AI Article Synopsis

  • - Betulin, a triterpenoid from birch tree bark, and its derivatives were studied for their potential anti-inflammatory properties, particularly against key inflammatory genes and pathways.
  • - Specific derivatives, particularly compounds 3, 4, and 5, showed selective inhibition of inducible nitric oxide synthase (iNOS) and reduced nitric oxide production, while a new compound (9) demonstrated broader anti-inflammatory effects by targeting multiple inflammatory mediators.
  • - The promising results, including effective in vivo reduction of inflammation in mice, suggest that these betulin derivatives could be valuable for future drug development aimed at treating inflammation.

Article Abstract

Betulin is a pharmacologically active triterpenoid found in the bark of the birch tree (Betula sp. L.). Betulin and betulinic acid are structurally related to anti-inflammatory steroids, but little is known about their potential anti-inflammatory properties. In the present study, the inflammatory gene expression and the anti-inflammatory properties of betulin, betulinic acid, and 16 semisynthetic betulin derivatives were investigated. Betulin derivatives 3, 4, and 5 selectively inhibited the expression of the inducible nitric oxide synthase (iNOS) in a post-transcriptional manner. They also inhibited nitric oxide (NO) production but had no effect on the other inflammatory factors studied. More interestingly, a new anti-inflammatory betulin derivative 9 with a wide-spectrum anti-inflammatory activity was discovered. Compound 9 was found to suppress the expression of cytokines interleukin-6 (IL-6) and monocyte chemotactic protein-1 (MCP-1), as well as that of prostaglandin synthase-2 (COX-2) in addition to iNOS. The in vivo anti-inflammatory effect of compound 9 was indicated via significant suppression of the carrageenan-induced paw inflammation in mice. The results show, for the first time, that the pyrazole-fused betulin derivative (9) and related compounds have anti-inflammatory properties that could be utilized in drug development.

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Source
http://dx.doi.org/10.1021/acs.jnatprod.5b00709DOI Listing

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