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Suppression of apomorphine-induced oral stereotypy in rats by microinjection of muscimol into midbrain.

作者信息

Dean P, Redgrave P, Eastwood L

出版信息

Life Sci. 1982 Jun 21;30(25):2171-9. doi: 10.1016/0024-3205(82)90291-0.

DOI:10.1016/0024-3205(82)90291-0
PMID:7202096
Abstract

Rats with large lesions of the superior colliculus do not display the oral stereotypy normally induced by high systemic doses of dopamine-agonists. It has been suggested that collicular lesions have such an effect because they destroy the GABAergic nigrotectal pathway. This suggestion was investigated by observing the effects of bilateral microinjections of the GABA-agonist muscimol into midbrain sites in rats given 8 mg/kg subcutaneous apomorphine. A low dose of muscimol (25 ng in 0.5 ul saline/side) injected into regions of the superior colliculus with nigrotectal innervation almost abolished apomorphine-induced licking and gnawing. Control microinjections of saline into the superior colliculus, or of muscimol into overlying cerebral cortex, were ineffective. This result is consistent with the GABAergic nigrotectal projection being important for the expression of dopamine-related oral stereotypy. It was also found, however, that 25 ng of muscimol suppressed oral stereotypy when microinjected into the mesencephalic reticular formation underlying the superior colliculus. The anatomical basis of this latter effect is uncertain.

摘要

相似文献

1
Suppression of apomorphine-induced oral stereotypy in rats by microinjection of muscimol into midbrain.
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2
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Superior colliculus lesions selectively attenuate apomorphine-induced oral stereotypy: a possible role for the nigrotectal pathway.
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Dissociation of stimulation-bound feeding and apomorphine-induced gnawing by lesions of superior colliculus.
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Enhanced GABA function in the angular complex (lateral periaqueductal grey matter and adjacent reticular formation) alters the postural component of striatal- or nigral-derived circling.
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Muscimol microinfused into the nigrotegmental target area blocks selected components of behavior elicited by amphetamine or cocaine.
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