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Transplacental passage and hemodynamic effects of esmolol in the gravid ewe.

Using a chronic maternal-fetal sheep preparation, the authors determined the transplacental passage and the hemodynamic changes consequent to maternal administration of esmolol. Fifteen experiments were performed in six chronically instrumented pregnant ewes near term. Each animal received esmolol iv, 500 micrograms.kg-1.min-1, for 4 min and then 300 micrograms.kg-1.min-1 for 6 min. Maternal and fetal blood esmolol concentrations (mean +/- SEM) were 1.2 +/- 0.28 and 0.1 +/- 0.03 micrograms/ml, respectively, at the completion of the infusion, and 0.03 +/- 0.01 microgram/ml in the mother and not detectable in the fetus 10 min after stopping the infusion. Despite the relatively low blood esmolol concentration in the fetus compared to the mother, the hemodynamic effects in the fetus were similar to those in the mother. The maximal decrease of maternal mean arterial pressure (MAP) and heart rate (HR) were 7 +/- 2 and 14 +/- 3% (mean +/- SEM), respectively (P less than .05). The maximal decrease of fetal MAP and HR were 7 +/- 2 and 12 +/- 3%, respectively (P less than .05). No changes were seen in maternal or fetal acid-base variables, and intra-amniotic pressure was not affected. The authors conclude that esmolol has a rapid but relatively small transplacental passage, and it is eliminated rapidly from both maternal and fetal plasma.

Adrenergic beta-Antagonists↗

Dose-dependent transplacental infection of murine encephalomyelitis virus GDVII in gravid uterus.

Intrauterine infection of murine encephalomyelitis virus GDVII was investigated by the indirect immunofluorescence method. Sixty-day-old pregnant mice were inoculated with 5 gradated doses of the virus ranging from 0.001 to 1.5 MLD50 via i.v. route on the 10th day of gestation. The mice exsanguinated on postinfection day 8 showed high incidences of viral antigen in the uterine walls, placentas, and fetal subcutaneous tissues with doses of 0.1-1.5 MLD50, regardless of the presence of maternal symptoms. Incidence of viral antigen-positive cells in fetal brains was high with a dose of 0.1 MLD50, but not by the other doses. However, the brains of the stillborn and newly-born mice derived from females infected by a dose of 0.5 MLD50 brought about still higher detection rates of viral antigen, as well as in the postpartum uteri. In effect, transplacental transmission of the virus was clearly demonstrated, and appeared to be dose-dependent.

Animals↗