1. Academic Validation
  2. Stylopine from Chelidonium majus inhibits LPS-induced inflammatory mediators in RAW 264.7 cells

Stylopine from Chelidonium majus inhibits LPS-induced inflammatory mediators in RAW 264.7 cells

  • Arch Pharm Res. 2004 Sep;27(9):923-9. doi: 10.1007/BF02975845.
Seon Il Jang 1 Byung Hee Kim Woo-Yiel Lee Sang Jin An Han Gil Choi Byung Hun Jeon Hun-Taeg Chung Jung-Rae Rho Young-Jun Kim Kyu-Yun Chai
Affiliations

Affiliation

  • 1 Department of Skin & beauty, Seojeong College, Yangju 482-860, Korea.
Abstract

Stylopine is a major component of the leaf of Chelidonium majus L. (Papaveraceae), which has been used for the removal of warts, papillomas and condylomas, as well as the treatment of liver disease, in oriental countries. Stylopine per se had no cytotoxic effect in unstimulated RAW 264.7 cells, but concentration-dependently reduced nitric oxide (NO), prostaglandin E2 (PGE2), tumor necrosis factor-alpha (TNF-alpha) and interleukin-1beta (IL-1beta), and the IL-6 production and cyclooxygenase-2 (COX-2) activity caused by the LPS stimulation. The levels of inducible nitric oxide synthase (iNOS) and COX-2 protein expressions were markedly suppressed by stylopine in a concentration dependent manner. These results suggest that stylopine suppress the NO and PGE2 production in macrophages by inhibiting the iNOS and COX-2 expressions. These biological activities of stylopine may contribute to the anti-inflammatory activity of Chelidonium majus.

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