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Inhibitory Activity of Natural cis-Khellactone on Soluble Epoxide Hydrolase and Proinflammatory Cytokine Production in Lipopolysaccharides-Stimulated RAW264.7 Cells.


ABSTRACT: The pursuit of anti-inflammatory agents has led to intensive research on the inhibition of soluble epoxide hydrolase (sEH) and cytokine production using medicinal plants. In this study, we evaluated the efficacy of cis-khellactone, a compound isolated for the first time from the roots of Peucedanum japonicum. The compound was found to be a competitive inhibitor of sEH, exhibiting an IC50 value of 3.1 ± 2.5 µM and ki value of 3.5 µM. Molecular docking and dynamics simulations illustrated the binding pose of (-)cis-khellactone within the active site of sEH. The results suggest that binding of the inhibitor to the enzyme is largely dependent on the Trp336-Gln384 loop within the active site. Further, cis-khellactone was found to inhibit pro-inflammatory cytokines, including NO, iNOS, IL-1β, and IL-4. These findings affirm that cis-khellactone could serve as a natural therapeutic candidate for the treatment of inflammation.

SUBMITTER: Kim JH 

PROVIDER: S-EPMC10610198 | biostudies-literature | 2023 Oct

REPOSITORIES: biostudies-literature

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Inhibitory Activity of Natural <i>cis</i>-Khellactone on Soluble Epoxide Hydrolase and Proinflammatory Cytokine Production in Lipopolysaccharides-Stimulated RAW264.7 Cells.

Kim Jang Hoon JH   Park Ji Hyeon JH   Koo Sung Cheol SC   Huh Yun-Chan YC   Hur Mok M   Park Woo Tae WT   Moon Youn-Ho YH   Kim Tae Il TI   Cho Byoung Ok BO  

Plants (Basel, Switzerland) 20231023 20


The pursuit of anti-inflammatory agents has led to intensive research on the inhibition of soluble epoxide hydrolase (sEH) and cytokine production using medicinal plants. In this study, we evaluated the efficacy of <i>cis</i>-khellactone, a compound isolated for the first time from the roots of <i>Peucedanum japonicum</i>. The compound was found to be a competitive inhibitor of sEH, exhibiting an IC<sub>50</sub> value of 3.1 ± 2.5 µM and <i>k</i><sub>i</sub> value of 3.5 µM. Molecular docking an  ...[more]

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