Equilibrative Nucleoside Transporter 1 (ENT1, SLC29A1 ) Facilitates Transfer of the Antiretroviral Drug Abacavir across the Placenta

Abacavir is a preferred antiretroviral drug for preventing mother-to-child human immunodeficiency virus transmission; however, mechanisms of its placental transfer have not been satisfactorily described to date. Because abacavir is a nucleoside-derived drug, we hypothesized that the nucleoside trans...

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Veröffentlicht in:Drug metabolism and disposition 2018-11, Vol.46 (11), p.1817-1826
Hauptverfasser: Cerveny, Lukas, Ptackova, Zuzana, Ceckova, Martina, Karahoda, Rona, Karbanova, Sara, Jiraskova, Lucie, Greenwood, Susan L, Glazier, Jocelyn D, Staud, Frantisek
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Sprache:eng
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Zusammenfassung:Abacavir is a preferred antiretroviral drug for preventing mother-to-child human immunodeficiency virus transmission; however, mechanisms of its placental transfer have not been satisfactorily described to date. Because abacavir is a nucleoside-derived drug, we hypothesized that the nucleoside transporters, equilibrative nucleoside transporters (ENTs, ) and/or Na -dependent concentrative nucleoside transporters (CNTs, ), may play a role in its passage across the placenta. To test this hypothesis, we performed uptake experiments using the choriocarcinoma-derived BeWo cell line, human fresh villous fragments, and microvillous plasma membrane (MVM) vesicles. Using endogenous substrates of nucleoside transporters, [ H]-adenosine (ENTs, CNT2, and CNT3) and [ H]-thymidine (ENTs, CNT1, and CNT3), we showed significant activity of ENT1 and CNT2 in BeWo cells, whereas experiments in the villous fragments and MVM vesicles, representing a model of the apical membrane of a syncytiotrophoblast, revealed only ENT1 activity. When testing [ H]-abacavir uptakes, we showed that of the nucleoside transporters, ENT1 plays the dominant role in abacavir uptake into placental tissues, whereas contribution of Na -dependent transport, most likely mediated by CNTs, was observed only in BeWo cells. Subsequent experiments with dually perfused rat term placentas showed that Ent1 contributes significantly to overall [ H]-abacavir placental transport. Finally, we quantified the expression of in first- and third-trimester placentas, revealing that is the dominant isoform. Neither nor expression changed over the course of placental development, but there was considerable interindividual variability in their expression. Therefore, drug-drug interactions and the effect of interindividual variability in placental ENT1 expression on abacavir disposition into fetal circulation should be further investigated to guarantee safe and effective abacavir-based combination therapies in pregnancy.
ISSN:0090-9556
1521-009X
DOI:10.1124/dmd.118.083329