Hepatic and neurobiological effects of foetal and breastfeeding and adulthood exposure to methylmercury in Wistar rats

Methylmercury (MeHg) is an organic bioaccumulated mercury derivative that strongly affects the environment and represents a public health problem primarily to riparian communities in South America. Our objective was to investigate the hepatic and neurological effects of MeHg exposure during the phas...

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Autores:
da Rosa-Silva, Helen Tais
Castro Panzenhagen, Alana
Schmidtt, Victória
Alves Teixeira, Alexsander
Espitia-Pérez, Pedro Juan
de Oliveira Franco, Álvaro
Mingori, Moara
Torres-Ávila, José F.
Schnorr, Carlos Eduardo
Silva Hermann, Paolla Rissi
Pompéu Moraes, Diogo
Farina Almeida, Roberto
Moreira, José Cláudio Fonseca
Tipo de recurso:
http://purl.org/coar/resource_type/c_816b
Fecha de publicación:
2020
Institución:
Corporación Universidad de la Costa
Repositorio:
REDICUC - Repositorio CUC
Idioma:
eng
OAI Identifier:
oai:repositorio.cuc.edu.co:11323/6248
Acceso en línea:
https://hdl.handle.net/11323/6248
https://doi.org/10.1016/j.chemosphere.2019.125400
https://repositorio.cuc.edu.co/
Palabra clave:
Methylmercury
Double exposure
Oxidative stress
Hepatotoxicity
Neurotoxicity
Akt/GSK3β/mTOR pathway
Rights
openAccess
License
CC0 1.0 Universal
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oai_identifier_str oai:repositorio.cuc.edu.co:11323/6248
network_acronym_str RCUC2
network_name_str REDICUC - Repositorio CUC
repository_id_str
dc.title.spa.fl_str_mv Hepatic and neurobiological effects of foetal and breastfeeding and adulthood exposure to methylmercury in Wistar rats
title Hepatic and neurobiological effects of foetal and breastfeeding and adulthood exposure to methylmercury in Wistar rats
spellingShingle Hepatic and neurobiological effects of foetal and breastfeeding and adulthood exposure to methylmercury in Wistar rats
Methylmercury
Double exposure
Oxidative stress
Hepatotoxicity
Neurotoxicity
Akt/GSK3β/mTOR pathway
title_short Hepatic and neurobiological effects of foetal and breastfeeding and adulthood exposure to methylmercury in Wistar rats
title_full Hepatic and neurobiological effects of foetal and breastfeeding and adulthood exposure to methylmercury in Wistar rats
title_fullStr Hepatic and neurobiological effects of foetal and breastfeeding and adulthood exposure to methylmercury in Wistar rats
title_full_unstemmed Hepatic and neurobiological effects of foetal and breastfeeding and adulthood exposure to methylmercury in Wistar rats
title_sort Hepatic and neurobiological effects of foetal and breastfeeding and adulthood exposure to methylmercury in Wistar rats
dc.creator.fl_str_mv da Rosa-Silva, Helen Tais
Castro Panzenhagen, Alana
Schmidtt, Victória
Alves Teixeira, Alexsander
Espitia-Pérez, Pedro Juan
de Oliveira Franco, Álvaro
Mingori, Moara
Torres-Ávila, José F.
Schnorr, Carlos Eduardo
Silva Hermann, Paolla Rissi
Pompéu Moraes, Diogo
Farina Almeida, Roberto
Moreira, José Cláudio Fonseca
dc.contributor.author.spa.fl_str_mv da Rosa-Silva, Helen Tais
Castro Panzenhagen, Alana
Schmidtt, Victória
Alves Teixeira, Alexsander
Espitia-Pérez, Pedro Juan
de Oliveira Franco, Álvaro
Mingori, Moara
Torres-Ávila, José F.
