P. De Gortari et al., Acute ethanol administration induces changes in TRH and proenkephalin expression in hypothalamic and limbic regions of rat brain, NEUROCHEM I, 37(5-6), 2000, pp. 483-496
Thyrotropin releasing hormone (TRH) present in several brain areas has been
proposed as a neuromodulator. Its administration produces opposite effects
to those observed with acute ethanol consumption. Opioid peptides, in cont
rast, have been proposed to mediate some of the effects of alcohol intoxica
tion. We measured TRH content and the levels of its mRNA in hypothalamic an
d limbic zones 1-24 h after acute ethanol injection. We report here fast an
d transient changes in the content of TRH and its mRNA in these areas. The
levels of proenkephalin mRNA varied differently from those of proTRH mRNA,
depending on the time and region studied. Wistar rats were administered one
dose of ethanol (intraperitoneal, 3 g/kg body weight) and brains dissected
in hypothalamus, hippocampus, amygdala, n. accumbens and frontal cortex, f
or TRH quantification by radioimmunoassay or for proTRH mRNA measurement by
RT-PCR. After 1 h injection, TRH levels were increased in hippocampus and
decreased in n. accumbens; after 4 h, it decreased in the hypothalamus, fro
ntal cortex and amygdala, recovering to control values in all regions at 24
h. ProTRH mRNA levels increased at 1 h post-injection in total hypothalamu
s and hippocampus. while they decreased in the frontal cortex. The effect o
f ethanol was also studied in primary culture of hypothalamic cells: a fast
and transient increase in proTRH mRNA was observed at 1 h of incubation (0
.001% final ethanol concentration). Changes in the mRNA levels of proTRH an
d proenkephalin were quantified by in situ hybridization in rats administer
ed ethanol intragastrically (2.5 g/kg). Opposite alterations were observed
for these two mRNAs in hippocampus and frontal cortex, while in n, accumben
s and the paraventricular nucleus of the hypothalamus, both mRNA levels wer
e increased but with different kinetics. These results give support for TRH
and enkephalin neurons as targets of ethanol and, as possible mediators of
some of its observed behavioral effects. (C) 2000 Elsevier Science Ltd. Al
l rights reserved.