STRIATAL GRAFTS IN INFARCT STRIATOPALLIDUM INCREASE GABA RELEASE, REORGANIZE GABA, RECEPTOR AND IMPROVE WATER-MAZE LEARNING IN THE RAT

We grafted fetal striatal cells in ischemic rat models, and investigat ed graft survival/growth, GABA release, GABA(A) receptor reorganizatio n and functional recovery. One hour intraluminal occlusion of the midd le cerebral artery (MCA) induced ischemic infarct in the lateral part of the striatum and adjacent cortex. In ischemic rats, the acquisition of Morris' water-maze learning was significantly slower than that of control rats. In these animals GABA level in the globus pallidus, dete cted by microdialysis, was about the half of that of controls. However , after the grafts of fetal striatal cells in the striatopallidum, the acquisition was improved, thus no difference was observed in the time course of learning curves in control and grafted animals. GABA level recovered to almost normal level by the graft. It further increased by the treatment of a GABA uptake blocker (nipecotic acids) in the perfu sion. In the grafts, GABA(A) receptor organization detected by autorad iography using [H-3] labeled SR95531 was restored for more than 1 year after the graft. Data suggest that fetal striatal cell grafts in infa rct striatum may partially reconstruct striatopallidal GABA projection and reorganize GABA(A) receptor. This might be a basis of improvement of function.