Schnorr, Carlos Eduardo
Silva Hermann, Paolla Rissi
Pompéu Moraes, Diogo
Farina Almeida, Roberto
Moreira, José Cláudio Fonseca
dc.subject.spa.fl_str_mv Methylmercury
Double exposure
Oxidative stress
Hepatotoxicity
Neurotoxicity
Akt/GSK3β/mTOR pathway
topic Methylmercury
Double exposure
Oxidative stress
Hepatotoxicity
Neurotoxicity
Akt/GSK3β/mTOR pathway
description Methylmercury (MeHg) is an organic bioaccumulated mercury derivative that strongly affects the environment and represents a public health problem primarily to riparian communities in South America. Our objective was to investigate the hepatic and neurological effects of MeHg exposure during the phases foetal and breast-feeding and adult in Wistar rats. Wistar rats (n = 10) were divided into 3 groups. Control group received mineral oil; The simple exposure (SE) group was exposed only in adulthood (0.5 mg/kg/day); and double exposure (DE) was pre-exposed to MeHg 0.5 mg/kg/day during pregnancy and breastfeeding (±40 days) and re-exposed to MeHg for 45 days from day 100. After, we evaluated possible abnormalities. Behavioral and biochemical parameters in liver and occipital cortex (CO), markers of liver injury, redox and AKT/GSK3β/mTOR signaling pathway. Our results showed that both groups treated with MeHg presented significant alterations, such as decreased locomotion and exploration and impaired visuospatial perception. The rats exposed to MeHg showed severe liver damage and increased hepatic glycogen concentration. The MeHg groups showed significant impairment in redox balance and oxidative damage to liver macromolecules and CO. MeHg upregulated the AKT/GSK3β/mTOR pathway and the phosphorylated form of the Tau protein. In addition, we found a reduction in NeuN and GFAP immunocontent. These results represent the first approach to the hepatotoxic and neural effects of foetal and adult MeHg exposure.
publishDate 2020
dc.date.accessioned.none.fl_str_mv 2020-05-04T22:12:13Z
dc.date.available.none.fl_str_mv 2020-05-04T22:12:13Z
dc.date.issued.none.fl_str_mv 2020
dc.type.spa.fl_str_mv Pre-Publicación
dc.type.coar.spa.fl_str_mv http://purl.org/coar/resource_type/c_816b
dc.type.content.spa.fl_str_mv Text
dc.type.driver.spa.fl_str_mv info:eu-repo/semantics/preprint
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dc.type.version.spa.fl_str_mv info:eu-repo/semantics/acceptedVersion
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status_str acceptedVersion
dc.identifier.uri.spa.fl_str_mv https://hdl.handle.net/11323/6248
dc.identifier.doi.spa.fl_str_mv https://doi.org/10.1016/j.chemosphere.2019.125400
dc.identifier.instname.spa.fl_str_mv Corporación Universidad de la Costa
dc.identifier.reponame.spa.fl_str_mv REDICUC - Repositorio CUC
dc.identifier.repourl.spa.fl_str_mv https://repositorio.cuc.edu.co/
url https://hdl.handle.net/11323/6248
https://doi.org/10.1016/j.chemosphere.2019.125400
https://repositorio.cuc.edu.co/
identifier_str_mv Corporación Universidad de la Costa
REDICUC - Repositorio CUC
dc.language.iso.none.fl_str_mv eng
language eng
dc.rights.spa.fl_str_mv CC0 1.0 Universal
dc.rights.uri.spa.fl_str_mv http://creativecommons.org/publicdomain/zero/1.0/
dc.rights.accessrights.spa.fl_str_mv info:eu-repo/semantics/openAccess
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rights_invalid_str_mv CC0 1.0 Universal
http://creativecommons.org/publicdomain/zero/1.0/
http://purl.org/coar/access_right/c_abf2
eu_rights_str_mv openAccess
dc.publisher.spa.fl_str_mv Universidad de la Costa
institution Corporación Universidad de la Costa
