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The regulation of inflammatory cytokine secretion in macrophage cell line by the chemical constituents of Rhus sylvestris.

Bioorganic & medicinal chemistry letters (2009-05-19)
Yan Ding, Huu Tung Nguyen, Sung In Kim, Ha Won Kim, Young Ho Kim
RESUMEN

In our preliminary screening study on the anti-inflammatory activity, eight triterpenes, one sterol, and one chalcone were isolated from the CH(2)Cl(2)-soluble extract of the stems and leaves of Rhus sylvestris Siebold and Zucc (Anacardiaceae). On the basis of their spectroscopic data, these compounds were identified as 10alpha-cucurbitadienol (1), glut-5-en-3-ol (2), beta-amyrin acetate (3), beta-amyrin (4) and lupeol (5), cycloart-24-en-3-one (6), cycloart-25-en-3,24-dione (7), 24-hydroxycycloart-25-en-3-one (8), beta-sitosterol (9), and 2'-hydroxy-4,4'-dimethoxychalcone (10). All of them were isolated from this plant for the first. Furthermore, the compounds in non-cytotoxic concentrations (0-1.0microM) were tested for their ability to block inflammatory cytokine secretion in the presence of LPS in the murine RAW264.7 macrophage cell line. Among the compounds that were tested, compounds 8 and 9 reduced the LPS-induced secretion of IL-6, as well as TNF-alpha, in a mouse RAW264.7 macrophage cell line. Moreover, compounds 2, 3, 7, and 10 specifically diminished only the secretion of TNF-alpha even in 0.01microM concentrations. It is thus suggested that they are potential therapeutics of TNF-alpha-related diseases and conditions, such as transplant rejection, type II diabetes, and atherosclerosis.

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Sigma-Aldrich
β-Sitosterol, synthetic, ≥95%
Sigma-Aldrich
β-Sitosterol, ≥70%
Sigma-Aldrich
Lupeol, ≥94%
Sigma-Aldrich
β-Sitosterol, from soybean, ≥96%
Supelco
β-Sitosterol, certified reference material, 100 μg/mL in chloroform