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Potential antidepressant effect of amantadine: a review of preclinical studies and clinical trials
OBJECTIVE: Amantadine blocks N-methyl-D-aspartate (NMDA) receptors and has dopaminergic and noradrenergic action, a neurochemical profile that suggests its potential as an antidepressant drug. We conducted a systematic review of preclinical and clinical studies addressing the effects of amantadine i...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Associação Brasileira de Psiquiatria
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6899375/ https://www.ncbi.nlm.nih.gov/pubmed/29898194 http://dx.doi.org/10.1590/1516-4446-2017-2393 |
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author | Raupp-Barcaro, Inara F. Vital, Maria A. Galduróz, José C. Andreatini, Roberto |
author_facet | Raupp-Barcaro, Inara F. Vital, Maria A. Galduróz, José C. Andreatini, Roberto |
author_sort | Raupp-Barcaro, Inara F. |
collection | PubMed |
description | OBJECTIVE: Amantadine blocks N-methyl-D-aspartate (NMDA) receptors and has dopaminergic and noradrenergic action, a neurochemical profile that suggests its potential as an antidepressant drug. We conducted a systematic review of preclinical and clinical studies addressing the effects of amantadine in animal models of depression and in patients with depression. METHODS: PubMed, Science Direct, and Web of Science were searched up to September 1, 2017 to identify clinical and preclinical studies. The following search terms were used: “amantadine AND depress*”; “amantadine AND mood”; “amantadine AND animal models AND antidepres*”; and “amantadine AND (forced swim, learned helplessness, reserpine, chronic mild stress, anhedonia, sucrose preference).” RESULTS: Amantadine had antidepressant-like effects in animal models and appeared to potentiate the antidepressant effects of other antidepressants. These preclinical findings have received some support from the results of small open-label clinical trials, suggesting that amantadine can reduce depressive symptomatology and potentiate the antidepressant effects of monoaminergic drugs. In addition to its glutamatergic and dopaminergic effects, the potential antidepressant-like effects of amantadine have been linked to molecular and cellular actions, such as increased expression of neurotrophic factors (e.g., brain-derived neurotrophic factor), activation of σ(1) receptors, decreased corticosterone levels, and decreased inflammatory response to stress. CONCLUSION: Amantadine is an interesting candidate as new antidepressant drug for the treatment of depression. |
format | Online Article Text |
id | pubmed-6899375 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Associação Brasileira de Psiquiatria |
record_format | MEDLINE/PubMed |
spelling | pubmed-68993752019-12-30 Potential antidepressant effect of amantadine: a review of preclinical studies and clinical trials Raupp-Barcaro, Inara F. Vital, Maria A. Galduróz, José C. Andreatini, Roberto Braz J Psychiatry Review Article OBJECTIVE: Amantadine blocks N-methyl-D-aspartate (NMDA) receptors and has dopaminergic and noradrenergic action, a neurochemical profile that suggests its potential as an antidepressant drug. We conducted a systematic review of preclinical and clinical studies addressing the effects of amantadine in animal models of depression and in patients with depression. METHODS: PubMed, Science Direct, and Web of Science were searched up to September 1, 2017 to identify clinical and preclinical studies. The following search terms were used: “amantadine AND depress*”; “amantadine AND mood”; “amantadine AND animal models AND antidepres*”; and “amantadine AND (forced swim, learned helplessness, reserpine, chronic mild stress, anhedonia, sucrose preference).” RESULTS: Amantadine had antidepressant-like effects in animal models and appeared to potentiate the antidepressant effects of other antidepressants. These preclinical findings have received some support from the results of small open-label clinical trials, suggesting that amantadine can reduce depressive symptomatology and potentiate the antidepressant effects of monoaminergic drugs. In addition to its glutamatergic and dopaminergic effects, the potential antidepressant-like effects of amantadine have been linked to molecular and cellular actions, such as increased expression of neurotrophic factors (e.g., brain-derived neurotrophic factor), activation of σ(1) receptors, decreased corticosterone levels, and decreased inflammatory response to stress. CONCLUSION: Amantadine is an interesting candidate as new antidepressant drug for the treatment of depression. Associação Brasileira de Psiquiatria 2018-06-11 /pmc/articles/PMC6899375/ /pubmed/29898194 http://dx.doi.org/10.1590/1516-4446-2017-2393 Text en http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article Raupp-Barcaro, Inara F. Vital, Maria A. Galduróz, José C. Andreatini, Roberto Potential antidepressant effect of amantadine: a review of preclinical studies and clinical trials |
title | Potential antidepressant effect of amantadine: a review of preclinical studies and clinical trials |
title_full | Potential antidepressant effect of amantadine: a review of preclinical studies and clinical trials |
title_fullStr | Potential antidepressant effect of amantadine: a review of preclinical studies and clinical trials |
title_full_unstemmed | Potential antidepressant effect of amantadine: a review of preclinical studies and clinical trials |
title_short | Potential antidepressant effect of amantadine: a review of preclinical studies and clinical trials |
title_sort | potential antidepressant effect of amantadine: a review of preclinical studies and clinical trials |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6899375/ https://www.ncbi.nlm.nih.gov/pubmed/29898194 http://dx.doi.org/10.1590/1516-4446-2017-2393 |
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