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Metformin ameliorates insulitis in STZ-induced diabetic mice
BACKGROUND & AIMS: Metformin is currently the most widely used first-line hypoglycemic agent for diabetes mellitus. Besides glucose-lowering action, there is increasingly interest in the potential anti-inflammatory action of this drug. In the present study, we investigated the actions of metform...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
PeerJ Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5399881/ https://www.ncbi.nlm.nih.gov/pubmed/28439456 http://dx.doi.org/10.7717/peerj.3155 |
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author | Han, Xue Tao, Yu-Long Deng, Ya-Ping Yu, Jia-Wen Cai, Jian Ren, Guo-Fei Sun, Yuan-Nan Jiang, Guo-Jun |
author_facet | Han, Xue Tao, Yu-Long Deng, Ya-Ping Yu, Jia-Wen Cai, Jian Ren, Guo-Fei Sun, Yuan-Nan Jiang, Guo-Jun |
author_sort | Han, Xue |
collection | PubMed |
description | BACKGROUND & AIMS: Metformin is currently the most widely used first-line hypoglycemic agent for diabetes mellitus. Besides glucose-lowering action, there is increasingly interest in the potential anti-inflammatory action of this drug. In the present study, we investigated the actions of metformin on experimental insulitis using STZ-induced diabetic mice. METHODS: Mice with acute diabetes induced by STZ were administered metformin by gavage. Changes of blood glucose and body weight, and the daily amount of food and water intake were measured. Pancreatic tissues were collected for histologic analyses. Pathological assessment and immunohistochemistry analysis were used to determine the effect of metformin on insulitis. Inflammatory cytokines in the pancreas and insulin levels were measured through ELISA analysis. RESULTS: Metformin significantly reduced blood glucose levels and improved aberrant water intake behavior in experimental diabetic mice. No significant differences were observed in terms of body weight and food intake behavior in metformin-treated animals. In the STZ-induced model of diabetes, we found the appearance of pronounced insulitis. However, metformin administration reduced the severity of insulitis assessed by blind pathological scoring. In addition, metformin treatment improved insulin levels in experimental diabetic mice. ELISA assay revealed decreased levels of inflammatory response marker IL-1β and TNF-α in the pancreatic tissues following metformin treatment. CONCLUSION: Metformin attenuated insulitis in the STZ-induced mice model of diabetes. This islet-protective effect might be partly correlated with the anti-inflammatory action of metformin. |
format | Online Article Text |
id | pubmed-5399881 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | PeerJ Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-53998812017-04-24 Metformin ameliorates insulitis in STZ-induced diabetic mice Han, Xue Tao, Yu-Long Deng, Ya-Ping Yu, Jia-Wen Cai, Jian Ren, Guo-Fei Sun, Yuan-Nan Jiang, Guo-Jun PeerJ Diabetes and Endocrinology BACKGROUND & AIMS: Metformin is currently the most widely used first-line hypoglycemic agent for diabetes mellitus. Besides glucose-lowering action, there is increasingly interest in the potential anti-inflammatory action of this drug. In the present study, we investigated the actions of metformin on experimental insulitis using STZ-induced diabetic mice. METHODS: Mice with acute diabetes induced by STZ were administered metformin by gavage. Changes of blood glucose and body weight, and the daily amount of food and water intake were measured. Pancreatic tissues were collected for histologic analyses. Pathological assessment and immunohistochemistry analysis were used to determine the effect of metformin on insulitis. Inflammatory cytokines in the pancreas and insulin levels were measured through ELISA analysis. RESULTS: Metformin significantly reduced blood glucose levels and improved aberrant water intake behavior in experimental diabetic mice. No significant differences were observed in terms of body weight and food intake behavior in metformin-treated animals. In the STZ-induced model of diabetes, we found the appearance of pronounced insulitis. However, metformin administration reduced the severity of insulitis assessed by blind pathological scoring. In addition, metformin treatment improved insulin levels in experimental diabetic mice. ELISA assay revealed decreased levels of inflammatory response marker IL-1β and TNF-α in the pancreatic tissues following metformin treatment. CONCLUSION: Metformin attenuated insulitis in the STZ-induced mice model of diabetes. This islet-protective effect might be partly correlated with the anti-inflammatory action of metformin. PeerJ Inc. 2017-04-13 /pmc/articles/PMC5399881/ /pubmed/28439456 http://dx.doi.org/10.7717/peerj.3155 Text en ©2017 Han et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited. |
spellingShingle | Diabetes and Endocrinology Han, Xue Tao, Yu-Long Deng, Ya-Ping Yu, Jia-Wen Cai, Jian Ren, Guo-Fei Sun, Yuan-Nan Jiang, Guo-Jun Metformin ameliorates insulitis in STZ-induced diabetic mice |
title | Metformin ameliorates insulitis in STZ-induced diabetic mice |
title_full | Metformin ameliorates insulitis in STZ-induced diabetic mice |
title_fullStr | Metformin ameliorates insulitis in STZ-induced diabetic mice |
title_full_unstemmed | Metformin ameliorates insulitis in STZ-induced diabetic mice |
title_short | Metformin ameliorates insulitis in STZ-induced diabetic mice |
title_sort | metformin ameliorates insulitis in stz-induced diabetic mice |
topic | Diabetes and Endocrinology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5399881/ https://www.ncbi.nlm.nih.gov/pubmed/28439456 http://dx.doi.org/10.7717/peerj.3155 |
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