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Central and Systemic Responses to Methionine-Induced Hyperhomocysteinemia in Mice

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 diffe...

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Autores principales: de Rezende, Marina Mastelaro, D’Almeida, Vânia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4143291/
https://www.ncbi.nlm.nih.gov/pubmed/25153079
http://dx.doi.org/10.1371/journal.pone.0105704
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author de Rezende, Marina Mastelaro
D’Almeida, Vânia
author_facet de Rezende, Marina Mastelaro
D’Almeida, Vânia
author_sort de Rezende, Marina Mastelaro
collection PubMed
description 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.
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spelling pubmed-41432912014-08-27 Central and Systemic Responses to Methionine-Induced Hyperhomocysteinemia in Mice de Rezende, Marina Mastelaro D’Almeida, Vânia PLoS One Research Article 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. Public Library of Science 2014-08-25 /pmc/articles/PMC4143291/ /pubmed/25153079 http://dx.doi.org/10.1371/journal.pone.0105704 Text en © 2014 Rezende, D'Almeida http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
de Rezende, Marina Mastelaro
D’Almeida, Vânia
Central and Systemic Responses to Methionine-Induced Hyperhomocysteinemia in Mice
title Central and Systemic Responses to Methionine-Induced Hyperhomocysteinemia in Mice
title_full Central and Systemic Responses to Methionine-Induced Hyperhomocysteinemia in Mice
title_fullStr Central and Systemic Responses to Methionine-Induced Hyperhomocysteinemia in Mice
title_full_unstemmed Central and Systemic Responses to Methionine-Induced Hyperhomocysteinemia in Mice
title_short Central and Systemic Responses to Methionine-Induced Hyperhomocysteinemia in Mice
title_sort central and systemic responses to methionine-induced hyperhomocysteinemia in mice
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4143291/
https://www.ncbi.nlm.nih.gov/pubmed/25153079
http://dx.doi.org/10.1371/journal.pone.0105704
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