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Momordica charantia extracts obtained by ultrasound-assisted extraction inhibit the inflammatory pathways

Ha-Rim Kim; Eun-Mi Noh; Seung-Hyeon Lee; Saerom Lee; Dong Hee Kim; Nam Hyouck Lee; Seon-Young Kim; Mi Hee Park
Molecular & Cellular Toxicology · Vol. 20, Issue 1 · pp. 67-74 · 2024

Abstract

Background Momordica charantia is a member of the Cucurbitaceae family and has traditionally been used for medical nutritional therapy to cure diabetes, and its various biological properties have been reported. However, several studies have demonstrated that M. charantia may exert toxic or adverse effects under different conditions. In this study, we prepared an M. charantia extract using ultrasound-assisted extraction, which is a green technology, and verified its anti-inflammatory effects. Objectives The aim of this study was to investigate the anti-inflammatory effects of M. charantia extract using ultrasound-assisted extraction in LPS-induced Raw264.7 macrophages and explore the potential mechanism mediated by the MAPK/NF-κB signaling pathway. Results We found that the M. charantia extract was non-toxic up to a concentration of 500 μg/mL in Raw264.7 cells. We verified that treatment with M. charantia extract significantly reduced the production of nitric oxide and proinflammatory cytokines, including TNF-α, IL-1β, IL-2, and IL-6, in LPS-stimulated RAW264.7 cells. Moreover, the anti-inflammatory cytokine IL-10 was dramatically increased by treatment with the M. charantia extract. In addition, the phosphorylation of the transcription factor NF-κB, which modulates the production of inflammatory proteins, including JNK, ERK, and p38, was reduced by downregulation of the MAPK signaling pathway. Conclusion These results indicate that the M. charantia extract collected using an industrial ultrasonic system is non-toxic and has an anti-inflammatory effect through regulation of the NF-κB and MAPK pathways, suggesting that it can act as a therapeutic candidate for the treatment of inflammatory diseases.

Bibliographic Information

JournalMolecular & Cellular Toxicology
PublisherSpringer
Publication Date2024-01-01
Publication Year2024
Volume20
Issue1
Pages67-74
Document TypeJournal Article
Print ISSN1738-642X
eISSN2092-8467
DOI10.1007/s13273-022-00320-3

Access Information

NARA Access Coverage2010-01-01~Current
Journal Homepagehttps://www.springer.com/journal/13273
Publisher PageOpen Publisher Page
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