RT Journal Article SR Electronic T1 Novobiocin Is a Potent Inhibitor for Human Organic Anion Transporters JF Drug Metabolism and Disposition JO Drug Metab Dispos FD American Society for Pharmacology and Experimental Therapeutics SP 1203 OP 1210 DO 10.1124/dmd.109.026880 VO 37 IS 6 A1 Peng Duan A1 Guofeng You YR 2009 UL http://dmd.aspetjournals.org/content/37/6/1203.abstract AB Organic anion transporters (OATs) mediate the body disposition of a diverse array of environmental toxins and clinically important drugs. Previous studies have shown that novobiocin, an inhibitor for breast cancer resistance proteins (BCRP), inhibited organic anion transport. However, its interactions with specific OATs are unknown. In the current study, we characterized the inhibitory effects of novobiocin on the function of human OATs (hOAT)1, hOAT3, and hOAT4. Kinetic study revealed that novobiocin inhibited OAT-mediated uptake in a competitive manner, with Ki of 14.87 ± 0.40 μM for hOAT1, Ki of 4.77 ± 1.12 μM for hOAT3, and Ki of 90.50 ± 7.50 μM for hOAT4. Furthermore, the cis- and trans-inhibition feature of novobiocin demonstrated that novobiocin was a potent inhibitor but not a substrate for hOAT1 (IC50 = 34.76 ± 0.31 μM), hOAT3 (IC50 = 4.987 ± 0.35 μM), and hOAT4 (IC50 = 92.68 ± 0.34 μM). We further showed that the effects of novobiocin on OATs were not mediated through a change in transporter protein abundance on the plasma membrane. Taken together, we conclude that novobiocin seems to interact with the substrate-binding sites of OATs from both the intracellular and the extracellular sides, and this interaction interferes with the substrate-binding site(s) on respective carriers, leading to an apparent reduction in carriers available for the substrates. Because BCRP is often expressed in the same tissue where multiple OATs are identified such as liver, kidney and placenta, when dissecting the contribution of BCRP to drug disposition using novobiocin as an inhibitor, its inhibitory effect to OATs has to be taken into consideration. The American Society for Pharmacology and Experimental Therapeutics