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首页> 外文期刊>Carbohydrate Polymers: Scientific and Technological Aspects of Industrially Important Polysaccharides >Cultured Cordyceps sinensis polysaccharides modulate intestinal mucosal immunity and gut microbiota in cyclophosphamide-treated mice
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Cultured Cordyceps sinensis polysaccharides modulate intestinal mucosal immunity and gut microbiota in cyclophosphamide-treated mice

机译:培养的冬虫夏草多糖调节环磷酰胺处理小鼠中的肠粘膜免疫和肠道微生物

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摘要

The present study aimed to investigate the protective effect of cultured Cordyceps sinensis polysaccharides (CSP) on cyclophosphamide (Cy)-induced intestinal mucosal immunosuppression and microbial dysbiosis in mice. Results showed that CSP stimulated cytokines secretion (IL-12, IFN-gamma, IL-4, IL-13, IL-6, IL-17, IL-10, TGF-beta 3, TNF-alpha, IL-2, IL-21) and transcription factors production (T-bet, GATA-3, ROR gamma t, Foxp3). TLRs (TLR-2, TLR-4, TLR-6) and NF-kappa B pathway key proteins (p-I kappa B-alpha, NF-kappa B p65) were also upregulated after CSP administration. Moreover, CSP recovered SCFAs levels which decreased by Cy treatment. Furthermore, 16S rRNA sequencing of fecal samples was performed. alpha-diversity and beta-diversity analysis revealed CSP improved microbial community diversity and modulated the overall structure of gut microbiota. Taxonomic composition analysis found that CSP increased the abundance of probiotics (Lactobacillus, Bifidobacterium, Bacteroides) and decreased pathogenic bacteria (Clostridium, Flexispira). These findings suggested the potential of CSP as a prebiotics to reduce side effects of Cy on intestinal mucosal immunity and gut microbiota.
机译:本研究旨在探讨培养的冬虫夏草(CSP)对小鼠环磷酰胺(CY)诱导的肠道粘膜免疫抑制和微生物消带病毒的保护作用。结果表明,CSP刺激细胞因子分泌(IL-12,IFN-γ,IL-4,IL-13,IL-6,IL-17,IL-10,TGF-β3,TNF-α,IL-2,IL -21)和转录因子生产(T-BET,GATA-3,ROR Gamma T,Foxp3)。 CSP给药后,还上调TLRS(TLR-2,TLR-4,TLR-6)和NF-Kappa途径键蛋白(P-I Kappa B-α,NF-Kappa B P65)。此外,CSP回收了Cy治疗减少的SCFA水平。此外,进行粪便样品的16S rRNA测序。 α-多样性和β-多样性分析显示CSP改善的微生物群落多样性,并调节了肠道微生物的整体结构。分类组成分析发现,CSP增加了益生菌(乳杆菌,双歧杆菌,诱导)和降低的致病菌(Clostridium,Flexispira)的丰富。这些发现表明CSP作为益生元的潜力,以减少Cy对肠粘膜免疫和肠道微生物症的副作用。

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