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ROTATION IN RESPONSE TO SELECTIVE DOPAMINE RECEPTOR AGONISTS IN RATS WITH ELECTROLYTIC SUBSTANTIA-NIGRA LESIONS
被引:3
|
作者
:
ASIN, KE
论文数:
0
引用数:
0
h-index:
0
机构:
Neuroscience Research Division Pharmaceutical Discovery, Dept. 47H Abbott Laboratories Abbott Park
ASIN, KE
BEDNARZ, L
论文数:
0
引用数:
0
h-index:
0
机构:
Neuroscience Research Division Pharmaceutical Discovery, Dept. 47H Abbott Laboratories Abbott Park
BEDNARZ, L
MONTANA, W
论文数:
0
引用数:
0
h-index:
0
机构:
Neuroscience Research Division Pharmaceutical Discovery, Dept. 47H Abbott Laboratories Abbott Park
MONTANA, W
机构
:
[1]
Neuroscience Research Division Pharmaceutical Discovery, Dept. 47H Abbott Laboratories Abbott Park
来源
:
LIFE SCIENCES
|
1990年
/ 46卷
/ 25期
关键词
:
D O I
:
10.1016/0024-3205(90)90232-G
中图分类号
:
R-3 [医学研究方法];
R3 [基础医学];
学科分类号
:
1001 ;
摘要
:
Rats with unilateral, electrolytic substantia nigra (ESN) lesions were tested for rotation following systemic injections of the D1 dopamine receptor agonist SKF38393 or the D2 agonist quinpirole. Only quinpirole produced significant levels of rotation, which was ipsilateral in direction. This rotation was potentiated by coadministration of the D1 agonist, and was significantly reduced by injections of either a D1 or D2 receptor antagonist. Other groups of lesioned animals were treated with reserpine for 5 days and were then tested for rotation in response to the agonists. In this case, SKF38393 produced significant levels of contralateral rotation, while quinpirole-induced rotation remained ipsilateral; coadministration of the D1 and D2 agonists resulted in pronounced ipsilateral rotation. These results stress a role for D1 receptor mechanisms in producing rotation, and suggest that different striatal efferent pathways mediate rotation in response to selective agonists following ESN lesions. © 1990.
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收藏
页码:1817 / 1823
页数:7
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