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Lipophilic 1,1-bisphosphonates are potent squalene synthase inhibitors and orally active cholesterol lowering agents in vivo.

1993; Elsevier BV; Volume: 268; Issue: 33 Linguagem: Inglês

10.1016/s0021-9258(19)74540-2

1083-351X

Carl P. Ciosek, David R. Magnin, Thomas Harrity, Janette V. H. Logan, John K. Dickson, Eric M. Gordon, Kenneth Hamilton, Kern G. Jolibois, Lori Kunselman, R. Michael Lawrence,

Cholesterol and Lipid Metabolism

Squalene synthase catalyzes the reductive dimerization of two molecules of farnesyl diphosphate to form squalene at the final branchpoint of the cholesterol biosynthetic pathway. We report herein that isoprenyl 1,1-bisphosphonates and related analogs are potent inhibitors of rat microsomal squalene synthase (I50 = 0.7-32 nM). In addition, members of this family are potent inhibitors of cholesterol biosynthesis in rats on intravenous and oral dosing, as well as cholesterol lowering agents in rats and hamsters. Significant inhibition of cholesterol biosynthesis in rats by lovastatin occurs with a concomitant inhibition of dolichol and coenzyme-Q9 synthesis. In contrast, bisphosphonate 4 has no effect on dolichol and coenzyme-Q9 biosynthesis in rats under conditions where cholesterol biosynthesis is > 90% inhibited.