Target intelligence / Profile preview

Solute carrier family 22 member 6 (hOAT1) and Solute carrier family 22 member 8 (hOAT3) (hOAT1/hOAT3)

Target
hOAT1/hOAT3
Molecular classification
Transporter, Solute carrier family 22 (SLC22), Organic anion transporter (OAT) subfamily
01

Overview

Renal organic anion transporters 1 (hOAT1) and 3 (hOAT3) are essential membrane transport proteins located on the basolateral membrane of renal proximal tubule cells. Encoded by the SLC22A6 and SLC22A8 genes, these transporters facilitate the uptake of a diverse array of organic anions from the blood into the tubular cells, representing a critical step in the renal secretion and systemic clearance of both endogenous metabolites and exogenous drugs. They handle a wide variety of substrates, including uremic toxins, signaling molecules like prostaglandins, and numerous therapeutic agents such as beta-lactam antibiotics, nonsteroidal anti-inflammatory drugs (NSAIDs), and antivirals. Because of their broad substrate specificity, hOAT1 and hOAT3 are major sites for drug-drug interactions, where the inhibition of one transporter can significantly alter the pharmacokinetics and toxicity profiles of co-administered medications. Furthermore, these transporters are implicated in drug-induced nephrotoxicity, as the rapid uptake of certain drugs can lead to high intracellular concentrations that damage tubular cells. Consequently, they are recognized by regulatory agencies as key targets for evaluating the safety and interaction potential of new drug candidates.

Other names
SLC22A6SLC22A8Organic anion transporter 1Organic anion transporter 3NKT (Novel Kidney Transporter)PAH transporterPara-aminohippurate transporter
02

Mechanism of action

Inhibition of basolateral uptake transporters in the renal proximal tubule, which reduces the secretion of substrate drugs into the urine or prevents the accumulation of nephrotoxic agents within tubular cells.

03

Biological functions

Renal excretion of organic anionsSystemic drug clearanceMaintenance of metabolic homeostasisTransport of uremic toxinsInter-organ communication via the gut-liver-kidney axisUptake of endogenous metabolites (e.g., prostaglandins, urate, dicarboxylates)
04

Disease associations

Chronic kidney disease (CKD)Drug-induced nephrotoxicityHyperuricemiaUremiaRenal failure
05

Safety considerations

Risk of clinically significant drug-drug interactions (DDIs) leading to increased systemic exposure and toxicity of co-administered drugsPotential for drug-induced nephrotoxicity due to high intracellular concentrations of transported toxinsAltered drug clearance and exposure in patients with renal impairment
06

Interacting drugs

Probenecid

11 more in the full profile.

07

Biomarkers

TaurineGlycochenodeoxycholate-3-sulfate (GCDCA-S)Pyridoxic acid (PDA)Homovanillic acid (HVA)6-carboxyfluorescein (6-CF)Creatinine (as a shared substrate)

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