Pregled bibliografske jedinice broj: 237363
Zimelidine decreases seizure susceptibility in stressed mice
Zimelidine decreases seizure susceptibility in stressed mice // Journal of Neural Transmission, 113 (2006), 12; 1863-1871 (međunarodna recenzija, članak, znanstveni)
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Naslov
Zimelidine decreases seizure susceptibility in stressed mice
Autori
Peričić, Danka ; Švob Štrac, Dubravka ; Vlainić (Lazić), Josipa
Izvornik
Journal of Neural Transmission (0300-9564) 113
(2006), 12;
1863-1871
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
Zimelidine; selective serotonin reuptake inhibitor (SSRI); 5-HT receptor antagonists; seizure threshold; picrotoxin; swim stress
Sažetak
To further evaluate whether selective serotonin reuptake inhibitors (SSRIs) have pro- or anticonvulsant properties and whether these properties will be modified by stress, we studied the effect of zimelidine on the convulsions produced by picrotoxin, a GABA-A receptor antagonist, in unstressed and swim stressed mice. Zimelidine potentiated the ability of swim stress to enhance the threshold doses of intravenously administered picrotoxin producing convulsant signs and death, without having an effect in unstressed mice. The anticonvulsant effect of zimelidine was counteracted with mianserin, the antagonist of 5-HT2A/2C, and diminished with WAY-100635, a selective antagonist of 5-HT1A receptors. In stressed mice, WAY-100635 prevented the anticonvulsant effect of 8-OH-DPAT, a 5-HT1A receptor agonist. SB-269970 and ketanserin, the antagonists of 5-HT7 and 5-HT2A receptors, respectively, failed to reduce the effect of zimelidine. The results suggest the involvement of 5-HT2C and 5-HT1A receptors in the anticonvulsant effects of zimelidine and possibly other SSRIs in stress.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE
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