首页> 外文期刊>International Journal of Biological Macromolecules: Structure, Function and Interactions >Isolation, structural characterization of polysaccharide from Cephalosporium sinensis mycelia and its anti-nephritic effects in adenine-induced CKD rats
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Isolation, structural characterization of polysaccharide from Cephalosporium sinensis mycelia and its anti-nephritic effects in adenine-induced CKD rats

机译:来自头孢菌孢菌菌丝体的多糖结构表征及其在腺嘌呤诱导的CKD大鼠中的抗肾病效应

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In this study, a new polysaccharide (CSMP, Mw = 16,685 Da) was isolated and purified from Cephalosporium sinensis mycelia. Monosaccharide composition analysis indicated that CSMP consists of mannose, glucose and galactose. A detailed structural analysis revealed that CSMP has a backbone consisting of -> 2,6)-beta-D-Manp-(1 -> and -> 3,6)-beta-D-Manp-(1 ->, as well as two branched chains including of alpha-D-Manp-(1 -> 6)-alpha-D-Glcp-(1 -> and alpha-D-Glcp-(1 -> 4)-alpha-D-Glcp-(1 -> 3)-beta-D-Galp-(1 -> 2)-beta-D-Manp-(1 -> attached to C6 of -> 2,6)-beta-D-Manp-(1 -> and -> 3,6)-beta-D-Manp-(1 ->. Orally administrated CSMP showed renal protection function in adenine-induced chronic kidney disease (CKD) rats. Further analysis demonstrated that CSMP increased relative abundance of the genera Lactobacillus group, Clostridium coccoides group and Bifidobacterium, and decreased Echerichia subgroup. CSMP increased acetate, propionate and butyrate levels both in colon and cecum. The mechanisms behind these effects could be related to the down-regulation nuclear factor kappa-B (NF-kappa B) level by up-regulating expression of G protein-coupled receptor 41 (GPR41) and improvement regulatory T cells (Tregs) ratio by inhibiting histone deacetylase (HDAC) activity. These results indicated that CSMP could be developed as one of the potential drugs in the treatment of CKD. (C) 2020 Published by Elsevier B.V.
机译:在该研究中,分离出一种新的多糖(CSMP,MW = 16,685Da),并从头孢菌孢子菌丝体纯化。单糖组成分析表明CSMP由甘露糖,葡萄糖和半乳糖组成。详细的结构分析表明,CSMP具有由 - > 2,6)-beta-d-manp-(1 - >和 - > 3,6)-beta-d-manp-(1 - >)组成的骨架作为两个分支链,包括α-D-MANP-(1 - > 6) - alpha-d-glcp-(1 - >和alpha-d-glcp-(1 - > 4)-alpha-d-glcp-( 1 - > 3)-beta-d-galp-(1 - > 2)-beta-d-manp-(1 - >连接到C6 - > 2,6)-beta-d-manp-(1 - > - > 3,6)-beta-d-manp-(1 - >。口服给药的csmp在腺嘌呤诱导的慢性肾病(CKD)大鼠中显示出肾脏保护功能。进一步的分析表明,CSMP增加了Genera乳酸杆菌的相对丰度组,Coccoides组和双歧杆菌,和肌胞间亚组减少。CSMP在结肠和盲肠中增加醋酸盐,丙酸盐和丁酸盐水平。这些效果背后的机制可能与下调核因子Kappa-B(NF-Kappa B )通过上调节G蛋白偶联受体41(GPR41)和改善调节T细胞(Tregs)比率的水平通过抑制组蛋白脱乙酰化酶(HDAC)活性。这些结果表明,CSMP可以作为治疗CKD治疗中的潜在药物之一。 (c)2020由elsevier b.v发布。

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