Comparative uptake of statins by hepatic organic anion transporting polypeptides

Uptake into hepatocytes by the organic anion transporting polypeptides (OATP) 1B1, 1B3, and 2B1 can form a rate-determining step in drug clearance. While several lipid-lowering statin drugs are substrates of the hepatic OATPs, the literature statin uptake profiles form a wide range with values obtained from different laboratories and systems. Therefore, this study aimed to characterize hepatic OATP-mediated transport of statins in a single-laboratory experimental setup, allowing comparison between the statins and OATPs. The uptake of atorvastatin, 3R,5S-fluvastatin, 3S,5R-fluvastatin, pravastatin, rosuvastatin, and simvastatin acid was assessed in human embryonic kidney 293 cells overexpressing OATP1B1, 1B3, or OATP2B1. All the three OATPs transported atorvastatin with K<sub>m</sub> values 2.6 μM (1B1), 1.9 μM (1B3), and 1.1 μM (2B1). Also rosuvastatin was transported by all the OATPs: OATP1B1 (as previously reported from our lab) and 2B1 affinities were similar (13 μM) while OATP1B3 had a K<sub>m</sub> of 40 μM. Although all OATPs also transported pravastatin, the uptake by OATP2B1 was not saturated at the studied concentration range, and affinity parameters could be determined only for OATP1B1 and 1B3 at K<sub>m</sub> 37 μM and 28 µM, respectively. OATP2B1 was the high-affinity transporter of the fluvastatin enantiomers (K<sub>m</sub> 0.57 μM for 3S,5R- and 2.5 μM for 3R,5S-fluvastatin) which were not taken up by OATP1B3. Importantly, active simvastatin acid uptake was observed only for OATP1B1 with a K<sub>m</sub> value of 2.1 μM. Taken together, only OATP1B1 could transport all statins and, in general, the affinities of the hydrophobic statins (atorvastatin, fluvastatin, simvastatin acid) were higher compared to the hydrophilic statins (pravastatin, rosuvastatin). These differences between the OATPs and statins can help to explain differences in clinically observed statin gene-drug interactions and have utility in the pharmacokinetic modeling of statins.

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Publication Details

Journal
European Journal of Pharmaceutical Sciences
Published
2025-03-17
DOI
https://doi.org/10.1016/j.ejps.2025.107073
Citations
6
Primary Topic
Drug Transport and Resistance Mechanisms
Type
article
Field-Weighted Citation Impact
6.27

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article

Comparative uptake of statins by hepatic organic anion transporting polypeptides

Alli Sinokki, Wilma Kiander, Mikko Niemi, Heidi Kidron et al.
6 citations
European Journal of Pharmaceutical Sciences
Drug Transport and Resistance Mechanisms
6.27
article

Comparative uptake of statins by hepatic organic anion transporting polypeptides

Alli Sinokki, Wilma Kiander, Mikko Niemi, Heidi Kidron, Mikko Neuvonen
article en
6 citations

Abstract

Uptake into hepatocytes by the organic anion transporting polypeptides (OATP) 1B1, 1B3, and 2B1 can form a rate-determining step in drug clearance. While several lipid-lowering statin drugs are substrates of the hepatic OATPs, the literature statin uptake profiles form a wide range with values obtained from different laboratories and systems. Therefore, this study aimed to characterize hepatic OATP-mediated transport of statins in a single-laboratory experimental setup, allowing comparison between the statins and OATPs. The uptake of atorvastatin, 3R,5S-fluvastatin, 3S,5R-fluvastatin, pravastatin, rosuvastatin, and simvastatin acid was assessed in human embryonic kidney 293 cells overexpressing OATP1B1, 1B3, or OATP2B1. All the three OATPs transported atorvastatin with K<sub>m</sub> values 2.6 μM (1B1), 1.9 μM (1B3), and 1.1 μM (2B1). Also rosuvastatin was transported by all the OATPs: OATP1B1 (as previously reported from our lab) and 2B1 affinities were similar (13 μM) while OATP1B3 had a K<sub>m</sub> of 40 μM. Although all OATPs also transported pravastatin, the uptake by OATP2B1 was not saturated at the studied concentration range, and affinity parameters could be determined only for OATP1B1 and 1B3 at K<sub>m</sub> 37 μM and 28 µM, respectively. OATP2B1 was the high-affinity transporter of the fluvastatin enantiomers (K<sub>m</sub> 0.57 μM for 3S,5R- and 2.5 μM for 3R,5S-fluvastatin) which were not taken up by OATP1B3. Importantly, active simvastatin acid uptake was observed only for OATP1B1 with a K<sub>m</sub> value of 2.1 μM. Taken together, only OATP1B1 could transport all statins and, in general, the affinities of the hydrophobic statins (atorvastatin, fluvastatin, simvastatin acid) were higher compared to the hydrophilic statins (pravastatin, rosuvastatin). These differences between the OATPs and statins can help to explain differences in clinically observed statin gene-drug interactions and have utility in the pharmacokinetic modeling of statins.

European Journal of Pharmaceutical SciencesVol. 209
University of Helsinki (FI), Helsinki University Hospital (FI)
Suomen Kulttuurirahasto, Sigrid Juséliuksen Säätiö, European Research Council
Openalex Percentile: Top 3%
Drug Transport and Resistance Mechanisms
6.27
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