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The antidepressant impact of minocycline in rodents: A systematic review and meta-analysis

Evidence from recent animal studies suggest that minocycline, a broad-spectrum antibiotic capable of regulating immune processes, may possess antidepressant properties. These studies, however, have yet to be comprehensively reviewed. Accordingly, this systematic review and meta-analysis summarizes t...

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Autores principales: Reis, Daniel J., Casteen, Emily J., Ilardi, Stephen S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6342970/
https://www.ncbi.nlm.nih.gov/pubmed/30670723
http://dx.doi.org/10.1038/s41598-018-36507-9
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author Reis, Daniel J.
Casteen, Emily J.
Ilardi, Stephen S.
author_facet Reis, Daniel J.
Casteen, Emily J.
Ilardi, Stephen S.
author_sort Reis, Daniel J.
collection PubMed
description Evidence from recent animal studies suggest that minocycline, a broad-spectrum antibiotic capable of regulating immune processes, may possess antidepressant properties. These studies, however, have yet to be comprehensively reviewed. Accordingly, this systematic review and meta-analysis summarizes the extant literature examining the effect of minocycline on depressive-like behavior in rodent models. PubMed, PsycINFO, and Web of Science databases were systematically searched for articles that met prespecified inclusion and exclusion criteria, and standardized mean differences (SMDs) were calculated for each continuous measure of depressive-like behavior. The overall effect of minocycline on depressive-like behavior was estimated using robust variance estimation meta-analysis. Separate subgroup analyses were conducted on diseased vs healthy animal models, different rodent species, and immobility-based vs anhedonia-based measures of depressive-like behavior. A total of 22 preclinical studies (816 animals) were included. Overall, minocycline reduced depressive-like behavior in rodents (SMD = −1.07, 95% CI −1.41–−0.74, p < 0.001). Subgroup analyses revealed that minocycline reduced depressive-like behavior in diseased, but not healthy, animal models. Finally, minocycline was found to reduce both immobility-based and anhedonia-based outcomes. These findings suggest that minocycline may be an effective treatment of core depressive symptoms, and that further investigation of minocycline treatment for clinically relevant depression in humans is warranted.
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spelling pubmed-63429702019-01-26 The antidepressant impact of minocycline in rodents: A systematic review and meta-analysis Reis, Daniel J. Casteen, Emily J. Ilardi, Stephen S. Sci Rep Article Evidence from recent animal studies suggest that minocycline, a broad-spectrum antibiotic capable of regulating immune processes, may possess antidepressant properties. These studies, however, have yet to be comprehensively reviewed. Accordingly, this systematic review and meta-analysis summarizes the extant literature examining the effect of minocycline on depressive-like behavior in rodent models. PubMed, PsycINFO, and Web of Science databases were systematically searched for articles that met prespecified inclusion and exclusion criteria, and standardized mean differences (SMDs) were calculated for each continuous measure of depressive-like behavior. The overall effect of minocycline on depressive-like behavior was estimated using robust variance estimation meta-analysis. Separate subgroup analyses were conducted on diseased vs healthy animal models, different rodent species, and immobility-based vs anhedonia-based measures of depressive-like behavior. A total of 22 preclinical studies (816 animals) were included. Overall, minocycline reduced depressive-like behavior in rodents (SMD = −1.07, 95% CI −1.41–−0.74, p < 0.001). Subgroup analyses revealed that minocycline reduced depressive-like behavior in diseased, but not healthy, animal models. Finally, minocycline was found to reduce both immobility-based and anhedonia-based outcomes. These findings suggest that minocycline may be an effective treatment of core depressive symptoms, and that further investigation of minocycline treatment for clinically relevant depression in humans is warranted. Nature Publishing Group UK 2019-01-22 /pmc/articles/PMC6342970/ /pubmed/30670723 http://dx.doi.org/10.1038/s41598-018-36507-9 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Reis, Daniel J.
Casteen, Emily J.
Ilardi, Stephen S.
The antidepressant impact of minocycline in rodents: A systematic review and meta-analysis
title The antidepressant impact of minocycline in rodents: A systematic review and meta-analysis
title_full The antidepressant impact of minocycline in rodents: A systematic review and meta-analysis
title_fullStr The antidepressant impact of minocycline in rodents: A systematic review and meta-analysis
title_full_unstemmed The antidepressant impact of minocycline in rodents: A systematic review and meta-analysis
title_short The antidepressant impact of minocycline in rodents: A systematic review and meta-analysis
title_sort antidepressant impact of minocycline in rodents: a systematic review and meta-analysis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6342970/
https://www.ncbi.nlm.nih.gov/pubmed/30670723
http://dx.doi.org/10.1038/s41598-018-36507-9
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