Paeoniae radix alba polysaccharides obtained via optimized extraction treat experimental autoimmune hepatitis effectively
The extraction process of Paeoniae radix alba polysaccharides (PRAP) was optimized as the liquid-solid ratio of 10.65 mL/g, the extraction time of 2.10 h, and the 2 extraction repetitions through a response surface methodology. The chemical profiles of the obtained PRAP were characterized by measuri...
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Veröffentlicht in: | International journal of biological macromolecules 2020-12, Vol.164, p.1554-1564 |
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creator | Wang, Siyu Xu, Jiazhi Wang, Changfu Li, Jianchun Wang, Qiuhong Kuang, Haixue Yang, Bingyou Chen, Rongying Luo, Zhongwen |
description | The extraction process of Paeoniae radix alba polysaccharides (PRAP) was optimized as the liquid-solid ratio of 10.65 mL/g, the extraction time of 2.10 h, and the 2 extraction repetitions through a response surface methodology. The chemical profiles of the obtained PRAP were characterized by measuring the contents of total carbohydrates, total phenolics, uronic acid and protein, and by analyzing the FT-IR spectrum and monosaccharide composition. To determine the therapeutic effects of PRAP on experimental autoimmune hepatitis (EAH), we established an EAH mice model. After treated with PRAP, liver and spleen injuries were reduced, and hepatocyte regeneration and liver function were improved. Further study of the mechanism by which PRAP treats EAH showed that PRAP significantly inhibited oxidative stress in the livers of EAH model mice. More importantly, PRAP inhibited immune inflammatory reactions in EAH model mice, including the hepatic infiltration of inflammatory CD4+ and CD8+ T cells, as well as overexpression of inflammatory cytokines IL-2, IL-6 and IL-10, via inhibition of the NF-κB signaling pathway.
•The optimal extraction process of PRAP has been determined by response surface methodology.•PRAP could recover the liver function and damages of EAH mice.•PRAP treat EAH in mice by inhibiting immune inflammatory reaction. |
doi_str_mv | 10.1016/j.ijbiomac.2020.07.214 |
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•The optimal extraction process of PRAP has been determined by response surface methodology.•PRAP could recover the liver function and damages of EAH mice.•PRAP treat EAH in mice by inhibiting immune inflammatory reaction.</description><identifier>ISSN: 0141-8130</identifier><identifier>EISSN: 1879-0003</identifier><identifier>DOI: 10.1016/j.ijbiomac.2020.07.214</identifier><identifier>PMID: 32735927</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Animals ; Carbohydrates - pharmacology ; CD4-Positive T-Lymphocytes - drug effects ; CD4-Positive T-Lymphocytes - metabolism ; CD8-Positive T-Lymphocytes - drug effects ; CD8-Positive T-Lymphocytes - metabolism ; Cytokines - metabolism ; Disease Models, Animal ; Drugs, Chinese Herbal - pharmacology ; Experimental autoimmune hepatitis ; Extraction process ; Hepatitis, Autoimmune - drug therapy ; Hepatitis, Autoimmune - metabolism ; Hepatocytes - drug effects ; Hepatocytes - metabolism ; Inflammation - drug therapy ; Inflammation - metabolism ; Liver - drug effects ; Liver - metabolism ; Male ; Mice ; Oxidative Stress - drug effects ; Paeonia - chemistry ; Paeoniae radix alba polysaccharides ; Phenols - pharmacology ; Polysaccharides - pharmacology ; Signal Transduction - drug effects ; Spleen - drug effects ; Spleen - metabolism ; Uronic Acids - pharmacology</subject><ispartof>International journal of biological macromolecules, 2020-12, Vol.164, p.1554-1564</ispartof><rights>2020 Elsevier B.V.</rights><rights>Copyright © 2020 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c368t-98dfe52756dc9c3efd0e7d05a0853fb11fde36a85ff1b8310eadb7fa59e6c3023</citedby><cites>FETCH-LOGICAL-c368t-98dfe52756dc9c3efd0e7d05a0853fb11fde36a85ff1b8310eadb7fa59e6c3023</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0141813020339763$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65534</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32735927$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Siyu</creatorcontrib><creatorcontrib>Xu, Jiazhi</creatorcontrib><creatorcontrib>Wang, Changfu</creatorcontrib><creatorcontrib>Li, Jianchun</creatorcontrib><creatorcontrib>Wang, Qiuhong</creatorcontrib><creatorcontrib>Kuang, Haixue</creatorcontrib><creatorcontrib>Yang, Bingyou</creatorcontrib><creatorcontrib>Chen, Rongying</creatorcontrib><creatorcontrib>Luo, Zhongwen</creatorcontrib><title>Paeoniae radix alba polysaccharides obtained via optimized extraction treat experimental autoimmune hepatitis effectively</title><title>International journal of biological macromolecules</title><addtitle>Int J Biol Macromol</addtitle><description>The extraction process of Paeoniae radix alba polysaccharides (PRAP) was optimized as the liquid-solid ratio of 10.65 mL/g, the extraction time of 2.10 h, and the 2 extraction repetitions through a response surface methodology. The chemical profiles of the obtained PRAP were characterized by measuring the contents of total carbohydrates, total phenolics, uronic acid and protein, and by analyzing the FT-IR spectrum and monosaccharide composition. To determine the therapeutic effects of PRAP on experimental autoimmune hepatitis (EAH), we established an EAH mice model. After treated with PRAP, liver and spleen injuries were reduced, and hepatocyte regeneration and liver function were improved. Further study of the mechanism by which PRAP treats EAH showed that PRAP significantly inhibited oxidative stress in the livers of EAH model mice. More importantly, PRAP inhibited immune inflammatory reactions in EAH model mice, including the hepatic infiltration of inflammatory CD4+ and CD8+ T cells, as well as overexpression of inflammatory cytokines IL-2, IL-6 and IL-10, via inhibition of the NF-κB signaling pathway.
