Pregled bibliografske jedinice broj: 154684
Acute and repeated fluoxetine treatment decrease the convulsant potency of picrotoxin in unstressed and stressed mice
Acute and repeated fluoxetine treatment decrease the convulsant potency of picrotoxin in unstressed and stressed mice // 4th Forum of European Neuroscience (FENS Forum) : Abstracts. Vol. 2 ; A219.13
Lisabon, 2004. (poster, međunarodna recenzija, sažetak, znanstveni)
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Naslov
Acute and repeated fluoxetine treatment decrease the convulsant potency of picrotoxin in unstressed and stressed mice
Autori
Peričić, Danka ; Lazić, Josipa ; Švob Štrac, Dubravka ; Jazvinšćak Jembrek, Maja
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
4th Forum of European Neuroscience (FENS Forum) : Abstracts. Vol. 2 ; A219.13
/ - Lisabon, 2004
Skup
Forum of European Neuroscience (4 ; 2004)
Mjesto i datum
Lisabon, Portugal, 08.07.2004. - 12.07.2004
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
fluoxetine; acute and chronic treatment; stress; convulsions; picrotoxin
Sažetak
The aim of this study was to assess whether fluoxetine, a well known antidepressant drug and 5-HT reuptake inhibitor, affects the seizure threshold in unstressed and/or stressed mice. Male CBA mice were prior to exposure to stress (10-min swimming at 18-19°C) and the i.v. infusion of picrotoxin (starting 15 min after termination of stress), pre-treated with fluoxetine either acutely (10 and 20 mg/kg i.p. 40 min prior to stress) or repeatedly (20 mg/kg once daily for 5 consecutive days) and the latency to the onset of two convulsant signs and death was registered. In accordance with our results published previously (Pericic et al., Psychopharmacology 158: 87-93, 2001), swim stress enhanced significantly the doses of picrotoxin needed to produce running bouncing (RB) clonus, tonic hindlimb extension (THE) and death. Fluoxetine (10 mg/kg) enhanced the dose of picrotoxin needed to produce tonic hindlimb extension (THE) in stressed but not in unstressed mice. A higher dose of this drug (20 mg/kg) increased the dose of picrotoxin producing THE and death in unstressed and swim stressed mice. Neither of this treatments affected running bouncing (RB) clonus. Repeated treatment with fluoxetine (20 mg/kg i.p.) exerted an even more pronounced anticonvulsant effect. This treatment significantly enhanced in unstressed and swim-stressed mice doses of picrotoxin needed to produce RB clonus, THE and death. The results demonstrate that acute fluoxetine treatment had a greater anticonvulsant effect in unstressed than in stressed animals. On the other hand, repeated fluoxetine treatment had a similar anticonvulsant activity in stressed and unstressed animals, at least against convulsions produced by the blockade of GABAergic transmission. While swim stress attenuated the anticonvulsant property of acute fluoxetine, it failed to affect this property of repeated fluoxetine treatment.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti
POVEZANOST RADA
Projekti:
0098103
Ustanove:
Institut "Ruđer Bošković", Zagreb
Profili:
Dubravka Švob Štrac
(autor)
Maja Jazvinšćak Jembrek
(autor)
Josipa Vlainić
(autor)
Danka Peričić
(autor)