Lack of interaction of digoxin and P-glycoprotein inhibitors, quinidine and verapamil in human placenta in vitro

Gershon Holcberg, Olga Sapir, Marina Tsadkin, Mahmoud Huleihel, Simcha Lazer, Miriam Katz, Moshe Mazor, Zvi Ben-Zvi

Research output: Contribution to journalArticlepeer-review

27 Scopus citations

Abstract

Objective: To determine the effect of quinidine and verapamil, known antiarrhythmic agents and P-glycoprotein (Pgp) inhibitors, on digoxin transport from the maternal to the fetal compartment in the isolated perfused human placenta. Study design: Isolated placental cotyledons from normal human placentae (n=20) were dually perfused with M199 medium enriched with albumin (0.3%) and glucose (0.1%). The maternal and the fetal circulation flow rates were 12 and 6ml/min, respectively. Closed circulations were used to evaluate steady state transplacental gradient formation. In six placentae quinindine was added to the maternal circuit; after 45min of perfusion, digoxin was added to the maternal circulation. The effect of verapamil on digoxin transfer from the maternal to the fetal compartments was explored in five placentae. In six additional placentae the transfer of digoxin was studied in the absence of quinidine. Transplacental passage of digoxin was calculated from repeated fetal and maternal perfusate samples. Digoxin levels were determined in perfusate samples by fluorescence polarization immunoassay. Antipyrine was added to the maternal reservoir of all placentae as reference substance. Results: The transfer of digoxin (alone) and in the presence of quinidine or verapamil was 10.93±3.71, 9.00±5.2 and 12.94±4.86%, respectively. The levels of digoxin in the fetal compartment, 0.62±0.20, 0.48±0.29 and 0.60±0.26ng/ml, respectively, were not significantly affected by quinidine and verapamil. These Pgp modulators, also did not influence significantly the steady state levels of digoxin in the maternal compartment. Conclusion: Neither quinidine nor verapamil affected the transplacental transfer of digoxin in vitro in normal human placentae. In contrast to the other tissues, they do not inhibit Pgp activity in term human placentae.

Original languageEnglish
Pages (from-to)133-137
Number of pages5
JournalEuropean Journal of Obstetrics, Gynecology and Reproductive Biology
Volume109
Issue number2
DOIs
StatePublished - 15 Aug 2003
Externally publishedYes

Keywords

  • Digoxin interaction
  • Human perfusion system
  • Human placenta

ASJC Scopus subject areas

  • Reproductive Medicine
  • Obstetrics and Gynecology

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