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金银花多糖对模型大鼠的降血尿酸及抗痛风性关节炎作用。

Anti-hyperuricemic and anti-gouty arthritis activities of polysaccharide purified from Lonicera japonica in model rats.

机构信息

Department of Pharmaceutics, School of Pharmacy, Center for Nano Drug/Gene Delivery and Tissue Engineering, Jiangsu University, Zhenjiang 212013, PR China.

Department of Pharmaceutics, School of Pharmacy, Center for Nano Drug/Gene Delivery and Tissue Engineering, Jiangsu University, Zhenjiang 212013, PR China.

出版信息

Int J Biol Macromol. 2019 Feb 15;123:801-809. doi: 10.1016/j.ijbiomac.2018.11.077. Epub 2018 Nov 13.

Abstract

In this present study, we investigated the anti-hyperuricemic and anti-gouty arthritis effect of a puried water-soluble polysaccharide (LJP-1) obtained from Lonicera japonica. A series of characterization of the purified polysaccharide were carried out in this paper. Monosaccharide analysis showed that LJP-1 composed of glucuronic acid, glucose, galactose, arabinose, and xylose at the ratio of 2.43:1:2.09:1.95:1.96, respectively. The estimated molecular weight of LJP-1 was 17.5 kDa. LJP-1 belonged to pyranose and possessed α- and β -glycosidic configurations. Congo red test showed that LJP-1 had a spatial triple helix structure. In pharmacodynamic experiments, the anti-hyperuricemic activity of LJP-1 was studied using hyperuricemic SD rat model induced via potassium oxonate and hypoxanthine. The result showed that LJP-1 could obviously decrease the serum uric acid level and suppress xanthine oxidase (XOD) activity. Moreover, in the gouty arthritis model established by sodium urate crystals, the degree of swelling of the ankle joint, IL-1β, IL-6, TNF-α and COX-2-related inflammatory factors levels in murine serum all declined. Taken together, these results demonstrated that LJP-1 has anti-gouty arthritis effect. Therefore, LJP-1 could serve as a promising candidate for developing novel natural anti-gouty agent.

摘要

在本研究中,我们研究了从忍冬中提取的一种纯化水溶性多糖(LJP-1)的抗高尿酸血症和抗痛风性关节炎作用。本文对纯化多糖进行了一系列的表征。单糖分析表明,LJP-1 由葡萄糖醛酸、葡萄糖、半乳糖、阿拉伯糖和木糖组成,摩尔比分别为 2.43:1:2.09:1.95:1.96。LJP-1 的估计分子量为 17.5 kDa。LJP-1 属于吡喃糖,具有α-和β-糖苷键构型。刚果红试验表明 LJP-1 具有空间三螺旋结构。在药效学实验中,采用氧嗪酸钾和次黄嘌呤诱导的高尿酸血症 SD 大鼠模型研究了 LJP-1 的抗高尿酸血症活性。结果表明,LJP-1 能明显降低血清尿酸水平,抑制黄嘌呤氧化酶(XOD)活性。此外,在尿酸盐晶体建立的痛风性关节炎模型中,LJP-1 可降低小鼠血清中踝关节肿胀程度、IL-1β、IL-6、TNF-α 和 COX-2 相关炎症因子水平。综上所述,这些结果表明 LJP-1 具有抗痛风性关节炎作用。因此,LJP-1 可以作为开发新型天然抗痛风药物的有前途的候选物。

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