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KMID : 1161420150180070762
Journal of Medicinal Food
2015 Volume.18 No. 7 p.762 ~ p.775
Lonicera japonica THUNB. Extract Inhibits Lipopolysaccharide-Stimulated Inflammatory Responses by Suppressing NF-¥êB Signaling in BV-2 Microglial Cells
Kwon Seung-Hwan

Ma Shi-Xun
Hong Sa-Ik
Lee Seok-Yong
Jang Choon-Gon
Abstract
In the current study, we evaluated the anti-inflammatory effects of Lonicera japonica THUNB. (LJ) and its underlying molecular mechanism in lipopolysaccharide (LPS)-stimulated BV-2 microglial cells. Our results indicated that LJ significantly inhibits LPS-stimulated production of nitric oxide (NO) and prostaglandin E2 (PGE2). In addition, LJ inhibited inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2) at both the protein and mRNA levels. In LPS-stimulated BV-2 microglial cells, LJ inhibited proinflammatory cytokines and chemokines, tumor necrosis factor-¥á (TNF-¥á), interleukin-1¥â (IL-1¥â), monocyte chemoattractant protein-1 (MCP-1), matrix metalloproteinase-9 (MMP-9) enzymatic activities, and/or mRNA expression, as well as reactive oxygen species (ROS) production. LJ significantly suppressed activation of nuclear factor-¥êB (NF-¥êB) and its translocation from the cytosol to the nucleus and suppressed the DNA-binding activity of NF-¥êB. Furthermore, LJ significantly inhibited phosphorylation of c-Jun N-terminal kinase (JNK), extracellular signal-regulated kinase 1/2 (ERK 1/2), p38 mitogen-activated protein kinases (MAPKs), phosphatidylinositol 3-kinases (PI3K)/Akt, and Janus kinase 1 (JAK1)/signal transducer and activator of transcription (STAT)1/3. Collectively, our findings indicated that the antineuroinflammatory properties of LJ in LPS-induced BV-2 microglial cells is due to downregulation of proinflammatory cytokines and chemokines downstream of inhibition of NF-¥êB activation.
KEYWORD
BV-2 microglial cells, Inflammatory responses, Lipopolysaccharide, Lonicera japonica THUNB, Nuclear factor-¥êB
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