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Anti-oxidant activity and protective effects of Lindera obtusiloba flower teas on inflammatory response in Raw 264.7 macrophages induced by lipopolysaccharideopen accessAnti-oxidant activity and protective effects of Lindera obtusiloba flower teas on inflammatory response in Raw 264.7 macrophages induced by lipopolysaccharide

Other Titles
Anti-oxidant activity and protective effects of Lindera obtusiloba flower teas on inflammatory response in Raw 264.7 macrophages induced by lipopolysaccharide
Authors
Song, Min ChaeShin, Seung MiSeo, Weon TaekKim, Hyun YoungKim, Ji Hyun
Issue Date
Mar-2024
Publisher
Korean Society for Applied Biological Chemistry
Keywords
Flower tea; Free radical; Inflammation; Lindera obtusiloba; Nitric oxide
Citation
Journal of Applied Biological Chemistry, v.67, no.1, pp 70 - 77
Pages
8
Indexed
SCOPUS
KCI
Journal Title
Journal of Applied Biological Chemistry
Volume
67
Number
1
Start Page
70
End Page
77
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/70042
DOI
10.3839/jabc.2024.010
ISSN
1976-0442
2234-7941
Abstract
We investigated the in vitro anti-oxidant activity and protective effects of Lindera obtusiloba flower tea extract (LFE) on lipopolysaccharide (LPS)-induced inflammatory response in Raw 264.7 macrophages. The polyphenol and flavonoid contents of LFE were 32.32 mg GAE/g and 213.83 mg QE/g, respectively. The LFE exhibited the highest 2,2-diphenyl-1-picrylhydrazyl and 2,2'-azino-bis (3-ethylbenzothiazoline-6-sulfonic acid) radical scavenging activities at a concentration of 100 μg/mL among stem and leaf of Lindera obtusiloba extracts. When treated with LFE at concentrations of 10-100 μg/mL, it dose-dependently reduced the production of nitric oxide (NO) in LPS-induced Raw 264.7 macrophages. The treatment of LFE significantly inhibited inflammatory cytokines such as interleukin (IL)-1β and IL-6 in Raw 264.7 macrophage induced by LPS. In particular, treatment of LFE showed a high suppression of IL-1β expression. To evaluate the anti-inflammatory mechanisms of LFE, we investigated protein expressions such as phospho-nuclear factor kappa-light-chain-enhancer of activated B cells (p-NF-kB), inducible NO synthase (iNOS), and cyclooxygenase-2 (COX-2). The LFE inhibited the expression of p-NF-kB, iNOS, and COX-2 compared with LPS-treated cells, resulting anti-inflammatory effects of LFE by inhibiting protein expression involved in NF-kB signaling. Therefore, LFE could be a considered as a functional material with anti-oxidant and anti-inflammatory properties. © The Korean Society for Applied Biological Chemistry 2024.
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농업생명과학대학 (식품공학부)
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