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海滨莲子草提取物和2″-O-α-L-鼠李糖基牡荆素对小鼠的抗痛觉过敏和抗炎活性

Anti-hyperalgesic and Anti-inflammatory Activity of Alternanthera Maritima Extract and 2″-O-α-L-rhamnopyranosylvitexin in Mice.

作者信息

de Santana Aquino Diana Figuereido, Piccinelli Ana Claudia, Soares Fabíola Lacerda Pires, Arena Arielle Cristina, Salvador Marcos José, Kassuya Candida Aparecida Leite

机构信息

College of Health Science, Federal University of Grande Dourados, Dourados, 79825-070, MS, Brazil.

Department of Morphology, Institute of Biosciences of Botucatu, São Paulo State University (UNESP), Botucatu, SP, Brazil.

出版信息

Inflammation. 2015 Dec;38(6):2057-66. doi: 10.1007/s10753-015-0187-0.

DOI:10.1007/s10753-015-0187-0
PMID:26045342
Abstract

Alternanthera maritima are used in Brazilian popular medicine for the treatment of inflammatory and infectious diseases. Species of Alternanthera have demonstrated biological activities in previous scientific studies. The aim of this study was to determine whether the ethanol extract of the aerial parts of A. maritima (EEAM) and the isolated compound 2″-O-α-L-rhamnopyranosyl-vitexin inhibit mechanical hyperalgesia and parameters of inflammation in mice. The oral administration of EEAM significantly inhibited carrageenan (Cg)-induced paw edema and reduced leukocyte migration into the pleural cavity. 2″-O-α-L-rhamnopyranosylvitexin significantly inhibited paw edema and reduced both leukocyte migration and the leakage of protein into the pleural cavity. Both EEAM and 2″-O-α-L-rhamnopyranosylvitexin significantly prevented the Cg-induced hyperalgesia. Local administration of 2″-O-α-L-rhamnopyranosylvitexin significantly prevented the Cg- and tumor necrosis factor (TNF)-induced hyperalgesia. In conclusion, this study demonstrated that EEAM is an anti-inflammatory and anti-hyperalgesic agent, and the results suggested that 2″-O-α-L-rhamnopyranosylvitexin is responsible for the effects of EEAM and the mechanism involves the TNF pathway.

摘要

滨海莲子草在巴西民间医学中用于治疗炎症和传染病。在先前的科学研究中,莲子草属植物已表现出生物活性。本研究的目的是确定滨海莲子草地上部分的乙醇提取物(EEAM)和分离出的化合物2″-O-α-L-鼠李糖基牡荆素是否能抑制小鼠的机械性痛觉过敏和炎症参数。口服EEAM可显著抑制角叉菜胶(Cg)诱导的爪肿胀,并减少白细胞向胸腔的迁移。2″-O-α-L-鼠李糖基牡荆素可显著抑制爪肿胀,并减少白细胞迁移和蛋白质向胸腔的渗漏。EEAM和2″-O-α-L-鼠李糖基牡荆素均能显著预防Cg诱导的痛觉过敏。局部施用2″-O-α-L-鼠李糖基牡荆素可显著预防Cg和肿瘤坏死因子(TNF)诱导的痛觉过敏。总之,本研究表明EEAM是一种抗炎和抗痛觉过敏剂,结果表明2″-O-α-L-鼠李糖基牡荆素是EEAM发挥作用的原因,其机制涉及TNF途径。

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