@article{oai:repo.qst.go.jp:00077713,
 author = {Kimura, Hiroyuki and Yagi, Yusuke and Mikamo, Mutsumi and Maeda, Kazuya and Kagawa, Shinya and Arimitsu, Kenji and Higashi, Tatsuya and Nishii, Ryuichi and Ono, Masahiro and Nakamoto, Yuji and Togashi, Kaori and Kusuhara, Hiroyuki and Saji, Hideo and Tatsuya, Higashi and Ryuichi, Nishii},
 issue = {5},
 journal = {Drug Metabolism and Pharmacokinetics},
 month = {Oct},
 note = {Quantitative evaluations of the functions of uptake and efflux transporters directly in vivo is desired to understand an efficient hepatobiliary transport of substrate drugs. Pitavastatin is a substrate of organic anion transporting polypeptides (OATPs) and canalicular efflux transporters; thus, it can be a suitable probe for positron-emission tomography (PET) imaging of hepatic transporter functions. To characterize the performance of [18F]PTV-F1, an analogue of pitavastatin, we investigated the impact of rifampicin (a typical OATP inhibitor) coadministration or Bcrp (breast cancer resistance protein) knockout on [18F]PTV-F1 hepatic uptake and efflux in rats by PET imaging. After intravenous administration, [18F]PTV-F1 selectively accumulated in the liver, and the radioactivity detected in plasma, liver, and bile mainly derived from the parent PTV-F1 during the PET study (∼40 min). Coadministration of rifampicin largely decreased the hepatic uptake of [18F]PTV-F1 by 73%. Because of its lower clearance in rats, [18F]PTV-F1 is more sensitive for monitoring changes in hepatic OATP1B function that other previously reported OATP1B PET probes. Rifampicin coadministration also significantly decreased the biliary excretion of radioactivity by 65%. Bcrp knockout did not show a significant impact on its biliary excretion.[18F]PTV-F1 enables quantitative analysis of the hepatobiliary transport system for organic anions.},
 pages = {317--324},
 title = {Evaluation of transporter-mediated hepatobiliary transport of newly developed 18F-labeled pitavastatin derivative, PTV-F1, in rats by PET imaging},
 volume = {34},
 year = {2019}
}