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神经肽FF(FLFQPQRFamide)受体在人类脊髓感觉系统中的放射自显影定位

Autoradiographic localization of receptors for neuropeptide FF, FLFQPQRFamide, in human spinal sensory system.

作者信息

Allard M, Jordan D, Zajac J M, Ries C, Martin D, Monkouanga D, Kopp N, Simonnet G

机构信息

Laboratoire de Psychobiologie des Comportements Adaptatifs, INSERM U259, Université de Bordeaux II, France.

出版信息

Brain Res. 1994 Jan 7;633(1-2):127-32. doi: 10.1016/0006-8993(94)91531-8.

Abstract

The regional distribution of FLFQPQRFamide binding sites on fresh unfixed cryostate sections from post mortem specimens of human spinal cord and lower medulla oblongata was studied by quantitative autoradiographic methods using [125I]YLFQPQRFamide as ligand. Samples were taken from five cases who had died with no history of neurological disease at ages ranging from 5 months to 66 years. The biochemical and pharmacological characteristics of [125I]YLFQPQRFamide binding to mounted tissue sections were comparable to those reported for the rat in a previous study. [125I]YLFQPQRFamide appeared to interact reversibly with high affinity binding sites (Kd = 0.06 nM), distinct from opiate receptors. Sites labelled with [125I]YLFQPQRFamide were distributed unevenly within the human spinal cord and lower medulla oblongata, with the highest density in the superficial layers of the dorsal horn and the spinal trigeminal nucleus. Although moderate labelling was observed in the ventral part of spinal grey matter, dense labelling appeared in the gracile and cuneate nuclei. No binding sites were detected in white matter. These results show that, as in the rat, FLFQPQRFamide receptors in the human spinal cord and lower medulla oblongata, are mainly concentrated within spinal areas implicated in the analgesic action of opiates. The possible role of these receptors in modulating spinal nociceptive information is discussed with respect to the pharmacological effects of substances acting on FLFQPQRFamide receptors in animals.

摘要

采用定量放射自显影法,以[125I]YLFQPQRFamide为配体,研究了人脊髓和延髓下部新鲜未固定冷冻切片上FLFQPQRFamide结合位点的区域分布。样本取自5例年龄在5个月至66岁之间、无神经疾病病史的死亡病例。[125I]YLFQPQRFamide与固定组织切片结合的生化和药理学特性与先前研究报道的大鼠的特性相当。[125I]YLFQPQRFamide似乎与高亲和力结合位点(Kd = 0.06 nM)可逆性相互作用,这些位点与阿片受体不同。用[125I]YLFQPQRFamide标记的位点在人脊髓和延髓下部分布不均匀,在背角浅层和三叉神经脊髓核中密度最高。虽然在脊髓灰质腹侧观察到中度标记,但在薄束核和楔束核中出现密集标记。在白质中未检测到结合位点。这些结果表明,与大鼠一样,人脊髓和延髓下部的FLFQPQRFamide受体主要集中在与阿片类药物镇痛作用相关的脊髓区域。结合作用于动物FLFQPQRFamide受体的物质的药理作用,讨论了这些受体在调节脊髓伤害性信息方面的可能作用。

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