Mas M, Zahradnik M A, Martino V, Davidson J M
Brain Res. 1985 Sep 2;342(1):128-34. doi: 10.1016/0006-8993(85)91360-5.
Penile erection and ejaculation are produced by spinal reflexes subject to tonic control from the brain. This study examines the possible involvement of serotonergic transmission in the supraspinal modulation of such reflexes. The effects of two drugs which facilitate serotonergic transmission by different mechanisms, namely the direct receptor agonist, 5-methoxy-N,N'-dimethyltryptamine (5-MeODMT), and the reuptake inhibitor, zimelidine, were compared in intact and spinal rats. Results show that serotonergic stimulation in intact rats by either drug produces a dose-related increase in the incidence of seminal emission as well as a definite decrease of the display of erectile responses. In the spinal animals 5-MeODMT treatment reproduced both effects. By contrast, zimelidine, which needs functional nerve endings to exert its agonistic action, was ineffective in the spinal rats. This is interpreted to exclude a peripheral mechanism for the effects of the serotonin agonists on penile reflexes of intact animals and makes a strong case for a spinal site of action. We postulate the existence of serotonergic receptors located in the lower segments of the spinal cord which, when stimulated, trigger seminal emission and suppress erection.
阴茎勃起和射精是由脊髓反射产生的,受大脑的紧张性控制。本研究探讨了5-羟色胺能传递在这种反射的脊髓上调制中的可能作用。比较了两种通过不同机制促进5-羟色胺能传递的药物,即直接受体激动剂5-甲氧基-N,N'-二甲基色胺(5-MeODMT)和再摄取抑制剂齐美利定,对完整大鼠和脊髓大鼠的影响。结果表明,两种药物对完整大鼠的5-羟色胺能刺激均产生与剂量相关的射精发生率增加以及勃起反应表现的明显降低。在脊髓动物中,5-MeODMT治疗重现了这两种效应。相比之下,需要功能性神经末梢来发挥其激动作用的齐美利定在脊髓大鼠中无效。这被解释为排除了5-羟色胺激动剂对完整动物阴茎反射作用的外周机制,并有力地证明了脊髓作用部位的存在。我们推测脊髓下段存在5-羟色胺能受体,当受到刺激时,会引发射精并抑制勃起。