4.8 Article

Insight Into Polysaccharides From Panax ginseng C. A. Meyer in Improving Intestinal Inflammation: Modulating Intestinal Microbiota and Autophagy

期刊

FRONTIERS IN IMMUNOLOGY
卷 12, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fimmu.2021.683911

关键词

Panax ginseng C. A. Meyer; polysaccharide; intestinal inflammation; gut microbiota; autophagy

资金

  1. National Key Research and Development Program of China [2017YFC1702100]
  2. National Natural Science Foundation of China [81603276, U19A2013, 82004099]
  3. Department of Science and Technology of Jilin Province [20190101010JH, 20200201419JC, 202002053JC]
  4. Science and Technology Projects in Jilin Province Department of Education [JJKH20200903KJ]

向作者/读者索取更多资源

The study isolated and studied a polysaccharide from Panax ginseng, finding that it exhibits significant intestinal anti-inflammatory activity by modulating gut microbiota structure and restoring autophagic function to suppress inflammation.
Polysaccharides from Panax ginseng C. A. Meyer (P. ginseng) are the main active component of P. ginseng and exhibit significant intestinal anti-inflammatory activity. However, the therapeutic mechanism of the ginseng polysaccharide is unclear, and this hinders the application for medicine or functional food. In this study, a polysaccharide was isolated from P. ginseng (GP). The primary structure and morphology of the GP were studied by HPLC, FT-IR spectroscopy, and scanning electron microscopy (SEM). Further, its intestinal anti-inflammatory activity and its mechanism of function were evaluated in experimental systems using DSS-induced rats, fecal microbiota transplantation (FMT), and LPS-stimulated HT-29 cells. Results showed that GP modulated the structure of gut microbiota and restored mTOR-dependent autophagic dysfunction. Consequently, active autophagy suppressed inflammation through the inhibition of NF-kappa B, oxidative stress, and the release of cytokines. Therefore, our research provides a rationale for future investigations into the relationship between microbiota and autophagy and revealed the therapeutic potential of GP for inflammatory bowel disease.

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