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三白草乙醇提取物的抗哮喘活性。

Anti-asthmatic activity of an ethanol extract from Saururus chinensis.

作者信息

Lee Eunkyung, Haa Kyungmi, Yook Ju Min, Jin Mei Hua, Seo Chang Seob, Son Kun Ho, Kim Hyun Pyo, Bae Ki Hwan, Kang Sam Sik, Son Jong Keun, Chang Hyeun Wook

机构信息

College of Pharmacy, Yeungnam University, Gyeongsan 712-749, Korea.

出版信息

Biol Pharm Bull. 2006 Feb;29(2):211-5. doi: 10.1248/bpb.29.211.

Abstract

As an attempt to find bioactive medicinal herbs exerting anti-asthmatic activity, the effects of an ethanol extract from the parts of Saururus chinensis were evaluated in both in vitro and in vivo. The ethanol extract of S. chinensis (ESC) inhibited generation of the cyclooxygenase-2 (COX-2) dependent phases of prostaglandin D(2) in bone marrow-derived mast cells in a concentration-dependent manner with an IC(50) value of 14.3 microg/ml. ESC also inhibited leukotriene C(4) production with an IC(50) value of 0.3 microg/ml. This demonstrates that ESC has COX-2/5-lipoxygenase dual inhibitory activity. In addition, this compound inhibited degranulation reaction in a dose dependent manner, with an IC(50) value of 1.3 microg/ml. An ovalbumin induced mouse asthmatic animal model was used to determine its in vivo anti-asthmatic activity. The oral administration (50-200 mg/kg) of ESC reduced the number of infiltrated eosinophil in a bronchoalveolar lavage fluid. Furthermore, ESC (100 mg/kg) inhibited the eotaxin and IL-4 mRNA expression levels. These results suggest that the anti-asthmatic activity of S. chinensis might in part occur via the inhibition of eicosanoid generation, degranulation as well as the down regulation of IL-4 and eotaxin mRNA expression.

摘要

作为寻找具有抗哮喘活性的生物活性草药的尝试,对中华三白草各部位乙醇提取物的体外和体内作用进行了评估。中华三白草乙醇提取物(ESC)以浓度依赖性方式抑制骨髓源性肥大细胞中前列腺素D2的环氧合酶-2(COX-2)依赖性生成阶段,IC50值为14.3微克/毫升。ESC还抑制白三烯C4的产生,IC50值为0.3微克/毫升。这表明ESC具有COX-2/5-脂氧合酶双重抑制活性。此外,该化合物以剂量依赖性方式抑制脱颗粒反应,IC50值为1.3微克/毫升。使用卵清蛋白诱导的小鼠哮喘动物模型来确定其体内抗哮喘活性。口服ESC(50-200毫克/千克)可减少支气管肺泡灌洗液中浸润的嗜酸性粒细胞数量。此外,ESC(100毫克/千克)抑制嗜酸性粒细胞趋化因子和IL-4 mRNA表达水平。这些结果表明,中华三白草的抗哮喘活性可能部分通过抑制类花生酸生成、脱颗粒以及下调IL-4和嗜酸性粒细胞趋化因子mRNA表达而发生。

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