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Ginsenoside Rg1 Exhibits Anti-asthmatic Activity in an Aspergillus Protease-Induced Asthma Model in Mice

机译:人参皂苷Rg1在小鼠中表现出曲霉蛋白酶诱导的哮喘模型的抗哮喘活性

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Asthma is one of the most common chronic airway diseases and is characterized by symptoms, such as, wheezing and coughing. Its prevalence in Korea is gradually increasing among children and adults, especially among those older than 60 years. In this study, we investigated the effects of ginsenoside Rgl (Rgl), one of the major constituents of Panax ginseng Meyer on ovalbumin (OVA) plus Aspergillus protease (A. protease) allergen-induced asthmatic mice. Mice were orally administered Rg I for 10 days from 8 days after OVA + A. protease sensitization and intranasally administered booster doses of OVA + A. protease for 4 days from 14 days after sensitization. The effects of Rgl administration on airway hyperresponsiveness (AHR), immune cell distributions in bronchoalveolar lavage fluid (BALF), and serum level of immunoglobulin E (IgE) were investigated at 18 days after sensitization. Histopathological changes in hematoxylin and eosin (H&E)-stained lung sections were also examined. Treatment of OVA + A. protease-sensitized/challenged asthmatic mice with Rgl significantly decreased total eosinophil counts in BALF as compared with those of phosphate-buffered saline (PBS)-treated sensitized/challenged controls, and significantly decreased methacholine-induced AHR. Furthermore, IgE serum levels were significantly lower in Rgl administered OVA + A. protease sensitized asthmatic mice than in PBS-treated sensitized/challenged controls. The study shows Rgl protects against A. protease allergen-induced asthma in mice.
机译:哮喘是最常见的慢性气道疾病之一,其特征在于症状,例如喘息和咳嗽。其在韩国的流行逐渐增加了儿童和成年人,特别是在60年龄较长的人中。在这项研究中,我们研究了人参皂苷RGL(RGL)的影响,Panax人参Meyer的主要成分之一在卵烧蛋白(OVA)加曲霉(A.蛋白酶)过敏原诱导的哮喘小鼠。在OVA + A A + A.蛋白+ A.蛋白酶致敏和鼻内给予的增强剂量,蛋白酶溶解和鼻内给予的增强剂量在敏化后14天,蛋白酶溶解和鼻内给予剂量的蛋白酶的蛋白酶4天。敏化后18天研究了RGL管理对气道高反应性(AHR),免疫细胞分布的影响(AHR),免疫细胞分布,以及敏化后18天。还检查了苏木精和曙红(H&E)肺切片的组织病理学变化。与磷酸盐缓冲盐水(PBS) - 治疗的致敏/攻击/攻击的对照相比,HALF的蛋白酶敏化/挑战哮喘小鼠的蛋白酶敏化/攻击的哮喘小鼠显着降低了BALF中的总嗜酸性粒细胞计数,并且显着降低了甲素诱导的AHR。此外,在施用的OVA + A A.蛋白酶溶解的哮喘小鼠中,IgE血清水平显着低于PBS处理的致病/攻击性对照。该研究表明RGL保护针对蛋白酶过敏原诱导小鼠的哮喘。

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