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评估μ和δ选择性配体与[3H]D-丙氨酸2-D-亮氨酸5-脑啡肽结合小鼠脑膜的相互作用。

Evaluation of the interactions of mu and delta selective ligands with [3H]D-Ala2-D-Leu5-enkephalin binding to mouse brain membranes.

作者信息

Barrett R W, Vaught J L

出版信息

Life Sci. 1983 Dec 12;33(24):2439-48. doi: 10.1016/0024-3205(83)90638-0.

Abstract

The interactions of putative mu and delta selective ligands with [3H]D-ala2-D-leu5 enkephalin (DADLE) binding to mouse brain membranes were investigated. Computerized curve fitting of displacement curves performed at three different concentrations of 3H-DADLE indicated that a one site competitive model was sufficient to explain the interactions of leu-enkephalin (LE) and D-ser2-thr6-leucine enkephalin with 3H-DADLE binding. Similar experiments with morphine and morphiceptin were unique in that the multiple displacement curves crossed over one another. A two-site competitive model was required to adequately describe the interactions of these mu selective ligands with 3H-DADLE. This two-site model was one in which the inhibitor had higher affinity for the site labeled with lower affinity by 3H-DADLE. However, this two site model did not correctly predict the interaction of LE with 3H-DADLE in the presence of morphiceptin. These data indicate that: 1) putative mu and delta selective ligands do not bind to a common high affinity site; 2) mu selective ligands are not simple mixed inhibitors of a single site labeled by 3H-DADLE; and 3) competitive binding models may not explain the interaction of mu ligands with 3H-DADLE binding.

摘要

研究了假定的μ和δ选择性配体与[³H]D-ala²-D-leu⁵脑啡肽(DADLE)结合小鼠脑膜的相互作用。在三种不同浓度的³H-DADLE下进行的位移曲线的计算机化曲线拟合表明,一个位点竞争模型足以解释亮氨酸脑啡肽(LE)和D-丝氨酸²-苏氨酸⁶-亮氨酸脑啡肽与³H-DADLE结合的相互作用。吗啡和吗啡肽的类似实验的独特之处在于多条位移曲线相互交叉。需要一个双位点竞争模型来充分描述这些μ选择性配体与³H-DADLE的相互作用。这个双位点模型是抑制剂对³H-DADLE标记的低亲和力位点具有更高亲和力的模型。然而,这个双位点模型不能正确预测在吗啡肽存在下LE与³H-DADLE的相互作用。这些数据表明:1)假定的μ和δ选择性配体不结合到共同的高亲和力位点;2)μ选择性配体不是³H-DADLE标记的单个位点的简单混合抑制剂;3)竞争结合模型可能无法解释μ配体与³H-DADLE结合的相互作用。

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