Te. Thiele et al., Ethanol-induced c-Fos expression in catecholamine- and neuropeptide Y-producing neurons in rat brainstem, ALC CLIN EX, 24(6), 2000, pp. 802-809
Background: Previous studies have used c-Fos-like immunoreactivity (cFLI) t
o examine the neuroanatomical location of cells that are activated in respo
nse to ethanol administration. However, the use of cFLI alone fails to reve
al the phenotypical identity of cells. Tn the present study we used double-
labeling procedures to identify the neurochemical phenotype of neurons that
showed ethanol-induced cFLI in the rat brainstem.
Methods: Individual groups of rats received intraperitoneal injection of et
hanol (1.5 g/kg or 3.5 g/kg) or isotonic saline (23 ml/kg). To assess the s
pecificity of cFLI induced by ethanol, we injected other rats with the drug
lithium chloride (LiCl; 76 mg/kg).Two hours after injection, rats were kil
led and their brains were processed for immunohistochemistry.
Results: Both doses of ethanol promoted cFLI in several brainstem regions,
including the nucleus of the solitary tract (NTS), the locus coeruleus (LC)
, and the ventrolateral medulla (VLM). Although LiCl caused significant cFT
I in the NTS, this drug promoted only minimal cFLI in the VLM and no signif
icant activation in the LC. We found that a significant proportion of tyros
ine hydroxylase (TH)-positive neurons coexpressed ethanol-induced cFLI in t
he VLM (similar to 75-85%), the NTS (similar to 65-75%), and the LC (simila
r to 30-65%). Additionally, a significant proportion of neuropeptide Y (NPY
)-producing neurons in the VLM coexpressed ethanol-induced cFLI (similar to
60-75%). On the other hand, LiCl promoted activation of TW-positive neuron
s in the VLM and the NTS but failed to stimulate cFLI in TH-producing neuro
ns in the LC or in NPY-producing neurons of the VLM
Conclusions: Neurons in the rat brainstem that show ethanol-induced c-Fos e
xpression produce catecholamines and NPY. This research demonstrates the us
efulness of double-labeling immunohistochemistry procedures for identifying
the neurochemical identity of neurons that are activated after ethanol adm
inistration.