Martin W R, Sloan J W, Hook R, Kaplan E, Wash C
Pharmacol Biochem Behav. 1986 Oct;25(4):843-8. doi: 10.1016/0091-3057(86)90396-5.
Four distinguishable nicotinic binding sites have been identified as well as four nicotinic ligands with different specificities: (+/-)-2-methylpiperidine which binds to a very high affinity site (Site 1) and produces up-regulation of the high affinity site (Site 2); (-)-nicotine which binds to Site 1 and Site 2 as well as to a low affinity site (Site 4); (+)-nicotine which binds to Site 1, Site 4 and Site 3 which is also a high affinity site; and (-)-cytisine which binds to Sites 1 and 2. These drugs were injected into the 4th ventricle of 5 dogs in graded concentrations (12.5 to 400 micrograms) and their effects on the EEG, skin twitch reflex latency, heart rate, rectal temperature, pupillary diameter, blood pressure and the amplitude of the flexor reflex were measured. Drugs which act predominantly on Site 1 [(+/-)-2-methylpiperidine and (+)-nicotine] produced EEG synchronization and hyperalgesia while drugs which interact with Sites 2 and 4 produce EEG desynchronization, analgesia and tachycardia. These data indicate that nicotinic ligands which have different binding specificities have different actions in medullary function and support the hypothesis that the different binding sites have different pharmacologic significance.
(±)-2-甲基哌啶与一个高亲和力位点(位点1)结合,并使高亲和力位点(位点2)上调;(-)-尼古丁与位点1和位点2以及一个低亲和力位点(位点4)结合;(+)-尼古丁与位点1、位点4和也是高亲和力位点的位点3结合;以及(-)-金雀花碱与位点1和位点2结合。将这些药物以分级浓度(12.5至400微克)注入5只狗的第四脑室,并测量它们对脑电图、皮肤抽搐反射潜伏期、心率、直肠温度、瞳孔直径、血压和屈肌反射幅度的影响。主要作用于位点1的药物[(±)-2-甲基哌啶和(+)-尼古丁]产生脑电图同步和痛觉过敏,而与位点2和4相互作用的药物产生脑电图去同步、镇痛和心动过速。这些数据表明,具有不同结合特异性的烟碱配体在延髓功能中具有不同作用,并支持不同结合位点具有不同药理学意义的假说。