نتایج جستجو برای: oatp1b1

تعداد نتایج: 379  

Journal: :Pharmaceutics 2015
Marie Brännström Pär Nordell Britta Bonn Andrew M Davis Anna-Pia Palmgren Constanze Hilgendorf Katarina Rubin Ken Grime

Clinical studies with montelukast show variability in effect and polymorphic OATP2B1-dependent absorption has previously been implicated as a possible cause. This claim has been challenged with conflicting data and here we used OATP2B1-transfected HEK293 cells to clarify the mechanisms involved. For montelukast, no significant difference in cell uptake between HEK-OATP2B1 and empty vector cell ...

2010

Contrast-enhancing magnetic resonance imaging with the liverspecific agent gadolinium-ethoxybenzyl-diethylenetriamine pentaacetic acid (Gd-EOB-DTPA) has been shown to improve the detection rate of focal lesions. There is evidence from preclinical studies that multidrug organic anion transporters are involved in hepatic uptake of Gd-EOB-DTPA. Therefore, we evaluated affinity of the contrast agen...

2017
KM Morrissey LZ Benet JA Ware

Approaches to predict and characterize drug–drug interactions (DDI) mediated by a single drug-metabolizing enzyme or a single transporter are well established. However, complex DDIs, where multiple metabolic and transport processes are involved, require an integrative translational approach.1,2 If a drug undergoes reversible metabolism, the net contribution of the processes of metabolism, uptak...

2013
Veronika Buxhofer-Ausch Lena Secky Katrin Wlcek Martin Svoboda Valentinos Kounnis Evangelos Briasoulis Andreas G. Tzakos Walter Jaeger Theresia Thalhammer

Members of the organic anion transporter family (OATP) mediate the transmembrane uptake of clinical important drugs and hormones thereby affecting drug disposition and tissue penetration. Particularly OATP subfamily 1 is known to mediate the cellular uptake of anticancer drugs (e.g., methotrexate, derivatives of taxol and camptothecin, flavopiridol, and imatinib). Tissue-specific expression was...

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2005
Cuiping Chen Rouchelle J Mireles Scott D Campbell Jian Lin Jessica B Mills Jinghai J Xu Teresa A Smolarek

The present study examined the interaction of four 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitors (atorvastatin, lovastatin, and simvastatin in acid and lactone forms, and pravastatin in acid form only) with multidrug resistance gene 1 (MDR1, ABCB1) P-glycoprotein, multidrug resistance-associated protein 2 (MRP2, ABCC2), and organic anion-transporting polypeptide 1B1 (OATP1B1, SLCO2...

Journal: :Pediatrics 2008
Zhili Lin Jamie Fontaine Jon F Watchko

OBJECTIVE The potential for genetically determined conditions to modulate the risk for developing neonatal hyperbilirubinemia is increasingly being recognized. The aims of this investigation were to (1) develop genotyping assays for an expanded panel of mutations and polymorphisms across 3 genes that are involved in bilirubin production and metabolism (glucose-6-phosphate dehydrogenase [G6PD], ...

2012
Nan Li Weifang Hong Hong Huang Hanping Lu Guangyun Lin Mei Hong

As an important structure in membrane proteins, transmembrane domains have been found to be crucial for properly targeting the protein to cell membrane as well as carrying out transport functions in transporters. Computer analysis of OATP sequences revealed transmembrane domain 2 (TM2) is among those transmembrane domains that have high amino acid identities within different family members. In ...

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