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Department of Physiology, Division of Neuroscience, University of Alberta, Edmonton, Alberta T6G 2S2, Canada
Received 30 October 1996; accepted in final form 21 March 1997.
Allan, Douglas W., and John J. Greer. Pathogenesis of
nitrofen-induced congenital diaphragmatic hernia in fetal rats. J. Appl. Physiol. 83(2): 338-347, 1997.
Congenital diaphragmatic hernia (CDH) is a developmental anomaly
characterized by the malformation of the diaphragm and impaired lung
development. In the present study, we tested several hypotheses
regarding the pathogenesis of CDH, including those suggesting that the
primary defect is due to abnormal 1)
lung development, 2) phrenic nerve
formation, 3) developmental
processes underlying diaphragmatic myotube formation, 4) pleuroperitoneal canal closure,
or 5) formation of the primordial diaphragm within the pleuroperitoneal fold. The
2,4-dichloro-phenyl-p-nitrophenyl ether (nitrofen)-induced CDH rat model was used for this
study. The following parameters were compared between normal and
herniated fetal rats at various stages of development:
1) weight, protein, and DNA content
of lungs; 2) phrenic nerve diameter,
axonal number, and motoneuron distribution;
3) formation of the phrenic nerve intramuscular branching pattern and diaphragmatic myotube formation; and 4) formation of the precursor of
the diaphragmatic musculature, the pleuroperitoneal fold. We
demonstrated that previously proposed theories regarding the primary
role of the lung, phrenic nerve, myotube formation, and the closure of
pleuroperitoneal canal in the pathogenesis of CDH are incorrect.
Rather, the primary defect associated with CDH, at least in the
nitrofen rat model, occurs at the earliest stage of diaphragm
development, the formation of the pleuroperitoneal fold.
breathing; lung; phrenic
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