Suppr超能文献

哇巴因在小鼠体内的抗炎和镇痛活性。

Anti-inflammatory and antinociceptive activity of ouabain in mice.

机构信息

Laboratório de Tecnologia Farmacêutica, Departamento de Fisiologia e Patologia, Centro de Ciências da Saúde, Universidade Federal da Paraíba, João Pessoa 58059-900, Brazil.

出版信息

Mediators Inflamm. 2011;2011:912925. doi: 10.1155/2011/912925. Epub 2011 May 26.

Abstract

Ouabain, an inhibitor of the Na(+)/K(+)-ATPase pump, was identified as an endogenous substance of human plasma. Ouabain has been studied for its ability to interfere with various regulatory mechanisms. Despite the studies portraying the ability of ouabain to modulate the immune response, little is known about the effect of this substance on the inflammatory process. The aim of this work was to study the effects triggered by ouabain on inflammation and nociceptive models. Ouabain produced a reduction in the mouse paw edema induced by carrageenan, compound 48/80 and zymosan. This anti-inflammatory potential might be related to the inhibition of prostaglandin E2, bradykinin, and mast-cell degranulation but not to histamine. Ouabain also modulated the inflammation induced by concanavalin A by inhibiting cell migration. Besides that, ouabain presented antinociceptive activity. Taken these data together, this work demonstrated, for the first time, that ouabain presented in vivo analgesic and anti-inflammatory effects.

摘要

哇巴因是 Na(+)/K(+)-ATP 酶泵的抑制剂,被鉴定为人血浆中的内源性物质。哇巴因因其干扰各种调节机制的能力而被研究。尽管研究表明哇巴因能够调节免疫反应,但人们对这种物质对炎症过程的影响知之甚少。本工作旨在研究哇巴因对炎症和痛觉模型的触发作用。哇巴因可减少角叉菜胶、化合物 48/80 和酵母聚糖诱导的小鼠爪肿胀。这种抗炎潜力可能与抑制前列腺素 E2、缓激肽和肥大细胞脱颗粒有关,但与组胺无关。哇巴因还通过抑制细胞迁移来调节伴刀豆球蛋白 A 诱导的炎症。此外,哇巴因具有镇痛活性。综上所述,这项工作首次证明哇巴因具有体内镇痛和抗炎作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c425/3136139/53ecfa0b4a30/MI2011-912925.001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验