Title : Comparative Hepatic and Intestinal Efflux Transport of Statins.

Pub. Date : 2021 Sep

PMID : 34162690






4 Functional Relationships(s)
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1 In our study, apically expressed breast cancer resistance protein (BCRP) and P-glycoprotein (P-gp) transported atorvastatin, fluvastatin, pitavastatin, and rosuvastatin. Atorvastatin ATP binding cassette subfamily B member 1 Homo sapiens
2 In our study, apically expressed breast cancer resistance protein (BCRP) and P-glycoprotein (P-gp) transported atorvastatin, fluvastatin, pitavastatin, and rosuvastatin. Atorvastatin ATP binding cassette subfamily B member 1 Homo sapiens
3 For atorvastatin, the corresponding values for P-gp-mediated efflux were 32-73% and 56%, respectively. Atorvastatin ATP binding cassette subfamily B member 1 Homo sapiens
4 These data indicate that BCRP may play an important role in limiting the intestinal absorption and facilitating the biliary excretion of rosuvastatin and that P-gp may restrict the intestinal absorption and mediate the biliary excretion of atorvastatin. Atorvastatin ATP binding cassette subfamily B member 1 Homo sapiens