Strychnine seizure potentiation by azaspirodecanedione anxiolytics in rats

Buspirone, gepirone and ipsaperone administered intraperitoneally (40 mg/kg) to naive rats were found to be proconvulsive for strychnine-induced seizures. The dose of strychnine required to induce seizures in 50% of test animals (CD 50) was 2.18 mg/kg in naive rats, while CD 50s for rats treated wit...

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Veröffentlicht in:European journal of pharmacology 1988-10, Vol.155 (3), p.279-283
Hauptverfasser: Anderson, Melissa C., Chung, Eunyong, Van Woert, Melvin H.
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Sprache:eng
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Zusammenfassung:Buspirone, gepirone and ipsaperone administered intraperitoneally (40 mg/kg) to naive rats were found to be proconvulsive for strychnine-induced seizures. The dose of strychnine required to induce seizures in 50% of test animals (CD 50) was 2.18 mg/kg in naive rats, while CD 50s for rats treated with the azaspirodecanediones ipsaperone, gepirone and buspirone were 1.65, 0.97 and 0.70 mg/kg respectively. Azaspirodecanediones have high affinity for the 5-HT 1A serotonin receptor, however, the specific 5-HT 1A agonist, 8-hydroxy-2-(di-n-propyl-amino)-tetralin (8-OH-DPAT) had no effect on strychnine seizure in naive rats (CD 50 = 2.0 mg/kg). The strychnine specific proconvulsive effects of inferior olive lesions and buspirone were additive, resulting in a CD 50 of 0.1 mg/kg. This observation indicates that the buspirone-induced decrease in strychnine seizure threshold does not require intact inferior olive-climbing fiber pathways. Cerebellar sites for possible azaspirodecanedione action are discussed.
ISSN:0014-2999
1879-0712
DOI:10.1016/0014-2999(88)90514-6