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209 related items for PubMed ID: 30488476
1. Effect of high uric acid on the disposition of metformin: in vivo and in vitro studies. Zhang G, Ma Y, Xi D, Rao Z, Sun X, Wu X. Biopharm Drug Dispos; 2019 Jan; 40(1):3-11. PubMed ID: 30488476 [Abstract] [Full Text] [Related]
2. Changes of drug pharmacokinetics mediated by downregulation of kidney organic cation transporters Mate1 and Oct2 in a rat model of hyperuricemia. Nishizawa K, Yoda N, Morokado F, Komori H, Nakanishi T, Tamai I. PLoS One; 2019 Jan; 14(4):e0214862. PubMed ID: 30951542 [Abstract] [Full Text] [Related]
3. Inhibitory effect of atenolol on urinary excretion of metformin via down-regulating multidrug and toxin extrusion protein 1 (rMate1) expression in the kidney of rats. Ma YR, Huang J, Shao YY, Ma K, Zhang GQ, Zhou Y, Zhi R, Qin HY, Wu XA. Eur J Pharm Sci; 2015 Feb 20; 68():18-26. PubMed ID: 25486332 [Abstract] [Full Text] [Related]
4. Organic cation transporter and multidrug and toxin extrusion 1 co-mediated interaction between metformin and berberine. Shi R, Xu Z, Xu X, Jin J, Zhao Y, Wang T, Li Y, Ma Y. Eur J Pharm Sci; 2019 Jan 15; 127():282-290. PubMed ID: 30428337 [Abstract] [Full Text] [Related]
5. Metformin is a superior substrate for renal organic cation transporter OCT2 rather than hepatic OCT1. Kimura N, Masuda S, Tanihara Y, Ueo H, Okuda M, Katsura T, Inui K. Drug Metab Pharmacokinet; 2005 Oct 15; 20(5):379-86. PubMed ID: 16272756 [Abstract] [Full Text] [Related]
6. Renal vectorial transport of berberine mediated by organic cation transporter 2 (OCT2) and multidrug and toxin extrusion proteins 1 (MATE1) in rats. Shi R, Yang Y, Xu Z, Dai Y, Zheng M, Wang T, Li Y, Ma Y. Biopharm Drug Dispos; 2018 Jan 15; 39(1):47-58. PubMed ID: 29065218 [Abstract] [Full Text] [Related]
8. A drug-drug interaction study to evaluate the impact of peficitinib on OCT1- and MATE1-mediated transport of metformin in healthy volunteers. Shibata M, Toyoshima J, Kaneko Y, Oda K, Nishimura T. Eur J Clin Pharmacol; 2020 Aug 15; 76(8):1135-1141. PubMed ID: 32472157 [Abstract] [Full Text] [Related]
12. N(1)-methylnicotinamide as an endogenous probe for drug interactions by renal cation transporters: studies on the metformin-trimethoprim interaction. Müller F, Pontones CA, Renner B, Mieth M, Hoier E, Auge D, Maas R, Zolk O, Fromm MF. Eur J Clin Pharmacol; 2015 Jan 15; 71(1):85-94. PubMed ID: 25552403 [Abstract] [Full Text] [Related]
13. Pregnancy Increases the Renal Secretion of N1-methylnicotinamide, an Endogenous Probe for Renal Cation Transporters, in Patients Prescribed Metformin. Bergagnini-Kolev MC, Hebert MF, Easterling TR, Lin YS. Drug Metab Dispos; 2017 Mar 15; 45(3):325-329. PubMed ID: 28069720 [Abstract] [Full Text] [Related]
16. Competitive inhibition of the luminal efflux by multidrug and toxin extrusions, but not basolateral uptake by organic cation transporter 2, is the likely mechanism underlying the pharmacokinetic drug-drug interactions caused by cimetidine in the kidney. Ito S, Kusuhara H, Yokochi M, Toyoshima J, Inoue K, Yuasa H, Sugiyama Y. J Pharmacol Exp Ther; 2012 Feb 15; 340(2):393-403. PubMed ID: 22072731 [Abstract] [Full Text] [Related]
18. Renal uptake of substrates for organic anion transporters Oat1 and Oat3 and organic cation transporters Oct1 and Oct2 is altered in rats with adenine-induced chronic renal failure. Komazawa H, Yamaguchi H, Hidaka K, Ogura J, Kobayashi M, Iseki K. J Pharm Sci; 2013 Mar 15; 102(3):1086-94. PubMed ID: 23280877 [Abstract] [Full Text] [Related]
19. Fampridine is a Substrate and Inhibitor of Human OCT2, but not of Human MATE1, or MATE2K. Xiao G, Rowbottom C, Boiselle C, Gan LS. Pharm Res; 2018 Jun 18; 35(8):159. PubMed ID: 29915999 [Abstract] [Full Text] [Related]
20. Altered pharmacokinetics of cationic drugs caused by down-regulation of renal rat organic cation transporter 2 (Slc22a2) and rat multidrug and toxin extrusion 1 (Slc47a1) in ischemia/reperfusion-induced acute kidney injury. Matsuzaki T, Morisaki T, Sugimoto W, Yokoo K, Sato D, Nonoguchi H, Tomita K, Terada T, Inui K, Hamada A, Saito H. Drug Metab Dispos; 2008 Apr 18; 36(4):649-54. PubMed ID: 18180268 [Abstract] [Full Text] [Related] Page: [Next] [New Search]