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 |
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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. |
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ISSN: | 0090-9556 1521-009X |
DOI: | 10.1124/dmd.118.083329 |