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首页> 外文期刊>Biomolecules & therapeutics >Therapeutic Potential of the Rhizomes of Anemarrhena asphodeloides and Timosaponin A-III in an Animal Model of Lipopolysaccharide-Induced Lung Inflammation
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Therapeutic Potential of the Rhizomes of Anemarrhena asphodeloides and Timosaponin A-III in an Animal Model of Lipopolysaccharide-Induced Lung Inflammation

机译:Anemarrhena Asphodeloides和Timosaponin A-III的疗效潜力在脂多糖诱导的肺炎的动物模型中

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摘要

Investigations into the development of new therapeutic agents for lung inflammatory disorders have led to the discovery of plant-based alternatives. The rhizomes of Anemarrhena asphodeloides have a long history of use against lung inflammatory disorders in traditional herbal medicine. However, the therapeutic potential of this plant material in animal models of lung inflammation has yet to be evaluated. In the present study, we prepared the alcoholic extract and derived the saponin-enriched fraction from the rhizomes of A. asphodeloides and isolated timosaponin A-III, a major constituent. Lung inflammation was induced by intranasal administration of lipopolysaccharide (LPS) to mice, representing an animal model of acute lung injury (ALI). The alcoholic extract (50-200 mg/kg) inhibited the development of ALI. Especially, the oral administration of the saponin-enriched fraction (10-50 mg/kg) potently inhibited the lung inflammatory index. It reduced the total number of inflammatory cells in the bronchoalveolar lavage fluid (BALF). Histological changes in alveolar wall thickness and the number of infiltrated cells of the lung tissue also indicated that the saponin-enriched fraction strongly inhibited lung inflammation. Most importantly, the oral administration of timosaponin A-III at 25-50 mg/kg significantly inhibited the inflammatory markers observed in LPS-induced ALI mice. All these findings, for the first time, provide evidence supporting the effectiveness of A. asphodeloides and its major constituent, timosaponin A-III, in alleviating lung inflammation.
机译:调查肺炎症患者新治疗剂的发展导致了植物替代品的发现。 Anemarrhena窒息的根茎在传统草药中对肺炎疾病的历史悠久。然而,这种植物材料在肺炎的动物模型中的治疗潜力尚未评估。在本研究中,我们制备了酒精提取物,并从Asphodeloides和分离的Timosaponin A-III,一个主要成分衍生富含皂苷富集的分数。通过鼻内施用脂多糖(LPS)给小鼠诱导肺炎,代表急性肺损伤的动物模型(ALI)。酒精萃取物(50-200mg / kg)抑制Ali的发育。特别是,富含皂苷级分(10-50mg / kg)的口服给药效果抑制了肺炎。它降低了支气管肺泡灌洗液(BALF)中的炎症细胞总数。肺泡壁厚和肺组织的渗透细胞数的组织学变化也表明富含皂苷的馏分强烈抑制肺炎。最重要的是,25-50mg / kg的Timosaponin A-III的口服给药显着抑制了LPS诱导的Ali小鼠中观察到的炎症标志物。所有这些调查结果首次提供了支持A. Asphodeloides及其主要成分,Timosaponin A-III的有效性的证据,以减轻肺炎。

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