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    Anti-inflammatory Effects of KOTMIN13: A Mixed Herbal Medicine in LPS-stimulated RAW 264.7 Cells and Mouse Edema Models

    Eujin Lee1, Sun-Gun Kim1, Na-Young Park1, Hyo-Hyun Park1, Kyu-Tae Jeong1, Jongkeun Choi2, In-Hae Lee2, Hwadong Lee1, Eunkyung Lee1 Corresponding author

    1. 1Research and Development Division, National Development Institute of Korean Medicine, Gyeongsan.
    2. 2Department of Cosmetic Science, Chungwoon University, Chungnam, Republic of Korea.

    CORRESPONDENCE

    Eunkyung Lee

    Research and Development Division, National Development Institute of Korean Medicine, Gyeongsan.

    eklee@ynu.ac.kr

    Received: 11-01-2016; Revised: 29-02-2016; Accepted: 29-02-2016.

    Volume 13, Issue 50 · pp. 216–21 · PUBLISHED 18 April 2017 · DOI: 10.4103/0973-1296.204548

    View on Pharmacogn. Mag. original site ↗

    ABSTRACT

    Background: A Korean herbal medicine, KOTMIN13, composed of Inula japonica Thunberg, Trichosanthes kirilowii Maximowicz var. japonica kitamura, Peucedanum praeruptorum Dunn, and Allium macrostemon Bge, has been used for anti-allergic and anti-asthmatic treatment in oriental clinics, but its activity has not been investigated. Materials and Methods: To evaluate the anti-inflammatory activity of KOTMIN13 for in vitro study, LPS-stimulated RAW 264.7 cells were used to induce the production and expression of inflammatory mediators and its mechanisms. 12-O-Tetradecanoylphorobol-13 aceate (TPA)-induced ear edema and carrageenan-induced paw edema models were also used to evaluate the effect of KOTMIN13 on acute inflammation in vivo. Results: KOTMIN13 reduced the release of inflammatory mediators [nitric oxide, prostaglandin E2, interleukin (IL)-1β, and IL-6] and the protein expression of inducible nitric oxide synthase and cyclooxygenase-2 in LPS-stimulated RAW 264.7 cells. Mechanism studies showed the attenuation of LPS-induced NF-κB activation by KOTMIN13 via IκBα degradation abrogation and a subsequent decrease in nuclear p65 levels. Activation of mitogen-activated protein kinases (ERK, JNK, and p38) was also suppressed. Furthermore, KOTMIN13 ameliorated the development of TPA-induced ear edema and carrageenan-induced paw edema in acute inflammatory edema mouse models. Conclusion: Our study demonstrates that KOTMIN13 inhibits inflammatory mediators through the inhibitions of NF-κB and MAPK activities in LPS-induced RAW 264.7 cells, as well as acute inflammation in edema models, indicating that KOTMIN13 is an effective suppressor for anti-inflammatory activities.

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      Lee, E., Kim, S., Park, N., Park, H., Jeong, K., Choi, J., Lee, I., Lee, H., & Lee, E. (2017). Anti-inflammatory Effects of KOTMIN13: A Mixed Herbal Medicine in LPS-stimulated RAW 264.7 Cells and Mouse Edema Models. Pharmacognosy Magazine, 13(50), 216–21. https://doi.org/10.4103/0973-1296.204548