The cycloartane glycosides cyclocarposide and cyclosieversioside F prevent an increase in the blood serum contents of cholesterol, triglycerides, and total fraction of pre-β- and β-lipoproteins in rabbits with atherosclerosis. They increase the ratio of α-cholesterol to total cholesterol and reduce the calculated coefficient of atherogenicity and the ratio of the total fraction of pre-β- and β-lipoproteins to α-cholesterol. In addition, the cycloartane glycosides restore the activity of antioxidant and NO-ergic systems in the heart muscle that is reduced in rabbits with atherosclerosis. The investigated cycloartane glycosides (especially cyclocarposide) had antiatherosclerotic action inferior to that of lovastatin, a drug from the statin group, and had certain advantages over lovastatin with respect to their effects on the antioxidant and NO-ergic systems.
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Translated from Khimiko-Farmatsevticheskii Zhurnal, Vol. 56, No. 5, pp. 14 – 18, May, 2022.
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Syrov, V.N., Kaipnazarov, T.N., Tsaruk, A.V. et al. Evaluation of the Pharmacotherapeutic Efficacy of Cycloartane Glycosides in Comparison to Lovastatin in Rabbits with Experimental Atherosclerosis. Pharm Chem J 56, 587–591 (2022). https://doi.org/10.1007/s11094-022-02680-5
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DOI: https://doi.org/10.1007/s11094-022-02680-5