Segal M
Brain Res. 1975 Aug 22;94(1):115-131. doi: 10.1016/0006-8993(75)90881-1.
Rat hippocampal pyramidal cells were studied for their response to serotonin applied iontophoretically and to stimulation of the midbrain raphe nuclei. Ninety-two percent of the cells studied were inhibited by serotonin. Fourty-eight percent of the cells responded by inhibition to dorsal and median raphe stimulation. The inhibitory response to raphe stimulation was absent when the rats were pretreated with p-chlorophenylalanine (PCPA), a serotonin synthesis inhibitor; PCPA effects were alleviated by 5-HTP or 5-HT administration. The response to raphe stimulation was blocked by emthysergide and cyproheptadine. The responses to raphe stimulation were potentiated by chlorimipramine, a serotonin reuptake blocker. These data satisfy several of the criteria required to identify serotonin as the inhibitory neurotransmitter for the raphe-hippocampal pathway
对大鼠海马锥体细胞进行了研究,观察其对离子电泳施加血清素以及对中脑缝核刺激的反应。所研究的细胞中有92%受到血清素的抑制。48%的细胞对背侧和中缝核刺激产生抑制反应。当用血清素合成抑制剂对氯苯丙氨酸(PCPA)预处理大鼠时,对缝核刺激的抑制反应消失;5-羟色氨酸(5-HTP)或5-羟色胺(5-HT)给药可减轻PCPA的作用。对缝核刺激的反应被麦角酰二乙胺(emthysergide)和赛庚啶阻断。血清素再摄取阻滞剂氯米帕明可增强对缝核刺激的反应。这些数据符合将血清素鉴定为缝核-海马通路抑制性神经递质所需的几个标准。