Effects of anticonvulsive drugs on pentylenetetrazol kindling and long-term potentiation in freely moving rats

• Published in: European journal of pharmacology 1998-09, Vol.356 (2), p.179-187
• Main Authors: Krug, Manfred, Becker, Axel, Grecksch, Gisela, Pfeiffer, Axel, Matthies, Renate, Wagner, Maria
• Format: Article
• Language: English
• Subjects: Animals; Anticonvulsants - pharmacology; Anticonvulsants. Antiepileptics. Antiparkinson agents; Biological and medical sciences; CGP 43487; Convulsants - pharmacology; Dentate gyrus; Diazepam; Diphenylhydantoin; Dizocilpine (MK 801); Drug Interactions; Electrodes; Field potential; Injections, Intraperitoneal; Kindling, Neurologic - drug effects; Long-term potentiation; Long-Term Potentiation - drug effects; Male; Medical sciences; Neuropharmacology; Pentobarbital; Pentylenetetrazol kindling; Pentylenetetrazole; Pharmacology. Drug treatments; Rat, freely moving; Rats; Rats, Wistar
• ISSN: 0014-2999; 1879-0712
• DOI: 10.1016/S0014-2999(98)00544-5

Drugs with anticonvulsive properties and different mechanisms of action were compared for their influence on long-term potentiation and pentylenetetrazol kindling in freely moving animals. Rats were chronically implanted with a stimulation electrode in the angular bundle and a recording electrode in the dentate gyrus. Field potentials in the dentate gyrus were elicited and long-term potentiation was induced by stimulation of the perforant pathway. The clinically used drugs or the potentially anticonvulsive drugs, diphenylhydantoin (50 mg/kg), diazepam (0.5 mg/kg), pentobarbital (10 mg/kg), dizocilpine (MK 801, 0.2 mg/kg) and CGP 43487 (2-amino-4-methyl-5-phosphono-3-pentenoic acid-carboxyethylester, 10 mg/kg), were injected before tetanization. In behavioural experiments pentylenetetrazol kindling was performed with pretreatment with the substances in dosages indicated above (except MK 801, 0.3 mg/kg). Field potentials recorded in the interval between drug administration and tetanization were influenced only by diphenylhydantoin which enhanced the population spike amplitude to 128% of control values. However, the substances showed different effects on long-term potentiation. MK 801, CGP 43487 and pentobarbital depressed potentiation; diazepam was without effect. Diphenylhydantoin had a minor influence on induction but significantly impaired maintenance of long-term potentiation. Furthermore, MK 801, CGP 43487, diazepam and pentobarbital differentially depressed kindling whereas phenytoin only slightly influenced it. The consequences as to hypothetical common cellular mechanisms for kindling development and long-term potentiation are discussed.