Proteomic approach underlying the hippocampal neurodegeneration caused by low doses of methylmercury after long-term exposure in adult rats
Authors:
- Leonardo Oliveira BittencourtLeonardo Oliveira Bittencourt
- Aline DionizioAline Dionizio
- Priscila Cunha NascimentoPriscila Cunha Nascimento
- Bruna PutyBruna Puty
- Luana Ketlen Reis LeãoLuana Ketlen Reis Leão
- Diandra Araújo LuzDiandra Araújo Luz
- Marcia Cristina Freitas SilvaMSMarcia Cristina Freitas Silva
- Lílian Lund AmadoLílian Lund Amado
- Aline LeiteAline Leite
- Marília Rabelo BuzalafMarília Rabelo Buzalaf
- Maria Elena Crespo-LopezMaria Elena Crespo-Lopez
- Cristiane Socorro Ferraz MaiaCristiane Socorro Ferraz Maia
Open Access
- 26 November 2018
- journal article
- research article
- Published by Oxford University Press (OUP) in Metallomics
- Vol. 11 (2) , 390-403
Abstract
Methylmercury (MeHg) is an important toxicant that causes cognitive dysfunctions in humans. This study aimed to investigate the proteomic and biochemical alterations of the hippocampus associated with behavioural consequences of low doses of MeHg in a long-term exposure model, and to realistically mimic in vivo the result of human exposure to this toxicant. Adult Wistar male rats were exposed to a dose of MeHg at 0.04 mg kg−1 day−1 by gavage for 60 days. Total mercury (Hg) content was significantly increased in the hippocampal parenchyma. The increase in the Hg levels was capable of reducing neuron and astrocyte cell density in the CA1, CA3, hilus and dentate gyrus regions, increasing both malondialdehyde and nitrite levels and decreasing antioxidant capacity against peroxyl radicals. The proteomic analysis detected 1041 proteins with altered expression due to MeHg exposure, including 364 proteins with no expression, 295 proteins with de novo expression and 382 proteins with up- or down-regulated expression. This proteomic approach revealed alterations in pathways related to chemical synapses, metabolism, amino acid transport, cell energy, neurodegenerative processes and myelin maintenance. Therefore, even at low doses of MeHg exposure, it is possible to cause hippocampal damage in adult rats at many organisational levels, triggering oxidative stress and proteome misbalance, featuring a neurodegenerative process and culminating in long- and short-term memory and learning deficits.Keywords
Funding Information
- Conselho Nacional de Desenvolvimento Científico e Tecnológico (Unassigned)
- Fundação de Amparo à Pesquisa do Estado de São Paulo (Unassigned)
- Fundação Amazônia Paraense de Amparo à Pesquisa (Unassigned)
- Ministério da Ciência, Tecnologia e Inovação (Unassigned)
- Conselho Nacional de Desenvolvimento Científico e Tecnológico
- Fundação de Amparo à Pesquisa do Estado de São Paulo
- Fundação Amazônia Paraense de Amparo à Pesquisa
- Ministério da Ciência, Tecnologia e Inovação
This publication has 94 references indexed in Scilit:
- Reactive oxygen species (ROS) homeostasis and redox regulation in cellular signalingCellular Signalling, 2012
- Mitochondrial calcium and its regulation in neurodegeneration induced by oxidative stressEuropean Journal of Neuroscience, 2011
- Norbin Is an Endogenous Regulator of Metabotropic Glutamate Receptor 5 SignalingScience, 2009
- Mitochondria, calcium and cell death: A deadly triad in neurodegenerationBiochimica et Biophysica Acta (BBA) - Bioenergetics, 2009
- ClueGO: a Cytoscape plug-in to decipher functionally grouped gene ontology and pathway annotation networksBioinformatics, 2009
- Developmental mercury exposure elicits acute hippocampal cell death, reductions in neurogenesis, and severe learning deficits during pubertyJournal of Neurochemistry, 2007
- Methylmercury induces oxidative injury, alterations in permeability and glutamine transport in cultured astrocytesBrain Research, 2007
- Mitochondrial dysfunction and oxidative stress in neurodegenerative diseasesNature, 2006
- Epsin Binds to Clathrin by Associating Directly with the Clathrin-terminal DomainJournal of Biological Chemistry, 2000
- A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye bindingAnalytical Biochemistry, 1976