Aguilar J S, Criado M, De Robertis E
Eur J Pharmacol. 1980 Dec 5;68(3):317-26. doi: 10.1016/0014-2999(80)90529-4.
[3H]Quinuclydinyl benzylate ([3H]QNB) binding was carried out on crude synaptosomal membranes isolated from cat cerebral cortex. The specific binding showed a single type of site with KD 0.25 nM, Hill number 0.89 and Bmax 114 pmol/g protein. The local anesthetics procaine, tetracaine and dibucaine, and the adrenergic antagonists phentolamine and propranolol, in concentrations between 1 nM and 500 microM, inhibited [3H]QNB binding with Ki varying between 9 microM for procaine and 80 microM for propranolol. The Hill coefficients obtained from logit/log plots suggested that there was no cooperativity between the binding sites for local anesthetics. At various concentrations the inhibition by procaine and propranolol may appear as competitive or non-competitive. The Hill numbers obtained from the saturation curves suggest that there was no cooperativity between anesthetics and [3H]QNB binding sites. Neither 1 mM Ca2+ nor Mg2+ affected [3H]QNB binding or the action of the drugs. The effect of local anesthetics and adrenergic antagonists was reversible and these drugs did not protect the muscarinic receptor from the deleterious effect of Triton X-100 as was the case with muscarinic agents. Our findings suggest that local anesthetics inhibit [3H]QNB binding to the muscarinic receptor by acting at some accessory site but not on the true receptor site. The possible mechanism of action and local anesthetics on synaptic transmission is discussed.
使用从猫脑皮层分离得到的粗制突触体膜进行了[3H]喹核酯苄酯([3H]QNB)结合实验。特异性结合显示出一种单一类型的位点,解离常数(KD)为0.25 nM,希尔系数为0.89,最大结合容量(Bmax)为114 pmol/g蛋白质。局部麻醉药普鲁卡因、丁卡因和布比卡因,以及肾上腺素能拮抗剂酚妥拉明和普萘洛尔,在1 nM至500 μM的浓度范围内,抑制了[3H]QNB结合,其抑制常数(Ki)在普鲁卡因为9 μM至普萘洛尔为80 μM之间变化。从对数几率/对数图获得的希尔系数表明,局部麻醉药的结合位点之间不存在协同性。在不同浓度下,普鲁卡因和普萘洛尔的抑制作用可能表现为竞争性或非竞争性。从饱和曲线获得的希尔系数表明,麻醉药与[3H]QNB结合位点之间不存在协同性。1 mM的Ca2+和Mg2+均未影响[3H]QNB结合或药物的作用。局部麻醉药和肾上腺素能拮抗剂的作用是可逆的,并且这些药物不像毒蕈碱剂那样能保护毒蕈碱受体免受Triton X - 100的有害影响。我们的研究结果表明,局部麻醉药通过作用于某些辅助位点而非真正的受体位点来抑制[3H]QNB与毒蕈碱受体的结合。本文讨论了局部麻醉药对突触传递可能的作用机制。