Nitrofen dose-dependent gestational day-specific murine lung hypoplasia and left-sided diaphragmatic hernia

被引:52
作者
Cilley, RE
Zgleszewski, SE
Krummel, TM
Chinoy, MR
机构
关键词
pulmonary hypoplasia; lung development;
D O I
10.1152/ajplung.1997.272.2.L362
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
2,4-Dichlorophenyl-p-nitrophenyl ether (nitrofen) is known to induce pulmonary hypoplasia (PH) with or without diaphragmatic hernias (DH) in rats and mice. We determined the timing of administration and dose of nitrofen needed to create left-sided DH and PH in fetal mice. Time-dated pregnant CD-1 mice were gavaged with various doses of nitrofen in the later one-half of gestational days (GD) 8-11. Fetuses were removed by laparotomy at GD 14, fixed, and evaluated histologically. Fetal lung size was inversely related to nitrofen dose. Morphometric analysis of normal and nitrofen-exposed hypoplastic lungs at the pseudoglandular stage revealed significant differences in lung length, surface area, and in the number of airways. Left-sided DH were observed in a ''dorsolateral'' position accompanied by PH in similar to 30% of GD 14 fetuses exposed to 25 mg nitrofen on GD 8. A minimal portion of liver was present in the hernia. The lungs of fetuses exposed on GD 9, 10, and 11 progressed to near normal size. Murine fetuses exposed to 25 mg nitrofen on GD 8 resulted in PH and DH, whereas other doses created dose-dependent PH alone or none at all on GD 11. Our study established that, to create left-sided DH and PH in murine fetuses, nitrofen dose specificity and time of administration during gestation were crucial.
引用
收藏
页码:L362 / L371
页数:10
相关论文
共 31 条
[1]   LUNG GROWTH AND MATURATION IN THE RAT MODEL OF EXPERIMENTALLY INDUCED CONGENITAL DIAPHRAGMATIC-HERNIA [J].
ALFONSO, LF ;
VILANOVA, J ;
ALDAZABAL, P ;
DETORRE, BL ;
TOVAR, JA .
EUROPEAN JOURNAL OF PEDIATRIC SURGERY, 1993, 3 (01) :6-11
[2]  
BALLARD PL, 1983, PEDIATR RES, V17, pA371
[3]  
BLACKBURN W R, 1977, American Review of Respiratory Disease, V115, P275
[4]   Bronchial ligation enhances murine fetal lung development ig whole-organ culture [J].
Blewett, CJ ;
Zgleszewski, SE ;
Chinoy, MR ;
Krummel, TM ;
Cilley, RE .
JOURNAL OF PEDIATRIC SURGERY, 1996, 31 (07) :869-877
[5]  
BRANDSMA AE, 1996, BIOCHIM BIOPHYS ACTA, V1201, P266
[6]   ELEMENTAL COMPOSITION OF LAMELLAR BODIES FROM FETAL AND ADULT HUMAN LUNG [J].
CHINOY, MR ;
GONZALES, LW ;
BALLARD, PL ;
FISHER, AB ;
ECKENHOFF, RG .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1995, 13 (01) :99-108
[7]  
CUNNINGHAM MD, 1980, OBSTET GYNECOL, V55, P439
[8]  
DIFIORE JW, 1995, PEDIATR SURG INT, V10, P2
[9]   EFFECT OF FETAL THYROIDECTOMY ON OVINE FETAL LUNG MATURATION [J].
ERENBERG, A ;
RHODES, ML ;
WEINSTEIN, MM ;
KENNEDY, RL .
PEDIATRIC RESEARCH, 1979, 13 (04) :230-235
[10]   PATHOPHYSIOLOGY OF CONGENITAL DIAPHRAGMATIC-HERNIA .2. THE FETAL LAMB CDH MODEL IS SURFACTANT DEFICIENT [J].
GLICK, PL ;
STANNARD, VA ;
LEACH, CL ;
ROSSMAN, J ;
HOSADA, Y ;
MORIN, FC ;
COONEY, DR ;
ALLEN, JE ;
HOLM, B .
JOURNAL OF PEDIATRIC SURGERY, 1992, 27 (03) :382-388