Onosma glomeratum Y. L. Liu polysaccharide alleviates LPS-induced pulmonary inflammation via NF-κB signal pathway
As a traditional Chinese medicinal and edible homologous plant, Onosma glomeratum Y. L. Liu has been used for treating lung diseases in Tibet. In this study, a pectin polysaccharide, OGY-LLPA, with a molecular weight of 62,184 Da, was isolated and characterized by GC–MS and NMR analysis. It mainly c...
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Veröffentlicht in: | International journal of biological macromolecules 2024-04, Vol.263 (Pt 2), p.130452-130452, Article 130452 |
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Sprache: | eng |
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Zusammenfassung: | As a traditional Chinese medicinal and edible homologous plant, Onosma glomeratum Y. L. Liu has been used for treating lung diseases in Tibet. In this study, a pectin polysaccharide, OGY-LLPA, with a molecular weight of 62,184 Da, was isolated and characterized by GC–MS and NMR analysis. It mainly consists of galacturonic acid (GalA), galactose (Gal), rhamnose (Rha), and arabinose (Ara), with a linear main chain of galacturonic acid (homogalacturonan, HG) inserted by part of rhamnose galacturonic acid (rhamnogalacturonan, RG), attaching with arabinogalactan (AG) branches at RG-I. Both in the LPS-induced A549 cell model and LPS-induced pneumonia mouse model, OGY-LLPA demonstrated strong anti-inflammatory effects, even comparable to DEX, indicating its potential as an anti-pneumonia candidate agent. Moreover, low-dose OGY-LLPA alleviated LPS-induced pulmonary inflammation by inhibiting the NF-κB signaling pathway. Overall, these findings could not only contribute to the utilization of Onosma glomeratum Y. L. Liu., but also provides a theoretical basis for the treatment of inflammation-related diseases.
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•A pectin polysaccharide, OGY-LLPA, was isolated from Onosma glomeratum Y. L. Liu.•It mainly consists of galactose uronic acid, galactose, rhamnose, and arabinose, with Mw of 62,184 Da.•It had a linear main chain of galacturonic acid inserted by part of rhamnose galacturonic acid.•It exhibited strong protective effects on both in vitro and in vivo pneumonia model.•It alleviated LPS-induced pulmonary inflammation by inhibiting the NF-κB signaling pathway. |
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ISSN: | 0141-8130 1879-0003 |
DOI: | 10.1016/j.ijbiomac.2024.130452 |