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The Journal of Lipid Research, Vol. 40, 464-474, March 1999
Copyright © 1999 by Lipid Research, Inc.
Comparison of synthetic saponin cholesterol absorption inhibitors in rabbits: evidence for a non-stoichiometric, intestinal mechanism of action
Lee A. Morehousea,
Faan-Wen Bangertera,
Michael P. DeNinnoa,
Philip B. Inskeepa,
Peter A. McCarthya,
Judith L. Pettinia,
Yvette E. Savoya,
Eliot D. Sugarmana,
Robert W. Wilkinsa,
Theresa C. Wilsona,
Heidi A. Woodya,
Lawrence M. Zaccaroa, and
Charles E. Chandlera
a Department of Cardiovascular and Metabolic Diseases, Pfizer Central Research, Eastern Point Road, Groton, CT 06340
Correspondence to:
Lee A. Morehouse
The hypocholesterolemic activities of pamaqueside and tiqueside, two structurally similar saponins, were evaluated in cholesterol-fed rabbits. The pharmacological profiles of the saponins were virtually identical: both dose-dependently decreased the intestinal absorption of labeled cholesterol 2575%, increased fecal neutral sterol excretion up to 2.5-fold, and decreased hepatic cholesterol content 1055%. High doses of pamaqueside (>5 mg/kg) or tiqueside (>125 mg/kg) completely prevented hypercholesterolemia. Decreases in plasma and hepatic cholesterol levels were strongly correlated with increased neutral sterol excretion. Ratios of neutral sterol excreted to pamaqueside administered were greater than 1:1 at all doses, in opposition to the formation of a stoichiometric complex previously suggested for tiqueside and other saponins. Ratios in tiqueside-treated rabbits were less than unity, a reflection of its lower potency. Pamaqueside-treated rabbits exhibited a more rapid decline in plasma cholesterol concentrations than control animals fed a cholesterol-free diet, indicating that the compound also inhibited the absorption of biliary cholesterol. Intravenous administration of pamaqueside had no effect on plasma cholesterol levels despite plasma levels twice those observed in rabbits given pamaqueside orally.
These data indicate that pamaqueside and tiqueside induce hypocholesterolemia by blocking lumenal cholesterol absorption via a mechanism that apparently differs from the stoichiometric complexation of cholesterol hypothesized for other saponins.Morehouse, L. A., F-W. Bangerter, M. P. DeNinno, P. B. Inskeep, P. A. McCarthy, J. L. Pettini, Y. E. Savoy, E. D. Sugarman, R. W. Wilkins, T. C. Wilson, H. A. Woody, L. M. Zaccaro, and C. E. Chandler. Comparison of synthetic saponin cholesterol absorption inhibitors in rabbits: evidence for a non-stoichiometric, intestinal mechanism of action. J. Lipid Res. 1999. 40: 464 474.
Supplementary key words:
tiqueside, pamaqueside, hypocholesterolemic, fecal neutral sterols

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Copyright © 1999 by the American Society for Biochemistry and Molecular Biology.
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