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双孢蘑菇褐藻糖胶:结构特征和药理作用研究。

Agaricus bisporus fucogalactan: structural characterization and pharmacological approaches.

机构信息

Departamento de Bioquímica e Biologia Molecular, Universidade Federal do Paraná, CP 19046, CEP 81531-980, Curitiba, PR, Brazil.

出版信息

Carbohydr Polym. 2013 Jan 30;92(1):184-91. doi: 10.1016/j.carbpol.2012.08.071. Epub 2012 Aug 24.

Abstract

The fucogalactan from Agaricus bisporus (EFP-Ab) obtained on aqueous extraction followed by purification had M(w) 37.1 × 10(4)g mol(-1) relative to a (1→6)-linked α-D-Galp main-chain partially methylated at HO-3, and partially substituted at O-2 by nonreducing end-units of α-L-Fucp or β-d-Galp. EFP-Ab also inhibited significantly the neurogenic and inflammatory phases of formalin-induced licking, however, the antinociceptive effect was more pronounced against the inflammatory phase with ID(50) of 36.0 (25.8-50.3)mg kg(-1). In addition, EFP-Ab decreased the lethality induced by CLP. Its administration reduced the late mortality rate by 40%, prevented neutrophil accumulation in lungs and markedly decreased iNOS and COX-2 protein expression by ileum cells. These data show for the first time that EFP-Ab has significant anti-sepsis, antinociceptive and anti-inflammatory actions, which seems to be related to the decreased iNOS and COX-2 expression. Collectively, the present results demonstrate that EFP-Ab could constitute an attractive molecule of interest for the development of new drugs.

摘要

从双孢蘑菇(EFP-Ab)的水提物中提取并经纯化得到的岩藻半乳聚糖,其重均分子量(M(w))为 37.1×10(4)g/mol,相对于(1→6)-连接的α-D-Galp 主链,HO-3 处部分甲基化,O-2 处被非还原端单元的α-L-Fucp 或β-d-Galp 部分取代。EFP-Ab 还显著抑制福尔马林诱导的舔舐的神经源性和炎症性阶段,然而,其对炎症阶段的镇痛作用更为明显,ID(50)为 36.0(25.8-50.3)mg/kg。此外,EFP-Ab 降低了 CLP 诱导的致死率。其给药可使晚期死亡率降低 40%,防止中性粒细胞在肺部聚集,并显著降低回肠细胞中 iNOS 和 COX-2 蛋白的表达。这些数据首次表明,EFP-Ab 具有显著的抗败血症、镇痛和抗炎作用,这似乎与 iNOS 和 COX-2 表达的降低有关。总之,目前的结果表明,EFP-Ab 可能成为开发新药的有吸引力的候选分子。

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