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甲硫氨酸脑啡肽与阿片受体的结合在功能上与生物降解无关。

Met-enkephalin binding to opiate receptors is not functionally coupled to biodegradation.

作者信息

Nagy A, Gráf L, Lajtha A

出版信息

Life Sci. 1983 Aug 29;33(9):835-40. doi: 10.1016/0024-3205(83)90621-5.

Abstract

Using synaptosomal rat brain membranes, the degradation of Met-enkephalin in both free and receptor-bound form was measured, together with the dissociation of Met-enkephalin from the receptors. The results show that the degradation rate of initially receptor-bound Met-enkephalin is significantly smaller than either the rate of dissociation from the receptors or that of the degradation of free Met-enkephalin. These data suggest that intact Met-enkephalin dissociates from the receptors and then it becomes a target for the same membrane-associated peptidases that split free Met-enkephalin. This view is supported by the good fitness of the measured degradation of initially receptor-bound Met-enkephalin to the predicted degradation curve calculated from the dissociation rate of receptor-bound Met-enkephalin and the degradation rate of free Met-enkephalin.

摘要

利用大鼠脑突触体膜,测定了游离形式和受体结合形式的甲硫氨酸脑啡肽的降解情况,以及甲硫氨酸脑啡肽从受体上的解离情况。结果表明,最初与受体结合的甲硫氨酸脑啡肽的降解速率明显小于其从受体上的解离速率或游离甲硫氨酸脑啡肽的降解速率。这些数据表明,完整的甲硫氨酸脑啡肽从受体上解离,然后成为与膜相关的肽酶的作用靶点,这些肽酶会分解游离的甲硫氨酸脑啡肽。最初与受体结合的甲硫氨酸脑啡肽的实测降解情况与根据受体结合的甲硫氨酸脑啡肽的解离速率和游离甲硫氨酸脑啡肽的降解速率计算出的预测降解曲线拟合良好,这支持了这一观点。

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