Modification of kindled amygdaloid seizures by opiate agonists and antagonists

• Published in: The Journal of pharmacology and experimental therapeutics Vol. 228; no. 3; pp. 620 - 627
• Main Authors: ALBERTSON, T. E, JOY, R. M, STARK, L. G
• Format: Journal Article
• Language: English
• Published: Bethesda, MD American Society for Pharmacology and Experimental Therapeutics 01.03.1984
• Subjects: Amygdala - drug effects; Analgesics; Animals; Biological and medical sciences; Electroencephalography; Kindling, Neurologic - drug effects; Male; Medical sciences; Narcotic Antagonists - pharmacology; Narcotics - pharmacology; Neuropharmacology; Pharmacology. Drug treatments; Rats; Rats, Inbred Strains; Receptors, Opioid - drug effects; Narcotic antagonist; Opiates; Convulsion; Narcotic analgesic
• ISSN: 0022-3565; 1521-0103

The effects of 19 opiate agonists and antagonists on kindled amygdaloid seizures in the rat were studied. The mu agonists tended to reduce the length of elicited afterdischarges and behavioral ranks, while markedly increasing postictal electroencephalogram spikes and behavioral arrest time. These effects were reversed by naloxone. The kappa agonists reduced behavioral rank and variably reduced afterdischarge length with a concomitant lengthening of postictal behavioral arrest time and number of electroencephalogram spikes. The putative sigma agonist, SKF 10,047, reduced afterdischarge durations only at the higher doses tested. The decreases found after the sigma agonists in postictal electroencephalogram spiking and time of behavioral arrest were not reversed by naloxone. Only the lower doses of normeperidine were found to decrease seizure thresholds. The mixed agonist/antagonists (MAA) cyclazocine and cyclorphan markedly increased seizure threshold and reduced afterdischarge duration and behavioral rank. Only the MAA pentazocine tended to increase threshold but not suprathreshold afterdischarge durations. The order of ability to modify the ictal events was MAA (selected) greater than kappa agonists greater than mu agonists greater than sigma agonists. The increase in postictal events (behavior arrest and spikes) was caused most effectively by pretreatment with mu agonist greater than kappa agonist greater than selected MAA greater than sigma agonists.