2019
DOI: 10.1016/j.foodhyd.2018.09.013
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Neuroimmunoregulatory potential of seleno-polymannuronate derived from alginate in lipopolysaccharide-stimulated BV2 microglia

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Cited by 12 publications
(4 citation statements)
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“…Selenylated alginate‐derived polymannuronate (Se‐PM) showed significantly higher neuroimmunoregulatory effect compared with native PM (Bi et al., 2019). In lipopolysaccharide (LPS)‐induced microglia, Se‐PM significantly attenuated the secretion of prostaglandin E2 and NO, expression of cyclooxygenase‐2 and inducible nitric oxide synthase (iNOS), and release of IL‐1β, IL‐12, IL‐6, and TNF‐α by overactivation of MAPK and NF‐κB signaling pathways.…”
Section: Biological Properties Structure‐activity Relationship and Un...mentioning
confidence: 99%
“…Selenylated alginate‐derived polymannuronate (Se‐PM) showed significantly higher neuroimmunoregulatory effect compared with native PM (Bi et al., 2019). In lipopolysaccharide (LPS)‐induced microglia, Se‐PM significantly attenuated the secretion of prostaglandin E2 and NO, expression of cyclooxygenase‐2 and inducible nitric oxide synthase (iNOS), and release of IL‐1β, IL‐12, IL‐6, and TNF‐α by overactivation of MAPK and NF‐κB signaling pathways.…”
Section: Biological Properties Structure‐activity Relationship and Un...mentioning
confidence: 99%
“…The modification of the carboxyl group in the C6 position of alginate is usually through esterification or amino reaction to introduce long alkyl groups or fatty acids, which makes alginate become amphiphilic molecules [31,32]. On the other hand, the hydroxyl group can be modified by sulfation [33,34], phosphorylation [35,36] and selenization [37][38][39][40] to improve the bioactivity of alginate. Due to the distribution of a large number of hydroxyl and carboxyl groups in the main chain of alginate, it can be easily chemically modified to improve its characteristics.…”
Section: Structure Derivatization and Analysismentioning
confidence: 99%
“…The protein expression in N2a-sw cells after treated respectively by PM, S-PM, and Se-PM, was determined using Western blot analysis as described previously (Bi et al, 2019). The cells were lysed on ice with RIPA buffer containing a protease and phosphatase inhibitor cocktail (Selleck, Shanghai, China).…”
Section: Western Blot Analysismentioning
confidence: 99%