Inhibitory effect of caffeic acid phenethyl ester (CAPE) on LPS-induced inflammation of human middle ear epithelial cells
- Authors
- Song, Jae-Jun; Cho, Jae Gu; Hwang, Soon-Jae; Cho, Chang Gun; Park, Seok-Won; Chae, Sung-Won
- Issue Date
- 2008
- Publisher
- TAYLOR & FRANCIS LTD
- Keywords
- Caffeic acid phenethyl ester; otitis media; NF-B
- Citation
- ACTA OTO-LARYNGOLOGICA, v.128, no.12, pp 1303 - 1307
- Pages
- 5
- Indexed
- SCIE
SCOPUS
- Journal Title
- ACTA OTO-LARYNGOLOGICA
- Volume
- 128
- Number
- 12
- Start Page
- 1303
- End Page
- 1307
- URI
- https://scholar.korea.ac.kr/handle/2021.sw.korea/125572
- DOI
- 10.1080/00016480801947082
- ISSN
- 0001-6489
1651-2251
- Abstract
- Conclusions. The results suggest that the anti-inflammatory effect of caffeic acid phenethyl ester (CAPE) is due to its inhibition of tumor necrosis factor (TNF)- expression and interleukin (IL)-8 production. The anti-inflammatory effect of CAPE is possibly through the inhibition of nuclear factor (NF)-B via the suppression of inhibitor-B- (IB-) degradation. Objectives. CAPE is a biologically active component of propolis, a resinous material obtained from bee hives, which originates from conifer bark. The effect of CAPE on lipopolysaccharide (LPS)-induced inflammatory reactions is not known. The aim of this study was to evaluate the anti-inflammatory effect of CAPE on cultured human middle ear epithelial cells (HMEECs). Materials and methods. The effect of CAPE on LPS-induced TNF- expression was evaluated in HMEECs by real-time reverse transcription polymerase chain reaction (RT-PCR). LPS-induced IL-8 production was determined by enzyme-linked immunosorbent assay (ELISA), and LPS-induced IB- degradation was followed by Western blot analysis. Results. CAPE significantly inhibited LPS-induced up-regulation of TNF- in a dose-dependent manner. IL-8 production by LPS was significantly suppressed by the CAPE pretreatment. Furthermore, LPS-induced IB- degradation was suppressed by the CAPE pretreatment.
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