Characterization of the efflux transport of 17β-estradiol-D-17β-glucuronide from the brain across the blood-brain barrier

Daisuke Sugiyama, Hiroyuki Kusuhara, Yoshihisa Shitara, Takaaki Abe, Peter J. Meier, Takashi Sekine, Hitoshi Endou, Hiroshi Suzuki, Yuichi Sugiyama

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161 Citations (Scopus)

Abstract

The contribution of organic anion transporters to the total efflux of 17β-estradiol-D-17β-glucuronide (E217βG) through the blood-brain barrier (BBB) was investigated using the Brain Efflux Index method by examining the inhibitory effects of probenecid, taurocholate (TCA), p-aminohippurate (PAH), and digoxin. E217βG was eliminated through the BBB with a rate constant of 0.037 min-1 after the microinjection into the brain. Probenecid and TCA inhibited this elimination with an IC50 value of 34 and 1.8 nmol/0.5 μl of injectate, respectively, whereas PAH and digoxin reduced the total efflux to about 80 and 60% of the control value, respectively. The selectivity of these inhibitors was confirmed by examining their inhibitory effects on the transport via organic anion transporting polypeptide 1 (Oatp1), Oatp2, organic anion transporter 1 (Oat1), and Oat3 transfectants using LLC-PK1 cells as hosts. Digoxin specifically inhibited the transport via Oatp2 (Ki = 0.037μM). The K1 values of TCA for Oatp1 and Oatp2 (11 and 39μM, respectively) were about 20 times lower than those for Oat1 and Oat3 (2.8 and 0.8 mM, respectively). PAH did not affect the transport via the Oatp family, but had a similar affinity for Oat1 and Oat3 (85 and 300μM, respectively). Probenecid had a similar affinity for these transporters (Oatp1, Oatp2, Oat1, and Oat3) examined in this study. Taking the selectivity of these inhibitors into consideration, the maximum contribution made by the Oatp2 and Oat family to the total efflux of E217βG from the brain appears to be about 40 and 20%, respectively.

Original languageEnglish
Pages (from-to)316-322
Number of pages7
JournalJournal of Pharmacology and Experimental Therapeutics
Volume298
Issue number1
Publication statusPublished - 2001

ASJC Scopus subject areas

  • Molecular Medicine
  • Pharmacology

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