The organic anion transporter (OAT) family: a systems biology perspective

SK Nigam, KT Bush, G Martovetsky… - Physiological …, 2015 - journals.physiology.org
The organic anion transporter (OAT) subfamily, which constitutes roughly half of the SLC22
(solute carrier 22) transporter family, has received a great deal of attention because of its …

Renal drug transporters and drug interactions

A Ivanyuk, F Livio, J Biollaz, T Buclin - Clinical pharmacokinetics, 2017 - Springer
Transporters in proximal renal tubules contribute to the disposition of numerous drugs.
Furthermore, the molecular mechanisms of tubular secretion have been progressively …

Organic anion transporters: discovery, pharmacology, regulation and roles in pathophysiology

AL VanWert, MR Gionfriddo… - Biopharmaceutics & drug …, 2010 - Wiley Online Library
Our understanding of the mechanisms behind inter‐and intra‐patient variability in drug
response is inadequate. Advances in the cytochrome P450 drug metabolizing enzyme field …

Abundance of drug transporters in the human kidney cortex as quantified by quantitative targeted proteomics

B Prasad, K Johnson, S Billington, C Lee… - Drug Metabolism and …, 2016 - ASPET
Protein expression of renal uptake and efflux transporters was quantified by quantitative
targeted proteomics using the surrogate peptide approach. Renal uptake transporters …

In vitro and in vivo evidence of the importance of organic anion transporters (OATs) in drug therapy

G Burckhardt, BC Burckhardt - Drug Transporters, 2011 - Springer
Abstract Organic anion transporters 1-10 (OAT1-10) and the urate transporter 1 (URAT1)
belong to the SLC22A gene family and accept a huge variety of chemically unrelated …

In vitro-in vivo extrapolation of transporter-mediated clearance in the liver and kidney

H Kusuhara, Y Sugiyama - Drug metabolism and pharmacokinetics, 2009 - jstage.jst.go.jp
Transporters govern drug movement into and out of tissues, thereby playing an important
role in drug disposition in plasma and to the site of action. The molecular cloning of such …

Characterisation of human tubular cell monolayers as a model of proximal tubular xenobiotic handling

CDA Brown, R Sayer, AS Windass, IS Haslam… - Toxicology and applied …, 2008 - Elsevier
The aim of this study was to determine whether primary human tubular cell monolayers
could provide a powerful tool with which to investigate the renal proximal tubular handling of …

Precision-cut tissue slices as a tool to predict metabolism of novel drugs

IAM Graaf, GMM Groothuis, P Olinga - Expert opinion on drug …, 2007 - Taylor & Francis
Precision-cut tissue slices have been applied by many researchers because they represent
an organ mini-model that closely resembles the organ from which it is prepared, with all cell …

Inhibitory effects of p-aminohippurate and probenecid on the renal clearance of adefovir and benzylpenicillin as probe drugs for organic anion transporter (OAT) 1 and …

K Maeda, Y Tian, T Fujita, Y Ikeda, Y Kumagai… - European Journal of …, 2014 - Elsevier
Probe substrates for, and inhibitors of, specific transporters are desired to evaluate
quantitatively the in vivo functions of transporters in humans. Based on published data …

Multiple human isoforms of drug transporters contribute to the hepatic and renal transport of olmesartan, a selective antagonist of the angiotensin II AT1-receptor

A Yamada, K Maeda, E Kamiyama, D Sugiyama… - Drug metabolism and …, 2007 - ASPET
Olmesartan, a novel angiotensin II AT1-receptor antagonist, is excreted into both bile and
urine, with minimal metabolism. Because olmesartan is a hydrophilic anionic compound …