Velazquez-Moctezuma J, Aguilar-Garcia A, Diaz-Ruiz O
Departamento de Biologia de la Reproduccion, Universidad Autonoma Metropolitana-Iztapalapa, Mexico City, Mexico.
Pharmacol Biochem Behav. 1993 Sep;46(1):215-7. doi: 10.1016/0091-3057(93)90343-r.
It has been suggested that REM sleep deprivation due to the administration of clomipramine, during early developmental stages, results in dramatic behavioral changes during adulthood. One of the main alterations is the impairment of masculine sexual behavior (MSB). Clomipramine increase monoaminergic availability at the synaptic level and also suppresses REM sleep. This study was performed to compare the effect on masculine sexual behavior of three different neonatal treatments: clomipramine, which increases monoaminergic availability at the synaptic level and suppresses REM sleep; scopolamine, a cholinergic antagonist that suppresses REM sleep; and idaxozan, a selective adrenergic agonist. Subjects (Ss) were treated neonatally and tested for masculine sexual behavior during adulthood with standard techniques. Results obtained with clomipramine administration showed a marked impairment of MSB, mainly reflected by the decrease in the percentage of active Ss and the decrease in the percentage of Ss reaching ejaculation. In contrast, idaxozan and scopolamine produce a facilitation of MSB. The effect of idaxozan was not significantly different when compared to saline control rats. The effect of scopolamine was greater, and the percentage of Ss reaching ejaculation was significantly larger than saline control. These results suggest that the alterations of sexual behavior induced with neonatally administered clomipramine are not due to early REM sleep deprivation. As idaxozan did not replicate clomipramine results, it is also possible that noradrenergic transmission is not involved in the generation of these effects. It remains possible that the serotonin system could be responsible for the impairment of sexual behavior due to neonatal clomipramine treatment.
有人提出,在发育早期阶段给予氯米帕明导致的快速眼动睡眠剥夺会在成年期引发显著的行为变化。主要变化之一是雄性性行为(MSB)受损。氯米帕明可提高突触水平的单胺能可用性,还能抑制快速眼动睡眠。本研究旨在比较三种不同的新生期处理对雄性性行为的影响:氯米帕明,可提高突触水平的单胺能可用性并抑制快速眼动睡眠;东莨菪碱,一种抑制快速眼动睡眠的胆碱能拮抗剂;以及伊达唑胺,一种选择性肾上腺素能激动剂。对实验对象(Ss)进行新生期处理,并在成年期用标准技术测试其雄性性行为。给予氯米帕明后获得的结果显示MSB明显受损,主要表现为活跃的Ss百分比下降以及达到射精的Ss百分比下降。相比之下,伊达唑胺和东莨菪碱则促进了MSB。与生理盐水对照大鼠相比,伊达唑胺的效果无显著差异。东莨菪碱的效果更强,达到射精的Ss百分比显著高于生理盐水对照。这些结果表明,新生期给予氯米帕明引起的性行为改变并非由于早期快速眼动睡眠剥夺。由于伊达唑胺未重现氯米帕明的结果,也有可能去甲肾上腺素能传递不参与这些效应的产生。仍有可能是5-羟色胺系统导致了新生期氯米帕明处理引起的性行为受损。