3h - n -甲基东莨菪碱与完整大鼠胸腺细胞结合的表征。

Endocrinologia experimentalis Pub Date : 1990-03-01
I Rinner, S Porta, K Schauenstein
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引用次数: 0

摘要

通过与3h - n -甲基东莨菪碱(3H-NMS)的竞争结合实验,确定了毒毒碱拮抗剂在完整大鼠胸腺细胞中的结合参数。毒蕈碱拮抗剂以剂量依赖的方式抑制3H-NMS的结合。位移曲线的非线性回归分析表明,毒蕈碱类化合物存在两种亲和状态。-阻断剂r -心得安、s -心得安和阿普萘洛尔抑制3H-NMS与大鼠胸腺淋巴细胞一个低亲和力结合位点的结合。神经节阻断物质六甲铵不影响3H-NMS的结合。结果表明,放射性配体在大鼠胸腺细胞上存在两个结合位点,其中只有一个是毒蕈碱受体拮抗剂特异性的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Characterization of 3H-N-methylscopolamine binding to intact rat thymocytes.

The binding parameters of muscarinic antagonists in intact rat thymocytes were determined from competitive binding experiments with 3H-N-methylscopolamine (3H-NMS). The muscarinic antagonists inhibited binding of 3H-NMS in a dose-dependent manner. Non-linear regression analysis of the displacement curves indicated the presence of two affinity states for the muscarinic compounds. The beta-blocking agents R-propranolol, S-propranolol and alprenolol inhibited the binding of 3H-NMS to one, low affinity binding site on rat thymic lymphocytes. The ganglionic blocking substance hexamethonium did not affect the binding of 3H-NMS. The results indicate the presence of two binding sites for the radioligand on rat thymocytes, of which only one is specific for muscarinic receptor antagonists.

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