The physiological sexual excitation is mediated both by the sympathetic and
the parasympathetic nervous system. The antagonism between testosterone (T
t) and estrogens (Es) as well as the fact that the dynamics of the sexual e
xcitation in the male are antagonistic to those in the female are nowadays
well-known; hence, the hypothesis was emitted that the sympathoparasympathe
tic sexual excitation is bihormonal mediated, consisting in a very active s
exual hormone associated with a weak antagonistic hormone.
Most studies show a serotonergic (ejaculatory) involvement in premature eja
culation (PE). Nevertheless, an effective treatment of PE is rather difficu
lt with selective serotonin reuptake inhibitor drugs and other clinical dat
a even suggest that changes in PE actually involve at first the sexual exci
tation process and only secondly the ejaculation reflex.
Thus, a therapeutic model for PE is set up, starting from the physiological
aspects described and from the presumed pathophysiological mechanism in PE
. (C) 2001 Harcourt Publishers Ltd.