Yamamura H I, Snyder S H
Proc Natl Acad Sci U S A. 1974 May;71(5):1725-9. doi: 10.1073/pnas.71.5.1725.
Binding sites with high affinity and specificity for [(3)H]quinuclidinyl benzilate (QNB) are present in homogenates of rat brain. The characteristics of the binding sites resemble those of muscarinic cholinergic receptors. Specific binding is saturable with respect to [(3)H]QNB and tissue concentration and is time-, temperature-, and pH-dependent. The bimolecular rate of association (2.0 x 10(8) M(-1) min(-1)) and dissociation (1.2 x 10(-2) min(-1)) at 35 degrees indicate a dissociation constant of 60 pM and a density of 65 pmol/g of brain. Muscarinic antagonists and agonists displace specific [(3)H]QNB binding, while nicotinic and non-cholinergic drugs possess little affinity for [(3)H]QNB-binding sites.
大鼠脑匀浆中存在对[³H]东莨菪碱(QNB)具有高亲和力和特异性的结合位点。这些结合位点的特征类似于毒蕈碱胆碱能受体。特异性结合对于[³H]QNB和组织浓度而言是可饱和的,并且依赖于时间、温度和pH值。在35℃时,双分子缔合速率(2.0×10⁸ M⁻¹ min⁻¹)和解离速率(1.2×10⁻² min⁻¹)表明解离常数为60 pM,脑密度为65 pmol/g。毒蕈碱拮抗剂和激动剂可取代特异性[³H]QNB结合,而烟碱和非胆碱能药物对[³H]QNB结合位点几乎没有亲和力。