| Literature DB >> 31102467 |
Sarah Billington1,2, Steven Shoner3, Scott Lee4, Kindra Clark-Snustad4, Matthew Pennington5, David Lewis3, Mark Muzi3, Shirley Rene3, Jean Lee3, Tot Bui Nguyen1, Vineet Kumar1, Kazuya Ishida1,6, Laigao Chen7, Xiaoyan Chu8, Yurong Lai9, Laurent Salphati10, Cornelis E C A Hop10, Guangqing Xiao11,12, Mingxiang Liao12, Jashvant D Unadkat1.
Abstract
Using positron emission tomography imaging, we determined the hepatic concentrations and hepatobiliary transport of [11 C]rosuvastatin (RSV; i.v. injection) in the absence (n = 6) and presence (n = 4 of 6) of cyclosporin A (CsA; i.v. infusion) following a therapeutic dose of unlabeled RSV (5 mg, p.o.) in healthy human volunteers. The sinusoidal uptake, sinusoidal efflux, and biliary efflux clearance (CL; mL/minute) of [11 C]RSV, estimated through compartment modeling were 1,205.6 ± 384.8, 16.2 ± 11.2, and 5.1 ± 1.8, respectively (n = 6). CsA (blood concentration: 2.77 ± 0.24 μM), an organic-anion-transporting polypeptide, Na+ -taurocholate cotransporting polypeptide, and breast cancer resistance protein inhibitor increased [11 C]RSV systemic blood exposure (45%; P < 0.05), reduced its biliary efflux CL (52%; P < 0.05) and hepatic uptake (25%; P > 0.05) but did not affect its distribution into the kidneys. CsA increased plasma concentrations of coproporphyrin I and III and total bilirubin by 297 ± 69%, 384 ± 102%, and 81 ± 39%, respectively (P < 0.05). These data can be used in the future to verify predictions of hepatic concentrations and hepatobiliary transport of RSV.Entities:
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Year: 2019 PMID: 31102467 PMCID: PMC6777999 DOI: 10.1002/cpt.1506
Source DB: PubMed Journal: Clin Pharmacol Ther ISSN: 0009-9236 Impact factor: 6.875