Ex vivo perfusion model of mouse liver and its application to analyze the effects of OCT1 deficiency

The method enables reproducible and reliable perfusion of mouse livers. We applied it to study the effects of Oct1 knockout on drug metabolism. Oct1 knockout affected the first-pass metabolism of codeine, including the formation of the metabolites morphine and morphine-3-glucuronide, as well as the first-pass metabolism of proguanil and the formation of cycloguanil. The model is applicable to any mouse strain, genetic background, and substrate of interest and is thus applicable to a wide variety of research questions.

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Journal
Frontiers in Pharmacology
Published
2025-11-14
DOI
https://doi.org/10.3389/fphar.2025.1629421
Primary Topic
Pharmacogenetics and Drug Metabolism
Type
article
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article

Ex vivo perfusion model of mouse liver and its application to analyze the effects of OCT1 deficiency

Marleen J. Meyer, Giuliano Ciarimboli, Mladen V. Tzvetkov, Markus Grube et al.
Frontiers in Pharmacology
Pharmacogenetics and Drug Metabolism
article

Ex vivo perfusion model of mouse liver and its application to analyze the effects of OCT1 deficiency

Marleen J. Meyer, Giuliano Ciarimboli, Mladen V. Tzvetkov, Markus Grube, Vincent Rönnpagel, Felix Morof
article en

Abstract

The method enables reproducible and reliable perfusion of mouse livers. We applied it to study the effects of Oct1 knockout on drug metabolism. Oct1 knockout affected the first-pass metabolism of codeine, including the formation of the metabolites morphine and morphine-3-glucuronide, as well as the first-pass metabolism of proguanil and the formation of cycloguanil. The model is applicable to any mouse strain, genetic background, and substrate of interest and is thus applicable to a wide variety of research questions.

Frontiers in PharmacologyVol. 16
Universitätsmedizin Greifswald (DE), University Hospital Münster (DE)
Openalex Percentile: Top 57%
Pharmacogenetics and Drug Metabolism
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