<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ren Y</submitter><funding>Top Talent Support Program for young and middle-aged people of Wuxi Health Committee</funding><funding>Traditional Chinese Medicine Research Project of Wuxi Health Committee</funding><funding>National Natural Science Foundation of China</funding><funding>China Postdoctoral Science Foundation</funding><funding>Talent Support Program for young and middle-aged people of Wuxi Health Committee</funding><pagination>739</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9920828</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>15(3)</volume><pubmed_abstract>Ulcerative colitis (UC), one of the typical inflammatory bowel diseases caused by dysregulated immunity, still requires novel therapeutic medicine with high efficacy and low toxicity. &lt;i>Hericium erinaceus&lt;/i> has been widely used to treat different health problems especially gastrointestinal sickness in China for thousands of years. Here, we isolated, purified, and characterized a novel low weight polysaccharide (HEP10, Mw: 9.9 kDa) from the mycelia of &lt;i>H. erinaceus&lt;/i> in submerged culture. We explored the therapeutic effect of HEP10 on UC and explored its underlying mechanisms. On one hand, HEP10 suppressed the production of TNF-α, IL-1β, IL-6, inducible iNOS, and COX-2 in LPS challenged murine macrophage RAW264.7 cells, as well as in colons from DSS-induced colitis mice. On the other hand, HEP10 treatment markedly suppressed the activation of NLRP3 inflammasome, NF-κB, AKT, and MAPK pathways. Moreover, HEP10 reversed DSS-induced alternation of the gut community composition and structure by significantly increasing &lt;i>Akkermansia muciniphila&lt;/i> and also promoting functional shifts in gut microbiota. Structural equation modeling also highlighted that HEP10 can change widely through gut microbiota. In conclusion, HEP10 has a better prebiotic effect than the crude polysaccharides of &lt;i>H. erinaceus&lt;/i>, which can be used as a novel dietary supplement and prebiotic to ameliorate colitis.</pubmed_abstract><journal>Nutrients</journal><pubmed_title>Low Weight Polysaccharide of &lt;i>Hericium erinaceus&lt;/i> Ameliorates Colitis via Inhibiting the NLRP3 Inflammasome Activation in Association with Gut Microbiota Modulation.</pubmed_title><pmcid>PMC9920828</pmcid><funding_grant_id>32001661</funding_grant_id><funding_grant_id>32101964</funding_grant_id><funding_grant_id>31970746</funding_grant_id><funding_grant_id>ZYKJ201910</funding_grant_id><funding_grant_id>2018M640455</funding_grant_id><funding_grant_id>HB2020055</funding_grant_id><pubmed_authors>Zhou L</pubmed_authors><pubmed_authors>Li H</pubmed_authors><pubmed_authors>Sheng Y</pubmed_authors><pubmed_authors>Yu L</pubmed_authors><pubmed_authors>Ren Y</pubmed_authors><pubmed_authors>Lu Z</pubmed_authors><pubmed_authors>Guan T</pubmed_authors><pubmed_authors>Xue Y</pubmed_authors><pubmed_authors>Li W</pubmed_authors><pubmed_authors>Gao R</pubmed_authors><pubmed_authors>Sun Q</pubmed_authors><pubmed_authors>Geng Y</pubmed_authors><pubmed_authors>Liu C</pubmed_authors><pubmed_authors>Shi J</pubmed_authors><pubmed_authors>Xu Z</pubmed_authors></additional><is_claimable>false</is_claimable><name>Low Weight Polysaccharide of &lt;i>Hericium erinaceus&lt;/i> Ameliorates Colitis via Inhibiting the NLRP3 Inflammasome Activation in Association with Gut Microbiota Modulation.</name><description>Ulcerative colitis (UC), one of the typical inflammatory bowel diseases caused by dysregulated immunity, still requires novel therapeutic medicine with high efficacy and low toxicity. &lt;i>Hericium erinaceus&lt;/i> has been widely used to treat different health problems especially gastrointestinal sickness in China for thousands of years. Here, we isolated, purified, and characterized a novel low weight polysaccharide (HEP10, Mw: 9.9 kDa) from the mycelia of &lt;i>H. erinaceus&lt;/i> in submerged culture. We explored the therapeutic effect of HEP10 on UC and explored its underlying mechanisms. On one hand, HEP10 suppressed the production of TNF-α, IL-1β, IL-6, inducible iNOS, and COX-2 in LPS challenged murine macrophage RAW264.7 cells, as well as in colons from DSS-induced colitis mice. On the other hand, HEP10 treatment markedly suppressed the activation of NLRP3 inflammasome, NF-κB, AKT, and MAPK pathways. Moreover, HEP10 reversed DSS-induced alternation of the gut community composition and structure by significantly increasing &lt;i>Akkermansia muciniphila&lt;/i> and also promoting functional shifts in gut microbiota. Structural equation modeling also highlighted that HEP10 can change widely through gut microbiota. In conclusion, HEP10 has a better prebiotic effect than the crude polysaccharides of &lt;i>H. erinaceus&lt;/i>, which can be used as a novel dietary supplement and prebiotic to ameliorate colitis.</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Feb</publication><modification>2026-04-08T14:15:21.356Z</modification><creation>2025-02-19T02:23:48.535Z</creation></dates><accession>S-EPMC9920828</accession><cross_references><pubmed>36771444</pubmed><doi>10.3390/nu15030739</doi></cross_references></HashMap>