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Sex Med Rev ; 6(2): 234-241, 2018 04.
Article in English | MEDLINE | ID: mdl-28827037

ABSTRACT

INTRODUCTION: It is common for men to develop erectile dysfunction after radical prostatectomy. The anatomy of the rat allows the cavernous nerve (CN) to be identified, dissected, and injured in a controlled fashion. Therefore, bilateral CN injury (BCNI) in the rat model is routinely used to study post-prostatectomy erectile dysfunction. AIM: To compare and contrast the available literature on pharmacologic intervention after BCNI in the rat. METHODS: A literature search was performed on PubMed for cavernous nerve and injury and erectile dysfunction and rat. Only articles with BCNI and pharmacologic intervention that could be grouped into categories of immune modulation, growth factor therapy, receptor kinase inhibition, phosphodiesterase type 5 inhibition, and anti-inflammatory and antifibrotic interventions were included. MAIN OUTCOME MEASURES: To assess outcomes of pharmaceutical intervention on erectile function recovery after BCNI in the rat model. The ratio of maximum intracavernous pressure to mean arterial pressure was the main outcome measure chosen for this analysis. RESULTS: All interventions improved erectile function recovery after BCNI based on the ratio of maximum intracavernous pressure to mean arterial pressure results. Additional end-point analysis examined the corpus cavernosa and/or the major pelvic ganglion and CN. There was extreme heterogeneity within the literature, making accurate comparisons between crush injury and therapeutic interventions difficult. CONCLUSIONS: BCNI in the rat is the accepted animal model used to study nerve-sparing post-prostatectomy erectile dysfunction. However, an important limitation is extreme variability. Efforts should be made to decrease this variability and increase the translational utility toward clinical trials in humans. Haney NM, Nguyen HMT, Honda M, et al. Bilateral Cavernous Nerve Crush Injury in the Rat Model: A Comparative Review of Pharmacologic Interventions. Sex Med Rev 2018;6:234-241.


Subject(s)
Disease Models, Animal , Erectile Dysfunction , Peripheral Nerve Injuries , Prostatectomy/adverse effects , Animals , Erectile Dysfunction/drug therapy , Erectile Dysfunction/etiology , Male , Peripheral Nerve Injuries/drug therapy , Peripheral Nerve Injuries/etiology , Rats , Urological Agents/therapeutic use
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