Andersen Monica L, Perry Juliana C, Tufik Sergio
Department of Psychobiology, Universidade Federal de São Paulo, Escola Paulista de Medicina, São Paulo, Brazil.
Scand J Psychol. 2007 Dec;48(6):443-7. doi: 10.1111/j.1467-9450.2007.00613.x.
Previous studies have demonstrated that paradoxical sleep deprivation (PSD) potentiates cocaine-induced genital reflexes in male rats and both D1 and D2 receptors may play a role in those effects, and to examine the possibility that such might involve other dopaminergic receptors, we investigated the effects of D3 and D4 receptor subtype antagonists on cocaine-induced reflexes in sleep-deprived rats. Separate groups of PSD rats received saline, D3 (U9919A; 0.75, 1.5 and 3 mg/kg) or D4 (L745870; 0.75, 1.5 and 3 mg/kg) antagonists prior to acute cocaine challenge. Results demonstrated that U9919A induced significant reduction in the number of animals that displayed erection and the frequency of erection at two smaller doses, while no significant difference was reported for the D4 receptor antagonist. Although our studies indicate that there is a relevant participation of D3 receptors in male sexual function, D4 receptors seem not to exert an essential role in this model.
先前的研究表明,矛盾睡眠剥夺(PSD)会增强雄性大鼠中可卡因诱导的生殖器反射,并且D1和D2受体可能在这些效应中发挥作用。为了研究这种情况是否可能涉及其他多巴胺能受体,我们研究了D3和D4受体亚型拮抗剂对睡眠剥夺大鼠中可卡因诱导反射的影响。在急性可卡因激发前,将单独的PSD大鼠组分别给予生理盐水、D3(U9919A;0.75、1.5和3mg/kg)或D4(L745870;0.75、1.5和3mg/kg)拮抗剂。结果表明,U9919A在两个较小剂量时可显著减少出现勃起的动物数量和勃起频率,而D4受体拮抗剂未报告有显著差异。尽管我们的研究表明D3受体在男性性功能中有相关参与,但D4受体在该模型中似乎并未发挥关键作用。