Several phytosterols, stigmasterol, campesterol and β-sitosterol, were shown to have potent anti-complementary activities. Stigmasterol was the most potent. A marked consumption of C4 was observed to have occurred when serum was incubated with these phytosterols, and β-sitosterol and stigmasterol showed higher C4 consumption than campesterol. After the incubation of serum with these phytosterols in the absence of Ca2+ ions, cleavage of C3 in the serum was detected by immunoelectrophoresis. Stigmasterol caused greater C3 cleavage than the other two compounds. Stigmasterol also showed higher consumption of complement than campesterol and β-sitosterol when rabbit erythrocytes were used in the assay system in the absence of Ca2+ ions. These results indicate that these phytosterols activate complement via both the alternative and classical pathways. © 1987, The Pharmaceutical Society of Japan. All rights reserved.
CITATION STYLE
Yamada, H., Yoshino, M., Matsumoto, T., Nagai, T., Kiyohara, H., Cyong, J. C., … Ōmura, S. (1987). Effects of Phytosterols on Anti-complementary Activity. Chemical and Pharmaceutical Bulletin, 35(12), 4851–4855. https://doi.org/10.1248/cpb.35.4851
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