I. Panocka et al., SENSITIVITY OF BRAIN SITES TO THE INHIBITORY EFFECT ON ALCOHOL INTAKEOF THE TACHYKININ AMINOSENKTIDE, Peptides (New York, N.Y. 1980), 19(5), 1998, pp. 897-905
The present study evaluated the sensitivity of several brain sites to
the inhibitory effect of the tachykinin (TK) NK-3 receptor agonist ami
nosenktide (NH2-SENK) on 10% ethanol intake in genetically selected Ma
rchigian Sardinian alcohol-preferring rats. Attention was focused on l
imbic structures involved in alcohol-seeking behavior and endowed with
TK NK-3 receptors. NH2-SENK was bilaterally injected into the shell o
f the nucleus accumbens (NACC), the medial amygdala (AMY), the dorsal
hippocampus (HIPP), the ventral tegmental area (VTA), the bed nucleus
of the stria terminalis (BNST), the lateral hypothalamus (LH), and the
nucleus basalis magnocellularis (NBM). NH2-SENK (injected up to 25-75
ng/site) into the NACC, AMY, HIPP, and VTA did not significantly modi
fy ethanol intake. Injection of NH2-SENK into the BNST reduced ethanol
intake at doses of 25 ng/site or higher, but the same doses also redu
ced water intake in water-deprived rats and food intake in food-depriv
ed rats. Injection of NH2-SENK into the LH or the NBM at doses of 0.5,
5, or 25 ng/site inhibited 10% ethanol intake even at the lowest dose
tested without affecting either food or water consumption in deprived
animals. Present results indicate that the LH and the NBM are highly
sensitive to the inhibitory effect of the TK NK-3 receptor agonist NH2
-SENK on ethanol intake. TK peptides have been shown to evoke conditio
ned place preference following injection in the LH or the NBM. suggest
ing that in these brain sites the effect of TK agonists on ethanol int
ake might be due to interference with reward processes. (C) 1998 Elsev
ier Science Inc.