AG-4 has been characterized as a nicotinic agonist by binding (K i = 26 ± 1.4 µM) and in vitro functional assays. The antinociceptive effect of AG-4 was examined in mice and rats, using the hot plate, abdominal constriction, and paw-pressure tests. In both species, AG-4 (25-150 µg per mouse icv; 100
Effect of flumazenil on the memory-enhancing properties of (−)-nicotine in rodents
✍ Scribed by Alyssa B. O'Neill; Jorge D. Brioni
- Publisher
- John Wiley and Sons
- Year
- 1994
- Tongue
- English
- Weight
- 695 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0272-4391
No coin nor oath required. For personal study only.
✦ Synopsis
The effect of the benzodiazepine-receptor antagonist flumazenil on the facilitatory effect of (-)-nicotine on memory in septal-lesioned rats in a spatial task and in the inhibitory avoidance test in mice was investigated. In the two-platform spatial discrimination test, septallesioned rats exhibited a significant number of errors in comparison to sham animals, an effect that can be reversed by the administration of (-)-nicotine during the training phase. Flumazenil did not affect the performance of septal-lesioned rats but it blocked the facilitatory effect of (-)-nicotine on lesioned rats. In the inhibitory avoidance test in mice, (-)-nicotine as well as flumazenil facilitated retention of the test at 0.62 and 10 p,mol/kg, respectively. However, a low-noneffective dose of flumazenil blocked the memory enhancing effect of (-)-nicotine. The blockade of the facilitatory effect of (-)-nicotine by flumazenil in normal and septal-lesioned animals suggests that the cognitive effect of (-)-nicotine requires the activation of benzodiazepine receptors.
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