RT Journal Article SR Electronic T1 Repurposing 99mTc-mebrofenin as a probe for molecular imaging of hepatocyte transporters JF Journal of Nuclear Medicine JO J Nucl Med FD Society of Nuclear Medicine SP jnumed.120.261321 DO 10.2967/jnumed.120.261321 A1 Solene Marie A1 Irene HERNANDEZ-LOZANO A1 Oliver Langer A1 Nicolas Tournier YR 2021 UL http://jnm.snmjournals.org/content/early/2021/03/19/jnumed.120.261321.abstract AB Hepatocyte transporters control the hepatobiliary elimination of many drugs, metabolites and endogenous substances. Hepatocyte transporter function is altered in several pathophysiological situations and can be modulated by certain drugs, with a potential impact for pharmacokinetics and drug-induced liver injury. Development of substrate probes with optimal properties for selective and quantitative imaging of hepatic transporters remains a challenge. [99mTc]mebrofenin has been used for decades for hepatobiliary scintigraphy, but the specific transporters controlling its liver kinetics have been characterized more recently. These include sinusoidal influx transporters (organic anion-transporting polypeptides, OATP) responsible for hepatic uptake of [99mTc]mebrofenin, and efflux transporters (multidrug resistance-associated proteins, MRP) mediating its canalicular (liver-to-bile) and sinusoidal (liver-to-blood) excretion. Pharmacokinetic modeling enables molecular interpretation of [99mTc]mebrofenin scintigraphy data, thus offering a widely available translational method to investigate transporter-mediated drug-drug interactions in vivo. [99mTc]mebrofenin allows for phenotyping transporter activity at the different poles of hepatocytes as a biomarker of liver function.