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(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

Central and Systemic Responses to Methionine-Induced Hyperhomocysteinemia in Mice

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Autor(es):
de Rezende, Marina Mastelaro [1] ; D'Almeida, Vania [1]
Número total de Autores: 2
Afiliação do(s) autor(es):
[1] Univ Fed Sao Paulo, Dept Psychobiol, Sao Paulo - Brazil
Número total de Afiliações: 1
Tipo de documento: Artigo Científico
Fonte: PLoS One; v. 9, n. 8 AUG 25 2014.
Citações Web of Science: 6
Resumo

Hyperhomocysteinemia has been considered a risk factor for neuropsychiatric disorders, but the mechanisms involved in this process have not been completely elucidated. The aim of this study was to analyze the influence of hyperhomocysteinemia induction by methionine supplementation considering different levels and periods of exposure in mice. For this purpose, methionine supplementation at concentrations of 0.5 and 1% were administered in water to increase homocysteinemia in male C57BL/6 mice, and was maintained for 3 time periods (2, 4 and 6 months of treatment). The results from one-carbon metabolism parameters, brain-derived neurotrophic factor (BDNF) concentrations and behavioral evaluation were compared. The 0.5% supplementation was efficient in increasing plasma homocysteine levels after 2 and 6 months. The 1% supplementation, increased plasma homocysteine after 2, 4 and 6 months. Little influence was observed in cysteine and glutathione concentrations. Frontal cortex BDNF levels showed a lack of treatment influence in all periods; only the expected decrease due to increasing age was observed. Moreover, the only behavioral alteration observed using a novel object recognition task was that which was expected with increasing age. We found that responses to hyperhomocysteinemia varied based on how it was reached, and the length of toxicity. Moreover, hyperhomocysteinemia can affect the normal pattern of one carbon metabolism during age increase in mice. These findings allow the establishment of a reliable animal model for studies in this field. (AU)

Processo FAPESP: 10/00075-2 - Hiper-homocisteinemia materna e alterações epigenéticas na programação fetal de genes envolvidos na etiopatogênese da Doença de Alzheimer
Beneficiário:Vânia D'Almeida
Modalidade de apoio: Auxílio à Pesquisa - Regular
Processo FAPESP: 11/15699-4 - Estresse oxidativo, comportamento e modificações epigenéticas em modelo animal de hiper-homocisteinemia
Beneficiário:Marina Mastelaro de Rezende
Modalidade de apoio: Bolsas no Brasil - Mestrado