Plasticity in the phenotypic expression of catecholamines and vasoactive intestinal peptide in adult rat superior cervical and stellate ganglia afterlong-term hypoxia in vivo
J. Peyronnet et al., Plasticity in the phenotypic expression of catecholamines and vasoactive intestinal peptide in adult rat superior cervical and stellate ganglia afterlong-term hypoxia in vivo, NEUROSCIENC, 91(3), 1999, pp. 1183-1194
Sympathetic ganglia in the adult rat contain various populations of nerve c
ells which demonstrate plasticity with respect to their transmitter phenoty
pe. The plasticity of the neuronal cell bodies and of the small intensely f
luorescent cells in the superior cervical and stellate ganglia in response
to hypoxia in vivo (10% O-2 for seven days) was assessed by studying the ex
pression of catecholamines and vasoactive intestinal peptide. The levels of
norepinephrine, dopamine, 3,4-dihydroxyphenylacetic acid and vasoactive in
testinal peptide immunoreactivity were determined. In addition, the density
of the immunohistochemical staining of cells for tyrosine hydroxylase and
vasoactive intestinal peptide was evaluated. In the intact superior cervica
l ganglion, hypoxia increased the dopamine level as well as the density of
small intensely fluorescent cells immunolabelled for tyrosine hydroxylase a
nd vasoactive intestinal peptide. In the axotomized ganglion, hypoxia elici
ted a twofold rise in the level of the vasoactive intestinal peptide as wel
l as enhancing the density of neuronal cell bodies immunostained for this p
eptide. Thus, the effect of hypoxia on the expression of vasoactive intesti
nal peptide expression in neurons was dependent on neural interactions. In
the intact stellate ganglion, hypoxia alone induced a 1.5-fold increase in
the density of neuronal cell bodies immunostained for vasoactive intestinal
peptide. Thus, ganglia-specific factors appeared to play a role in determi
ning changes in neuronal phenotype in response to hypoxia.
The present study provides evidence for the involvement of dopamine and vas
oactive intestinal peptide in ganglionic responses to long-term hypoxia as
well as for differential responses by the two ganglionic cell populations,
i.e. neuronal cell bodies and small intensely fluorescent cells. Changes in
the expression of the vasoactive intestinal peptide during long-term hypox
ia may be of energetic, trophic and/or synaptic significance. Hypoxia may b
e considered to be a vasoactive intestinal peptide-inducing factor in sympa
thetic ganglia. (C) 1999 IBRO. Published by Elsevier Science Ltd.