The dopamine agonists lisuride and piribedil protect against behavioural and histological changes following 4-vessel occlusion in the rat

被引:15
作者
Caldwell, MA
Reymann, JM
BentueFerrer, D
Allain, H
Leonard, BE
机构
[1] NATL UNIV IRELAND UNIV COLL GALWAY, DEPT PHARMACOL, GALWAY, IRELAND
[2] CHU RENNES, LAB PHARMACOL CLIN, RENNES, FRANCE
关键词
4-vesselocclusion; ischaemia; dopamine agonists; lisuride; piribedil; Morris water maze; 14-unit T-maze; histology; TRANSIENT FOREBRAIN ISCHEMIA; CEREBRAL-ARTERY OCCLUSION; INTRACEREBRAL MICRODIALYSIS; PARKINSONS-DISEASE; QUANTITATIVE AUTORADIOGRAPHY; EXTRACELLULAR CONCENTRATIONS; STRIATAL DOPAMINE; TEMPORAL PROFILE; GERBIL BRAIN; MATURE-YOUNG;
D O I
10.1159/000119302
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The 4-vessel occlusion model of ischaemia in the rat was used to assess the effects of two dopaminergic agonists, lisuride and piribedil, on some behavioural and histological changes. Animals were either sham-operated, subjected to 20 min 4-vessel occlusion, or administered lisuride (0.5 mg/kg i.p.) or piribedil (10 mg/kg i.p.) 1 h before 20 min 4-vessel occlusion. Both drugs attenuated deficits in neurological testing, Morris water maze and 14-unit T-maze (p < 0.05). Extensive neuronal death was observed in the CA(1), CA(3) and CA(4) regions of the hippocampus of 4-vessel-occluded animals. Pretreatment with both lisuride and piribedil provided protection against cell death in the hippocampal regions. These findings suggest dopamine may play a role in cerebral ischaemia and dopaminergic agonists may be beneficial in preventing ischaemia-induced neurodegeneration.
引用
收藏
页码:117 / 124
页数:8
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