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A Protective Role of Glibenclamide in Inflammation-Associated Injury

Glibenclamide is the most widely used sulfonylurea drug for the treatment of type 2 diabetes mellitus (DM). Recent studies have suggested that glibenclamide reduced adverse neuroinflammation and improved behavioral outcomes following central nervous system (CNS) injury. We reviewed glibenclamide...

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Detalles Bibliográficos
Autores principales: Zhang, Gensheng, Lin, Xiuhui, Zhang, Shufang, Xiu, Huiqing, Pan, Chuli, Cui, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5504948/
https://www.ncbi.nlm.nih.gov/pubmed/28740332
http://dx.doi.org/10.1155/2017/3578702
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author Zhang, Gensheng
Lin, Xiuhui
Zhang, Shufang
Xiu, Huiqing
Pan, Chuli
Cui, Wei
author_facet Zhang, Gensheng
Lin, Xiuhui
Zhang, Shufang
Xiu, Huiqing
Pan, Chuli
Cui, Wei
author_sort Zhang, Gensheng
collection PubMed
description Glibenclamide is the most widely used sulfonylurea drug for the treatment of type 2 diabetes mellitus (DM). Recent studies have suggested that glibenclamide reduced adverse neuroinflammation and improved behavioral outcomes following central nervous system (CNS) injury. We reviewed glibenclamide's anti-inflammatory effects: abundant evidences have shown that glibenclamide exerted an anti-inflammatory effect in respiratory, digestive, urological, cardiological, and CNS diseases, as well as in ischemia-reperfusion injury. Glibenclamide might block K(ATP) channel, Sur1-Trpm4 channel, and NOD-like receptor pyrin domain containing 3 (NLRP3) inflammasome activation, decrease the production of proinflammatory mediators (TNF-α, IL-1β, and reactive oxygen species), and suppress the accumulation of inflammatory cells. Glibenclamide's anti-inflammation warrants further investigation.
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spelling pubmed-55049482017-07-24 A Protective Role of Glibenclamide in Inflammation-Associated Injury Zhang, Gensheng Lin, Xiuhui Zhang, Shufang Xiu, Huiqing Pan, Chuli Cui, Wei Mediators Inflamm Review Article Glibenclamide is the most widely used sulfonylurea drug for the treatment of type 2 diabetes mellitus (DM). Recent studies have suggested that glibenclamide reduced adverse neuroinflammation and improved behavioral outcomes following central nervous system (CNS) injury. We reviewed glibenclamide's anti-inflammatory effects: abundant evidences have shown that glibenclamide exerted an anti-inflammatory effect in respiratory, digestive, urological, cardiological, and CNS diseases, as well as in ischemia-reperfusion injury. Glibenclamide might block K(ATP) channel, Sur1-Trpm4 channel, and NOD-like receptor pyrin domain containing 3 (NLRP3) inflammasome activation, decrease the production of proinflammatory mediators (TNF-α, IL-1β, and reactive oxygen species), and suppress the accumulation of inflammatory cells. Glibenclamide's anti-inflammation warrants further investigation. Hindawi 2017 2017-06-27 /pmc/articles/PMC5504948/ /pubmed/28740332 http://dx.doi.org/10.1155/2017/3578702 Text en Copyright © 2017 Gensheng Zhang et al. https://creativecommons.org/licenses/by/4.0/ 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 Review Article
Zhang, Gensheng
Lin, Xiuhui
Zhang, Shufang
Xiu, Huiqing
Pan, Chuli
Cui, Wei
A Protective Role of Glibenclamide in Inflammation-Associated Injury
title A Protective Role of Glibenclamide in Inflammation-Associated Injury
title_full A Protective Role of Glibenclamide in Inflammation-Associated Injury
title_fullStr A Protective Role of Glibenclamide in Inflammation-Associated Injury
title_full_unstemmed A Protective Role of Glibenclamide in Inflammation-Associated Injury
title_short A Protective Role of Glibenclamide in Inflammation-Associated Injury
title_sort protective role of glibenclamide in inflammation-associated injury
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5504948/
https://www.ncbi.nlm.nih.gov/pubmed/28740332
http://dx.doi.org/10.1155/2017/3578702
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