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Bilateral megaureters in the Adriamycin rat model
A Mortell1, L Fourcade, V Solari
1The Children's Research Centre, Our Lady's Hospital for Sick Children, Crumlin, Dublin 12, Ireland.
Pediatric Surgery International
|December 4, 2004
Summary
Prenatal exposure to Adriamycin in rats between gestational days 7-9 causes significant urinary tract anomalies, primarily bilateral megaureters with a small bladder. This model aids research into congenital obstructive uropathy.
Area of Science:
- Developmental biology
- Toxicology
- Urology
Background:
- Congenital obstructive uropathy presents a significant health challenge in neonates, yet its underlying pathophysiology remains unclear.
- Existing experimental models for prenatal urinary tract obstruction are limited, necessitating new approaches.
- Prenatal Adriamycin exposure in rats is known to induce various malformations, including urinary tract anomalies.
Purpose of the Study:
- To investigate the incidence of urinary tract anomalies resulting from Adriamycin administration during specific gestational windows in rat embryos.
- To identify the critical period of Adriamycin exposure that maximizes the occurrence of these anomalies.
Main Methods:
- Pregnant rats received Adriamycin (1.75 mg/kg) intraperitoneally on gestational days 6-10.
- Control groups received saline.
- Embryos were recovered on day 21, examined for external and internal urinary tract malformations, and processed for histological analysis.
Main Results:
- Adriamycin administration on gestational days 7-9 resulted in a 91.6% incidence of urinary tract anomalies, compared to 16% in controls.
- The most frequent anomaly was bilateral megaureters with a hypoplastic bladder (81%).
- Other observed anomalies included ureterohydronephrosis, duplex kidney, and renal agenesis.
Conclusions:
- Gestational days 7-9 represent a critical window for Adriamycin-induced bilateral megaureters with a small bladder in the rat model.
- This Adriamycin-induced rat model offers a valuable tool for further investigation into the pathophysiology of congenital obstructive uropathy.