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[125I]麦角酸二乙酰胺在人额叶皮质和血小板组织中的结合比较。

Comparison of [125I]iodolysergic acid diethylamide binding in human frontal cortex and platelet tissue.

作者信息

Elliott J M, Kent A

机构信息

Department of Pharmacology and Toxicology, St. Mary's Hospital Medical School, London, England.

出版信息

J Neurochem. 1989 Jul;53(1):191-6. doi: 10.1111/j.1471-4159.1989.tb07313.x.

DOI:10.1111/j.1471-4159.1989.tb07313.x
PMID:2723656
Abstract

The human platelet contains a functional 5-hydroxytryptamine (5-HT) receptor that appears to resemble the 5-HT2 subtype. In this study, we have used the iodinated derivative [125I]iodolysergic acid diethylamide ([125I]iodoLSD) in an attempt to label 5-HT receptors in human platelet and frontal cortex membranes under identical assay conditions to compare the sites labelled in these two tissues. In human frontal cortex, [125I]iodoLSD labelled a single high-affinity site (KD = 0.35 +/- 0.02 nM). Displacement of specific [125I]iodoLSD binding indicated a typical 5-HT2 receptor inhibition profile, which demonstrated a significant linear correlation (r = 0.97, p less than 0.001, n = 17) with that observed using [3H]ketanserin. However, [125I]iodoLSD (Bmax = 136 +/- 7 fmol/mg of protein) labelled significantly fewer sites than [3H]ketanserin (Bmax = 258 +/- 19 fmol/mg of protein) (p less than 0.001, n = 6). In human platelet membranes, [125I]iodoLSD labelled a single site with affinity (KD = 0.37 +/- 0.03 nM) similar to that in frontal cortex. The inhibition profile in the platelet showed significant correlation with that in frontal cortex (r = 0.96, p less than 0.001, n = 16). We conclude that the site labelled by [125I]iodoLSD in human platelet membranes is biochemically similar to that in frontal cortex and most closely resembles the 5-HT2 receptor subtype, although the discrepancy in binding capacities of [125I]iodoLSD and [3H]ketanserin raises a question about the absolute nature of this receptor.

摘要

人类血小板含有一种功能性5-羟色胺(5-HT)受体,该受体似乎类似于5-HT2亚型。在本研究中,我们使用了碘化衍生物[125I]碘麦角酸二乙酰胺([125I]碘-LSD),试图在相同的测定条件下标记人类血小板和额叶皮质膜中的5-HT受体,以比较这两种组织中标记的位点。在人类额叶皮质中,[125I]碘-LSD标记了一个单一的高亲和力位点(KD = 0.35±0.02 nM)。特异性[125I]碘-LSD结合的置换表明了典型的5-HT2受体抑制谱,与使用[3H]酮色林观察到的结果显示出显著的线性相关性(r = 0.97,p < 0.001,n = 17)。然而,[125I]碘-LSD(Bmax = 136±7 fmol/mg蛋白质)标记的位点明显少于[3H]酮色林(Bmax = 258±19 fmol/mg蛋白质)(p < 0.001,n = 6)。在人类血小板膜中,[125I]碘-LSD标记了一个亲和力(KD = 0.37±0.03 nM)与额叶皮质相似的单一位点。血小板中的抑制谱与额叶皮质中的抑制谱显示出显著相关性(r = 0.96,p < 0.001,n = 16)。我们得出结论,[125I]碘-LSD在人类血小板膜中标记的位点在生化性质上与额叶皮质中的位点相似,并且最类似于5-HT2受体亚型,尽管[125I]碘-LSD和[3H]酮色林结合能力的差异对该受体的绝对性质提出了疑问。

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Concurrence of cortex and platelet serotonin2 receptor binding characteristics in the individual and the putative regulation by serotonin.个体中皮质与血小板5-羟色胺2受体结合特性的一致性以及5-羟色胺的假定调节作用。
J Neural Transm Gen Sect. 1993;93(1):27-35. doi: 10.1007/BF01244935.
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Human platelet 5-HT2 receptor binding sites re-evaluated: a criticism of current techniques [corrected].
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J Neural Transm Gen Sect. 1993;92(1):11-24. doi: 10.1007/BF01245158.
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Molecular structural basis of ligand selectivity for 5-HT2 versus 5-HT1C cortical receptors.5-HT2与5-HT1C皮质受体配体选择性的分子结构基础。
Naunyn Schmiedebergs Arch Pharmacol. 1992 Jul;346(1):4-11. doi: 10.1007/BF00167563.