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Cited 11 time in webofscience Cited 13 time in scopus
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Melittin has a chondroprotective effect by inhibiting MMP-1 and MMP-8 expressions via blocking NF-kappa B and AP-1 signaling pathway in chondrocytes

Authors
Jeong, Yun-JeongShin, Jae-MoonBae, Young-SeukCho, Hyun-JiPark, Kwan-KyuChoe, Jung-YoonHan, Sang-MiMoon, Sung-KwonKim, Wun-JaeChoi, Yung HyunKim, Cheorl-HoChang, Hyeun-WookChang, Young-Chae
Issue Date
Apr-2015
Publisher
ELSEVIER SCIENCE BV
Keywords
Bee venom; Melittin; Chondrocyte; Type II collagen
Citation
INTERNATIONAL IMMUNOPHARMACOLOGY, v.25, no.2, pp 400 - 405
Pages
6
Journal Title
INTERNATIONAL IMMUNOPHARMACOLOGY
Volume
25
Number
2
Start Page
400
End Page
405
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/9710
DOI
10.1016/j.intimp.2015.02.021
ISSN
1567-5769
1878-1705
Abstract
Bee venom is a natural ingredient produced by the honey bee (Apis mellifera), and has been widely used in China, Korea and Japan as a traditional medicine for various diseases such as arthritis, rheumatism, and skin diseases However, the regulation of the underlying molecular mechanisms of the anti-arthritis by bee venom and its major peptides is largely unknown. In this study, we investigated the potential molecular mechanisms underlying the anti-arthritis effect of bee venom and its major peptides, melittin and apamin, in tumor necrosis factor-alpha (TNF-alpha) responsive C57BL/6 mice chondrocyte cells. The bee venom and melittin significantly and selectively suppressed the TNF-alpha-mediated decrease of type II collagen expression, whereas the apamin had no effects on the type II collagen expression. We, furthermore, found that the bee venom and melittin inhibited the protein expression of matrix metalloproteinase (MMP)-1 and MMP-8, which suggests that the chondroprotective effect of bee venom may be caused by melittin. The inhibitory effects of melittin on the TNF-alpha-induced MMP-1 and MMP-8 protein expression were regulated by the inhibition of NF-kappa B and AP-1. In addition, melittin suppressed the TNF-alpha-induced phosphorylation of Akt, JNK and ERK1/2, but did not affect the phosphorylation of p38 kinase. These results suggest that melittin suppresses TNF-alpha-stimulated decrease of type II collagen expression by the inhibiting MMP-1 and MMP-8 through regulation of the NF-kappa B and AP-1 pathway and provision of a novel role for melittin in anti-arthritis action. (C) 2015 Elsevier B.V. All rights reserved.
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Moon, Sung Kwon
생명공학대학 (식품영양)
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