Fuller R W, Wong D T
Fed Proc. 1977 Jul;36(8):2154-8.
An uptake system on the serotonin neuronal membrane apparently functions to inactivate serotonin that has been released into the synaptic cleft. Various inhibitors of this active transport system on serotonin neurons are known, and some are specific in the sense that they do not inhibit the active uptake system on norepinephrine neurons. The most widely studied specific inhibitor of the serotonin neuron pump is fluoxetine, 3-(p-trifluoromethylphenoxy-N-methyl-3-phenyl propylamine (Lilly 110140). When fluoxetine or other effective but less specific serotonin uptake inhibitors are given, a rapid decrease in serotonin turnover occurs and the rate of firing of single neural units in the serotonin rich raphe area of brain is reduced. This decrease in serotonin turnover and release may be a compensatroy mechanism in response to an enhanced action of serotonin on synaptic receptors. Through the use of fluoxetine and other serotonin uptake inhibitors, the role of serotonin neurons in various brain functions--behavior, sleep, regulation of pituitary hormone release, thermoregulation, pain responsiveness, and so on--can be studied.
血清素神经元膜上的摄取系统显然起着使释放到突触间隙中的血清素失活的作用。已知血清素神经元上这种主动转运系统的各种抑制剂,其中一些具有特异性,即它们不会抑制去甲肾上腺素能神经元上的主动摄取系统。对血清素神经元泵研究最广泛的特异性抑制剂是氟西汀,即3-(对-三氟甲基苯氧基-N-甲基-3-苯基丙胺)(礼来110140)。当给予氟西汀或其他有效但特异性较低的血清素摄取抑制剂时,血清素周转率会迅速下降,且富含血清素的脑桥中缝区域单个神经单元的放电率会降低。血清素周转率和释放的这种下降可能是一种补偿机制,以应对血清素对突触受体作用增强的情况。通过使用氟西汀和其他血清素摄取抑制剂,可以研究血清素能神经元在各种脑功能(行为、睡眠、垂体激素释放调节、体温调节、疼痛反应性等)中的作用。