Abstract
The interactions of sulfonylureas and a novel anti-diabetic drug, nateglinide, with rat renal organic anion transporter (rOAT1) expressed in Xenopus laevis oocytes were studied. Uptake of p-aminohippurate via rOAT1 was markedly inhibited by glibenclamide and nateglinide, and moderately by chlorpropamide and tolbutamide. The inhibition constant values (K(i)) for chlorpropamide, glibenclamide, tolbutamide and nateglinide were 39.5, 1.6, 55.5 and 9.2 microM, respectively. Kinetic analysis showed that the inhibition of p-aminohippurate uptake by glibenclamide was competitive. Sulfonylureas examined and nateglinide did not show a trans-stimulation effect on [14C]p-aminohippurate efflux from rOAT1-expressing oocytes. There was no stimulation of [3H]glibenclamide uptake via rOAT1. These findings suggested that sulfonylureas and nateglinide interact with rOAT1, but these drugs are not translocated via the transporter.
Publication types
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Comparative Study
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Anion Transport Proteins
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Binding, Competitive / drug effects
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Carbon Radioisotopes
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Carrier Proteins / antagonists & inhibitors*
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Carrier Proteins / genetics
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Carrier Proteins / metabolism
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Chlorpropamide / pharmacology
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Cyclohexanes / pharmacology*
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Dose-Response Relationship, Drug
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Female
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Glyburide / pharmacology
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Hypoglycemic Agents / pharmacology*
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Kinetics
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Nateglinide
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Oocytes
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Phenylalanine / analogs & derivatives*
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Phenylalanine / pharmacology
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RNA, Complementary / administration & dosage
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RNA, Complementary / genetics
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Rats
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Sulfonylurea Compounds / pharmacology
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Tolbutamide / pharmacology
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Xenopus
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p-Aminohippuric Acid / metabolism
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p-Aminohippuric Acid / pharmacokinetics
Substances
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Anion Transport Proteins
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Carbon Radioisotopes
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Carrier Proteins
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Cyclohexanes
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Hypoglycemic Agents
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RNA, Complementary
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Sulfonylurea Compounds
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Nateglinide
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Phenylalanine
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Tolbutamide
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Glyburide
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Chlorpropamide
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p-Aminohippuric Acid