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人β-酪蛋白水解产物的阿片样活性。

Opioid activities of human beta-casomorphins.

作者信息

Koch G, Wiedemann K, Teschemacher H

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1985 Dec;331(4):351-4. doi: 10.1007/BF00500818.

Abstract

Opioid activities of human beta-casomorphin-4, -5, -7 and -8 and, for comparison, of the corresponding bovine beta-casomorphins were studied in the guinea-pig ileum preparation. Binding parameters, i.e. KD-values and binding site concentrations, for the interaction of human and bovine beta-casomorphins with opioid receptors in rat brain homogenates were determined in inhibition experiments, using [3H]-(D-Ala2, MePhe4, Gly-ol5)enkephalin, [3H]-(D-Ala2, D-Leu5)enkephalin and [3H]ethylketazocin as mu-, delta- and kappa-opioid receptor ligands. Analysis of binding data was performed using a non-linear curve fitting program. All beta-casomorphins examined displayed opioid activity. The affinity was highest for mu-receptors, less so for delta-receptors and lowest for kappa-receptors. It is suggested that human beta-casomorphins might play a role as "food hormones".

摘要

在豚鼠回肠制备物中研究了人β-酪蛋白衍生吗啡肽-4、-5、-7和-8的阿片样活性,并比较了相应的牛β-酪蛋白衍生吗啡肽的阿片样活性。在抑制实验中,使用[3H]-(D-丙氨酸2,甲硫氨酸4,甘氨酸-ol5)脑啡肽、[3H]-(D-丙氨酸2,D-亮氨酸5)脑啡肽和[3H]乙基酮唑辛作为μ-、δ-和κ-阿片样受体配体,测定了人和牛β-酪蛋白衍生吗啡肽与大鼠脑匀浆中阿片样受体相互作用的结合参数,即KD值和结合位点浓度。使用非线性曲线拟合程序对结合数据进行分析。所有检测的β-酪蛋白衍生吗啡肽均表现出阿片样活性。对μ-受体的亲和力最高,对δ-受体的亲和力较低,对κ-受体的亲和力最低。有人提出,人β-酪蛋白衍生吗啡肽可能作为“食物激素”发挥作用。

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