If meningomyelocele is indeed a progressive intrauterine process, then
early delivery or possibly intrauterine repair of meningomyelocele be
comes an issue. Utilizing the delayed splotch (Spd) mouse, a genetical
ly transmitted neural tube defect model, we looked for evidence of abn
ormalities of neural tissue exposed to amniotic fluid. Affected embryo
nic and fetal mice were examined with the light microscope, and also w
ith the transmission and scanning electron microscope. Neuronal develo
pment and programmed cell death paralleled normal fetal development. N
o evidence of inflammation on or within the exposed neural tissue was
observed. Because the Vascular supply to the alar and basilar plate ar
e different, vascular development was also examined and no difference
could be found. In conclusion, we found no evidence of deterioration o
f the exposed neural tube during the gestational period of a mouse, wh
ich suggests that exposure of unneurulated spinal cord to amniotic flu
id is not a risk factor to the fetus with a neural tube defect.