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[大鼠吗啡耐受性形成过程中脑阿片受体特性的变化]

[Changes in the properties of brain opiate receptors during the development of morphine tolerance in rats].

作者信息

Zaĭtsev S V, Sergeeva M G, Chichenkov O N, Petrov V E, Varfolomeev S D

出版信息

Biokhimiia. 1986 Aug;51(8):1334-40.

PMID:3021240
Abstract

The effects of prolonged administration of morphine on the properties of opiate receptors of rat brain were studied. For this purpose the isotherms of binding of labeled mu-, delta-, and chi-ligands--morphine, D-Ala2, D-Leu5-enkephalin and ethylketocyclazocine--with brain membrane preparations of morphine-tolerant rats as well as those of control animals were analyzed. For quantitative determination of dissociation constants of the ligand-receptor complexes (K) and receptor concentrations ([Q]), the difference and simulation methods were used. It was shown that the values of K and [Q] vary within broad ranges in individual animals, whereas the individual variations of the [Q]/[K] ratios in controls or in morphine-tolerant rats are not so significant. This suggests [Q]/K to be one of the basic criteria for a comparison of properties of opiate receptors in different groups of animals. The use of this criterion and of the simulation method demonstrated that the development of tolerance causes changes in the properties of delta-receptors (the [Q]/K ratio decreases by greater than 50%). Unlike delta-receptors, the tolerance has no appreciable effect on the properties of mu- or chi-receptors or on the superhigh affinity binding sites of the ligands tested.

摘要

研究了长期给予吗啡对大鼠脑阿片受体特性的影响。为此,分析了标记的μ、δ和κ配体——吗啡、D-丙氨酸²、D-亮氨酸⁵-脑啡肽和乙基酮环唑辛——与吗啡耐受大鼠以及对照动物的脑膜制剂的结合等温线。为了定量测定配体-受体复合物的解离常数(K)和受体浓度([Q]),使用了差值法和模拟法。结果表明,K和[Q]的值在个体动物中变化范围很广,而对照动物或吗啡耐受大鼠中[Q]/[K]比值的个体差异并不显著。这表明[Q]/K是比较不同动物组中阿片受体特性的基本标准之一。使用该标准和模拟法表明,耐受性的发展会导致δ受体特性发生变化([Q]/K比值降低超过50%)。与δ受体不同,耐受性对μ或κ受体的特性或所测试配体的超高亲和力结合位点没有明显影响。

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