TIME-COURSE OF THE NEUROPROTECTIVE EFFECT OF TRANSPLANTATION ON QUINOLINIC ACID-INDUCED LESIONS OF THE STRIATUM

被引:24
作者
LEVIVIER, M
GASH, DM
PRZEDBORSKI, S
机构
[1] UNIV KENTUCKY,CHANDLER MED CTR,DEPT ANAT & NEUROBIOL,LEXINGTON,KY 40536
[2] FREE UNIV BRUSSELS,HOP ERASME,DEPT NEUROSURG,B-1070 BRUSSELS,BELGIUM
[3] COLUMBIA UNIV,DEPT NEUROL,MOVEMENT DISORDERS GRP,NEW YORK,NY 10032
基金
美国国家卫生研究院;
关键词
HUNTINGTONS DISEASE; EXCITOTOXICITY; QUANTITATIVE BINDING AUTORADIOGRAPHY; DOPAMINE D1 RECEPTOR; ADENOSINE A2 RECEPTORS; CYTOCHROME C OXIDASE;
D O I
10.1016/0306-4522(95)00230-G
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Injection of quinolinic acid in the rat striatum mimics neurochemical changes observed in Huntington's disease. We previously demonstrated that intrastriatal transplantation of fetal striatum or gelfoam protects against toxicity induced by a subsequent intrastriatal injection of quinolinic acid performed one week later, Herein, we examined whether fetal striatum or sham transplantation provides protection against quinolinic acid that lasts up to four weeks. Intrastriatal quinolinic acid injection produces neuronal loss and gliosis in Nissl staining, loss of cytochrome oxidase histochemical staining, decrease in autoradiographic binding of [H-3]SCH 23390-labeled dopamine D1 and [H-3]CGS 21680-labeled adenosine A2 receptors, and increase in autoradiographic binding of[H-3]PK 11195-labeled peripheral benzodiazepine binding sites, None of these changes was observed in rats transplanted with fetal striatum one, two or four weeks before quinolinic acid injection. In animals transplanted with fetal striatal tissue, Nissl staining showed healthy grafts located in normal appearing striata. Although sham transplantation performed one week before quinolinic acid injection also protected against histological, histochemical and binding changes, sham transplantation performed two or four weeks before quinolinic acid injection was less effective in attenuating quinolinic acid-induced striatal toxicity. Thus, sham transplantation provides transient protection against quinolinic acid-induced striatal toxicity, whereas implantation of tissue such as fetal striatum seems to be required for long-lasting protection. Our study suggests that intracerebral transplantation may also act through other mechanisms than restoration of deficient neurotransmitters or damaged pathways, a finding which may have significant clinical implications in assessing the potential benefit of this approach for the treatment of neurodegenerative disorders such as Huntington's disease.
引用
收藏
页码:43 / 50
页数:8
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