Pharmaceutical Research

, Volume 20, Issue 5, pp 720–727

Expression and Functional Involvement of Organic Anion Transporting Polypeptide Subtype 3 (Slc21a7) in Rat Choroid Plexus

  • Hiroyuki Kusuhara
  • Zhonggui He
  • Yoshinori Nagata
  • Yoshitane Nozaki
  • Takashi Ito
  • Hiroyuki Masuda
  • Peter J. Meier
  • Takaaki Abe
  • Yuichi Sugiyama
Article

DOI: 10.1023/A:1023473216759

Cite this article as:
Kusuhara, H., He, Z., Nagata, Y. et al. Pharm Res (2003) 20: 720. doi:10.1023/A:1023473216759

Abstract

Purpose. It has been shown that transport(s) are involved in the uptake of estradiol 17β glucuronide (E217βG) by the choroid plexus (CP). The purpose of this study is to compare the substrate specificity of the transporter in the CP with those of rat organic anion transporting polypeptide 1 (rOatp1) and rOatp3.

Methods. The expression of rOatp1 and rOatp3 in rat CP was confirmed by RT-PCR and Western blot analyses. The substrate specificity of rOatp1 and rOatp3 was compared using cDNA-transfected LLC-PK1 cells. The uptake of E217βG by rat isolated CP was determined by centrifugal filtration technique.

Results. PCR analyses demonstrated that the mRNA expression of rOatp3 was abundant in the CP, whereas that of rOatp1 was low. Immunohistochemical staining revealed that rOatp3 is expressed on the apical membrane of the CP. Kinetic parameters (Km and Ki values) of rOatp3 were similar to those for rOatp1. The results of mutual inhibition study suggest that E217βG and taurocholate share the same mechanism in the CP. Corticosterone, estrone-3-sulfate and indomethacin are moderate inhibitors, but no effects by digoxin, p-aminohippurate, benzylpenicillin and cimetidine were observed.

Conclusions. rOatp3 is most possible candidate transporter involved in the uptake of organic anions on the brush border membrane of the choroid epithelial cells.

choroid plexus blood-CSF barrier efflux transport Oatp organic anion 

Copyright information

© Plenum Publishing Corporation 2003

Authors and Affiliations

  • Hiroyuki Kusuhara
    • 1
  • Zhonggui He
    • 1
  • Yoshinori Nagata
    • 1
  • Yoshitane Nozaki
    • 1
  • Takashi Ito
    • 2
  • Hiroyuki Masuda
    • 2
  • Peter J. Meier
    • 3
  • Takaaki Abe
    • 4
  • Yuichi Sugiyama
    • 1
  1. 1.Department of Biopharmaceutics, Graduate School of Pharmaceutical SciencesThe University of TokyoTokyoJapan
  2. 2.Drug Metabolism & Physicochemical Property Research LaboratoryDaiichi PharmaceuticalTokyoJapan
  3. 3.Division of Clinical Pharmacology and Toxicology, Department of MedicineUniversity Hospital ZurichZurichSwitzerland
  4. 4.Division of Nephrology, Endocrinology, and Vascular Medicine, Department of MedicineTohoku University Graduate School of MedicineSendaiJapan

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