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Inhibitory effect of caffeic acid phenethyl ester (CAPE) on LPS-induced inflammation of human middle ear epithelial cells

Authors
Song, Jae-JunCho, Jae GuHwang, Soon-JaeCho, Chang GunPark, Seok-WonChae, 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
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
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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