A study of the role of the cholinergic system in amygdaloid kindling in rats
โ Scribed by Douglas H. R. Blackwood; Michael J. Martin; James G. Howe
- Publisher
- Springer
- Year
- 1982
- Tongue
- English
- Weight
- 428 KB
- Volume
- 76
- Category
- Article
- ISSN
- 0033-3158
No coin nor oath required. For personal study only.
โฆ Synopsis
The effect of atropine on kindling the amygdala of rats was tested by administering the drug in a dose of 25 mg/kg 1 h before each stimulus was applied. Rats tested with atropine kindled at the same rate as saline-treated controls. Cholinergic activity in the amygdala of rats was assessed, 4 weeks after the completion of kindling, by measuring both muscarinic receptor numbers and sodiumdependent high affinity choline uptake in tissue homogenates. There was no change in either of these parameters attributable to kindling. These results suggest that changes in the cholinergic system are not fundamental either to the development or the maintenance of kindling in the rat amygdala.
๐ SIMILAR VOLUMES
The anticonvulsant properties of the endogenous excitatory amino acid antagonist, kynurenic acid (KYA), were studied in prepubescent and adult rats using the amygdaloid kindling model of epilepsy. Treatment with intracerebroventricular KYA (360 nmoles (adult dose) or 240 nmoles (prepuhescent dose))
One hundred-four Wistar rats were implanted with a bipolar electrode aimed at the right baso!ateral amygdala, and stimulated bipolarly twice daily (interval between stimulations 30 rain) with a 150 uA, 4-s train of biphasic square-wave l-ms pulses (100 pulses/s). Seventy-four animals developed a sti
The anticonvulsant effectiveness of AHR-11748 (3-[3-(trifluoromethyl)phenoxy]-1-azetidinecarboxamide) was evaluated in the kindled amygdaloid seizure model in rats. Doses of AHR-11748 that did not cause prestimulation toxicity significantly attenuated elicited afterdischarge durations and the severi