•The optimal extraction process of PRAP has been determined by response surface methodology.•PRAP could recover the liver function and damages of EAH mice.•PRAP treat EAH in mice by inhibiting immune inflammatory reaction.</description><subject>Animals</subject><subject>Carbohydrates - pharmacology</subject><subject>CD4-Positive T-Lymphocytes - drug effects</subject><subject>CD4-Positive T-Lymphocytes - metabolism</subject><subject>CD8-Positive T-Lymphocytes - drug effects</subject><subject>CD8-Positive T-Lymphocytes - metabolism</subject><subject>Cytokines - metabolism</subject><subject>Disease Models, Animal</subject><subject>Drugs, Chinese Herbal - pharmacology</subject><subject>Experimental autoimmune hepatitis</subject><subject>Extraction process</subject><subject>Hepatitis, Autoimmune - drug therapy</subject><subject>Hepatitis, Autoimmune - metabolism</subject><subject>Hepatocytes - drug effects</subject><subject>Hepatocytes - metabolism</subject><subject>Inflammation - drug therapy</subject><subject>Inflammation - metabolism</subject><subject>Liver - drug effects</subject><subject>Liver - metabolism</subject><subject>Male</subject><subject>Mice</subject><subject>Oxidative Stress - drug effects</subject><subject>Paeonia - chemistry</subject><subject>Paeoniae radix alba polysaccharides</subject><subject>Phenols - pharmacology</subject><subject>Polysaccharides - pharmacology</subject><subject>Signal Transduction - drug effects</subject><subject>Spleen - drug effects</subject><subject>Spleen - metabolism</subject><subject>Uronic Acids - pharmacology</subject><issn>0141-8130</issn><issn>1879-0003</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE9v1DAQxS0EokvhK1Q-cknwn03s3EAVBaRKcICzNbHHqldJHGxn1eXT49W2XDmN5um9Gb0fITectZzx_sOhDYcxxBlsK5hgLVOt4PsXZMe1GhrGmHxJdozveaO5ZFfkTc6HqvYd16_JlRRKdoNQO3L6ARiXAEgTuPBIYRqBrnE6ZbD2AVJwmGkcC4QFHT0GoHEtYQ5_6oaPJYEtIS60JIRShRVTmHEpMFHYSgzzvC1IH3CFEkrIFL3HmjjidHpLXnmYMr57mtfk193nn7dfm_vvX77dfrpvrOx1aQbtPHZCdb2zg5XoHUPlWAdMd9KPnHuHsgfdec9HLTlDcKPy0A3YW8mEvCbvL3fXFH9vmIuZQ7Y4TbBg3LIRezEozZQ4W_uL1aaYc0Jv1loH0slwZs7YzcE8Yzdn7IYpU7HX4M3Tj22c0f2LPXOuho8XA9amx4DJZBtwsehCqkCMi-F_P_4C9KObig</recordid><startdate>20201201</startdate><enddate>20201201</enddate><creator>Wang, Siyu</creator><creator>Xu, Jiazhi</creator><creator>Wang, Changfu</creator><creator>Li, Jianchun</creator><creator>Wang, Qiuhong</creator><creator>Kuang, Haixue</creator><creator>Yang, Bingyou</creator><creator>Chen, Rongying</creator><creator>Luo, Zhongwen</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>20201201</creationdate><title>Paeoniae radix alba polysaccharides obtained via optimized extraction treat experimental autoimmune hepatitis effectively</title><author>Wang, Siyu ; Xu, Jiazhi ; Wang, Changfu ; Li, Jianchun ; Wang, Qiuhong ; Kuang, Haixue ; Yang, Bingyou ; Chen, Rongying ; Luo, Zhongwen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c368t-98dfe52756dc9c3efd0e7d05a0853fb11fde36a85ff1b8310eadb7fa59e6c3023</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Animals</topic><topic>Carbohydrates - pharmacology</topic><topic>CD4-Positive T-Lymphocytes - drug effects</topic><topic>CD4-Positive T-Lymphocytes - metabolism</topic><topic>CD8-Positive T-Lymphocytes - drug effects</topic><topic>CD8-Positive T-Lymphocytes - metabolism</topic><topic>Cytokines - metabolism</topic><topic>Disease Models, Animal</topic><topic>Drugs, Chinese Herbal - pharmacology</topic><topic>Experimental autoimmune hepatitis</topic><topic>Extraction process</topic><topic>Hepatitis, Autoimmune - drug therapy</topic><topic>Hepatitis, Autoimmune - metabolism</topic><topic>Hepatocytes - drug effects</topic><topic>Hepatocytes - metabolism</topic><topic>Inflammation - drug therapy</topic><topic>Inflammation - metabolism</topic><topic>Liver - drug effects</topic><topic>Liver - metabolism</topic><topic>Male</topic><topic>Mice</topic><topic>Oxidative Stress - drug effects</topic><topic>Paeonia - chemistry</topic><topic>Paeoniae