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Anti-inflammatory effects of Salvia plebeia R. Br extract in vitro and in ovalbumin-induced mouse model

机译:丹参提取物的抗炎作用在体外和卵清蛋白诱导的小鼠模型中

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Asthma is an increasing global health problem, and novel strategies to prevent or ameliorate the condition are needed. Here, the effects of 80?% ethanol extracts of Salvia plebeia R. Br. (SE) on an induced inflammatory response were investigated. Salvia plebeia R. Br. inhibited production of pro-inflammatory cytokines, such as TNF-α and IL-6, as well as nitric oxide (NO) in LPS-stimulated RAW 264.7 cells. NO and pro-inflammatory cytokine production was suppressed more effectively by SE of the aerial parts (SE-A) than of the roots (SE-R) of S. plebeia. In BEAS-2B cells, both SE-A and SE-R inhibited the increase in production of the inflammatory cytokines IL-6 and IL-8. We also investigated the anti-asthmatic effects of SE in an ovalbumin (OVA)-induced BALB/c mouse model. SE-A treatment significantly reduced the number of airway eosinophils, IL-4 and IL-13 levels, mucus production, and inflammatory infiltration, as compared with the corresponding levels in the untreated, OVA-induced mice, and had similar effects to dexamethasone. Salvia plebeia ethanol extract ameliorated the induced inflammatory response in RAW 264.7 and BEAS-2B cells, with more effective inhibition noted for SE-A than for SE-R. SE-A treatment was effective in improving the histopathological changes in the lungs of asthma model mice via modulation of eosinophils and Th2 cytokines. These results suggest that SE-A can be considered as a therapeutic agent that can potentially relieve asthma.
机译:哮喘是一个日益严重的全球性健康问题,需要预防或改善这种状况的新策略。在这里,丹参80%乙醇提取物的作用。 (SE)对诱导的炎症反应进行了研究。丹参抑制LPS刺激的RAW 264.7细胞中促炎性细胞因子(例如TNF-α和IL-6)以及一氧化氮(NO)的产生。 SE和A.plebeia的根部(SE-R)能更有效地抑制NO和促炎性细胞因子的产生。在BEAS-2B细胞中,SE-A和SE-R均抑制炎性细胞因子IL-6和IL-8产量的增加。我们还研究了SE在卵清蛋白(OVA)诱导的BALB / c小鼠模型中的抗哮喘作用。与未经治疗的OVA诱发小鼠的相应水平相比,SE-A治疗显着减少了气道嗜酸性粒细胞的数量,IL-4和IL-13水平,粘液产生和炎性浸润,并且具有与地塞米松相似的作用。丹参紫菜乙醇提取物改善了RAW 264.7和BEAS-2B细胞中诱导的炎症反应,对SE-A的抑制作用比对SE-R的抑制作用更有效。 SE-A治疗可通过调节嗜酸性粒细胞和Th2细胞因子有效改善哮喘模型小鼠肺部的组织病理学变化。这些结果表明SE-A可以被认为是可以潜在地缓解哮喘的治疗剂。

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