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Effects of molecular weight of chitosan on anti-inflammatory activity and modulation of intestinal microflora in an ulcerative colitis model
This study investigated the therapeutic effects and mechanisms of chitosans (CSs) with different molecular weights on ulcerative colitis (UC). Three size classes of CSs (Mw ≤ 3, 50, and 200 kDa) were used in this study. The effect of large CSs (Mw ≤ 200 kDa) on UC was the best, followed by that of m...
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Published in: | International journal of biological macromolecules 2021-12, Vol.193 (Pt B), p.1927-1936 |
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container_end_page | 1936 |
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container_start_page | 1927 |
container_title | International journal of biological macromolecules |
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creator | Niu, Wei Dong, Yuelin Fu, Ziwei Lv, Jiajie Wang, Ligui Zhang, Zhenhai Huo, Jiege Ju, Jianming |
description | This study investigated the therapeutic effects and mechanisms of chitosans (CSs) with different molecular weights on ulcerative colitis (UC). Three size classes of CSs (Mw ≤ 3, 50, and 200 kDa) were used in this study. The effect of large CSs (Mw ≤ 200 kDa) on UC was the best, followed by that of medium CSs (Mw ≤ 50 kDa), and that of small CSs (Mw ≤ 3 kDa) was the least in the LPS-induced Raw 264.7 cell model and DSS-induced UC mice model. The therapeutic mechanisms of three CSs are related to anti-oxidation, anti-inflammation, and regulation of immunoglobulin and intestinal flora by attenuating body weight loss, decreasing the disease activity index (DAI) and MPO activity, suppressing proinflammatory cytokines and IgG levels, down-regulating the level of oxidative stress, increasing anti-inflammatory cytokines, SOD activity and Prevotellaceae_UCG-001 levels, and reducing the abundance of Proteobacteria, Actinobacteria, and Escherichia-Shigella. In general, the molecular weight of CSs influences their efficacy against UC. CSs with an optimal molecular weight demonstrate good development prospects for ameliorating UC.
•The therapeutic effects of chitosans against UC vary with molecular weight.•Chitosans inhibit inflammatory cytokines, regulate immunoglobulin, and alter intestinal flora.•Higher molecular weight chitosans are more beneficial than lower weight ones. |
doi_str_mv | 10.1016/j.ijbiomac.2021.11.024 |
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•The therapeutic effects of chitosans against UC vary with molecular weight.•Chitosans inhibit inflammatory cytokines, regulate immunoglobulin, and alter intestinal flora.•Higher molecular weight chitosans are more beneficial than lower weight ones.</description><identifier>ISSN: 0141-8130</identifier><identifier>EISSN: 1879-0003</identifier><identifier>DOI: 10.1016/j.ijbiomac.2021.11.024</identifier><identifier>PMID: 34748786</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Animals ; Anti-Inflammatory Agents - pharmacology ; Anti-inflammatory mechanism ; Cell Line ; Chitosan ; Chitosan - pharmacology ; Colitis, Ulcerative - drug therapy ; Colitis, Ulcerative - metabolism ; Colitis, Ulcerative - microbiology ; Cytokines - metabolism ; Disease Models, Animal ; Gastrointestinal Microbiome - drug effects ; Inflammation - drug therapy ; Inflammation - metabolism ; Inflammation Mediators - metabolism ; Intestinal flora ; Male ; Mice ; Mice, Inbred ICR ; Molecular Weight ; RAW 264.7 Cells ; Ulcerative colitis</subject><ispartof>International journal of biological macromolecules, 2021-12, Vol.193 (Pt B), p.1927-1936</ispartof><rights>2021</rights><rights>Copyright © 2021. Published by Elsevier B.V.