Role of P-glycoprotein in pharmacokinetics: clinical implications

JH Lin, M Yamazaki - Clinical pharmacokinetics, 2003 - Springer
P-glycoprotein, the most extensively studied ATP-binding cassette (ABC) transporter, functions
as a biological barrier by extruding toxins and xenobiotics out of cells. In vitro and in vivo …

In vitro substrate identification studies for p-glycoprotein-mediated transport: species difference and predictability of in vivo results

M Yamazaki, WE Neway, T Ohe, IW Chen… - … of Pharmacology and …, 2001 - ASPET
Two different cellular assay models were assessed as in vitro systems for P-glycoprotein (P-gp)
substrate identification: cellular accumulation studies with KB-V1, a human MDR1P-gp-…

Clinical relevance of P-glycoprotein in drug therapy

JH Lin, M Yamazaki - Drug metabolism reviews, 2003 - Taylor & Francis
The drug efflux transporter P-glycoprotein (P-gp) is known to confer multidrug resistance in
cancer chemotherapy. The P-gp is highly expressed in many types of tumor cells, as well as …

Recent advances in carrier-mediated hepatic uptake and biliary excretion of xenobiotics

M Yamazaki, H Suzuki, Y Sugiyama - Pharmaceutical research, 1996 - Springer
Purpose. Besides renal excretion, hepatic metabolism and biliary excretion are the major
pathways involved in the removal of xenobiotics. Recently, for many endogenous and …

Methotrexate is excreted into the bile by canalicular multispecific organic anion transporter in rats

M Masuda, Y I'izuka, M Yamazaki, R Nishigaki, Y Kato… - Cancer Research, 1997 - AACR
Methotrexate [(+) amethopterin, L-MTX] has two carboxyl groups in its structure and is eliminated
mainly by excretion into urine and bile. To investigate the biliary excretion mechanism …

Na (+)-independent multispecific anion transporter mediates active transport of pravastatin into rat liver

M Yamazaki, H Suzuki, M Hanano… - American Journal …, 1993 - journals.physiology.org
To examine whether the relatively selective inhibition of hepatic cholesterol synthesis by the
hydrophilic 3-hydroxyl-3-methylglutaryl-coenzyme A (HMG-CoA) reductase inhibitor …

Interactions of human P-glycoprotein with simvastatin, simvastatin acid, and atorvastatin

JH Hochman, N Pudvah, J Qiu, M Yamazaki… - Pharmaceutical …, 2004 - Springer
Purpose. In this study, P-glycoprotein (P-gp) mediated efflux of simvastatin (SV), simvastatin
acid (SVA), and atorvastatin (AVA) and inhibition of P-gp by SV, SVA, and AVA were …

Influence of P-glycoprotein on the transport and metabolism of indinavir in Caco-2 cells expressing cytochrome P-450 3A4

JH Hochman, M Chiba, J Nishime, M Yamazaki… - Journal of pharmacology …, 2000 - ASPET
Caco-2 cells grown in the presence of 1α,25-di-OH vitamin D 3 (di-OH vit D 3 ) were used
as a model to evaluate the effects of P-glycoprotein (Pgp) efflux on CYP3A4-mediated …

Biliary excretion of pravastatin in rats: contribution of the excretion pathway mediated by canalicular multispecific organic anion transporter (cMOAT)

M Yamazaki, S Akiyama, K Ni'inuma, R Nishigaki… - Drug Metabolism and …, 1997 - ASPET
The biliary excretion of pravastatin in normal rats and Eisai hyperbiliruminemic rats (EHBRs)
was examined in vivo andin vitro using bile canalicular membrane vesicles (CMVs).In vivo, …

Hepatic uptake of the novel antifungal agent caspofungin

P Sandhu, W Lee, X Xu, BF Leake, M Yamazaki… - Drug metabolism and …, 2005 - ASPET
Caspofungin (CANCIDAS, a registered trademark of Merck & Co., Inc.) is a novel echinocandin
antifungal agent used in the treatment of esophageal and invasive candidiases, invasive …