Pregled bibliografske jedinice broj: 73346
The involvement of alpha(2)-adrenoceptors in the anticonvulsive effect of swim stress in mice
The involvement of alpha(2)-adrenoceptors in the anticonvulsive effect of swim stress in mice // Psychopharmacology, 158 (2001), 1; 87-93 (međunarodna recenzija, članak, znanstveni)
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Naslov
The involvement of alpha(2)-adrenoceptors in the anticonvulsive effect of swim stress in mice
Autori
Peričić, Danka ; Švob, Dubravka ; Jazvinšćak Jembrek, Maja ; Mirković Kos, Kety
Izvornik
Psychopharmacology (0033-3158) 158
(2001), 1;
87-93
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
Swim stress; Picrotoxin-induced convulsions; alpha (2)-adrenoceptor; Clonidine; Yohimbine; Idazoxan
Sažetak
Rationale: Various studies have shown that stressful manipulations in rats and mice lower the convulsant potency of GABA-related, but also some GABA-unrelated convulsants.The mechanism of this anticonvulsive effect of stress is still unknown. Objectives: We tested the possible involvement of alpha (2)-adrenoceptors in the previously observed anticonvulsive effect of swim stress. Methods: The mice were, prior to exposure to swim stress and the IV infusion of picrotoxin, pre-treated with clonidine (an alpha (2)-adrenoceptor agonist), yohimbine (a non-selective alpha (2)-adrenoceptor antagonist), idazoxan (a selective alpha (2)-adrenoceptor antagonist), or niguldipine (an alpha (1)-adrenoceptor antagonist), and the latency to the onset of two convulsant signs was registered. Results: In control unstressed animals clonidine (0.1 and 1 mg/kG IP), yohimbine (2 mg/kg IP) and idazoxan (1 mg/kg IP) failed to affect the doses of picrotoxin needed to produce convulsant signs, while niguldipine (5 mg/kg IP) prolonged the latency, i.e. it enhanced the doses of picrotoxin producing running/bouncing clonus and tonic hindlimb extension. In swim stressed mice clonidine enhanced, while idazoxan decreased doses of picrotoxin needed to produce two convulsive signs. Yohimbine decreased the dose of convulsant needed to produce tonic hindlimb extension, while niguldipine enhanced doses of picrotoxin needed to produce both symptoms. Conclusions: The results demonstrate the alpha (2)-adrenoceptor agonist-induced potentiation and alpha (2)-adrenoceptor antagonist-induced diminution of the anticonvulsive effect of stress. Additionally, they show the anticonvulsive effect of niguldipine in unstressed and stressed animals. Hence, the results suggest that alpha (2)-adrenoceptors are involved in the anticonvulsive effect of swim stress in mice.
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