Trospium Chloride Transport by Mouse Drug Carriers of the Slc22 and Slc47 Families
العنوان: | Trospium Chloride Transport by Mouse Drug Carriers of the Slc22 and Slc47 Families |
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المؤلفون: | Matthias Gorecki, Simon F. Müller, Regina Leidolf, Joachim Geyer |
المصدر: | International Journal of Molecular Sciences Volume 22 Issue 1 International Journal of Molecular Sciences, Vol 22, Iss 22, p 22 (2021) |
بيانات النشر: | MDPI, 2020. |
سنة النشر: | 2020 |
مصطلحات موضوعية: | Mice, Knockout, drug transport, Organic Cation Transport Proteins, Nortropanes, Organic Cation Transporter 2, Biological Transport, Muscarinic Antagonists, Benzilates, Article, trospium, lcsh:Chemistry, Mice, Inbred C57BL, Kinetics, HEK293 Cells, lcsh:Biology (General), lcsh:QD1-999, OCT, drug excretion, transport, MATE, Animals, Humans, Catecholamine Plasma Membrane Transport Proteins, lcsh:QH301-705.5 |
الوصف: | Background: The muscarinic receptor antagonist trospium chloride (TCl) is used for pharmacotherapy of the overactive bladder syndrome. TCl is a hydrophilic positively charged drug. Therefore, it has low permeability through biomembranes and requires drug transporters for distribution and excretion. In humans, the organic cation transporters OCT1 and OCT2 and the multidrug and toxin extrusion MATE1 and MATE2-K carriers showed TCl transport. However, their individual role for distribution and excretion of TCl is unclear. Knockout mouse models lacking mOct1/mOct2 or mMate1 might help to clarify their role for the overall pharmacokinetics of TCl. Method: In preparation of such experiments, TCl transport was analyzed in HEK293 cells stably transfected with the mouse carriers mOct1, mOct2, mMate1, and mMate2, respectively. Results: Mouse mOct1, mOct2, and mMate1 showed significant TCl transport with Km values of 58.7, 78.5, and 29.3 µ M, respectively. In contrast, mMate2 did not transport TCl but showed MPP+ transport with Km of 60.0 µ M that was inhibited by the drugs topotecan, acyclovir, and levofloxacin. Conclusion: TCl transport behavior as well as expression pattern were quite similar for the mouse carriers mOct1, mOct2, and mMate1 compared to their human counterparts. |
وصف الملف: | application/pdf |
اللغة: | English |
تدمد: | 1422-0067 |
الوصول الحر: | https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::6e4efa7b700f063170bc96d38015fd89Test http://europepmc.org/articles/PMC7792585Test |
حقوق: | OPEN |
رقم الانضمام: | edsair.pmid.dedup....6e4efa7b700f063170bc96d38015fd89 |
قاعدة البيانات: | OpenAIRE |
تدمد: | 14220067 |
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