Hepatic and neurobiological effects of foetal and breastfeeding and adulthood exposure to methylmercury in Wistar rats
Autor: | Álvaro de Oliveira Franco, Roberto Farina de Almeida, Pedro Espitia-Pérez, Diogo P. Moraes, Moara Rodrigues Mingori, José Cláudio Fonseca Moreira, Alexsander Alves Teixeira, José F. Torres-Ávila, Victória Schmidtt, Alana Castro Panzenhagen, Carlos Eduardo Schnorr, Paolla Rissi Silva Hermann, Helen Tais da Rosa-Silva |
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Rok vydání: | 2019 |
Předmět: |
Male
Health Toxicology and Mutagenesis 0208 environmental biotechnology 02 engineering and technology 010501 environmental sciences medicine.disease_cause 01 natural sciences Nervous System chemistry.chemical_compound Double exposure Pregnancy Methylmercury Liver injury biology General Medicine Methylmercury Compounds Pollution Breast Feeding Liver Environmental Pollutants Female Oxidation-Reduction Locomotion Signal Transduction medicine.medical_specialty Environmental Engineering Fetus Internal medicine medicine Neurotoxicity Environmental Chemistry Animals Humans Rats Wistar Protein kinase B PI3K/AKT/mTOR pathway 0105 earth and related environmental sciences business.industry Hepatotoxicity Public Health Environmental and Occupational Health General Chemistry South America medicine.disease 020801 environmental engineering Rats Endocrinology chemistry biology.protein NeuN business Oxidative stress |
Zdroj: | Chemosphere Repositorio Digital USB Universidad Simón Bolívar instacron:Universidad Simón Bolívar |
ISSN: | 1879-1298 |
DOI: | 10.1016/j.chemosphere.2019.125400 |
Popis: | 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. |
Databáze: | OpenAIRE |
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