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大鼠脑中神经肽Y受体亚型的比较特征及放射自显影分布

Comparative characterization and autoradiographic distribution of neuropeptide Y receptor subtypes in the rat brain.

作者信息

Dumont Y, Fournier A, St-Pierre S, Quirion R

机构信息

Douglas Hospital Research Center, McGill University, Montréal, Québec, Canada.

出版信息

J Neurosci. 1993 Jan;13(1):73-86. doi: 10.1523/JNEUROSCI.13-01-00073.1993.

Abstract

Some evidence has suggested the existence and differential distribution of neuropeptide Y (NPY) receptor subtypes in the mammalian brain (Dumont et al., 1990; Aicher et al., 1991). We now report on the extensive characterization and visualization of at least two classes of NPY receptor sites using a highly selective Y1 analog, [Leu31,Pro34]-NPY or [Pro34]-NPY, and a relatively specific Y2 competitor, NPY13-36. Autoradiographic studies using 125I-peptide YY (125I-PYY) clearly reveal that the Y1 receptor subtype is most abundant in various cortical areas, the dentate gyrus of the hippocampal formation, the claustrum, and the reuniens nucleus of the thalamus. In most other regions, 125I-PYY binding is potently inhibited by increasing concentrations of either NPY2-36 or NPY13-36, suggesting a Y2-like profile. Furthermore, binding assays using homogenates from discrete brain regions clearly demonstrate that various NPY fragments and analogs compete for 125I-PYY labeling with profiles indicative of heterogeneity of NPY receptor subtypes, even in the presence of a selective Y1 blocker. Thus, it is likely that, in addition to the Y1 receptor, which is particularly concentrated in cortical areas, the rat brain is enriched with a receptor class (Y2) that can exist under high- or low-affinity states or with additional receptor subtypes that are recognized by 125I-PYY. These findings cannot be explained by the existence of the very recently reported Y3 receptor subtype, since PYY does not possess significant affinity to this site (Grundemar et al., 1991). Further experiments are currently in progress to determine the nature and functional significance of each of these NPY/PYY receptor sites.

摘要

一些证据表明,神经肽Y(NPY)受体亚型在哺乳动物大脑中存在且分布有差异(Dumont等人,1990年;Aicher等人,1991年)。我们现在报告使用高度选择性的Y1类似物[Leu31,Pro34]-NPY或[Pro34]-NPY以及相对特异性的Y2拮抗剂NPY13-36对至少两类NPY受体位点进行的广泛表征和可视化研究。使用125I-肽YY(125I-PYY)的放射自显影研究清楚地表明,Y1受体亚型在各个皮质区域、海马结构的齿状回、屏状核和丘脑的 reunien 核中最为丰富。在大多数其他区域,增加NPY2-36或NPY13-36的浓度可有效抑制125I-PYY结合,表明具有Y2样特征。此外,使用离散脑区匀浆进行的结合测定清楚地表明,即使存在选择性Y1阻滞剂,各种NPY片段和类似物也能以表明NPY受体亚型异质性的特征竞争125I-PYY标记。因此,除了特别集中在皮质区域的Y1受体外,大鼠大脑可能还富含一种可以以高亲和力或低亲和力状态存在的受体类型(Y2)或其他可被125I-PYY识别的受体亚型。这些发现无法用最近报道的Y3受体亚型的存在来解释,因为PYY对该位点不具有显著亲和力(Grundemar等人,1991年)。目前正在进行进一步的实验,以确定这些NPY/PYY受体位点各自的性质和功能意义。

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