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Forsythiaside A Exhibits Anti-inflammatory Effects in LPS-Stimulated BV2 Microglia Cells Through Activation of Nrf2/HO-1 Signaling Pathway
by
Ren, Jie
, Zhang, Shizhong
, Wang, Yue
, Zhao, Hongfei
, Lin, Chuangxin
in
Animals
/ Anti-Inflammatory Agents - pharmacology
/ Biochemistry
/ Biomedical and Life Sciences
/ Biomedicine
/ Cell Biology
/ Cell Line
/ Cell Survival - drug effects
/ Cytokines - biosynthesis
/ Forsythia suspensa
/ Glycosides - pharmacology
/ Heme Oxygenase-1 - metabolism
/ Lipopolysaccharides - pharmacology
/ Membrane Proteins - metabolism
/ Mice
/ Microglia - drug effects
/ Microglia - metabolism
/ Neurochemistry
/ Neurology
/ Neurosciences
/ NF-E2-Related Factor 2 - metabolism
/ NF-kappa B p52 Subunit - metabolism
/ Nitric Oxide - biosynthesis
/ Original Paper
/ Protein Transport
/ Rats
/ Rats, Wistar
/ Signal Transduction
2016
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Forsythiaside A Exhibits Anti-inflammatory Effects in LPS-Stimulated BV2 Microglia Cells Through Activation of Nrf2/HO-1 Signaling Pathway
by
Ren, Jie
, Zhang, Shizhong
, Wang, Yue
, Zhao, Hongfei
, Lin, Chuangxin
in
Animals
/ Anti-Inflammatory Agents - pharmacology
/ Biochemistry
/ Biomedical and Life Sciences
/ Biomedicine
/ Cell Biology
/ Cell Line
/ Cell Survival - drug effects
/ Cytokines - biosynthesis
/ Forsythia suspensa
/ Glycosides - pharmacology
/ Heme Oxygenase-1 - metabolism
/ Lipopolysaccharides - pharmacology
/ Membrane Proteins - metabolism
/ Mice
/ Microglia - drug effects
/ Microglia - metabolism
/ Neurochemistry
/ Neurology
/ Neurosciences
/ NF-E2-Related Factor 2 - metabolism
/ NF-kappa B p52 Subunit - metabolism
/ Nitric Oxide - biosynthesis
/ Original Paper
/ Protein Transport
/ Rats
/ Rats, Wistar
/ Signal Transduction
2016
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Forsythiaside A Exhibits Anti-inflammatory Effects in LPS-Stimulated BV2 Microglia Cells Through Activation of Nrf2/HO-1 Signaling Pathway
by
Ren, Jie
, Zhang, Shizhong
, Wang, Yue
, Zhao, Hongfei
, Lin, Chuangxin
in
Animals
/ Anti-Inflammatory Agents - pharmacology
/ Biochemistry
/ Biomedical and Life Sciences
/ Biomedicine
/ Cell Biology
/ Cell Line
/ Cell Survival - drug effects
/ Cytokines - biosynthesis
/ Forsythia suspensa
/ Glycosides - pharmacology
/ Heme Oxygenase-1 - metabolism
/ Lipopolysaccharides - pharmacology
/ Membrane Proteins - metabolism
/ Mice
/ Microglia - drug effects
/ Microglia - metabolism
/ Neurochemistry
/ Neurology
/ Neurosciences
/ NF-E2-Related Factor 2 - metabolism
/ NF-kappa B p52 Subunit - metabolism
/ Nitric Oxide - biosynthesis
/ Original Paper
/ Protein Transport
/ Rats
/ Rats, Wistar
/ Signal Transduction
2016
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Forsythiaside A Exhibits Anti-inflammatory Effects in LPS-Stimulated BV2 Microglia Cells Through Activation of Nrf2/HO-1 Signaling Pathway
Journal Article
Forsythiaside A Exhibits Anti-inflammatory Effects in LPS-Stimulated BV2 Microglia Cells Through Activation of Nrf2/HO-1 Signaling Pathway
2016
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Overview
Inflammation and oxidative stress have been reported to play critical roles in the pathogenesis of neurodegenerative disease. Forsythiaside A, a phenylethanoside product isolated from air-dried fruits of
Forsythia suspensa
, has been reported to have anti-inflammatory and antioxidant effects. In this study, the anti-inflammatory effects of forsythiaside A on LPS-stimulated BV2 microglia cells and primary microglia cells were investigated. The production of inflammatory mediators TNF-α, IL-1β, NO and PGE
2
were detected in this study. NF-κB, nuclear factor-erythroid 2-related factor 2 (Nrf2), heme oxygenase-1 (HO-1) expression were detected by western blot analysis. Our results showed that forsythiaside A significantly inhibited LPS-induced inflammatory mediators TNF-α, IL-1β, NO and PGE
2
production. LPS-induced NF-κB activation was suppressed by forsythiaside A. Furthermore, forsythiaside A was found to up-regulate the expression of Nrf2 and HO-1. In conclusion, this study demonstrates that forsythiaside A inhibits LPS-induced inflammatory responses in BV2 microglia cells and primary microglia cells through inhibition of NF-κB activation and activation of Nrf2/HO-1 signaling pathway.
Publisher
Springer US,Springer Nature B.V
Subject
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