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大鼠新皮质中的选择性去甲肾上腺素能神经支配与³H-哌唑嗪结合位点

Selective noradrenergic denervation and 3H-prazosin binding sites in rat neocortex.

作者信息

Reader T A, Brière R

出版信息

Brain Res Bull. 1983 Jan;10(1):155-8. doi: 10.1016/0361-9230(83)90087-4.

Abstract

Biochemical determinations of alpha 1-noradrenergic binding sites were performed in the neocortex of normal rats and of rats which had been subjected to a selective noradrenergic deafferentation obtained by microinjecting 6-OHDA in the dorsal noradrenergic bundle. The extent and the specificity of the deafferentation was assessed by measuring the catecholamines dopamine, epinephrine and norepinephrine, as well as the indoleamine serotonin using radioenzymatic assays. In the denervated animals (90% reduction in NE levels) specific binding of the alpha 1-noradrenergic antagonist prazosin revealed an increase only in the number of binding sites (Bmax) without changes in the dissociation constant (Kd).

摘要

在正常大鼠以及通过向去甲肾上腺素能背束微量注射6-羟基多巴胺实现选择性去甲肾上腺素能脱失的大鼠的新皮质中,进行了α1-去甲肾上腺素能结合位点的生化测定。通过使用放射酶分析法测量儿茶酚胺多巴胺、肾上腺素和去甲肾上腺素以及吲哚胺5-羟色胺,评估脱失的程度和特异性。在去神经支配的动物中(去甲肾上腺素水平降低90%),α1-去甲肾上腺素能拮抗剂哌唑嗪的特异性结合仅显示结合位点数量(Bmax)增加,而解离常数(Kd)无变化。

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