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PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
11
pubmed:dateCreated
2007-10-22
pubmed:abstractText
The role of transporters in the disposition of (+)-2-[4-({[2-(benzo[1,3]dioxol-5-yloxy)-pyridine-3-carbonyl]-amino}-methyl)-3-fluoro-phenoxy]-propionic acid (CP-671,305), an orally active inhibitor of phosphodiesterase-4, was examined. In bile duct-exteriorized rats, a 7.4-fold decrease in the half-life of CP-671,305 was observed, implicating enterohepatic recirculation. Statistically significant differences in CP-671,305 pharmacokinetics (clearance and area under the curve) were discernible in cyclosporin A- or rifampicin-pretreated rats. Considering that cyclosporin A and rifampicin inhibit multiple uptake/efflux transporters, the interactions of CP-671,305 with major human hepatic drug transporters, multidrug resistance protein 1 (MDR1), multidrug resistance-associated protein 2 (MRP2), breast cancer resistant protein (BCRP), and organic anion-transporting polypeptide (OATPs) were evaluated in vitro. CP-671,305 was identified as a substrate of MRP2 and BCRP, but not MDR1. CP-671,305 was a substrate of human OATP2B1 with a high affinity (Km = 4 microM) but not a substrate for human OATP1B1 or OATP1B3. Consistent with these results, examination of hepatobiliary transport of CP-671,305 in hepatocytes indicated active uptake followed by efflux into bile canaliculi. Upon examination as a substrate for major rat hepatic Oatps, CP-671,305 displayed high affinity (Km = 12 microM) for Oatp1a4. The role of rat Mrp2 in the biliary excretion was also examined in Mrp2-deficient rats. The observations that CP-671,305 pharmacokinetics were largely unaltered suggested that compromised biliary clearance of CP-671,305 was compensated by increased urinary clearance. Overall, these studies suggest that hepatic transporters play an important role in the disposition and clearance of CP-671,305 in rat and human, and as such, these studies should aid in the design of clinical drug-drug interaction studies.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/ABCB1 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/ABCG2 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/ATP-Binding Cassette Transporters, http://linkedlifedata.com/resource/pubmed/chemical/Abcc2 protein, rat, http://linkedlifedata.com/resource/pubmed/chemical/Membrane Transport Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Multidrug Resistance-Associated..., http://linkedlifedata.com/resource/pubmed/chemical/Neoplasm Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Organic Anion Transporters, http://linkedlifedata.com/resource/pubmed/chemical/Organic Anion Transporters..., http://linkedlifedata.com/resource/pubmed/chemical/P-Glycoprotein, http://linkedlifedata.com/resource/pubmed/chemical/Phosphodiesterase 4 Inhibitors, http://linkedlifedata.com/resource/pubmed/chemical/Phosphodiesterase Inhibitors, http://linkedlifedata.com/resource/pubmed/chemical/Propionic Acids, http://linkedlifedata.com/resource/pubmed/chemical/Pyridines, http://linkedlifedata.com/resource/pubmed/chemical/SLCO2B1 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Slco1a4 protein, rat, http://linkedlifedata.com/resource/pubmed/chemical/multidrug resistance-associated...
pubmed:status
MEDLINE
pubmed:month
Nov
pubmed:issn
0090-9556
pubmed:author
pubmed:issnType
Print
pubmed:volume
35
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
2111-8
pubmed:dateRevised
2010-11-18
pubmed:meshHeading
pubmed-meshheading:17686907-ATP-Binding Cassette Transporters, pubmed-meshheading:17686907-Animals, pubmed-meshheading:17686907-Bile, pubmed-meshheading:17686907-CHO Cells, pubmed-meshheading:17686907-Cell Line, pubmed-meshheading:17686907-Cricetinae, pubmed-meshheading:17686907-Cricetulus, pubmed-meshheading:17686907-Hepatocytes, pubmed-meshheading:17686907-Humans, pubmed-meshheading:17686907-Male, pubmed-meshheading:17686907-Membrane Transport Proteins, pubmed-meshheading:17686907-Molecular Structure, pubmed-meshheading:17686907-Multidrug Resistance-Associated Proteins, pubmed-meshheading:17686907-Neoplasm Proteins, pubmed-meshheading:17686907-Organic Anion Transporters, pubmed-meshheading:17686907-Organic Anion Transporters, Sodium-Independent, pubmed-meshheading:17686907-P-Glycoprotein, pubmed-meshheading:17686907-Phosphodiesterase 4 Inhibitors, pubmed-meshheading:17686907-Phosphodiesterase Inhibitors, pubmed-meshheading:17686907-Propionic Acids, pubmed-meshheading:17686907-Pyridines, pubmed-meshheading:17686907-Rats, pubmed-meshheading:17686907-Rats, Mutant Strains, pubmed-meshheading:17686907-Rats, Sprague-Dawley, pubmed-meshheading:17686907-Rats, Wistar, pubmed-meshheading:17686907-Transfection
pubmed:year
2007
pubmed:articleTitle
Role of transporters in the disposition of the selective phosphodiesterase-4 inhibitor (+)-2-[4-({[2-(benzo[1,3]dioxol-5-yloxy)-pyridine-3-carbonyl]-amino}-methyl)-3-fluoro-phenoxy]-propionic acid in rat and human.
pubmed:affiliation
Pharmacokinetics, Dyamics, and Metabolism Department, Pfizer Global Research and Development, Eastern Point Road, Groton, CT 06340, USA. amit.kalgutkar@pfizer.com
pubmed:publicationType
Journal Article