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c368t-ccc0dd46f71fee5ebf483e34daa139413d2d6305b8a5163a2ea327070bdba36f3</citedby><cites>FETCH-LOGICAL-c368t-ccc0dd46f71fee5ebf483e34daa139413d2d6305b8a5163a2ea327070bdba36f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34748786$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Niu, Wei</creatorcontrib><creatorcontrib>Dong, Yuelin</creatorcontrib><creatorcontrib>Fu, Ziwei</creatorcontrib><creatorcontrib>Lv, Jiajie</creatorcontrib><creatorcontrib>Wang, Ligui</creatorcontrib><creatorcontrib>Zhang, Zhenhai</creatorcontrib><creatorcontrib>Huo, Jiege</creatorcontrib><creatorcontrib>Ju, Jianming</creatorcontrib><title>Effects of molecular weight of chitosan on anti-inflammatory activity and modulation of intestinal microflora in an ulcerative colitis model</title><title>International journal of biological macromolecules</title><addtitle>Int J Biol Macromol</addtitle><description>This study investigated the therapeutic effects and mechanisms of chitosans (CSs) with different molecular weights on ulcerative colitis (UC). Three size classes of CSs (Mw ≤ 3, 50, and 200 kDa) were used in this study. The effect of large CSs (Mw ≤ 200 kDa) on UC was the best, followed by that of medium CSs (Mw ≤ 50 kDa), and that of small CSs (Mw ≤ 3 kDa) was the least in the LPS-induced Raw 264.7 cell model and DSS-induced UC mice model. The therapeutic mechanisms of three CSs are related to anti-oxidation, anti-inflammation, and regulation of immunoglobulin and intestinal flora by attenuating body weight loss, decreasing the disease activity index (DAI) and MPO activity, suppressing proinflammatory cytokines and IgG levels, down-regulating the level of oxidative stress, increasing anti-inflammatory cytokines, SOD activity and Prevotellaceae_UCG-001 levels, and reducing the abundance of Proteobacteria, Actinobacteria, and Escherichia-Shigella. In general, the molecular weight of CSs influences their efficacy against UC. CSs with an optimal molecular weight demonstrate good development prospects for ameliorating UC.
•The therapeutic effects of chitosans against UC vary with molecular weight.•Chitosans inhibit inflammatory cytokines, regulate immunoglobulin, and alter intestinal flora.•Higher molecular weight chitosans are more beneficial than lower weight ones.</description><subject>Animals</subject><subject>Anti-Inflammatory Agents - pharmacology</subject><subject>Anti-inflammatory mechanism</subject><subject>Cell Line</subject><subject>Chitosan</subject><subject>Chitosan - pharmacology</subject><subject>Colitis, Ulcerative - drug therapy</subject><subject>Colitis, Ulcerative - metabolism</subject><subject>Colitis, Ulcerative - microbiology</subject><subject>Cytokines - metabolism</subject><subject>Disease Models, Animal</subject><subject>Gastrointestinal Microbiome - drug effects</subject><subject>Inflammation - drug therapy</subject><subject>Inflammation - metabolism</subject><subject>Inflammation Mediators - metabolism</subject><subject>Intestinal flora</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred ICR</subject><subject>Molecular Weight</subject><subject>RAW 264.7 Cells</subject><subject>Ulcerative colitis</subject><issn>0141-8130</issn><issn>1879-0003</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNqFkcFuFSEUhonR2Gv1FRqWbmaEgWHm7jRNqyZN3OiaMHCw54aBCsw1fQcfWm5u69YNkJPv43D4CbnirOeMqw-HHg8LptXYfmAD7znv2SBfkB2fp33HGBMvyY5xybuZC3ZB3pRyaFU18vk1uRBykvM0qx35c-M92Fpo8nRNAewWTKa_AX_e11PN3mNNxUSaIjWxYofRB7Oupqb8SI2teMTaDtE13TW5YiObiLFCqRhNoCvanHxI2bRqQ-kWLORGHoHaFLBiOckQ3pJX3oQC7572S_Lj9ub79Zfu7tvnr9ef7jor1Fw7ay1zTio_cQ8wwuLlLEBIZwwXe8mFG5wSbFxmM3IlzABGDBOb2OIWI5QXl-T9-d6HnH5t7Zl6xWIhBBMhbUUP434cR9nWhqoz2kYoJYPXDxlXkx81Z_qUhD7o5yT0KQnNuW5JNPHqqce2rOD-ac9f34CPZwDapEeErItFiBYc5paIdgn_1-Mv4JahdQ</recordid><startdate>20211215</startdate><enddate>20211215</enddate><creator>Niu, Wei</creator><creator>Dong, Yuelin</creator><creator>Fu, Ziwei</creator><creator>Lv, Jiajie</creator><creator>Wang, Ligui</creator><creator>Zhang, Zhenhai</creator><creator>Huo, Jiege</creator><creator>Ju, Jianming</creator><general>Elsevier B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20211215</creationdate><title>Effects of molecular weight of chitosan on anti-inflammatory activity and modulation of intestinal microflora in an ulcerative colitis model</title><author>Niu, Wei ; Dong, Yuelin ; Fu, Ziwei ; Lv, Jiajie ; Wang, Ligui ; Zhang, Zhenhai ; Huo, Jiege ; Ju, Jianming</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c368t-ccc0dd46f71fee5ebf483e34daa139413d2d6305b8a5163a2ea327070bdba36f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Animals</topic><topic>Anti-Inflammatory