Cargando…
Astragaloside IV attenuates gestational diabetes mellitus via targeting NLRP3 inflammasome in genetic mice
BACKGROUND: As the most ordinary metabolic disorder during pregnancy, gestational diabetes mellitus (GDM) has become a severe risk for the health of both pregnant female and fetus. Astragaloside IV (AS-IV) is the dominant active component in Astragalus membranaceus. It has been proved that AS-IV has...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6764134/ https://www.ncbi.nlm.nih.gov/pubmed/31558153 http://dx.doi.org/10.1186/s12958-019-0522-7 |
_version_ | 1783454314239361024 |
---|---|
author | Zhang, Ruixue Zhang, Xuelei Xing, Baoheng Zhao, Jianyong Zhang, Peipei Shi, Dandan Yang, Fengzhen |
author_facet | Zhang, Ruixue Zhang, Xuelei Xing, Baoheng Zhao, Jianyong Zhang, Peipei Shi, Dandan Yang, Fengzhen |
author_sort | Zhang, Ruixue |
collection | PubMed |
description | BACKGROUND: As the most ordinary metabolic disorder during pregnancy, gestational diabetes mellitus (GDM) has become a severe risk for the health of both pregnant female and fetus. Astragaloside IV (AS-IV) is the dominant active component in Astragalus membranaceus. It has been proved that AS-IV has anti-inflammation and immune-regulation function. We aimed to demonstrate the function of AS-IV in the therapy of GDM and the molecular mechanism in this process. METHODS: C57BL/KsJ-Lepdb/+ female mice were used as GDM model. The mRNA levels of relative genes in this research were detected by qRT-PCR. The protein levels of relative genes were analyzed by western blot. Serum concentration of interleukin-6 (IL-6) and tumor necrosis factor alpha (TNF-α) were analyzed by ELISA. RESULTS: Glucose and insulin levels in GDM mice model were decreased by AS-IV treatment. AS-IV down-regulated the expression of inflammatory gene IL-6 and TNF-α in GDM mice model. AS-IV treatment inhibited the expression of NLR family pyrin domain containing-3 (NLRP3) inflammasome relative proteins in the pancreas of GDM mice. CONCLUSION: This study demonstrated that AS-IV treatment has an effective therapeutic function of GDM in mice model through the inhibition of NLRP3 inflammasome in the pancreas. |
format | Online Article Text |
id | pubmed-6764134 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-67641342019-09-30 Astragaloside IV attenuates gestational diabetes mellitus via targeting NLRP3 inflammasome in genetic mice Zhang, Ruixue Zhang, Xuelei Xing, Baoheng Zhao, Jianyong Zhang, Peipei Shi, Dandan Yang, Fengzhen Reprod Biol Endocrinol Research BACKGROUND: As the most ordinary metabolic disorder during pregnancy, gestational diabetes mellitus (GDM) has become a severe risk for the health of both pregnant female and fetus. Astragaloside IV (AS-IV) is the dominant active component in Astragalus membranaceus. It has been proved that AS-IV has anti-inflammation and immune-regulation function. We aimed to demonstrate the function of AS-IV in the therapy of GDM and the molecular mechanism in this process. METHODS: C57BL/KsJ-Lepdb/+ female mice were used as GDM model. The mRNA levels of relative genes in this research were detected by qRT-PCR. The protein levels of relative genes were analyzed by western blot. Serum concentration of interleukin-6 (IL-6) and tumor necrosis factor alpha (TNF-α) were analyzed by ELISA. RESULTS: Glucose and insulin levels in GDM mice model were decreased by AS-IV treatment. AS-IV down-regulated the expression of inflammatory gene IL-6 and TNF-α in GDM mice model. AS-IV treatment inhibited the expression of NLR family pyrin domain containing-3 (NLRP3) inflammasome relative proteins in the pancreas of GDM mice. CONCLUSION: This study demonstrated that AS-IV treatment has an effective therapeutic function of GDM in mice model through the inhibition of NLRP3 inflammasome in the pancreas. BioMed Central 2019-09-26 /pmc/articles/PMC6764134/ /pubmed/31558153 http://dx.doi.org/10.1186/s12958-019-0522-7 Text en © The Author(s). 2019 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 Zhang, Ruixue Zhang, Xuelei Xing, Baoheng Zhao, Jianyong Zhang, Peipei Shi, Dandan Yang, Fengzhen Astragaloside IV attenuates gestational diabetes mellitus via targeting NLRP3 inflammasome in genetic mice |
title | Astragaloside IV attenuates gestational diabetes mellitus via targeting NLRP3 inflammasome in genetic mice |
title_full | Astragaloside IV attenuates gestational diabetes mellitus via targeting NLRP3 inflammasome in genetic mice |
title_fullStr | Astragaloside IV attenuates gestational diabetes mellitus via targeting NLRP3 inflammasome in genetic mice |
title_full_unstemmed | Astragaloside IV attenuates gestational diabetes mellitus via targeting NLRP3 inflammasome in genetic mice |
title_short | Astragaloside IV attenuates gestational diabetes mellitus via targeting NLRP3 inflammasome in genetic mice |
title_sort | astragaloside iv attenuates gestational diabetes mellitus via targeting nlrp3 inflammasome in genetic mice |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6764134/ https://www.ncbi.nlm.nih.gov/pubmed/31558153 http://dx.doi.org/10.1186/s12958-019-0522-7 |
work_keys_str_mv | AT zhangruixue astragalosideivattenuatesgestationaldiabetesmellitusviatargetingnlrp3inflammasomeingeneticmice AT zhangxuelei astragalosideivattenuatesgestationaldiabetesmellitusviatargetingnlrp3inflammasomeingeneticmice AT xingbaoheng astragalosideivattenuatesgestationaldiabetesmellitusviatargetingnlrp3inflammasomeingeneticmice AT zhaojianyong astragalosideivattenuatesgestationaldiabetesmellitusviatargetingnlrp3inflammasomeingeneticmice AT zhangpeipei astragalosideivattenuatesgestationaldiabetesmellitusviatargetingnlrp3inflammasomeingeneticmice AT shidandan astragalosideivattenuatesgestationaldiabetesmellitusviatargetingnlrp3inflammasomeingeneticmice AT yangfengzhen astragalosideivattenuatesgestationaldiabetesmellitusviatargetingnlrp3inflammasomeingeneticmice |