دورية أكاديمية

Involvement of Organic Anion Transporting Polypeptide 1a5 (Oatp1a5) in the Intestinal Absorption of Endothelin Receptor Antagonist in Rats.

التفاصيل البيبلوغرافية
العنوان: Involvement of Organic Anion Transporting Polypeptide 1a5 (Oatp1a5) in the Intestinal Absorption of Endothelin Receptor Antagonist in Rats.
المؤلفون: Takeshi Tani1, Hiroshi Arakawa2, Akihiro Kikuchi2, Masato Chiba1, Yasuyuki Ishii1, Bente Steffansen3, Ikumi Tamai2
المصدر: Pharmaceutical Research. May2008, Vol. 25 Issue 5, p1085-1091. 7p.
مصطلحات موضوعية: *ABSORPTION, *HYDROGEN-ion concentration, *INTESTINAL absorption, *MALABSORPTION syndromes
مستخلص: Abstract Purpose  To assess the contribution of organic anion transporting polypeptide 1a5 (Oatp1a5/Oatp3) in the intestinal absorption of an orally active endothelin receptor antagonist, ()-(5S,6R,7R)-2-butyl-7-[2-((2S)-2-carboxypropyl)-4-methoxyphenyl]-5-(3,4-methylene-dioxyphenyl)cyclopenteno[1,2-b]pyridine-6-carboxylic acid (compound-A) in rats. Methods  Uptakes of [14C]compound-A by Oatp1a5-expressing Xenopus laevis oocytes and isolated rat enterocytes were evaluated. Results  The uptake of compound-A by Oatp1a5-expressing oocytes was significantly higher than that by water-injected oocytes and Oatp1a5-mediated uptake was saturable with K m value of 116 μM. Compound-A was taken up into isolated enterocytes in time- and concentration-dependent manners and the estimated K m value was 83 μM, which was close to that for the Oatpt1a5-mediated uptake in oocytes. Both uptakes of compound-A by Oatp1a5-expressing oocytes and enterocytes were pH-sensitive with significantly higher uptake at acidic pH than those at neutral pH. Uptakes of compound-A into Oatp1a5-expressing oocytes and enterocytes were significantly decreased in the presence of Oatp1a5 substrates such as bromosulfophthalein and taurocholic acid. Conclusions  These results consistently suggested that Oatp1a5 is contributing to the intestinal absorption of compound-A at least in part, and the transporter-mediated absorption seems to be maximized at the acidic microenvironment of epithelial cells in the small intestine in rats. [ABSTRACT FROM AUTHOR]
قاعدة البيانات: Academic Search Index
الوصف
تدمد:07248741
DOI:10.1007/s11095-007-9472-4