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Long-Term NMDAR Antagonism Correlates Weight Loss With Less Eating

Memantine hydrochloride is an uncompetitive N-methyl-D-aspartate (NMDA) antagonist for treatment of moderate-to-severe Alzheimer's disease. Several studies have shown that memantine can significantly correct the binge-like eating behavior in human and animal models. People with overeating behav...

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Autores principales: Deng, Shi-Ning, Yan, Yu-Hua, Zhu, Tai-Lin, Ma, Bing-Ke, Fan, Hui-Ran, Liu, Yan-Mei, Li, Wei-Guang, Li, Fei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6375831/
https://www.ncbi.nlm.nih.gov/pubmed/30800078
http://dx.doi.org/10.3389/fpsyt.2019.00015
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author Deng, Shi-Ning
Yan, Yu-Hua
Zhu, Tai-Lin
Ma, Bing-Ke
Fan, Hui-Ran
Liu, Yan-Mei
Li, Wei-Guang
Li, Fei
author_facet Deng, Shi-Ning
Yan, Yu-Hua
Zhu, Tai-Lin
Ma, Bing-Ke
Fan, Hui-Ran
Liu, Yan-Mei
Li, Wei-Guang
Li, Fei
author_sort Deng, Shi-Ning
collection PubMed
description Memantine hydrochloride is an uncompetitive N-methyl-D-aspartate (NMDA) antagonist for treatment of moderate-to-severe Alzheimer's disease. Several studies have shown that memantine can significantly correct the binge-like eating behavior in human and animal models. People with overeating behavior are more likely to be obese. Therefore, we suppose that memantine would be a good candidate for the treatment of obesity. In this study, memantine was shown to increase weight loss in obese mice induced by high fat diet. Memantine was shown to decrease food intake without inducing abdominal discomfort and anxiety, suggesting that this compound would be a good candidate drug for obesity control.
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spelling pubmed-63758312019-02-22 Long-Term NMDAR Antagonism Correlates Weight Loss With Less Eating Deng, Shi-Ning Yan, Yu-Hua Zhu, Tai-Lin Ma, Bing-Ke Fan, Hui-Ran Liu, Yan-Mei Li, Wei-Guang Li, Fei Front Psychiatry Psychiatry Memantine hydrochloride is an uncompetitive N-methyl-D-aspartate (NMDA) antagonist for treatment of moderate-to-severe Alzheimer's disease. Several studies have shown that memantine can significantly correct the binge-like eating behavior in human and animal models. People with overeating behavior are more likely to be obese. Therefore, we suppose that memantine would be a good candidate for the treatment of obesity. In this study, memantine was shown to increase weight loss in obese mice induced by high fat diet. Memantine was shown to decrease food intake without inducing abdominal discomfort and anxiety, suggesting that this compound would be a good candidate drug for obesity control. Frontiers Media S.A. 2019-02-08 /pmc/articles/PMC6375831/ /pubmed/30800078 http://dx.doi.org/10.3389/fpsyt.2019.00015 Text en Copyright © 2019 Deng, Yan, Zhu, Ma, Fan, Liu, Li and Li. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Psychiatry
Deng, Shi-Ning
Yan, Yu-Hua
Zhu, Tai-Lin
Ma, Bing-Ke
Fan, Hui-Ran
Liu, Yan-Mei
Li, Wei-Guang
Li, Fei
Long-Term NMDAR Antagonism Correlates Weight Loss With Less Eating
title Long-Term NMDAR Antagonism Correlates Weight Loss With Less Eating
title_full Long-Term NMDAR Antagonism Correlates Weight Loss With Less Eating
title_fullStr Long-Term NMDAR Antagonism Correlates Weight Loss With Less Eating
title_full_unstemmed Long-Term NMDAR Antagonism Correlates Weight Loss With Less Eating
title_short Long-Term NMDAR Antagonism Correlates Weight Loss With Less Eating
title_sort long-term nmdar antagonism correlates weight loss with less eating
topic Psychiatry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6375831/
https://www.ncbi.nlm.nih.gov/pubmed/30800078
http://dx.doi.org/10.3389/fpsyt.2019.00015
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