Abstract
Lesioning of serotonergic afferents increases hippocampal ACh release and attenuates memory deficits produced by cholinergic lesions. Improved memory performance described in 5-HT 1B-knockout (KO) mice might thus be due to a weaker 5-HT 1B-mediated inhibitory influence of 5-HT on hippocampal ACh release. The selective delay-dependent impairment of working memory observed in these KO mice suggests, however, that cortical regions also participate in task performance, possibly via indirect influences of 5-HT on ACh release. To provide neuropharmacological support for these hypotheses we measured evoked ACh and 5-HT release in hippocampal and cortical slices of wild-type (WT) and 5-HT 1B KO mice. Superfused slices (preincubated with [ 3H]choline or [ 3H]5-HT) were electrically stimulated in the absence or presence of 5-HT 1B receptor ligands. In hippocampus and cortex, 5-HT 1B agonists decreased and antagonists increased 5-HT release in WT, but not in 5-HT 1B KO mice. In 5-HT 1B KO mice, 5-HT release was enhanced in both structures, while ACh release (in nCi) was reduced. ACh release was inhibited by 5-HT 1B agonists in hippocampal (not cortical) slices of WT but not of 5-HT 1B KO mice. Our data (i) confirm the absence of autoinhibition of 5-HT release in 5-HT 1B-KO mice, (ii) demonstrate a reduced release of ACh, and the absence of 5-HT 1B-receptor-mediated inhibition of ACh release, in the hippocampus and cortex of 5-HT 1B-KO mice, and (iii) are compatible with an indirect role of cortical ACh in the working memory impairment observed in these KO mice.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have