Your browser doesn't support javascript.
loading
Montrer: 20 | 50 | 100
Résultats 1 - 2 de 2
Filtre
Ajouter des filtres








Gamme d'année
1.
Journal of Zhejiang University. Medical sciences ; (6): 609-614, 2013.
Article Dans Chinois | WPRIM | ID: wpr-252581

Résumé

<p><b>OBJECTIVE</b>To compare seizure induced by different epileptic drugs in ICR mice.</p><p><b>METHODS</b>Male adult ICR mice were injected with pilocarpine (Pilo), kainic acid (KA) and pentylenetetrazole (PTZ) to induce status epilepticus (SE). After 2 h of SE, seizures were terminated by injection of diazepam. Mice were sacrificed and sectioned for assessment of neuronal cell death by Fluro-Jade B staining after 7 d and mossy fiber sprouting by Timm staining after 28 d, respectively. Spontaneous seizures were detected by video for 28 d.</p><p><b>RESULTS</b>Pilo and KA induced typical SE in ICR mice, which was identical to those observed in rats and C57/BL6 mice. Timm staining showed evident mossy fiber sprouting in both Pilo and KA treated mice. The incidences of spontaneous seizure were 57.1% and 35.7% in Pilo and KA treated mice, respectively. Mice treated with PTZ represented kindling model. No mossy fiber sprouting and spontaneous seizures were observed. No cell death was detected in all three groups.</p><p><b>CONCLUSION</b>Similar seizure pattern is observed in ICR mice as in rats and C57/BL6 mice. Both Pilo and KA model are the ideal models for chronic temporal lobe epilepsy. ICR mice can be widely used as a cheaper substitute in epilepsy research.</p>


Sujets)
Animaux , Mâle , Souris , Modèles animaux de maladie humaine , Épilepsie , Acide kaïnique , Toxicité , Souris de lignée ICR , Pentétrazol , Toxicité , Pilocarpine , Toxicité
2.
Journal of Zhejiang University. Medical sciences ; (6): 615-619, 2013.
Article Dans Chinois | WPRIM | ID: wpr-252580

Résumé

<p><b>OBJECTIVE</b>To explore the synergistic antidepressant effect of quercetin and hyperforin (HF, extracted from Hypericum perforatum).</p><p><b>METHODS</b>Male ICR mice were divided into nine groups:blank control, positive control (Paroxetine, 10 mg/kg), quercetin groups (A: 5 mg/kg, B: 10 mg/kg, C: 20 mg/kg), Hypericum perforatum extract (HF 10 mg/kg),combination groups (A: quercetin 2.5 mg/kg + HF 5 mg/kg,B:quercetin 5 mg/kg + HF 5 mg/kg,C: quercetin 10 mg/kg + HF 5 mg/kg). All drugs were administered intragastrically. Reserpine reversal tests were used to compare the reversal effects of drugs on body temperature decline, eyelid ptosis and akinesia. Tail suspension test was used to compare immobility time in each group.</p><p><b>RESULTS</b>Combination group B showed no significant difference (P>0.05) compared with combination group C in reserpine reversal tests and tail suspension test. However, its body temperature reversal effect was significantly higher (P<0.01) than that of quercetin group B, and its effect in shortening immobility time was stronger than that of HF 10 mg/kg group (P<0.05) and quercetin group B (P<0.01).</p><p><b>CONCLUSION</b>The combination of quercetin and Hypericum perforatum extract in certain ratio has significant synergistic antidepressant effect in ICR mice.</p>


Sujets)
Animaux , Mâle , Souris , Antidépresseurs , Pharmacologie , Dépression , Traitement médicamenteux , Modèles animaux de maladie humaine , Hypericum , Chimie , Souris de lignée ICR , Extraits de plantes , Pharmacologie , Quercétine , Pharmacologie
SÉLECTION CITATIONS
Détails de la recherche