In vitro analysis of esophageal atresia using a whole-embryo culture system

Eur J Pediatr Surg. 2002 Feb;12(1):3-7. doi: 10.1055/s-2002-25086.

Abstract

Background/purpose: Administration of Adriamycin to pregnant rats leads to the development of esophageal atresia with tracheo-esophageal fistula. This defect arises from failure of the trachea to develop normally from the primitive foregut; instead,the upper foregut differentiates into trachea, then continues to the lower esophageal segment as a tracheo-esophageal fistula. Our aim was to explore the possibility of growing Adriamycin-exposed embryos using a whole-embryo culture technique and to determine whether or not esophageal atresia with tracheo-esophageal fistula could be prevented in an Adriamycin-treated rat model.

Methods: Rat embryos were exposed to Adriamycin in utero on days 6 - 9 of gestation, removed on day 10 and grown in vitro as described by New (11) for 48 hours using 100% serum from animals not exposed to Adriamycin.

Results: Thirty Adriamycin-exposed embryos were grown in vitro using normal serum. Histologic assessment of tracheo-esophageal development showed that 14 embryos had normal development, while 16 developed esophageal atresia.

Conclusions: Growth of Adriamycin-exposed embryos was successful using "whole-embryo culture technique"; abnormal tracheo-esophageal development could in some cases be altered by removing the embryos at day 10 and exposing them to normal serum for 48 hours.

MeSH terms

  • Abnormalities, Drug-Induced
  • Animals
  • Antibiotics, Antineoplastic / adverse effects*
  • Antineoplastic Agents / adverse effects*
  • Culture Media
  • Doxorubicin / adverse effects*
  • Embryo, Mammalian / drug effects*
  • Esophageal Atresia / chemically induced*
  • Esophageal Atresia / prevention & control
  • Female
  • Maternal Exposure
  • Organ Culture Techniques / methods*
  • Pregnancy
  • Rats
  • Rats, Sprague-Dawley
  • Time Factors
  • Tracheoesophageal Fistula / chemically induced
  • Tracheoesophageal Fistula / prevention & control

Substances

  • Antibiotics, Antineoplastic
  • Antineoplastic Agents
  • Culture Media
  • Doxorubicin