Piscroside C, a novel iridoid glycoside isolated from Pseudolysimachion rotundum var. subinegrum suppresses airway inflammation induced by cigarette smoke
- Authors
- Song, Hyuk-Hwan; Shin, In-Sik; Woo, So Yeun; Lee, Su Ui; Sung, Min Hee; Ryu, Hyung Won; Kim, Doo-Young; Ahn, Kyung-Seop; Lee, Hyeong-Kyu; Lee, Dongho; Oh, Sei-Ryang
- Issue Date
- 21-7월-2015
- Publisher
- ELSEVIER IRELAND LTD
- Keywords
- Pseudolysimachion rotundum var. subintegrum; Piscroside C; Cigarette smoke; Inflammation; NF-kappa B
- Citation
- JOURNAL OF ETHNOPHARMACOLOGY, v.170, pp.20 - 27
- Indexed
- SCIE
SCOPUS
- Journal Title
- JOURNAL OF ETHNOPHARMACOLOGY
- Volume
- 170
- Start Page
- 20
- End Page
- 27
- URI
- https://scholar.korea.ac.kr/handle/2021.sw.korea/92994
- DOI
- 10.1016/j.jep.2015.04.043
- ISSN
- 0378-8741
- Abstract
- Ethnopharmacological relevance: Pseudolysimachion rotundum var. subintegrum (Speedwell, Plantaginaceae) is used as a traditional herbal medicine for treating bronchitis, cough and asthma in Korea, China, Russia, and Europe. Aim of the study: In this study, we investigated the protective effects of the novel iridoid glycoside, piscroside C (compound 1) isolated from the methanolic extract of P. rotundum var. subintegrum against inflammatory responses using a cigarette smoke induced chronic obstructive pulmonary disease (COPD) and TNF-alpha-stimulated human airway epithelial NCI-H292 cells. Materials and methods: The novel iridoid glycoside piscroside C was isolated from the methanolic extract of P. rotundum var. subintegrum. The chemical structure was established by NMR, HRESIMS, and optical rotation. In in vivo experiment, the mice received 1 h of cigarette smoke for 3 days. Piscroside C was administered to mice by oral gavage I h before cigarette smoke exposure for 3 days. In in vitro experiment, we evaluated the effect of piscroside C on proinflammatory mediators in H292 cells stimulated with TNF-alpha. Results: Piscroside C significantly reduced the neutrophil influx, reactive oxygen species production, IL-6, TNF-alpha, and elastase activity in bronchoalveolar lavage fluid in COPD animals. In addition, piscroside C attenuated NF-kappa B and ha phosphorylation, leading to reduced recruitment of inflammatory cells into the lung tissue. Consistent with the results of in vivo experiment, piscroside C significantly inhibited the expression of inflammatory cytokines (IL-6, IL-8 and IL-10) by inhibiting NF-kappa B activation, as resulting decrease in the phosphorylation of IKK beta, I kappa B alpha and TAK1 in TNF-alpha-stimulated H292 cells. Conclusion: These findings indicate that piscroside C effectively inhibits inflammatory responses, which is an important process in the development of COPD through suppression of IKK/NF-kappa B activation. Our study suggest that piscroside C might represent a useful therapeutic for the treatment of inflammatory airway disease. (C) 2015 Elsevier Ireland Ltd. All rights reserved.
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