Heym J, Rasmussen K, Jacobs B L
Eur J Pharmacol. 1984 May 18;101(1-2):57-68. doi: 10.1016/0014-2999(84)90030-x.
Although central serotonergic systems appear to be linked importantly to the mechanism of action of a variety of hallucinogenic drugs, the nature of this interaction has remained unclear. In the present study, the question of whether the critical link is presynaptic or postsynaptic was examined in cats. Behaviorally inactive doses (1.0 mg/kg) of the serotonin receptor antagonists mianserin, ketanserin or metergoline effectively blocked behavior, as measured by the cat limb flick response, elicited by either LSD (50 micrograms/kg) or DOM (250 micrograms/kg) but not that resulting either from lisuride (50 micrograms/kg) or a high dose of apomorphine (4 mg/kg). Pretreatment with 1.0 mg/kg of mianserin, which completely attenuated LSD's behavioral effect, failed to alter LSD-induced depression of mesencephalic serotonergic neuron discharge. These results demonstrate that at least some of the behavioral effects of LSD can be blocked by pharmacological antagonism of postsynaptic serotonin receptors which leaves LSD's presynaptic effect unaffected. Thus, the behavioral, and possibly psychoactive, effects of hallucinogens appear to be attributable to an action at 5HT2 receptors, presumably located postsynaptically.
尽管中枢5-羟色胺能系统似乎与多种致幻药物的作用机制密切相关,但这种相互作用的本质仍不清楚。在本研究中,在猫身上研究了关键联系是突触前还是突触后的问题。行为上无活性剂量(1.0毫克/千克)的5-羟色胺受体拮抗剂米安色林、酮色林或麦角苄酯能有效阻断由LSD(50微克/千克)或DOM(250微克/千克)引起的、通过猫肢体轻弹反应测量的行为,但不能阻断由利苏瑞得(50微克/千克)或高剂量阿扑吗啡(4毫克/千克)引起的行为。用1.0毫克/千克的米安色林预处理可完全减弱LSD的行为效应,但未能改变LSD引起的中脑5-羟色胺能神经元放电的抑制。这些结果表明,LSD的至少一些行为效应可通过对突触后5-羟色胺受体的药理拮抗作用来阻断,而LSD的突触前效应不受影响。因此,致幻剂的行为效应以及可能的精神活性效应似乎归因于对5HT2受体的作用,推测该受体位于突触后。