Agents - pharmacology</topic><topic>Anti-inflammatory mechanism</topic><topic>Cell Line</topic><topic>Chitosan</topic><topic>Chitosan - pharmacology</topic><topic>Colitis, Ulcerative - drug therapy</topic><topic>Colitis, Ulcerative - metabolism</topic><topic>Colitis, Ulcerative - microbiology</topic><topic>Cytokines - metabolism</topic><topic>Disease Models, Animal</topic><topic>Gastrointestinal Microbiome - drug effects</topic><topic>Inflammation - drug therapy</topic><topic>Inflammation - metabolism</topic><topic>Inflammation Mediators - metabolism</topic><topic>Intestinal flora</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred ICR</topic><topic>Molecular Weight</topic><topic>RAW 264.7 Cells</topic><topic>Ulcerative colitis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Niu, Wei</creatorcontrib><creatorcontrib>Dong, Yuelin</creatorcontrib><creatorcontrib>Fu, Ziwei</creatorcontrib><creatorcontrib>Lv, Jiajie</creatorcontrib><creatorcontrib>Wang, Ligui</creatorcontrib><creatorcontrib>Zhang, Zhenhai</creatorcontrib><creatorcontrib>Huo, Jiege</creatorcontrib><creatorcontrib>Ju, Jianming</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>International journal of biological macromolecules</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Niu, Wei</au><au>Dong, Yuelin</au><au>Fu, Ziwei</au><au>Lv, Jiajie</au><au>Wang, Ligui</au><au>Zhang, Zhenhai</au><au>Huo, Jiege</au><au>Ju, Jianming</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of molecular weight of chitosan on anti-inflammatory activity and modulation of intestinal microflora in an ulcerative colitis model</atitle><jtitle>International journal of biological macromolecules</jtitle><addtitle>Int J Biol Macromol</addtitle><date>2021-12-15</date><risdate>2021</risdate><volume>193</volume><issue>Pt B</issue><spage>1927</spage><epage>1936</epage><pages>1927-1936</pages><issn>0141-8130</issn><eissn>1879-0003</eissn><abstract>This study investigated the therapeutic effects and mechanisms of chitosans (CSs) with different molecular weights on ulcerative colitis (UC). Three size classes of CSs (Mw ≤ 3, 50, and 200 kDa) were used in this study. The effect of large CSs (Mw ≤ 200 kDa) on UC was the best, followed by that of medium CSs (Mw ≤ 50 kDa), and that of small CSs (Mw ≤ 3 kDa) was the least in the LPS-induced Raw 264.7 cell model and DSS-induced UC mice model. The therapeutic mechanisms of three CSs are related to anti-oxidation, anti-inflammation, and regulation of immunoglobulin and intestinal flora by attenuating body weight loss, decreasing the disease activity index (DAI) and MPO activity, suppressing proinflammatory cytokines and IgG levels, down-regulating the level of oxidative stress, increasing anti-inflammatory cytokines, SOD activity and Prevotellaceae_UCG-001 levels, and reducing the abundance of Proteobacteria, Actinobacteria, and Escherichia-Shigella. In general, the molecular weight of CSs influences their efficacy against UC. CSs with an optimal molecular weight demonstrate good development prospects for ameliorating UC.
•The therapeutic effects of chitosans against UC vary with molecular weight.•Chitosans inhibit inflammatory cytokines, regulate immunoglobulin, and alter intestinal flora.•Higher molecular weight chitosans are more beneficial than lower weight ones.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>34748786</pmid><doi>10.1016/j.ijbiomac.2021.11.024</doi><tpages>10</tpages></addata></record> |
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subjects | Animals Anti-Inflammatory Agents - pharmacology Anti-inflammatory mechanism Cell Line Chitosan Chitosan - pharmacology Colitis, Ulcerative - drug therapy Colitis, Ulcerative - metabolism Colitis, Ulcerative - microbiology Cytokines - metabolism Disease Models, Animal Gastrointestinal Microbiome - drug effects Inflammation - drug therapy Inflammation - metabolism Inflammation Mediators - metabolism Intestinal flora Male Mice Mice, Inbred ICR Molecular Weight RAW 264.7 Cells Ulcerative colitis |
title | Effects of molecular weight of chitosan on anti-inflammatory activity and modulation of intestinal microflora in an ulcerative colitis model |
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