THE ROLE OF THE MEDIAL PREFRONTAL CORTEX OF RATS IN SHORT-TERM-MEMORYFUNCTIONING - FURTHER SUPPORT FOR INVOLVEMENT OF CHOLINERGIC, RATHER THAN DOPAMINERGIC MECHANISMS
Lm. Broersen et al., THE ROLE OF THE MEDIAL PREFRONTAL CORTEX OF RATS IN SHORT-TERM-MEMORYFUNCTIONING - FURTHER SUPPORT FOR INVOLVEMENT OF CHOLINERGIC, RATHER THAN DOPAMINERGIC MECHANISMS, Brain research, 674(2), 1995, pp. 221-229
The putative involvement of the dopaminergic innervation of the medial
part of the prefrontal cortex (PFC) in short-term memory functioning
was investigated by evaluating the effects of local infusions of dopam
inergic drugs into the ventral part of the medial PFC of rats in an op
erant delayed-matching-to-position (DMTP) task. Two separate groups of
rats were tested after bilateral microinfusion of several doses of ei
ther the dopamine receptor agonist apomorphine (APO) or the dopamine r
eceptor antagonist cis-flupenthixol (FLU) into the ventromedial PFC. I
n addition, all animals were tested after infusion of several doses of
the muscarinic receptor antagonist scopolamine (SCO) and the dopamine
D1 receptor antagonist SCH-23390 (SCH). The drugs tested affected DMT
P performance differentially. APO had no effect on response accuracy,
although it dose-dependently affected nose poke activity and response
latencies. FLU and SCH both induced a dose-dependent, but delay-indepe
ndent deterioration of response accuracy that was parallelled by incre
ases in response latencies and decreases in nose poke frequencies, cau
sing some animals to stop responding after infusion of the highest dos
es of both drugs. In contrast, SCO infusions into the ventromedial PFC
induced a dose- and delay-dependent deterioration of response accurac
y, that was accompanied by an increase in response latencies only. Tak
en together, these results provide additional support for the involvem
ent of cholinergic, rather than dopaminergic mechanisms in short-term
memory processes supported by the medial PFC of the rat, and they are
not in favor of a functional dissociation between the dorsomedial PFC
and the ventromedial PFC in this role.