Y. Chen et al., PERINATAL ASPHYXIA-INDUCED CHANGES IN RAT-BRAIN TYROSINE HYDROXYLASE-IMMUNOREACTIVE CELL BODY NUMBER - EFFECTS OF NICOTINE TREATMENT, Neuroscience letters, 221(2-3), 1997, pp. 77-80
Perinatal asphyxia (15-22 min) was induced to male Sprague-Dawley rat
pups during the last day of gestation and the surviving pups were sacr
ificed at 4 weeks of age. Brain sections were stained for tyrosine hyd
roxylase immunoreactivity and Cresyl violet. With increasing duration
of perinatal asphyxia a reduction in the number of tyrosine hydroxylas
e immunoreactive (TH-IR) nerve cell bodies was found in the locus ceru
leus, probably reflecting an increased death of noradrenaline nerve ce
ll bodies. In contrast, perinatal asphyxia (15-20 min) resulted in an
increased number of TH-IR nerve cell bodies in the A9 (zona compacta o
f the substantia nigra) and the A10 (ventral tegmental area) regions o
f the mesencephalon, probably reflecting an increased survival of dopa
mine nerve cell bodies. Perinatal asphyxia for longer than 20 min peri
ods reduced the number of TH-IR cell bodies in the 4 week old rat, eve
n below those found in control animals, indicating that when asphyxia
is induced for a period leading to almost 100% mortality, a long-term
reduction of the number of mesencephalic dopamine neurons is produced.
It has previously been shown that a 4 week postnatal nicotine (0.2 mu
mol/kg per h) treatment counteracts the asphyxia-induced increase in
TH-IR cell body number in the substantia nigra and ventral tegmental a
rea, Such nicotine treatment did not influence the reduction in TH-IR
cell bodies in the locus ceruleus following 15-20 min of perinatal asp
hyxia. (C) 1997 Elsevier Science Ireland Ltd.