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Regulation of microbiota—GLP1 axis by sennoside A in diet-induced obese mice
Sennoside A (SA) is a bioactive component of Chinese herbal medicines with an activity of irritant laxative, which is often used in the treatment of constipation and obesity. However, its activity remains unknown in the regulation of insulin sensitivity. In this study, the impact of SA on insulin se...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6663941/ https://www.ncbi.nlm.nih.gov/pubmed/31384536 http://dx.doi.org/10.1016/j.apsb.2019.01.014 |
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author | Le, Jiamei Zhang, Xiaoying Jia, Weiping Zhang, Yong Luo, Juntao Sun, Yongning Ye, Jianping |
author_facet | Le, Jiamei Zhang, Xiaoying Jia, Weiping Zhang, Yong Luo, Juntao Sun, Yongning Ye, Jianping |
author_sort | Le, Jiamei |
collection | PubMed |
description | Sennoside A (SA) is a bioactive component of Chinese herbal medicines with an activity of irritant laxative, which is often used in the treatment of constipation and obesity. However, its activity remains unknown in the regulation of insulin sensitivity. In this study, the impact of SA on insulin sensitivity was tested in high fat diet (HFD)-induced obese mice through dietary supplementation. At a dosage of 30 mg/kg/day, SA improved insulin sensitivity in the mice after 8-week treatment as indicated by HOMA-IR (homeostatic model assessment for insulin resistance) and glucose tolerance test (GTT). SA restored plasma level of glucagon-like peptide 1 (GLP1) by 90% and mRNA expression of Glp1 by 80% in the large intestine of HFD mice. In the mechanism, SA restored the gut microbiota profile, short chain fatty acids (SCFAs), and mucosal structure in the colon. A mitochondrial stress was observed in the enterocytes of HFD mice with ATP elevation, structural damage, and complex dysfunction. The mitochondrial response was induced in enterocytes by the dietary fat as the same responses were induced by palmitic acid in the cell culture. The mitochondrial response was inhibited in HFD mice by SA treatment. These data suggest that SA may restore the function of microbiota–GLP1 axis to improve glucose metabolism in the obese mice. |
format | Online Article Text |
id | pubmed-6663941 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-66639412019-08-05 Regulation of microbiota—GLP1 axis by sennoside A in diet-induced obese mice Le, Jiamei Zhang, Xiaoying Jia, Weiping Zhang, Yong Luo, Juntao Sun, Yongning Ye, Jianping Acta Pharm Sin B Original article Sennoside A (SA) is a bioactive component of Chinese herbal medicines with an activity of irritant laxative, which is often used in the treatment of constipation and obesity. However, its activity remains unknown in the regulation of insulin sensitivity. In this study, the impact of SA on insulin sensitivity was tested in high fat diet (HFD)-induced obese mice through dietary supplementation. At a dosage of 30 mg/kg/day, SA improved insulin sensitivity in the mice after 8-week treatment as indicated by HOMA-IR (homeostatic model assessment for insulin resistance) and glucose tolerance test (GTT). SA restored plasma level of glucagon-like peptide 1 (GLP1) by 90% and mRNA expression of Glp1 by 80% in the large intestine of HFD mice. In the mechanism, SA restored the gut microbiota profile, short chain fatty acids (SCFAs), and mucosal structure in the colon. A mitochondrial stress was observed in the enterocytes of HFD mice with ATP elevation, structural damage, and complex dysfunction. The mitochondrial response was induced in enterocytes by the dietary fat as the same responses were induced by palmitic acid in the cell culture. The mitochondrial response was inhibited in HFD mice by SA treatment. These data suggest that SA may restore the function of microbiota–GLP1 axis to improve glucose metabolism in the obese mice. Elsevier 2019-07 2019-01-29 /pmc/articles/PMC6663941/ /pubmed/31384536 http://dx.doi.org/10.1016/j.apsb.2019.01.014 Text en © 2019 Chinese Pharmaceutical Association and Institute of Materia Medica, Chinese Academy of Medical Sciences. Production and hosting by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original article Le, Jiamei Zhang, Xiaoying Jia, Weiping Zhang, Yong Luo, Juntao Sun, Yongning Ye, Jianping Regulation of microbiota—GLP1 axis by sennoside A in diet-induced obese mice |
title | Regulation of microbiota—GLP1 axis by sennoside A in diet-induced obese mice |
title_full | Regulation of microbiota—GLP1 axis by sennoside A in diet-induced obese mice |
title_fullStr | Regulation of microbiota—GLP1 axis by sennoside A in diet-induced obese mice |
title_full_unstemmed | Regulation of microbiota—GLP1 axis by sennoside A in diet-induced obese mice |
title_short | Regulation of microbiota—GLP1 axis by sennoside A in diet-induced obese mice |
title_sort | regulation of microbiota—glp1 axis by sennoside a in diet-induced obese mice |
topic | Original article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6663941/ https://www.ncbi.nlm.nih.gov/pubmed/31384536 http://dx.doi.org/10.1016/j.apsb.2019.01.014 |
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