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Wogonin inhibits microglial cell migration via suppression of nuclear factor-kappa B activity

Authors
Piao, Hua ZiChoi, In YoungPark, Jin-SunKim, Hee-SunCheong, Jae HoonSon, Kun HoJeon, Su JinKo, Kwang HoKim, Won-Ki
Issue Date
10-Dec-2008
Publisher
ELSEVIER
Keywords
Wogonin; MCP-1; Microglia; Migration; NF-kappa B; cAMP
Citation
INTERNATIONAL IMMUNOPHARMACOLOGY, v.8, no.12, pp.1658 - 1662
Indexed
SCIE
SCOPUS
Journal Title
INTERNATIONAL IMMUNOPHARMACOLOGY
Volume
8
Number
12
Start Page
1658
End Page
1662
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/134842
DOI
10.1016/j.intimp.2008.07.018
ISSN
1567-5769
Abstract
Previously, we and others have demonstrated that wogonin, an active component from the root of Scutellaria baicalensis Georgi, has a neuroprotective effect in cerebral ischemic insult. The neuroprotective effect of wogonin may at least in part be due to its anti-inflammatory properties. Microglial cells, well-known residential macrophages in the central nervous system, migrate to the ischemic lesion and play a pivotal role in the development of chronic inflammation. In the present study, we observed that wogonin potently inhibited microglial migration toward a chemokine, monocyte chemoattractant protein-1 (MCP-1). The anti-migratory effect of wogonin was provoked at nanomolar concentrations, at which wogonin did not significantly inhibit the production of cytokines and chemokines. NF-kappa B has previously shown to regulate microglial cell migration, and activation of cAMP-signaling pathway has also been associated with inhibition of microglial cell motility. in the present study, wogonin at low micromolar concentrations completely suppressed the activity of NF-kappa B in MCP-1-stimulated microglia, and NF-kappa B inhibitors such as N-acetyl cysteine and pyrroliclinedithiocarbamate inhibited the MCP-1-induced migration of microglial cells. However, wogonin did not stimulate the production of cAMP in microglial cells. Our results indicate that the anti-inflammatory activity of wogonin is exerted at least in part by suppressing microglial cell motility via inhibition of NF-kappa B activity. (c) 2008 Elsevier B.V. All rights reserved.
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