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DOI: 10.1055/s-0039-3400145
Plaunol A isolated from Croton stellatopilosus suppress inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2)
Publikationsverlauf
Publikationsdatum:
20. Dezember 2019 (online)
A cyclic diterpene, namely plaunotol from Croton stellatopilosus Ohba or plaunoi (Thai name) has long been used in the treatment of gastric ulcer and it has been manufactured in a gelatin capsule under the trade name as Kelnac® (Sankyo Daiichi, Japan) [1]. Other cyclic diterpenes have also isolated from plaunoi including labdane-, kaurene-, clerodane-type diterpenes[2], [3]. Previously, plaunotol, plaunol E and plaunol F been reportedanti-inflammatory activity in lipopolysaccharide (LPS)-induced murine macrophage RAW264.7 cells [4]. In the present study, plaunol A, isolated from the stem, was assessed for an anti-inflammatory activity in the LPS-induced RAW264.7 cells model. The result showed that plaunol A exhibited an inhibitory effect on nitric oxide (NO) production with an IC50 of 11.69 µM and cytotoxicity at the concentration more than30 µM. In addition, the transcription profile analysis of inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2) genes in the RAW264.7 cells using qRT-PCR technique that plaunol A inhibited the NO production by suppressing the iNOS and COX-2 mRNAs. In conclusion, plaunol A possessed an anti-inflammatory effect by suppressing the iNOS and COX-2 in the macrophage RAW cells.
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References
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