radix alba polysaccharides</topic><topic>Phenols - pharmacology</topic><topic>Polysaccharides - pharmacology</topic><topic>Signal Transduction - drug effects</topic><topic>Spleen - drug effects</topic><topic>Spleen - metabolism</topic><topic>Uronic Acids - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Siyu</creatorcontrib><creatorcontrib>Xu, Jiazhi</creatorcontrib><creatorcontrib>Wang, Changfu</creatorcontrib><creatorcontrib>Li, Jianchun</creatorcontrib><creatorcontrib>Wang, Qiuhong</creatorcontrib><creatorcontrib>Kuang, Haixue</creatorcontrib><creatorcontrib>Yang, Bingyou</creatorcontrib><creatorcontrib>Chen, Rongying</creatorcontrib><creatorcontrib>Luo, Zhongwen</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>Wang, Siyu</au><au>Xu, Jiazhi</au><au>Wang, Changfu</au><au>Li, Jianchun</au><au>Wang, Qiuhong</au><au>Kuang, Haixue</au><au>Yang, Bingyou</au><au>Chen, Rongying</au><au>Luo, Zhongwen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Paeoniae radix alba polysaccharides obtained via optimized extraction treat experimental autoimmune hepatitis effectively</atitle><jtitle>International journal of biological macromolecules</jtitle><addtitle>Int J Biol Macromol</addtitle><date>2020-12-01</date><risdate>2020</risdate><volume>164</volume><spage>1554</spage><epage>1564</epage><pages>1554-1564</pages><issn>0141-8130</issn><eissn>1879-0003</eissn><abstract>The extraction process of Paeoniae radix alba polysaccharides (PRAP) was optimized as the liquid-solid ratio of 10.65 mL/g, the extraction time of 2.10 h, and the 2 extraction repetitions through a response surface methodology. The chemical profiles of the obtained PRAP were characterized by measuring the contents of total carbohydrates, total phenolics, uronic acid and protein, and by analyzing the FT-IR spectrum and monosaccharide composition. To determine the therapeutic effects of PRAP on experimental autoimmune hepatitis (EAH), we established an EAH mice model. After treated with PRAP, liver and spleen injuries were reduced, and hepatocyte regeneration and liver function were improved. Further study of the mechanism by which PRAP treats EAH showed that PRAP significantly inhibited oxidative stress in the livers of EAH model mice. More importantly, PRAP inhibited immune inflammatory reactions in EAH model mice, including the hepatic infiltration of inflammatory CD4+ and CD8+ T cells, as well as overexpression of inflammatory cytokines IL-2, IL-6 and IL-10, via inhibition of the NF-κB signaling pathway.
•The optimal extraction process of PRAP has been determined by response surface methodology.•PRAP could recover the liver function and damages of EAH mice.•PRAP treat EAH in mice by inhibiting immune inflammatory reaction.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>32735927</pmid><doi>10.1016/j.ijbiomac.2020.07.214</doi><tpages>11</tpages></addata></record> |
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subjects | Animals Carbohydrates - pharmacology CD4-Positive T-Lymphocytes - drug effects CD4-Positive T-Lymphocytes - metabolism CD8-Positive T-Lymphocytes - drug effects CD8-Positive T-Lymphocytes - metabolism Cytokines - metabolism Disease Models, Animal Drugs, Chinese Herbal - pharmacology Experimental autoimmune hepatitis Extraction process Hepatitis, Autoimmune - drug therapy Hepatitis, Autoimmune - metabolism Hepatocytes - drug effects Hepatocytes - metabolism Inflammation - drug therapy Inflammation - metabolism Liver - drug effects Liver - metabolism Male Mice Oxidative Stress - drug effects Paeonia - chemistry Paeoniae radix alba polysaccharides Phenols - pharmacology Polysaccharides - pharmacology Signal Transduction - drug effects Spleen - drug effects Spleen - metabolism Uronic Acids - pharmacology |
title | Paeoniae radix alba polysaccharides obtained via optimized extraction treat experimental autoimmune hepatitis effectively |
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