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Naringenin improves insulin sensitivity in gestational diabetes mellitus mice through AMPK

BACKGROUND: Gestational diabetes mellitus (GDM) is a temporary form of diabetes during pregnancy, which influences the health of maternal-child in clinical practice. It is still urgent to develop new effective treatment for GDM. Naringenin is a bioactive ingredient with multiple activities including...

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Autores principales: Li, Sen, Zhang, Yan, Sun, Yewu, Zhang, Guangzhen, Bai, Jie, Guo, Jianfei, Su, Xudong, Du, Hongquan, Cao, Xi, Yang, Jinkui, Wang, Ting
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6779739/
https://www.ncbi.nlm.nih.gov/pubmed/31591391
http://dx.doi.org/10.1038/s41387-019-0095-8
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author Li, Sen
Zhang, Yan
Sun, Yewu
Zhang, Guangzhen
Bai, Jie
Guo, Jianfei
Su, Xudong
Du, Hongquan
Cao, Xi
Yang, Jinkui
Wang, Ting
author_facet Li, Sen
Zhang, Yan
Sun, Yewu
Zhang, Guangzhen
Bai, Jie
Guo, Jianfei
Su, Xudong
Du, Hongquan
Cao, Xi
Yang, Jinkui
Wang, Ting
author_sort Li, Sen
collection PubMed
description BACKGROUND: Gestational diabetes mellitus (GDM) is a temporary form of diabetes during pregnancy, which influences the health of maternal-child in clinical practice. It is still urgent to develop new effective treatment for GDM. Naringenin is a bioactive ingredient with multiple activities including anti-diabetic. In current study, the effects of naringenin on GDM symptoms, insulin tolerance, inflammation, and productive outcomes were evaluated and the underlying mechanisms were explored. METHODS: We administrated naringenin to GDM mice and monitored the GDM symptoms, glucose and insulin tolerance, inflammation and productive outcomes. We established tumor necrosis factor alpha (TNF-α)-induced insulin resistance skeletal muscle cell model and evaluated the effects of naringenin on reactive oxygen species (ROS) production, glucose uptake and glucose transporter type 4 (GLUT4) membrane translocation. RESULTS: We found that naringenin ameliorated GDM symptoms, improved glucose and insulin tolerance, inhibited inflammation, and improved productive outcomes. It was further found that naringenin inhibited TNF-α-induced ROS production, enhanced GLUT4 membrane translocation, and glucose uptake, which were abolished by inhibition of AMP-activated protein kinase (AMPK). CONCLUSION: Naringenin improves insulin sensitivity in gestational diabetes mellitus mice in an AMPK-dependent manner.
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spelling pubmed-67797392019-10-10 Naringenin improves insulin sensitivity in gestational diabetes mellitus mice through AMPK Li, Sen Zhang, Yan Sun, Yewu Zhang, Guangzhen Bai, Jie Guo, Jianfei Su, Xudong Du, Hongquan Cao, Xi Yang, Jinkui Wang, Ting Nutr Diabetes Article BACKGROUND: Gestational diabetes mellitus (GDM) is a temporary form of diabetes during pregnancy, which influences the health of maternal-child in clinical practice. It is still urgent to develop new effective treatment for GDM. Naringenin is a bioactive ingredient with multiple activities including anti-diabetic. In current study, the effects of naringenin on GDM symptoms, insulin tolerance, inflammation, and productive outcomes were evaluated and the underlying mechanisms were explored. METHODS: We administrated naringenin to GDM mice and monitored the GDM symptoms, glucose and insulin tolerance, inflammation and productive outcomes. We established tumor necrosis factor alpha (TNF-α)-induced insulin resistance skeletal muscle cell model and evaluated the effects of naringenin on reactive oxygen species (ROS) production, glucose uptake and glucose transporter type 4 (GLUT4) membrane translocation. RESULTS: We found that naringenin ameliorated GDM symptoms, improved glucose and insulin tolerance, inhibited inflammation, and improved productive outcomes. It was further found that naringenin inhibited TNF-α-induced ROS production, enhanced GLUT4 membrane translocation, and glucose uptake, which were abolished by inhibition of AMP-activated protein kinase (AMPK). CONCLUSION: Naringenin improves insulin sensitivity in gestational diabetes mellitus mice in an AMPK-dependent manner. Nature Publishing Group UK 2019-10-07 /pmc/articles/PMC6779739/ /pubmed/31591391 http://dx.doi.org/10.1038/s41387-019-0095-8 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
Li, Sen
Zhang, Yan
Sun, Yewu
Zhang, Guangzhen
Bai, Jie
Guo, Jianfei
Su, Xudong
Du, Hongquan
Cao, Xi
Yang, Jinkui
Wang, Ting
Naringenin improves insulin sensitivity in gestational diabetes mellitus mice through AMPK
title Naringenin improves insulin sensitivity in gestational diabetes mellitus mice through AMPK
title_full Naringenin improves insulin sensitivity in gestational diabetes mellitus mice through AMPK
title_fullStr Naringenin improves insulin sensitivity in gestational diabetes mellitus mice through AMPK
title_full_unstemmed Naringenin improves insulin sensitivity in gestational diabetes mellitus mice through AMPK
title_short Naringenin improves insulin sensitivity in gestational diabetes mellitus mice through AMPK
title_sort naringenin improves insulin sensitivity in gestational diabetes mellitus mice through ampk
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6779739/
https://www.ncbi.nlm.nih.gov/pubmed/31591391
http://dx.doi.org/10.1038/s41387-019-0095-8
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