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黑质内注射谷氨酸拮抗剂可调节多巴胺 D1 介导的旋转行为和纹状体 c-fos 表达。

Intranigral injections of glutamate antagonists modulate dopamine D1-mediated turning behavior and striatal c-fos expression.

作者信息

Fenu S, Carta A, Morelli M

机构信息

Department of Toxicology, University of Cagliari, Italy.

出版信息

J Neural Transm Suppl. 1995;45:75-81.

PMID:8748612
Abstract

The contribution of the substantia nigra (SN) in the positive interaction between dopamine D1 receptor agonists and glutamate antagonists was studied in rats with a unilateral 6-hydroxydopamine (6-OHDA) lesion of dopaminergic nigro-striatal pathway. Local infusion into the SN of the 6-OHDA lesioned side of NMDA glutamate antagonists MK 801 and CPP or the AMPA antagonist NBQX at doses inducing none or minimal behavioral effects, significantly increased the turning behavior and the expression of c-fos induced, in the lesioned caudate-putamen (CPu), by a parenteral administration of SKF 38393. High doses of MK 801 or CPP infused into the SN produced intense contralateral turning per-se but induced only sparse c-fos expression in the lesioned CPu. The results show that a depression of SN pars reticulata efferent neurons, potentiates D1-mediated responses and suggest that this area may play a role in the positive interaction between glutamate antagonists and D1 receptor agonists.

摘要

在患有多巴胺能黑质纹状体通路单侧6-羟基多巴胺(6-OHDA)损伤的大鼠中,研究了黑质(SN)在多巴胺D1受体激动剂与谷氨酸拮抗剂之间正向相互作用中的作用。将NMDA谷氨酸拮抗剂MK 801和CPP或AMPA拮抗剂NBQX以不产生或仅产生最小行为效应的剂量局部注入6-OHDA损伤侧的SN,显著增加了由胃肠外给予SKF 38393在损伤的尾状核-壳核(CPu)中诱导的旋转行为和c-fos表达。向SN注入高剂量的MK 801或CPP本身会产生强烈的对侧旋转,但在损伤的CPu中仅诱导稀疏的c-fos表达。结果表明,黑质网状部传出神经元的抑制增强了D1介导的反应,并表明该区域可能在谷氨酸拮抗剂与D1受体激动剂之间的正向相互作用中发挥作用。

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