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κ-阿片受体基因敲除小鼠中μ、δ和κ1阿片受体的定量放射自显影

Quantitative autoradiography of mu-,delta- and kappa1 opioid receptors in kappa-opioid receptor knockout mice.

作者信息

Slowe S J, Simonin F, Kieffer B, Kitchen I

机构信息

Pharmacology Research Group, School of Biological Sciences, University of Surrey, Guildford, Surrey, GU2 5XH, UK.

出版信息

Brain Res. 1999 Feb 13;818(2):335-45. doi: 10.1016/s0006-8993(98)01201-3.

Abstract

Mice deficient in the kappa-opioid receptor (KOR) gene have recently been developed by the technique of homologous recombination and shown to lack behavioural responses to the selective kappa1-receptor agonist U-50,488H. We have carried out quantitative autoradiography of mu-, delta- and kappa1 receptors in the brains of wild-type (+/+), heterozygous (+/-) and homozygous (-/-) KOR knockout mice to determine if there is any compensatory expression of mu- and delta-receptor subtypes in mutant animals. Adjacent coronal sections were cut from the brains of +/+, +/- and -/- mice for the determination of binding of [3H]CI-977, [3H]DAMGO (D-Ala2-MePhe4-Gly-ol5 enkephalin) or [3H]DELT-I (D-Ala2 deltorphin I) to kappa1-, mu- and delta-receptors, respectively. In +/- mice there was a decrease in [3H]CI-977 binding of approximately 50% whilst no kappa1-receptors could be detected in any brain region of homozygous animals confirming the successful disruption of the KOR gene. There were no major changes in the number or distribution of mu- or delta-receptors in any brain region of mutant mice. There were, however some non-cortical regions where a small up-regulation of delta-receptors was observed in contrast to an opposing down-regulation of delta-receptors evident in mu-knockout brains. This effect was most notable in the nucleus accumbens and the vertical limb of the diagonal band, and suggests there may be functional interactions between mu- and delta-receptors and kappa1- and delta-receptors in mouse brain.

摘要

最近通过同源重组技术培育出了缺乏κ-阿片受体(KOR)基因的小鼠,这些小鼠对选择性κ1受体激动剂U-50,488H缺乏行为反应。我们对野生型(+/+)、杂合子(+/-)和纯合子(-/-)KOR基因敲除小鼠的大脑进行了μ、δ和κ1受体的定量放射自显影,以确定突变动物中μ和δ受体亚型是否存在代偿性表达。从+/+、+/-和-/-小鼠的大脑中切取相邻的冠状切片,分别用于测定[3H]CI-977、[3H]DAMGO(D-丙氨酸2-甲基苯丙氨酸4-甘氨醇5脑啡肽)或[3H]DELT-I(D-丙氨酸2 强啡肽I)与κ1、μ和δ受体的结合。在+/-小鼠中,[3H]CI-977的结合减少了约50%,而在纯合子动物的任何脑区都未检测到κ1受体,这证实了KOR基因的成功破坏。突变小鼠的任何脑区中μ或δ受体的数量或分布均无重大变化。然而在一些非皮质区域,观察到δ受体有小幅度上调,这与μ受体敲除大脑中明显的δ受体下调相反。这种效应在伏隔核和斜角带垂直支最为明显,表明小鼠大脑中μ和δ受体以及κ1和δ受体之间可能存在功能相互作用。

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