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Oxiracetam and aniracetam increase acetylcholine release from the rat hippocampus in vivo

✍ Scribed by Maria Grazia Giovannini; Paola Rodinò; Donatella Mutolo; Gincarlo Pepeu


Publisher
John Wiley and Sons
Year
1993
Tongue
English
Weight
644 KB
Volume
28
Category
Article
ISSN
0272-4391

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✦ Synopsis


The effect of two nootropic drugs, oxiracetam and aniracetam, on cholinergic neurotransmission in vivo was investigated in the rat b y means of the transversal microdialysis technique. The basal release of acetylcholine (ACh) from the hippocampus and parietal cortex was 2.93 ? 0.17 and 3.10 c 0.18 pmol/20 min (mean * s.e.m.), respectively, and remained stable for at least 3 h, while the initial efflux of choline was 51.9 I+_ 2.6 and 42.8 I+_ 6.4 pmolRO min (mean 2 s.e.m.), respectively, and decreased by about 50% during the first 60 min of collection. Oxiracetam, tested at doses of 50,100, and 300 mg/kg ip, elicted a 63% increase in ACh release from the hippocampus at the dose of 100 mg/kg only. This effect of oxiracetam was inhibited by perfusion with tetrodotoxin (TTX), 5 x lo-' M. In oxiracetam-treated rats the decrease in choline efflux was less pronounced than in controls (-23% of the initial value) at the dose o f 100 mg/kg. Aniracetam (100 mg/kg, orally) elicited a sustained increase of ACh release from the hippocampus (+58%, 120 min after the administration), without affecting choline efflux. Doses of 50 and 300 mg/kg, orally, o f aniracetam were ineffective. Oxiracetam and aniracetam (50 and 100 mg/kg) neither modified the output of ACh or choline from the parietal cortex nor induced gross behavioral changes. These results indicate that oxiracetam and aniracetarn could act on cognitive processes by stimulating the hippocampal cholinergic pathways.


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