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

苦瓜 促炎细胞因子 一氧化氮 MAPK/ERK通路 车站3 p38丝裂原活化蛋白激酶 药理学 炎症 NF-κB 消炎药 下调和上调 医学 信号转导 化学 生物化学 免疫学 传统医学 内科学 基因
作者
Ha-Rim Kim,Eun‐Mi Noh,Seung-Hyeon Lee,Saerom Lee,Dong Hee Kim,Nam Hyouck Lee,Seon‐Young Kim,Mi Hee Park
出处
期刊:Molecular & Cellular Toxicology [Springer Science+Business Media]
卷期号:20 (1): 67-74 被引量:5
标识
DOI:10.1007/s13273-022-00320-3
摘要

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.
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