Ma. Caldwell et al., THE DOPAMINE AGONISTS LISURIDE AND PIRIBEDIL PROTECT AGAINST BEHAVIORAL AND HISTOLOGICAL-CHANGES FOLLOWING 4-VESSEL OCCLUSION IN THE RAT, Neuropsychobiology, 34(3), 1996, pp. 117-124
The 4-vessel occlusion model of ischaemia in the rat was used to asses
s the effects of two dopaminergic agonists, lisuride and piribedil, on
some behavioural and histological changes. Animals were either sham-o
perated, subjected to 20 min 4-vessel occlusion, or administered lisur
ide (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 testi
ng, Morris water maze and 14-unit T-maze (p < 0.05). Extensive neurona
l death was observed in the CA(1), CA(3) and CA(4) regions of the hipp
ocampus of 4-vessel-occluded animals. Pretreatment with both lisuride
and piribedil provided protection against cell death in the hippocampa
l regions. These findings suggest dopamine may play a role in cerebral
ischaemia and dopaminergic agonists may be beneficial in preventing i
schaemia-induced neurodegeneration.