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dc.date.accessioned2023-03-06T18:25:32Z
dc.date.available2023-03-06T18:25:32Z
dc.date.created2022-11-17T12:46:34Z
dc.date.issued2022
dc.identifier.citationLi, Li-Xia Chen, Meng-Si Zhang, Zi-Yu Paulsen, Berit Smestad Rise, Frode Huang, Chao Feng, Bin Chen, Xing-Fu Jia, Ren-Yong Ding, Chun-Bang Feng, Shi-Ling Li, Yang-Ping Chen, Yu-Long Huang, Zhen Zhao, Xing-Hong Yin, Zhong-Qiong Zou, Yuanfeng . Structural features and antioxidant activities of polysaccharides from different parts of Codonopsis pilosula var. modesta (Nannf.) L. T. Shen. Frontiers in Pharmacology. 2022, 13, 937581
dc.identifier.urihttp://hdl.handle.net/10852/100953
dc.description.abstractIn this study, three acidic polysaccharides from different plant parts of Codonopsis pilosula var. Modesta (Nannf.) L. T. Shen were obtained by ion exchange chromatography and gel filtration chromatography, and the yields of these three polysaccharides were different. According to the preliminary experimental results, the antioxidant activities of the polysaccharides from rhizomes and fibrous roots (CLFP-1) were poor, and was thus not studied further. Due to this the structural features of polysaccharides from roots (CLRP-1) and aerial parts (CLSP-1) were the object for this study and were structurally characterized, and their antioxidant activities were evaluated. As revealed by the results, the molecular weight of CLRP-1and CLSP-1 were 15.9 kDa and 26.4 kDa, respectively. The monosaccharide composition of CLRP-1 was Ara , Rha, Fuc, Xyl, Man, Gal, GlcA, GalA in a ratio of 3.8: 8.4: 1.0: 0.8: 2.4: 7.4: 7.5: 2.0: 66.7, and Ara , Rha, Gal, GalA in a ratio of 5.8: 8.9: 8.0: 77.0 in for CLSP-1. The results of structural elucidation indicated that both CLRP-1 and CLSP-1 were pectic polysaccharides, mainly composed of 1, 4-linked galacturonic acid with long homogalacturonan regions. Arabinogalactan type I and arabinogalactan type II were presented as side chains. The antioxidant assay in IPEC-J2 cells showed that both CLRP-1 and CLSP-1 promoted cell viability and antioxidant activity, which significantly increase the level of total antioxidant capacity and the activity of superoxide dismutase, catalase, and decrease the content of malondialdehyde. Moreover, CLRP-1 and CLSP-1 also showed powerful antioxidant abilities in Caenorhabditis elegans and might regulate the nuclear localization of DAF-16 transcription factor, induced antioxidant enzymes activities, and further reduced reactive oxygen species and malondialdehyde contents to increase the antioxidant ability of Caenorhabditis elegans . Thus, these finding suggest that CLRP-1 and CLSP-1 could be used as potential antioxidants.
dc.languageEN
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.titleStructural features and antioxidant activities of polysaccharides from different parts of Codonopsis pilosula var. modesta (Nannf.) L. T. Shen
dc.title.alternativeENEngelskEnglishStructural features and antioxidant activities of polysaccharides from different parts of Codonopsis pilosula var. modesta (Nannf.) L. T. Shen
dc.typeJournal article
dc.creator.authorLi, Li-Xia
dc.creator.authorChen, Meng-Si
dc.creator.authorZhang, Zi-Yu
dc.creator.authorPaulsen, Berit Smestad
dc.creator.authorRise, Frode
dc.creator.authorHuang, Chao
dc.creator.authorFeng, Bin
dc.creator.authorChen, Xing-Fu
dc.creator.authorJia, Ren-Yong
dc.creator.authorDing, Chun-Bang
dc.creator.authorFeng, Shi-Ling
dc.creator.authorLi, Yang-Ping
dc.creator.authorChen, Yu-Long
dc.creator.authorHuang, Zhen
dc.creator.authorZhao, Xing-Hong
dc.creator.authorYin, Zhong-Qiong
dc.creator.authorZou, Yuanfeng
cristin.unitcode185,15,23,20
cristin.unitnameSeksjon for farmasøytisk kjemi
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.cristin2075563
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Frontiers in Pharmacology&rft.volume=13&rft.spage=937581&rft.date=2022
dc.identifier.jtitleFrontiers in Pharmacology
dc.identifier.volume13
dc.identifier.doihttps://doi.org/10.3389/fphar.2022.937581
dc.type.documentTidsskriftartikkel
dc.type.peerreviewedPeer reviewed
dc.source.issn1663-9812
dc.type.versionPublishedVersion
cristin.articleid937581
dc.relation.projectNFR/226244/F50
dc.relation.projectNFR/226244


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