Brain opioidergic mechanisms participate in the regulation of motivati
onal and ingestive behaviours. Since alcohol is believed to activate e
ndogenous opiold systems and to produce opioid-mediated antinociceptio
n, the present experiments were performed to find out if alcohol-induc
ed antinociception differs between the alcohol-preferring AA and alcoh
ol-avoiding ANA rat lines. Alcohol doses relevant to the voluntary alc
ohol intake by the AA rats (0.5-1.0 g/kg, intraperitoneally) failed to
alter tail-flick (TF) latency in a 55 degrees C water bath by either
rat line. However, repeated measurement of TF latency, even without an
y alcohol treatment, prolonged tail-flick latencies in AA but not in A
NA rats. Prolongation of TF latency was also seen in non-selected Wist
ar rats, indicating that the ANA rats respond abnormally in this test.
The antinociceptive effects of swimming-induced stress (3 min at 15 d
egrees C) and those of cumulative morphine administration (0.5-16.0 mg
/kg, subcutaneously) were similar in both rat lines. Using higher, mot
or-impairing alcohol doses with repeated baseline TF determinations, i
t was observed that a dose of 1.5 g/kg induced slight antinociception
only in the AA rats, while 2.0 g/kg produced similar effects in both r
at lines. It is thus concluded that the alcohol-preferring AA rats do
not show any enhanced alcohol-induced antinociception at relevant alco
hol doses. However, the alcohol-avoiding ANA rats appear to have a def
ective ability to habituate to repeated sensory stimuli, which could c
ontribute to their alcohol avoidance by preventing the development of
tolerance to aversive effects of alcohol.