Lee J H, el-Fakahany E E
J Pharmacol Exp Ther. 1985 Jun;233(3):707-14.
The binding properties of (-)-[3H]quinuclidinyl benzilate and [3H] N-methylscopolamine to muscarinic acetylcholine receptors have been investigated in rat brain homogenates. The binding of both antagonists demonstrated high affinity and saturability. Analysis of the binding data resulted in linear Scatchard plots. However, (-)-[3H]quinuclidinyl benzilate showed a significantly higher maximal binding capacity than that of [3H]N-methylscopolamine. Displacement of both ligands with several muscarinic receptor antagonists resulted in competition curves in accordance with the law of mass-action for quinuclidinyl benzilate, atropine and scopolamine. A similar profile was found for the quaternary ammonium analogs of atropine and scopolamine when [3H]N-methylscopolamine was used to label the receptors. However, when these hydrophilic antagonists were used to displace (-)-[3H] quinuclidinyl benzilate binding, they showed interaction with high- and low-affinity binding sites. On the other hand, the nonclassical muscarinic receptor antagonist, pirenzepine, was able to displace both ligands from two binding sites. The present data are discussed in terms of the relationship of this anomalous heterogenity of binding of these hydrophilic muscarinic receptor antagonists and the proposed M1 and M2 receptor subtypes.
已在大鼠脑匀浆中研究了(-)-[3H]东莨菪碱和[3H]N-甲基东莨菪碱与毒蕈碱型乙酰胆碱受体的结合特性。两种拮抗剂的结合均表现出高亲和力和饱和性。结合数据的分析产生了线性Scatchard图。然而,(-)-[3H]东莨菪碱的最大结合容量明显高于[3H]N-甲基东莨菪碱。用几种毒蕈碱受体拮抗剂置换两种配体,得到的竞争曲线符合东莨菪碱、阿托品和东莨菪碱的质量作用定律。当用[3H]N-甲基东莨菪碱标记受体时,阿托品和东莨菪碱的季铵类似物也有类似的情况。然而,当用这些亲水性拮抗剂置换(-)-[3H]东莨菪碱结合时,它们显示出与高亲和力和低亲和力结合位点的相互作用。另一方面,非经典毒蕈碱受体拮抗剂哌仑西平能够从两个结合位点置换两种配体。本文根据这些亲水性毒蕈碱受体拮抗剂结合的异常异质性与所提出的M1和M2受体亚型之间的关系对现有数据进行了讨论。