Some proposals regarding the organization of the central nervous system control of penile erection

• Published in: Neuroscience and Biobehavioral Reviews 2000-07, Vol.24 (5), p.535-540
• Main Author: McKenna, K.E.
• Format: Article
• Language: English
• Subjects: Animals; Central Nervous System - physiology; Erectile dysfunction; Humans; Impotence; Male; Penile Erection - physiology; Penis; Sexual responses; Spinal Cord - physiology
• ISSN: 0149-7634; 1873-7528
• DOI: 10.1016/S0149-7634(00)00021-X

Recent research on the central nervous control of penile erection is discussed. A framework for this control is based upon principles put forward by Frank Beach regarding the neuroendocrine regulation of male copulatory behavior. The current discussion is focused primarily on a subset, penile erection. The spinal cord contains all the necessary components for the production of penile erection. This requires a multisegmental coordination among penile vasodilator and vasoconstrictor autonomic neurons, pudendal motoneurons responsible for penile rigidity and autonomic neurons which control extra-penile blood flow. Genital sensory stimulation can activate this spinal network. The spinal cord is also under excitatory and inhibitory control from supraspinal sites. Penile erection can be driven by supraspinal input alone and supraspinal control can inhibit the erectile effects of genital stimulation. An important aspect of the CNS control of penile erection is that there are extensive interconnections between most of the brain sites identified to date. Most of the pathways are characterized by reciprocal connections. A large number of the CNS sites also receive genital sensory information. Thus, descending control may itself be modulated by ascending sensory pathways which relay information from the genitalia. This raises the possibility that penile erection may involve a positive feedback system. Receptors for gonadal hormones have been identified throughout the neuraxis. However, strong evidence for the control of male sexual function by gonadal hormones has been identified only for forebrain sites. The functional role of brainstem and spinal gonadal hormone receptors has not yet been clarified.