HMG-CoA reductase inhibitors (statins) and their drug interactions involving CYP enzymes, P-glycoprotein and OATP transporters-an overview

R Balasubramanian, NMP Maideen - Current drug metabolism, 2021 - ingentaconnect.com
… and it is also known to inhibit the OATP1B1-mediated hepatic uptake of substrates [49]. The
… of cyclosporine, as they are all the substrates of OATP1B1 transporter [50, 51]. Cyclosporine …

Drug-drug interactions of P-gp substrates unrelated to CYP metabolism

Y Akamine, N Yasui-Furukori, T Uno - Current drug metabolism, 2019 - ingentaconnect.com
drug-drug interactions (DDIs) has highlighted the clinical importance of hepatic organic
anion-transporting polypeptide transporters (OATPs), ABC drug … their broad substrate specificity …

Clinical aspects of transporter‐mediated drugdrug interactions

A Gessner, J König, MF Fromm - Clinical Pharmacology & …, 2019 - Wiley Online Library
… victim drugs due to OATP-mediated drugdrug interactions … of OATP1B1/1B3 and CYP3A4.
Moreover, most statins are not specifically transported by OATPs, but they are also substrates

[HTML][HTML] Drugdrug interaction potential of darolutamide: in vitro and clinical studies

C Zurth, M Koskinen, R Fricke, O Prien… - … Journal of Drug …, 2019 - Springer
… a low potential for clinically relevant DDIs with drugs that are substrates for CYP or P-gp;
increased exposure of BCRP and probably OATP substrates was the main interaction of note. …

Role of Oatp2b1 in drug absorption and drug-drug interactions

M Chen, S Hu, Y Li, AA Gibson, Q Fu, SD Baker… - Drug Metabolism and …, 2020 - ASPET
… Since several TKIs were previously determined to affect the function of OATPs, … drugs used
in various therapeutic areas that may cause drug-drug interactions with OATP2B1 substrates. …

Effect of cyclosporin A and impact of dose staggering on OATP1B1/1B3 endogenous substrates and drug probes for assessing clinical drug interactions

T Mochizuki, MJ Zamek‐Gliszczynski… - Clinical …, 2022 - Wiley Online Library
… (OATP) 1B1/1B3-mediated drug-drug interactions (DDIs… OATP1B1/1B3 substrates are
anticipated to serve as surrogate probes to assess OATP1B1/1B3-mediated drug-drug interactions

Transporter-mediated drug-drug interactions and their significance

X Liu - Drug Transporters in Drug Disposition, Effects and …, 2019 - Springer
drug interaction) in human and their clinical significances. … regarding clinical relevance are
OATP1B1 and OATP1B3 mainly … between OATP1B1 substrates and several OATP inhibitors. …

[HTML][HTML] Role of OATP1B1 and OATP1B3 in drug-drug interactions mediated by tyrosine kinase inhibitors

DA Garrison, Z Talebi, ED Eisenmann, A Sparreboom… - Pharmaceutics, 2020 - mdpi.com
… As hypertension and diabetes are among the prevalent comorbidities in cancer patients,
many xenobiotic OATP1B1 and OATP1B3 substrate drugs are likely to be co-administrated with …

Assessment of pharmacokinetic drugdrug interactions in humans: in vivo probe substrates for drug metabolism and drug transport revisited

U Fuhr, C Hsin, X Li, W Jabrane… - Annual review of …, 2019 - annualreviews.org
… include the following compounds: Rosuvastatin is a substrate for breast cancer resistance
protein (BCRP) and organic anion transporting polypeptides OATP1B1 and OATP1B3 (10, 93)…

[HTML][HTML] Effect of P-glycoprotein (P-gp) inducers on exposure of P-gp substrates: review of clinical drugdrug interaction studies

M Elmeliegy, M Vourvahis, C Guo, DD Wang - Clinical pharmacokinetics, 2020 - Springer
… While the main focus of our review was P-gp induction, we also noted that the exposure
of pravastatin, an OATP substrate, was reduced by a similar extent as that for dabigatran …