Department of Pharmacology, College of Korean Medicine, Kyung Hee University, Seoul, 130-701, Republic of Korea.
Department of Science in Korean Medicine, Graduate School, Kyung Hee University, Seoul, 02447, Republic of Korea.
Inflamm Res. 2019 May;68(5):387-395. doi: 10.1007/s00011-019-01226-y. Epub 2019 Mar 14.
AST2017-01 is developed to be used for treatment and prevention of allergic diseases and composed of processed-Cordyceps militaris and processed-Rumex crispus. But, effect of AST2017-01 remains unclear in an allergic rhinitis (AR). So, this study aimed to explore the effects of AST2017-01 in ovalbumin (OVA)-induced AR animal model.
OVA-induced AR animals were orally administered AST2017-01 and chrysophanol, an active component of AST2017-01 for 10 days.
In mice with AR, AST2017-01 and chrysophanol markedly decreased number of rubs, IgE, histamine, thymic stromal lymphopoietin, tumor necrosis factor-α, interleukin (IL)-1β, IL-4, IL-5, and IL-13 in serum or nasal mucosa tissues. Moreover, activities and protein levels of caspase-1 were markedly diminished by oral administration of AST2017-01 and chrysophanol. Declines of macrophage inflammatory protein-2, intercellular adhesion molecules-1, eosinophil, and mast cells were also noted in nasal mucosa tissues of AST2017-01 and chrysophanol groups.
Taken together, these findings indicate that AST2017-01 has an anti-allergic effect as a therapeutic agent or functional food for treating and preventing AR.
AST2017-01 被开发用于治疗和预防过敏性疾病,由蛹虫草和酸模制成。但是,AST2017-01 在过敏性鼻炎(AR)中的作用尚不清楚。因此,本研究旨在探讨 AST2017-01 在卵清蛋白(OVA)诱导的 AR 动物模型中的作用。
OVA 诱导的 AR 动物经口给予 AST2017-01 和大黄素,AST2017-01 的一种活性成分,连续 10 天。
在 AR 小鼠中,AST2017-01 和大黄素显著减少了搔抓次数、IgE、组胺、胸腺基质淋巴细胞生成素、肿瘤坏死因子-α、白细胞介素(IL)-1β、IL-4、IL-5 和 IL-13 在血清或鼻黏膜组织中的含量。此外,口服 AST2017-01 和大黄素显著降低了半胱天冬酶-1的活性和蛋白水平。在 AST2017-01 和大黄素组的鼻黏膜组织中,巨噬细胞炎症蛋白-2、细胞间黏附分子-1、嗜酸性粒细胞和肥大细胞的数量也有所减少。
综上所述,这些发现表明,AST2017-01 具有抗过敏作用,可作为治疗和预防 AR 的治疗剂或功能性食品。