Qi B, Diez-Pardo J A, Navarro C, Tovar J A
Department of Pediatric Surgery, Hospital Infantil Universitario "La Paz", E-28046, Madrid, Spain.
Pediatr Surg Int. 1996 Aug;11(7):444-7. doi: 10.1007/BF00180079.
We recently reported on a new fetal rat model of esophageal atresia (EA) with tracheoesophageal fistula (TEF) induced by prenatal exposure to adriamycin (1.75 mg/kg i. p. injected daily to the pregnant dam from the 6th to 9th gestational days). With this treatment regime, many fetuses were resorbed and the number of associated malformations was very high. The present study demonstrates that similar doses of the drug administered only on the 8th and 9th gestational days allow higher fetal survival (9.7 ∓ 3.9 vs. 6.8 ∓ 4.7 fetuses per litter, P < 0.01) with a similar incidence of EA-TEF (41.2% vs. 56.4%, n. s.) and decreased occurence of associated anorectal and genitourinary malformations. Since this model is an instrument for further investigation of the disturbed cellular and morphogenetic events leading to EA and TEF, the narrowing of the embryologic window obtained by the present study will allow better focusing of the research on the critical period of time involved.
我们最近报道了一种新的食管闭锁(EA)合并气管食管瘘(TEF)的胎鼠模型,该模型是通过在孕期第6至9天每天给孕鼠腹腔注射阿霉素(1.75 mg/kg)诱导产生的。采用这种治疗方案时,许多胎儿被吸收,且相关畸形的数量非常高。本研究表明,仅在孕期第8天和第9天给予相似剂量的药物,可使胎儿存活率更高(每窝胎儿数为9.7±3.9 vs. 6.8±4.7,P<0.01),EA-TEF的发生率相似(41.2% vs. 56.4%,无统计学差异),且相关肛门直肠和泌尿生殖系统畸形的发生率降低。由于该模型是进一步研究导致EA和TEF的细胞和形态发生事件紊乱的工具,本研究获得的胚胎学窗口变窄将使研究能够更好地聚焦于所涉及的关键时间段。