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Inhibitory Effect of NMDA Receptors in the Ventral Tegmental Area on Hormonal and Eating Behavior Responses to Stress in Rats

Background. Stress and its consequences are among the causes of accidents. Objective. The effects of intraventral tegmental area (I-VTA) memantine on the plasma corticosterone and eating parameters disturbance induced by acute stress were investigated. Methods. Male Wistar rats (W: 250–300 g) were d...

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Autores principales: Nasihatkon, Zohreh Sadat, Khosravi, Maryam, Bourbour, Zahra, Sahraei, Hedayat, Ranjbaran, Mina, Hassantash, Seyedeh Maryam, Sahraei, Mohammad, Baghlani, Kefayat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4143587/
https://www.ncbi.nlm.nih.gov/pubmed/25177106
http://dx.doi.org/10.1155/2014/294149
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author Nasihatkon, Zohreh Sadat
Khosravi, Maryam
Bourbour, Zahra
Sahraei, Hedayat
Ranjbaran, Mina
Hassantash, Seyedeh Maryam
Sahraei, Mohammad
Baghlani, Kefayat
author_facet Nasihatkon, Zohreh Sadat
Khosravi, Maryam
Bourbour, Zahra
Sahraei, Hedayat
Ranjbaran, Mina
Hassantash, Seyedeh Maryam
Sahraei, Mohammad
Baghlani, Kefayat
author_sort Nasihatkon, Zohreh Sadat
collection PubMed
description Background. Stress and its consequences are among the causes of accidents. Objective. The effects of intraventral tegmental area (I-VTA) memantine on the plasma corticosterone and eating parameters disturbance induced by acute stress were investigated. Methods. Male Wistar rats (W: 250–300 g) were divided into control and experiential groups, each of which received memantine either intra-VTA or peripherally. One week after bilateral cannulation, the rats received memantine (1 and 5 μg/Rat) five min before electroshock stress. The other experimental groups received memantine (1 and 5 mg/kg) intraperitoneally 30 min before stress. The control groups received saline or memantine but did not experience stress. Food and water intake and plasma corticosterone level were recorded. Results. Results showed that stress decreases food intake but does not change water intake and increase in plasma corticosterone level. Intraperitoneal memantine administration slightly inhibits the stress effects on food intake. However, water intake and plasma corticosterone level were increased. Intra-VTA memantine reduces the effects of stress on corticosterone and water intake. Conclusion. It could be concluded that inhibition of glutamate NMDA receptors in the VTA by memantine leads to the inhibition of the eating behavior parameters and plasma corticosterone level disturbance induced by stress in rats.
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spelling pubmed-41435872014-08-31 Inhibitory Effect of NMDA Receptors in the Ventral Tegmental Area on Hormonal and Eating Behavior Responses to Stress in Rats Nasihatkon, Zohreh Sadat Khosravi, Maryam Bourbour, Zahra Sahraei, Hedayat Ranjbaran, Mina Hassantash, Seyedeh Maryam Sahraei, Mohammad Baghlani, Kefayat Behav Neurol Research Article Background. Stress and its consequences are among the causes of accidents. Objective. The effects of intraventral tegmental area (I-VTA) memantine on the plasma corticosterone and eating parameters disturbance induced by acute stress were investigated. Methods. Male Wistar rats (W: 250–300 g) were divided into control and experiential groups, each of which received memantine either intra-VTA or peripherally. One week after bilateral cannulation, the rats received memantine (1 and 5 μg/Rat) five min before electroshock stress. The other experimental groups received memantine (1 and 5 mg/kg) intraperitoneally 30 min before stress. The control groups received saline or memantine but did not experience stress. Food and water intake and plasma corticosterone level were recorded. Results. Results showed that stress decreases food intake but does not change water intake and increase in plasma corticosterone level. Intraperitoneal memantine administration slightly inhibits the stress effects on food intake. However, water intake and plasma corticosterone level were increased. Intra-VTA memantine reduces the effects of stress on corticosterone and water intake. Conclusion. It could be concluded that inhibition of glutamate NMDA receptors in the VTA by memantine leads to the inhibition of the eating behavior parameters and plasma corticosterone level disturbance induced by stress in rats. Hindawi Publishing Corporation 2014 2014-08-07 /pmc/articles/PMC4143587/ /pubmed/25177106 http://dx.doi.org/10.1155/2014/294149 Text en Copyright © 2014 Zohreh Sadat Nasihatkon et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Nasihatkon, Zohreh Sadat
Khosravi, Maryam
Bourbour, Zahra
Sahraei, Hedayat
Ranjbaran, Mina
Hassantash, Seyedeh Maryam
Sahraei, Mohammad
Baghlani, Kefayat
Inhibitory Effect of NMDA Receptors in the Ventral Tegmental Area on Hormonal and Eating Behavior Responses to Stress in Rats
title Inhibitory Effect of NMDA Receptors in the Ventral Tegmental Area on Hormonal and Eating Behavior Responses to Stress in Rats
title_full Inhibitory Effect of NMDA Receptors in the Ventral Tegmental Area on Hormonal and Eating Behavior Responses to Stress in Rats
title_fullStr Inhibitory Effect of NMDA Receptors in the Ventral Tegmental Area on Hormonal and Eating Behavior Responses to Stress in Rats
title_full_unstemmed Inhibitory Effect of NMDA Receptors in the Ventral Tegmental Area on Hormonal and Eating Behavior Responses to Stress in Rats
title_short Inhibitory Effect of NMDA Receptors in the Ventral Tegmental Area on Hormonal and Eating Behavior Responses to Stress in Rats
title_sort inhibitory effect of nmda receptors in the ventral tegmental area on hormonal and eating behavior responses to stress in rats
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4143587/
https://www.ncbi.nlm.nih.gov/pubmed/25177106
http://dx.doi.org/10.1155/2014/294149
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