Interactions of cationic drugs and cardiac glycosides at the hepatic uptake level: Studies in the rat in vivo, isolated perfused rat liver, isolated rat hepatocytes and oocytes expressing oatp2

Archives of Pharmacal Research

Volumn 25, Issue 4, 2002, Pages 397-415

  Meijer, Dirk K F ^a,b   Van Montfoort, Jessica E ^a  

^a UNIVERSITY OF GRONINGEN   (Netherlands)

^b UNIVERSITY OF GRONINGEN   (Netherlands)

Author keywords

Basic drugs; Cardiac glycosides; Curare like agents; Digitoxin; Drug interactions; Hepatic Uptake; K Strophanthoside; oatp2; Organic cations; Oubain; Rocuronium

Indexed keywords

ADENOSINE TRIPHOSPHATASE (POTASSIUM SODIUM); CARDIAC GLYCOSIDE; CATION; DIGITOXIN; K STROPHANTHIN GAMMA; K-STROPHANTHOSIDE; ORGANIC ANION TRANSPORTER 2; OUABAIN; STROPHANTHIN; TUBOCURARINE CHLORIDE;

ANIMAL; ARTICLE; BILE; BIOSYNTHESIS; DRUG EFFECT; DRUG INTERACTION; ENZYMOLOGY; GENETICS; IN VITRO STUDY; KINETICS; LIVER; LIVER CELL; MALE; METABOLISM; OOCYTE; RAT; WISTAR RAT; XENOPUS LAEVIS;

ANIMALS; BILE; CARDIAC GLYCOSIDES; CATIONS; DIGITOXIN; DRUG INTERACTIONS; HEPATOCYTES; KINETICS; LIVER; MALE; NA(+)-K(+)-EXCHANGING ATPASE; OOCYTES; ORGANIC ANION TRANSPORT POLYPEPTIDE C; OUABAIN; RATS; RATS, WISTAR; STROPHANTHINS; TUBOCURARINE; XENOPUS LAEVIS;

EID: 0036689055     PISSN: 02536269     EISSN: 02536269     Source Type: Journal    
DOI: 10.1007/BF02976592     Document Type: Review

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