Suppr超能文献

使用高选择性配体对大鼠脑中μ和δ阿片受体进行放射自显影分布研究。

Autoradiographic distribution of mu and delta opiate receptors in rat brain using highly selective ligands.

作者信息

Quirion R, Zajac J M, Morgat J L, Roques B P

出版信息

Life Sci. 1983;33 Suppl 1:227-30. doi: 10.1016/0024-3205(83)90484-8.

Abstract

We have characterized the autoradiographic distribution of mu and delta opiate receptors in rat brain using [3H]-Tyr-D-Ala-Gly-NMe-Phe-Gly-ol (DAGO) and [3H]D-Thr2, Thr6leu-enkephalin (DTLET), two highly selective ligands for mu and delta opiate receptors, respectively. Both ligands label an apparent single class of sites. Ligand selectivity shows that [3H]DAGO and [3H]DTLET are more selective ligands for their respective receptors than [3H]dihydromorphine (DHM) and [3H][D-Ala2,D-Leu5]enkephalin (DADLE). Autoradiographically, mu opiate receptors are highly discretely distributed in certain areas. High densities are found in "patches" in caudate-putamen, nucleus accumbens, cingulate cortex, habenula, various thalamic nuclei, amygdala, superior colliculus, and interpeduncular nucleus. Delta opiate receptors are mostly concentrated in the external plexiform layers of the olfactory bulb, caudate-putamen, olfactory tubercule, claustrum, and deep layers (layers V and VI) of the cortex. Since [3H]DAGO and [3H]DTLET are more selective ligands for their respective opiate receptor subtypes, they should be better ligands to characterize the fine distribution of mu and delta opiate receptors.

摘要

我们使用[3H]-酪氨酸-D-丙氨酸-甘氨酸-N-甲基苯丙氨酸-甘醇(DAGO)和[3H]D-苏氨酸2,苏氨酸6亮氨酸脑啡肽(DTLET)这两种分别对μ和δ阿片受体具有高度选择性的配体,对大鼠脑中μ和δ阿片受体的放射自显影分布进行了表征。两种配体均标记出一类明显的位点。配体选择性表明,与[3H]二氢吗啡(DHM)和[3H][D-丙氨酸2,D-亮氨酸5]脑啡肽(DADLE)相比,[3H]DAGO和[3H]DTLET对其各自的受体具有更高的选择性。通过放射自显影,μ阿片受体在某些区域高度离散分布。在尾状核-壳核、伏隔核、扣带回皮质、缰核、各种丘脑核、杏仁核、上丘和脚间核的“斑块”中发现高密度分布。δ阿片受体主要集中在嗅球、尾状核-壳核、嗅结节、屏状核以及皮质深层(V层和VI层)的外丛状层。由于[3H]DAGO和[3H]DTLET对其各自的阿片受体亚型具有更高的选择性,它们应该是用于表征μ和δ阿片受体精细分布的更好配体。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验