Involvement of multiple transporters in the efflux of 3-hydroxy-3- methylglutaryl-CoA reductase inhibitors across the blood-brain barrier

Ryota Kikuchi, Hiroyuki Kusuhara, Takaaki Abe, Hitoshi Endou, Yuichi Sugiyama

Research output: Contribution to journalArticle

34 Citations (Scopus)

Abstract

Statins, 3-hydroxy-3-methylglutaryl-CoA reductase inhibitors, are frequently used for the treatment of hypercholesterolemia. The present study aimed to examine the involvement of organic anion transporters in the efflux transport of pravastatin and pitavastatin across the blood-brain barrier (BBB). Transport studies using cDNA-transfected cells revealed that these statins are substrates of multispecific organic anion transporters expressed at the BBB (rOat3:S/c22a8 and rOatp2:S/co1a4). The efflux of these statins across the BBB was characterized using the brain efflux index method. The efflux clearance of pitavastatin across the BBB, obtained from the elimination rate constant and the distribution volume in the brain, was greater than that of pravastatin (364 versus 59 μ/min/g brain). The efflux of pravastatin and pitavastatin was saturable (apparent Km values: 18 and 5 μM, respectively) and inhibited by probenecid but unaffected by tetraethylammonium. Furthermore, an inhibitor of the efflux pathway for hydrophilic organic anions across the BBB (p-aminohippurate), and inhibitors of the efflux pathway for amphipathic organic anions (taurocholate and digoxin) inhibited the efflux of both statins. The degree of inhibition by p-aminohippurate was similar and partial for the efflux of pravastatin and pitavastatin. Taurocholate and digoxin completely inhibited the efflux of pitavastatin, whereas their effect was partial for the efflux of pravastatin. The results of the present study suggest the involvement of multiple transporters, including rOat3 and rOatp2, in the efflux transport of pravastatin and pitavastatin across the BBB, each making a different contribution.

Original languageEnglish
Pages (from-to)1147-1153
Number of pages7
JournalJournal of Pharmacology and Experimental Therapeutics
Volume311
Issue number3
DOIs
Publication statusPublished - 2004 Dec

ASJC Scopus subject areas

  • Molecular Medicine
  • Pharmacology

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