Ferrari F, Giuliani D
Department of Biomedical Sciences, University of Modena, Italy.
Life Sci. 1994;55(14):1155-62. doi: 10.1016/0024-3205(94)00244-4.
The selective D2 antagonist eticlopride, at a dose (0.01 mg/kg, s.c.) that fails to modify the normal behavior of rats, significantly reversed all the behavioral effects exerted by the selective D2 agonist SND 919 (0.1 mg/kg, i.p.), namely, the stimulation of stretching-yawning, penile erection and sedation and the inhibition of grooming. In the copulatory test, eticlopride at the same dose did not affect animal sexual behavior but potently counteracted the reduction in mount and intromission frequency and latency to ejaculation induced by SND 919 at 0.1 mg/kg, a behavioral pattern which might possibly be proposed as an animal model for human ejaculatio praecox.
选择性D2拮抗剂依托必利,以未能改变大鼠正常行为的剂量(0.01毫克/千克,皮下注射),显著逆转了选择性D2激动剂SND 919(0.1毫克/千克,腹腔注射)所产生的所有行为效应,即对伸展-打哈欠、阴茎勃起和镇静的刺激以及对梳理行为的抑制。在交配试验中,相同剂量的依托必利不影响动物的性行为,但有力地对抗了0.1毫克/千克的SND 919所诱导的骑跨和插入频率降低以及射精潜伏期延长,这种行为模式可能被提议作为人类早泄的动物模型。