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The analgesic and anti-inflammatory effects of Litsea japonica fruit are mediated via suppression of NF-kappa B and JNK/p38 MAPK activation

Authors
Koo, Hyun JungYoon, Weon-JongSohn, Eun-HwaHam, Young-MinJang, Seon-AKwon, Jung-EunJeong, Yong JoonKwak, Jong HwanSohn, EunsooPark, Soo-YoungJang, Ki-HyoNamkoong, SeungHan, Hyo-SangJung, Yong-HwanKang, Se Chan
Issue Date
Sep-2014
Publisher
ELSEVIER SCIENCE BV
Keywords
Cyclooxygenase-2; Litsea japonica; Analgesic; Anti-inflammatory; Hamabiwalactone
Citation
INTERNATIONAL IMMUNOPHARMACOLOGY, v.22, no.1, pp.84 - 97
Journal Title
INTERNATIONAL IMMUNOPHARMACOLOGY
Volume
22
Number
1
Start Page
84
End Page
97
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/12336
DOI
10.1016/j.intimp.2014.06.007
ISSN
1567-5769
Abstract
Fruits of the Litsea family of trees and shrubs contain biologically active compounds, some of which have been used as natural nutrients and flavoring agents in food. In this study, we identified novel anti-nociceptive effects of the 30% ethanol extract, the CH2Cl2 fraction and the associated active components (Hamabiwalactone A and B) from Litsea japonica fruit by using in vivo peripheral and central nervous pain models. In addition, we compared the anti-inflammatory effects of several fractions from L japonica fruit extracts using lipopolysaccharide (LPS)-stimulated Raw264.7 cells. The CH2Cl2 fraction of L japonica fruit (LJM) had an optimal combination of anti-inflammatory effects and low cytotoxicity. Dose response studies were performed to determine the inhibitory effects of LJM on the pro-inflammatory enzymes, COX-2/PGE(2) and NO/iNOS, and pro-inflammatory cytokines, IL-1 beta, IL-6,and TNF-alpha. Molecular profiling revealed that LJM exerts anti-inflammatory effects through inhibition of NF-kappa B and JNK/p38 MAPK signaling in LPS-induced macrophages. This study suggests that CH2Cl2 fraction of L japonica fruit and its bioactive components are potential candidates as anti-inflammatory and analgesic agents (painkillers) for the treatment of inflammatory diseases. (C) 2014 Elsevier B.V. All rights reserved.
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