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spelling da Rosa-Silva, Helen TaisCastro Panzenhagen, AlanaSchmidtt, VictóriaAlves Teixeira, AlexsanderEspitia-Pérez, Pedro Juande Oliveira Franco, ÁlvaroMingori, MoaraTorres-Ávila, José F.Schnorr, Carlos EduardoSilva Hermann, Paolla RissiPompéu Moraes, DiogoFarina Almeida, RobertoMoreira, José Cláudio Fonseca2020-05-04T22:12:13Z2020-05-04T22:12:13Z2020https://hdl.handle.net/11323/6248https://doi.org/10.1016/j.chemosphere.2019.125400Corporación Universidad de la CostaREDICUC - Repositorio CUChttps://repositorio.cuc.edu.co/Methylmercury (MeHg) is an organic bioaccumulated mercury derivative that strongly affects the environment and represents a public health problem primarily to riparian communities in South America. Our objective was to investigate the hepatic and neurological effects of MeHg exposure during the phases foetal and breast-feeding and adult in Wistar rats. Wistar rats (n = 10) were divided into 3 groups. Control group received mineral oil; The simple exposure (SE) group was exposed only in adulthood (0.5 mg/kg/day); and double exposure (DE) was pre-exposed to MeHg 0.5 mg/kg/day during pregnancy and breastfeeding (±40 days) and re-exposed to MeHg for 45 days from day 100. After, we evaluated possible abnormalities. Behavioral and biochemical parameters in liver and occipital cortex (CO), markers of liver injury, redox and AKT/GSK3β/mTOR signaling pathway. Our results showed that both groups treated with MeHg presented significant alterations, such as decreased locomotion and exploration and impaired visuospatial perception. The rats exposed to MeHg showed severe liver damage and increased hepatic glycogen concentration. The MeHg groups showed significant impairment in redox balance and oxidative damage to liver macromolecules and CO. MeHg upregulated the AKT/GSK3β/mTOR pathway and the phosphorylated form of the Tau protein. In addition, we found a reduction in NeuN and GFAP immunocontent. These results represent the first approach to the hepatotoxic and neural effects of foetal and adult MeHg exposure.da Rosa-Silva, Helen TaisCastro Panzenhagen, Alana-will be generated-orcid-0000-0002-8844-3468-600Schmidtt, VictóriaAlves Teixeira, AlexsanderEspitia-Pérez, Pedro-will be generated-orcid-0000-0002-2487-9967-600de Oliveira Franco, Álvaro-will be generated-orcid-0000-0003-0601-6348-600Mingori, MoaraTorres-Ávila, José F.Schnorr, Carlos Eduardo-will be generated-orcid-0000-0002-2047-2107-600Silva Hermann, Paolla RissiPompéu Moraes, DiogoFarina Almeida, RobertoMoreira, José Cláudio Fonseca-will be generated-orcid-0000-0002-0619-4913-600engUniversidad de la CostaCC0 1.0 Universalhttp://creativecommons.org/publicdomain/zero/1.0/info:eu-repo/semantics/openAccesshttp://purl.org/coar/access_right/c_abf2MethylmercuryDouble exposureOxidative stressHepatotoxicityNeurotoxicityAkt/GSK3β/mTOR pathwayHepatic and neurobiological effects of foetal and breastfeeding and adulthood exposure to methylmercury in Wistar ratsPre-Publicaciónhttp://purl.org/coar/resource_type/c_816bTextinfo:eu-repo/semantics/preprinthttp://purl.org/redcol/resource_type/ARTOTRinfo:eu-repo/semantics/acceptedVersionPublicationORIGINALHepatic and neurobiological effects of foetal and breastfeeding and adulthood exposure to methylmercury in Wistar rats.pdfHepatic and neurobiological effects of foetal and breastfeeding and adulthood exposure to methylmercury in Wistar rats.pdfapplication/pdf292980https://repositorio.cuc.edu.co/bitstreams/f5c8aff0-ba81-40f8-ba15-d7817c9f4a24/download3c939414659a1c0e26dcbaf064d13526MD51CC-LICENSElicense_rdflicense_rdfapplication/rdf+xml; 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