Barrett R J, Blackshear M A, Sanders-Bush E
Psychopharmacology (Berl). 1982;76(1):29-35. doi: 10.1007/BF00430750.
Rats were trained to discriminate the stimulus properties of L-5-hydroxytryptophan (L-5-HTP) (30 mg/kg SC), the immediate precursor of serotonin (5-HT). The peripheral decarboxylase inhibitor R04-4602, administered prior to L-5-HTP, greatly attenuated the disruptive effects observed on responding when L-5-HTP alone was injected. Following acquisition, the discrimination was dose-dependent and generalized to fenfluramine, a 5-HT-releasing drug, but not to amphetamine, a catecholamine-releasing agent. Further evidence for the involvement of 5-HT receptor stimulation in mediating the discrimination was that pretreatment with fluoxetine, a highly specific 5-HT uptake inhibitor, markedly potentiated the cue. Nevertheless, the classical 5-HT antagonists methysergide, cyproheptadine, metergoline, and methiothepin did not block the L-5-HTP-related discriminative stimulus. This finding suggested that the cue properties of L-5-HTP might be mediated by a population of 5-HT receptors previously identified electrophysiologically in limbic structures. As in the present experiment, the putative 5-HT antagonists did not block the synaptic effects of 5-HT in these structures.
大鼠接受训练以辨别5-羟色胺(5-HT)的直接前体L-5-羟色氨酸(L-5-HTP)(30mg/kg,皮下注射)的刺激特性。在注射L-5-HTP之前给予外周脱羧酶抑制剂R04-4602,可大大减弱单独注射L-5-HTP时对反应所观察到的干扰作用。习得后,辨别呈剂量依赖性,并可泛化至5-HT释放药物芬氟拉明,但不会泛化至儿茶酚胺释放剂苯丙胺。5-HT受体刺激参与介导辨别这一观点的进一步证据是,用高度特异性的5-HT摄取抑制剂氟西汀预处理可显著增强该线索。然而,经典的5-HT拮抗剂麦角新碱、赛庚啶、美替拉林和甲硫噻平并未阻断与L-5-HTP相关的辨别性刺激。这一发现表明,L-5-HTP的线索特性可能由先前在边缘结构中通过电生理学鉴定的一群5-HT受体介导。正如在本实验中一样,推定的5-HT拮抗剂并未阻断5-HT在这些结构中的突触效应。