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The "specific" P-glycoprotein inhibitor zosuquidar (LY335979) also weakly inhibits human organic cation transporters.
- Source :
-
Naunyn-Schmiedeberg's archives of pharmacology [Naunyn Schmiedebergs Arch Pharmacol] 2024 Dec 24. Date of Electronic Publication: 2024 Dec 24. - Publication Year :
- 2024
- Publisher :
- Ahead of Print
-
Abstract
- Zosuquidar (LY335979) is a widely used experimental P-glycoprotein (P-gp) inhibitor, which is commended as very potent but also as very specific for P-gp. In this in vitro and in silico study, we demonstrated for the first time that zosuquidar also inhibits organic cation transporters (OCT) 1-3, albeit less potently than P-gp. This still has to be kept in mind when zosuquidar is used to inhibit cellular efflux of P-gp substrates that are concurrently transported into the cells by OCTs. To avoid interference in these assays, zosuquidar concentrations should be kept below 1 µM.<br />Competing Interests: Declarations. Competing interest: The authors declare no competing interests.<br /> (© 2024. The Author(s).)
Details
- Language :
- English
- ISSN :
- 1432-1912
- Database :
- MEDLINE
- Journal :
- Naunyn-Schmiedeberg's archives of pharmacology
- Publication Type :
- Academic Journal
- Accession number :
- 39718614
- Full Text :
- https://doi.org/10.1007/s00210-024-03743-y