| Warning:  Undefined variable $zfal in C:\Inetpub\vhosts\kidney.de\httpdocs\mlpefetch.php on line 525
 
 Deprecated:  str_replace(): Passing null to parameter #3 ($subject) of type array|string is deprecated in C:\Inetpub\vhosts\kidney.de\httpdocs\mlpefetch.php on line 525
 
  
 Warning:  Undefined variable $sterm in C:\Inetpub\vhosts\kidney.de\httpdocs\mlpefetch.php on line 530
 
 Warning:  Undefined variable $sterm in C:\Inetpub\vhosts\kidney.de\httpdocs\mlpefetch.php on line 531
 
   English Wikipedia
 
 Nephropedia Template TP (
 
 Twit Text
 
 
 DeepDyve
 Pubget Overpricing
 | lüll   
 
 Impact of genetic polymorphisms of transporters on the pharmacokinetic,  pharmacodynamic and toxicological properties of anionic drugs Maeda K; Sugiyama YDrug Metab Pharmacokinet  2008[]; 23 (4): 223-35As the importance of drug transporters in the clinical pharmacokinetics of drugs  is recognized, genetic polymorphisms of drug transporters have emerged as one of  the determinant factors to produce the inter-individual variability of  pharmacokinetics. Many clinical studies have shown the influence of genetic  polymorphisms of drug transporters on the pharmacokinetics and subsequent  pharmacological and toxicological effects of drugs. The functional change in a  transporter in clearance organs such as liver and kidney affects the drug  concentration in the blood circulation, while that in the pharmacological or  toxicological target can alter the local concentration at the target sites  without changing its plasma concentration. As for the transporters for organic  anions, some single nucleotide polymorphisms (SNPs) or haplotypes occurring with  high frequency in organic anion transporting polypeptide (OATP) 1B1, multidrug  resistance 1 (MDR1), and breast cancer resistance protein (BCRP) have been  extensively investigated in both human clinical studies and in vitro functional  assays. We introduce some examples showing the relationship between haplotypes in  transporters and pharmacokinetics and pharmacological effects of drugs. We also  discuss how to predict the effect of functional changes in drug transporters  caused by genetic polymorphisms on the pharmacokinetics of drugs from in vitro  data.|*Polymorphism, Genetic[MESH]|ATP Binding Cassette Transporter, Subfamily B, Member 1/*genetics[MESH]|ATP Binding Cassette Transporter, Subfamily G, Member 2[MESH]|ATP-Binding Cassette Transporters/*genetics[MESH]|Haplotypes[MESH]|Humans[MESH]|Liver-Specific Organic Anion Transporter 1[MESH]|Membrane Transport Proteins/*genetics[MESH]|Multidrug Resistance-Associated Protein 2[MESH]|Multidrug Resistance-Associated Proteins/*genetics[MESH]|Mutation[MESH]|Neoplasm Proteins/*genetics[MESH]|Organic Anion Transporters/*genetics[MESH]|Polymorphism, Single Nucleotide[MESH]
 |