10316/104748https://doi.org/10.3390/ijms22063101eng1422-0067338035851422-0067Novo, João P.Martins, BeatrizRaposo, Ramon S.Pereira, Frederico C.Oriá, Reinaldo BMalva, João O.Fontes-Ribeiro, Carlosinfo:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2025-02-26T12:29:50Zoai:estudogeral.uc.pt:10316/104748Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-29T05:54:57.098790Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse |
dc.title.none.fl_str_mv |
Cellular and Molecular Mechanisms Mediating Methylmercury Neurotoxicity and Neuroinflammation |
title |
Cellular and Molecular Mechanisms Mediating Methylmercury Neurotoxicity and Neuroinflammation |
spellingShingle |
Cellular and Molecular Mechanisms Mediating Methylmercury Neurotoxicity and Neuroinflammation Novo, João P. mercury cycle Methylmercury neuroinflammation neurotoxicity microglia oligodendrocytes astrocytes neurons oxidative stress |
title_short |
Cellular and Molecular Mechanisms Mediating Methylmercury Neurotoxicity and Neuroinflammation |
title_full |
Cellular and Molecular Mechanisms Mediating Methylmercury Neurotoxicity and Neuroinflammation |
title_fullStr |
Cellular and Molecular Mechanisms Mediating Methylmercury Neurotoxicity and Neuroinflammation |
title_full_unstemmed |
Cellular and Molecular Mechanisms Mediating Methylmercury Neurotoxicity and Neuroinflammation |
title_sort |
Cellular and Molecular Mechanisms Mediating Methylmercury Neurotoxicity and Neuroinflammation |
author |
Novo, João P. |
author_facet |
Novo, João P. Martins, Beatriz Raposo, Ramon S. Pereira, Frederico C. Oriá, Reinaldo B Malva, João O. Fontes-Ribeiro, Carlos |
author_role |
author |
author2 |
Martins, Beatriz Raposo, Ramon S. Pereira, Frederico C. Oriá, Reinaldo B Malva, João O. Fontes-Ribeiro, Carlos |
author2_role |
author author author author author author |
dc.contributor.author.fl_str_mv |
Novo, João P. Martins, Beatriz Raposo, Ramon S. Pereira, Frederico C. Oriá, Reinaldo B Malva, João O. Fontes-Ribeiro, Carlos |
dc.subject.por.fl_str_mv |
mercury cycle Methylmercury neuroinflammation neurotoxicity microglia oligodendrocytes astrocytes neurons oxidative stress |
topic |
mercury cycle Methylmercury neuroinflammation neurotoxicity microglia oligodendrocytes astrocytes neurons oxidative stress |
description |
Methylmercury (MeHg) toxicity is a major environmental concern. In the aquatic reservoir, MeHg bioaccumulates along the food chain until it is consumed by riverine populations. There has been much interest in the neurotoxicity of MeHg due to recent environmental disasters. Studies have also addressed the implications of long-term MeHg exposure for humans. The central nervous system is particularly susceptible to the deleterious effects of MeHg, as evidenced by clinical symptoms and histopathological changes in poisoned humans. In vitro and in vivo studies have been crucial in deciphering the molecular mechanisms underlying MeHg-induced neurotoxicity. A collection of cellular and molecular alterations including cytokine release, oxidative stress, mitochondrial dysfunction, Ca2+ and glutamate dyshomeostasis, and cell death mechanisms are important consequences of brain cells exposure to MeHg. The purpose of this review is to organize an overview of the mercury cycle and MeHg poisoning events and to summarize data from cellular, animal, and human studies focusing on MeHg effects in neurons and glial cells. This review proposes an up-to-date compendium that will serve as a starting point for further studies and a consultation reference of published studies. |
publishDate |
2021 |
dc.date.none.fl_str_mv |
2021-03-18 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
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publishedVersion |
dc.identifier.uri.fl_str_mv |
https://hdl.handle.net/10316/104748 https://hdl.handle.net/10316/104748 https://doi.org/10.3390/ijms22063101 |
url |
https://hdl.handle.net/10316/104748 https://doi.org/10.3390/ijms22063101 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
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1422-0067 33803585 1422-0067 |
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info:eu-repo/semantics/openAccess |
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openAccess |
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MDPI AG |
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MDPI AG |
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