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KGC3P 草药配方及其单体成分川陈皮素对煤飞尘诱导的气道炎症的影响。

Effects of a herbal formulation, KGC3P, and its individual component, nepetin, on coal fly dust-induced airway inflammation.

机构信息

Laboratory of Physiology and Cell Signalling, Department of Veterinary Medicine, College of Veterinary Medicine, Kyungpook National University, Daegu, 41566, Republic of Korea.

Herbal Medicine Research Division, Korea Institute of Oriental Medicine, 1672 Yuseong-daero, Yuseong-gu, Dajeon, 34054, Republic of Korea.

出版信息

Sci Rep. 2020 Aug 20;10(1):14036. doi: 10.1038/s41598-020-68965-5.

Abstract

Coal fly dust (CFD)-induced asthma model is used as an ambient particulate matter model of serious pulmonary damage. We aimed to evaluate the effects of a combination of ginseng and Salvia plebeia R. Br extract (KGC-03-PS; KG3P) and its individual components (hispidulin, nepetin and rosmarinic acid) in a CFD-induced mouse model of airway inflammation (asthma). We also evaluated signal transduction by KG3P and its individual components in the alveolar macrophage cell line, MH-S cells. In vitro, KG3P and its individual components inhibited nitric oxide production and expression of pro-inflammatory mediators and cytokines (iNOS, COX-2, IL-1β, IL-6 and TNF-α) through the NF-κB and MAPK pathways in coal fly ash (CFA)-induced inflammation in MH-S cells. Moreover, in the CFD-induced asthma model in mice, KG3P and its predominant individual component, nepetin, inhibited Asymmetric Dimethyl arginine (ADMA) and Symmetric Dimethyl arginine (SDMA) in serum, and decreased the histopathologic score in the lungs. A significant reduction in the neutrophils and immune cells in BALF and lung tissue was demonstrated, with significant reduction in the expression of the pro-inflammatory cytokines. Finally, IRAK-1 localization was also potently inhibited by KG3P and nepetin. Thus, KG3P extract can be considered as a potent candidate for amelioration of airway inflammation.

摘要

煤飞尘(CFD)诱导的哮喘模型被用作严重肺部损伤的环境颗粒物模型。我们旨在评估人参和丹参提取物(KGC-03-PS;KG3P)及其单个成分(哈巴俄苷、川陈皮素和迷迭香酸)在 CFD 诱导的气道炎症(哮喘)小鼠模型中的组合作用。我们还评估了 KG3P 及其单个成分在肺泡巨噬细胞系 MH-S 细胞中的信号转导作用。在体外,KG3P 及其单个成分通过 NF-κB 和 MAPK 通路抑制煤飞尘(CFA)诱导的 MH-S 细胞中一氧化氮的产生和促炎介质和细胞因子(iNOS、COX-2、IL-1β、IL-6 和 TNF-α)的表达。此外,在 CFD 诱导的哮喘小鼠模型中,KG3P 及其主要成分川陈皮素抑制了血清中的不对称二甲基精氨酸(ADMA)和对称二甲基精氨酸(SDMA),并降低了肺部的组织病理学评分。在 BALF 和肺组织中,中性粒细胞和免疫细胞的数量显著减少,促炎细胞因子的表达也显著降低。最后,KG3P 和川陈皮素也能强烈抑制 IRAK-1 的定位。因此,KG3P 提取物可被视为改善气道炎症的有效候选物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2914/7441173/3559e462e87c/41598_2020_68965_Fig1_HTML.jpg

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