Melanotan-II:: Investigation of the inducer and facilitator effects on penile erection in anaesthetized rat

被引:15
作者
Giuliano, F
Clément, P
Droupy, S
Alexandre, L
Bernabé, J
机构
[1] Raymond Poincare Hosp, Dept Neurol Rehabil, Neuro Urol Unit, AP HP, F-92380 Garches, France
[2] CNRS, Pelvipharm Labs, F-91190 Gif Sur Yvette, France
[3] Med Univ Paris S, UPRES, Grp Rech Urol, F-94270 Le Kremlin Bicetre, France
关键词
melanocortin receptor; paraventricular nucleus; spinal cord; sympathetic nervous system;
D O I
10.1016/j.neuroscience.2005.11.008
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
The effects of melanotan-II, a non-specific agonist of melanocortin receptors, on erection and its possible sites of action were investigated in anesthetized rats. Delivered i.v. (0.1, 0.3 and 1 mg/kg) or within the paraventricular nucleus of the hypothalamus (0.1 and mu g), melanotan-II exerted a dose-dependent inducer activity on erection by eliciting erectile events and shortening latency of the first erectile event to occur. Erectile events were of higher amplitude in rats treated with melanotan-II i.t. (0.2 mu g) delivered at the L6-S1 level than in animals treated with the vehicle i.t. delivered. Erectile responses elicited by cavernous nerve stimulation were increased after i.v. melanotan-II (11 mg/kg), thereby exerting facilitator effect on erection. In contrast, melanotan-II injected within the corpus cavernosum (1 mu g) did not display any facilitator activity. To investigate the neural pathways involved in the facilitator effect of melanotan-II, we performed acute spinalization (T8 level) and differential selective nerve transections. Neither spinalization nor bilateral transection of pelvic nerves or dorsal penile nerves impaired facilitator activity of i.v. melanotan-II (1 mg/kg). Conversely, the facilitator effect of melanotan-II was abolished after acute removal of the lumbar paravertebral sympathetic chain. These results lead to the conclusion that central and peripheral melanocortin pathways are recruited by melanotan-II, depending on its route of delivery, to exert both inducer and facilitator activities on erection. (c) 2005 Published by Elsevier Ltd on behalf of IBRO.
引用
收藏
页码:293 / 301
页数:9
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