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首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >Quantitative autoradiographic distribution of NPFF(1) neuropeptide FF receptor in the rat brain and comparison with NPFF(2) receptor by using ((125)I)YVP and ((125)I)EYF as selective radioligands.
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Quantitative autoradiographic distribution of NPFF(1) neuropeptide FF receptor in the rat brain and comparison with NPFF(2) receptor by using ((125)I)YVP and ((125)I)EYF as selective radioligands.

机译:NPFF(1)神经肽FF受体在大鼠脑中的放射自显影定量分布,并通过使用((125)I)YVP和((125)I)EYF作为选择性放射性配体与NPFF(2)受体进行比较。

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摘要

The selectivity of two new radioligands, [(125)I]YVP ([(125)I]YVPNLPQRF-NH(2)) and [(125)I]EYF ([(125)I]EYWSLAAPQRF-NH(2)), for neuropeptide FF (NPFF) receptor subtypes was determined using HEK293 cells expressing hNPFF(1) and CHO cells expressing hNPFF(2) receptors. Saturation binding and displacement experiments showed that [(125)I]YVP and [(125)I]EYF bound selectively with a very high affinity, K(D)=0.18 nM and 0.06 nM, to NPFF(1) and NPFF(2) receptors respectively.By using in vitro autoradiography with these radioligands and frog pancreatic polypeptide (PP) as selective unlabelled competitor of NPFF(2) binding sites, NPFF(1) and NPFF(2) receptor distribution was analyzed throughout the rat CNS.The highest densities of [(125)I]EYF binding sites were seen in the most external layers of the dorsal horn of the spinal cord, the parafascicular thalamic nucleus, laterodorsal thalamic nucleus and presubiculum of hippocampus. All specific binding of this radioligand was inhibited by 200 nM frog PP. The density of 0.1 nM [(125)I]YVP binding was much smaller in all brain areas and frog PP-insensitive binding sites (NPFF(1) receptor subtype) were detected in septal, thalamic and hypothalamic areas but were absent in the spinal cord.The restricted distribution of NPFF(1) receptors in the CNS supports its specific role in a limited number of neuronal functions. In contrast to the rat spinal cord where the NPFF(1) system is absent, there is no strict separation between NPFF(1) and NPFF(2) system at the supraspinal level.
机译:两种新的放射性配体[[(125)I] YVP([(125)I] YVPNLPQRF-NH(2))和[(125)I] EYF([[125)I] EYWSLAAPQRF-NH(2))的选择性,对于神经肽FF(NPFF)受体亚型,使用表达hNPFF(1)的HEK293细胞和表达hNPFF(2)受体的CHO细胞确定。饱和结合和置换实验表明,[(125)I] YVP和[(125)I] EYF与NPFF(1)和NPFF(2)有很高的亲和力,K(D)= 0.18 nM和0.06 nM选择性结合。通过将这些放射性配体和青蛙胰多肽(PP)作为NPFF(2)结合位点的选择性未标记竞争者的体外放射自显影,分析了NPFF(1)和NPFF(2)受体在整个大鼠中枢神经系统中的分布。最高密度的[(125)I] EYF结合位点出现在脊髓背角,束旁丘脑丘脑核,后背丘脑丘脑核和海马前突的最外层。该放射性配体的所有特异性结合均被200 nM青蛙PP抑制。在所有脑区域中,0.1 nM [(125)I] YVP结合的密度要小得多,并且在隔膜,丘脑和下丘脑区域检测到青蛙PP不敏感的结合位点(NPFF(1)受体亚型),但在脊髓中则没有NPFF(1)受体在CNS中的分布受限,支持了其在有限数量的神经元功能中的特定作用。与不存在NPFF(1)系统的大鼠脊髓相反,在脊髓上水平,NPFF(1)和NPFF(2)系统之间没有严格的分隔。

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