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Roflumilast ameliorates obesity-induced airway hyper-responsiveness and pulmonary fibrosis in a murine model
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | 박혜정 | - |
| dc.date.accessioned | 2017-07-07T16:10:48Z | - |
| dc.date.available | 2017-07-07T16:10:48Z | - |
| dc.date.issued | 2016 | - |
| dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/148882 | - |
| dc.description | 의과대학/박사 | - |
| dc.description.abstract | Background: Obese asthma patients respond poorly to conventional asthma medications, resulting in severe symptoms and poor prognosis. Roflumilast, a phosphodiesterase-4 inhibitor that lowers the levels of various cytokines and reactive oxygen species (ROS) which are implicated in obese asthmatics, may be effective to treat obese asthmatics. Objectives: We evaluated the potential of roflumilast as a novel therapeutic agent for obese asthmatics. Methods: We designed three models (diet-induced obesity [DIO], DIO with ovalbumin [OVA], and OVA). We fed C57BL/6J mice a high-fat (60%) diet for 3 months with or without OVA sensitization and challenge. Roflumilast or dexamethasone was administered orally thrice at 2-day intervals at the last experimental week. Airway hyper-responsiveness (AHR), bronchoalveolar fluid (BALF), lung pathology, mRNA and protein levels of cytokines and adipokines, ROS levels, and T cell activation were evaluated. Results: AHR resulting from DIO significantly improved in the roflumilast-treated group, compared with dexamethasone-treated groups. Although DIO did not affect the cell proliferation in BALF, increased fibrosis was seen in the DIO group, which significantly improved by the treatment of roflumilast. DIO-induced changes in adiponectin and leptin levels were improved by roflumilast, while dexamethasone aggravated them. Messenger RNA levels and proteins of tumor necrosis factor (TNF)-α, transforming growth factor (TGF)-β, interleukin (IL)-1β, and interferon (IFN)- γ increased in the DIO group, and decreased by roflumilast. The ROS levels was also increased in the DIO group, and decreased by roflumilast. In the DIO-with-OVA and OVA models, roflumilast improved Th1 and Th2 cell activation to a greater extent than dexamethasone. Conclusions: Roflumilast is significantly more effective than dexamethasone against AHR and fibrosis caused by DIO in the murine model, as roflumilast treatment led to improved levels of adiponectin, leptin, TNF-α, TGF-β, IL-1β, IFN- γ and ROS. Roflumilast may represent a promising therapeutic agent for the treatment of obese asthma patients. | - |
| dc.description.statementOfResponsibility | open | - |
| dc.format | application/pdf | - |
| dc.publisher | Graduate School, Yonsei University | - |
| dc.rights | CC BY-NC-ND 2.0 KR | - |
| dc.rights.uri | https://creativecommons.org/licenses/by-nc-nd/2.0/kr/ | - |
| dc.title | Roflumilast ameliorates obesity-induced airway hyper-responsiveness and pulmonary fibrosis in a murine model | - |
| dc.title.alternative | 식이요법으로 유도된 비만 쥐 모델에서의 기도과민성 및 폐섬유화에 대한 roflumilast의 효과 | - |
| dc.type | Thesis | - |
| dc.contributor.department | Dept. of Internal Medicine (내과학교실) | - |
| dc.contributor.localId | A01769 | - |
| dc.contributor.alternativeName | Park, Hye Jung | - |
| dc.contributor.affiliatedAuthor | 박혜정 | - |
| dc.type.local | Dissertation | - |
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