Anti-Inflammatory Effects of Fermented and Aged Mountain-Cultivated Ginseng Sprouts via Suppression of MAPK-NF-κB Pathway in Lipopolysaccharide-Stimulated RAW264.7 Macrophagesopen access
- Authors
- Cao, Dang Long; Woo, Min-Seok; Kim, Eun-Jin; Ahn, Byeonggyu; Prayoga, Anjas Happy; Kang, Sang Soo; Cho, Kye Man; Kang, Dawon
- Issue Date
- Nov-2024
- Publisher
- John Wiley and Sons Ltd
- Keywords
- fermented and aged mountain-cultivated ginseng sprout; inflammation; macrophage; MAPK; NF-κB
- Citation
- Food Science and Nutrition, v.12, no.11, pp 9566 - 9576
- Pages
- 11
- Indexed
- SCIE
SCOPUS
- Journal Title
- Food Science and Nutrition
- Volume
- 12
- Number
- 11
- Start Page
- 9566
- End Page
- 9576
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/74514
- DOI
- 10.1002/fsn3.4518
- ISSN
- 2048-7177
2048-7177
- Abstract
- Fermented and aged mountain-cultivated ginseng sprouts (FAMCGS) exhibit superior antioxidant and anti-inflammatory properties compared to mountain-cultivated ginseng sprouts (MCGS). However, the mechanisms behind these properties of FAMCGSE remain unclear. This study explores the anti-inflammatory effects of FAMCGS extract (FAMCGSE) on LPS-stimulated RAW 264.7 macrophages and the underlying mechanisms. The MTT assay confirmed that FAMCGSE (0 to 0.1%) maintained cell viability without inducing morphological changes. Pretreatment with FAMCGSE significantly mitigated LPS-induced morphological alterations dose-dependently. RT-PCR and Western blot analyses showed that FAMCGSE significantly reduced the mRNA and protein levels of proinflammatory mediators such as TNF-α, IL-1β, IL-6, iNOS, and COX-2. Additionally, FAMCGSE decreased the production of TNF-α, IL-1β, IL-6, nitric oxide, and PGE2 in LPS-activated RAW264.7 cells. Mechanistically, FAMCGSE inhibited the phosphorylation of mitogen-activated protein kinases (MAPKs; ERK, p38, and JNK) and prevented the LPS-induced nuclear translocation of NF-κB, with effects comparable to compound K (CK) or dexamethasone. Notably, FAMCGSE was particularly effective in inhibiting ERK and JNK activation, with less impact on p38, suggesting a specific inhibitory action on certain MAPK pathways. These findings highlight FAMCGSE's potential as an inhibitor of MAPK and NF-κB pathways, indicating that FAMCGSE, including its main component CK, may be a promising therapeutic agent for inflammation-related conditions. © 2024 The Author(s). Food Science & Nutrition published by Wiley Periodicals LLC.
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