The ventral hippocampus and fear conditioning in rats - Different anterograde amnesias of fear after tetrodotoxin inactivation and infusion of the GABA(A) agonist muscimol
T. Bast et al., The ventral hippocampus and fear conditioning in rats - Different anterograde amnesias of fear after tetrodotoxin inactivation and infusion of the GABA(A) agonist muscimol, EXP BRAIN R, 139(1), 2001, pp. 39-52
Studies on the involvement of the rat hippocampus in classical fear conditi
oning have focused mainly on the dorsal hippocampus and conditioning to a c
ontext. However, the ventral hippocampus has intimate connections with the
amygdala and the nucleus accumbens, which are involved in classical fear co
nditioning to explicit and contextual cues. Consistently, a few recent lesi
on studies have indicated a role for the ventral hippocampus in classical f
ear conditioning to explicit and contextual cues. The present study examine
d whether neuronal activity within the ventral hippocampus is important for
the formation of fear memory to explicit and contextual cues by classical
fear conditioning. Tetrodotoxin (TTX; 10 ng/side), which completely blocks
neuronal activity, or muscimol (1 mug/side), which increases GABA(A) recept
or-mediated inhibition, were bilaterally infused into the ventral hippocamp
us of Wistar rats before the conditioning session of a classical fear-condi
tioning experiment. Conditioning to a tone and the context were assessed us
ing freezing as a measure of conditioned fear. TTX blocked fear conditionin
g to both tone and context. Muscimol only blocked fear conditioning to the
context. The data of the present study indicate that activity of neurons in
the ventral hippocampus is necessary for the formation of fear memory to b
oth explicit and contextual cues and that neurons in the ventral hippocampu
s that bear the GABA, receptor are important for the formation of fear cond
itioning to a context. In addition, both bilateral muscimol (0.5 mug/side a
nd 1 mug/side) and TTX (5 ng/side and 10 ng/side) infusion into the ventral
hippocampus dose-dependently decreased locomotor activity in an open-field
experiment.