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磺酸脑啡肽:对大鼠脑阿片受体的结合特异性

Sulfonic acid enkephalin: binding specificity to rat brain opiate receptors.

作者信息

Martin J L, Coletti-Previero M A, Roques B P, Descomps B

出版信息

Neuropeptides. 1985 Jul;6(4):293-302. doi: 10.1016/0143-4179(85)90002-2.

Abstract

We tested sulfonic-acid enkephalin, a SO3H-Tyr derivative of the Leu-enkephalin, for its binding capacity to rat brain opiate receptors, by competition against several tritiated enkephalins. Using [3H]DADLE as the competitor, we demonstrated that sulfonic-acid enkephalin binds to rat brain opiate receptors, and using [3H]DSLET and [3H]DAGO as the competitors, we demonstrated that sulfonic-acid enkephalin binds preferentially to delta-opiate receptors. The affinity ratio of sulfonic-acid enkephalin for delta-opiate receptors versus mu-opiate receptors, is considerably higher than that of the parent compound, Leu-enkephalin, and of DADLE and is similar to the affinity ratio of DSLET for the same receptors.

摘要

我们通过与几种氚标记脑啡肽竞争,测试了磺酸脑啡肽(亮氨酸脑啡肽的一种SO3H - 酪氨酸衍生物)与大鼠脑阿片受体的结合能力。以[3H]DADLE作为竞争者,我们证明磺酸脑啡肽能与大鼠脑阿片受体结合;以[3H]DSLET和[3H]DAGO作为竞争者,我们证明磺酸脑啡肽优先与δ-阿片受体结合。磺酸脑啡肽对δ-阿片受体与μ-阿片受体的亲和比,明显高于母体化合物亮氨酸脑啡肽和DADLE,且与DSLET对相同受体的亲和比相似。

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