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Antidiabetic drug glyburide modulates depressive-like behavior comorbid with insulin resistance

BACKGROUND: Abundant reports indicated that depression was often comorbid with type 2 diabetes and even metabolic syndrome. Considering they might share common biological origins, it was tentatively attributed to the chronic cytokine-mediated inflammatory response which was induced by dysregulation...

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Autores principales: Su, Wen-Jun, Peng, Wei, Gong, Hong, Liu, Yun-Zi, Zhang, Yi, Lian, Yong-Jie, Cao, Zhi-Yong, Wu, Ran, Liu, Lin-Lin, Wang, Bo, Wang, Yun-Xia, Jiang, Chun-Lei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5663104/
https://www.ncbi.nlm.nih.gov/pubmed/29084550
http://dx.doi.org/10.1186/s12974-017-0985-4
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author Su, Wen-Jun
Peng, Wei
Gong, Hong
Liu, Yun-Zi
Zhang, Yi
Lian, Yong-Jie
Cao, Zhi-Yong
Wu, Ran
Liu, Lin-Lin
Wang, Bo
Wang, Yun-Xia
Jiang, Chun-Lei
author_facet Su, Wen-Jun
Peng, Wei
Gong, Hong
Liu, Yun-Zi
Zhang, Yi
Lian, Yong-Jie
Cao, Zhi-Yong
Wu, Ran
Liu, Lin-Lin
Wang, Bo
Wang, Yun-Xia
Jiang, Chun-Lei
author_sort Su, Wen-Jun
collection PubMed
description BACKGROUND: Abundant reports indicated that depression was often comorbid with type 2 diabetes and even metabolic syndrome. Considering they might share common biological origins, it was tentatively attributed to the chronic cytokine-mediated inflammatory response which was induced by dysregulation of HPA axis and overactivation of innate immunity. However, the exact mechanisms remain obscure. Herein, we mainly focused on the function of the NLRP3 inflammasome to investigate this issue. METHODS: Male C57BL/6 mice were subjected to 12 weeks of chronic unpredictable mild stress (CUMS), some of which were injected with glyburide or fluoxetine. After CUMS procedure, behavioral and metabolic tests were carried out. In order to evaluate the systemic inflammation associated with inflammasome activation, IL-1β and inflammasome components in hippocampi and pancreases, as well as corticosterone and IL-1β in serum were detected separately. Moreover, immunostaining was performed to assess morphologic characteristics of pancreases. RESULTS: In the present study, we found that 12 weeks’ chronic stress resulted in depressive-like behavior comorbid with insulin resistance. Furthermore, antidiabetic drug glyburide, an inhibitor of the NLRP3 inflammasome, was discovered to be effective in preventing the experimental comorbidity. In brief, it improved behavioral performance, ameliorated insulin intolerance as well as insulin signaling in the hippocampus possibly through inhibiting NLRP3 inflammasome activation by suppressing the expression of TXNIP. CONCLUSIONS: All these evidence supported our hypothesis that chronic stress led to comorbidity of depressive-like behavior and insulin resistance via long-term mild inflammation. More importantly, based on the beneficial effects of blocking the activation of the NLRP3 inflammasome, we provided a potential therapeutic target for clinical comorbidity and a new strategy for management of both diabetes and depression.
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spelling pubmed-56631042017-11-01 Antidiabetic drug glyburide modulates depressive-like behavior comorbid with insulin resistance Su, Wen-Jun Peng, Wei Gong, Hong Liu, Yun-Zi Zhang, Yi Lian, Yong-Jie Cao, Zhi-Yong Wu, Ran Liu, Lin-Lin Wang, Bo Wang, Yun-Xia Jiang, Chun-Lei J Neuroinflammation Research BACKGROUND: Abundant reports indicated that depression was often comorbid with type 2 diabetes and even metabolic syndrome. Considering they might share common biological origins, it was tentatively attributed to the chronic cytokine-mediated inflammatory response which was induced by dysregulation of HPA axis and overactivation of innate immunity. However, the exact mechanisms remain obscure. Herein, we mainly focused on the function of the NLRP3 inflammasome to investigate this issue. METHODS: Male C57BL/6 mice were subjected to 12 weeks of chronic unpredictable mild stress (CUMS), some of which were injected with glyburide or fluoxetine. After CUMS procedure, behavioral and metabolic tests were carried out. In order to evaluate the systemic inflammation associated with inflammasome activation, IL-1β and inflammasome components in hippocampi and pancreases, as well as corticosterone and IL-1β in serum were detected separately. Moreover, immunostaining was performed to assess morphologic characteristics of pancreases. RESULTS: In the present study, we found that 12 weeks’ chronic stress resulted in depressive-like behavior comorbid with insulin resistance. Furthermore, antidiabetic drug glyburide, an inhibitor of the NLRP3 inflammasome, was discovered to be effective in preventing the experimental comorbidity. In brief, it improved behavioral performance, ameliorated insulin intolerance as well as insulin signaling in the hippocampus possibly through inhibiting NLRP3 inflammasome activation by suppressing the expression of TXNIP. CONCLUSIONS: All these evidence supported our hypothesis that chronic stress led to comorbidity of depressive-like behavior and insulin resistance via long-term mild inflammation. More importantly, based on the beneficial effects of blocking the activation of the NLRP3 inflammasome, we provided a potential therapeutic target for clinical comorbidity and a new strategy for management of both diabetes and depression. BioMed Central 2017-10-30 /pmc/articles/PMC5663104/ /pubmed/29084550 http://dx.doi.org/10.1186/s12974-017-0985-4 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Su, Wen-Jun
Peng, Wei
Gong, Hong
Liu, Yun-Zi
Zhang, Yi
Lian, Yong-Jie
Cao, Zhi-Yong
Wu, Ran
Liu, Lin-Lin
Wang, Bo
Wang, Yun-Xia
Jiang, Chun-Lei
Antidiabetic drug glyburide modulates depressive-like behavior comorbid with insulin resistance
title Antidiabetic drug glyburide modulates depressive-like behavior comorbid with insulin resistance
title_full Antidiabetic drug glyburide modulates depressive-like behavior comorbid with insulin resistance
title_fullStr Antidiabetic drug glyburide modulates depressive-like behavior comorbid with insulin resistance
title_full_unstemmed Antidiabetic drug glyburide modulates depressive-like behavior comorbid with insulin resistance
title_short Antidiabetic drug glyburide modulates depressive-like behavior comorbid with insulin resistance
title_sort antidiabetic drug glyburide modulates depressive-like behavior comorbid with insulin resistance
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5663104/
https://www.ncbi.nlm.nih.gov/pubmed/29084550
http://dx.doi.org/10.1186/s12974-017-0985-4
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