首页> 外文期刊>Planta medica: Natural products and medicinal plant research >Antiallergic effects of pigments isolated from green sea urchin (Strongylocentrotus droebachiensis) shells
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Antiallergic effects of pigments isolated from green sea urchin (Strongylocentrotus droebachiensis) shells

机译:从绿海胆(Strongylocentrotus droebachiensis)贝壳中分离出的色素的抗过敏作用

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摘要

This study was undertaken to evaluate possible antiallergic effects of an extract of pigments from green sea urchin (Strongylocentrotus droebachiensis) shells. Effects were studied on animal models - guinea pig ileum contraction, rabbit eyes allergic conjunctivitis, and rabbit local skin irritation. The extract significantly reduced, in a dose-dependent manner, the histamine-induced contractions of the isolated guinea pig ileum with ID50 = 1.2 μg/mL (in equivalents of spinochrome B), had an inhibitory effect on the model of ocular allergic inflammation surpassing the reference drug olopatadine, and did not show any irritating effect in rabbits. The extract predominantly contained polyhydroxy-1,4-naphthoquinone which would be responsible for the pharmacological activity. The active compounds of the extract were evaluated in silico with molecular docking. Molecular docking into H1R receptor structures obtained from molecular dynamic simulations showed that all spinochrome derivatives bind to the receptor active site, but spinochrome monomers fit better to it. The results of the present study suggest possibilities for the development of new agents for treating allergic diseases on the base of pigments from sea urchins shells.
机译:进行这项研究以评估从绿海胆(Strongylocentrotus droebachiensis)贝壳中提取的色素的可能的抗过敏作用。研究了对动物模型的影响-豚鼠回肠收缩,兔眼过敏性结膜炎和兔局部皮肤刺激。提取物以剂量依赖性方式显着降低ID50 = 1.2μg/ mL(等效于旋转色素B)的组胺诱导的豚鼠回肠收缩,对超过眼睛的过敏性炎症模型具有抑制作用参比药物奥洛他定,对兔子没有刺激作用。提取物主要含有多羟基-1,4-萘醌,其可负责药理活性。通过分子对接在计算机上评估提取物的活性化合物。从分子动力学模拟获得的分子对接到H1R受体结构中显示,所有spinochrome衍生物均与受体活性位点结合,但spinochrome单体更适合它。本研究的结果表明开发基于海胆壳色素的新型药物治疗过敏性疾病的可能性。

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