Arteriogenic Erectile Dysfunction Alters Protein Expression within the Cavernosal Tissue in an Animal Model
Article first published online: 17 FEB 2005
The Journal of Sexual Medicine
Volume 2, Issue 2, pages 199–206, March 2005
How to Cite
De Young, L., Bella, A., Howard, J. and Brock, G. (2005), Arteriogenic Erectile Dysfunction Alters Protein Expression within the Cavernosal Tissue in an Animal Model. Journal of Sexual Medicine, 2: 199–206. doi: 10.1111/j.1743-6109.2005.20229.x
- Issue published online: 17 FEB 2005
- Article first published online: 17 FEB 2005
- Arteriogenic Erectile Dysfunction;
- Nitric Oxide;
Introduction. Erectile dysfunction (ED) is a highly prevalent and often untreated condition. It may be a marker of underlying chronic illness and negatively impacts quality of life. Penile arterial insufficiency, frequently found in association with hypertension, dyslipidemia, diabetes mellitus, pelvic irradiation, trauma, and smoking, is the most common cause of ED.
Aim. This study was designed to measure the effect of penile hypoperfusion-induced alteration and injury on erectile tissue at the cellular and protein level.
Methods. Eighteen 4-month-old male Sprague Dawley rats were placed into three groups (n = 6): sham surgery, unilateral internal iliac artery ligation (UIIAL), and bilateral internal iliac artery ligation (BIIAL).
Main Outcome Measure. Erectile function was assessed 4 weeks following arterial ligation surgery as measured by a rise in intracavernosal pressure induced by cavernosal nerve stimulation. Penile tissue alterations were characterized by immunohistochemistry, protein content measured by western blot, and “global” protein expression profile carried out by using surface-enhanced laser desorption/ionization time-of-flight mass spectrometry (SELDI-TOF-MS) ProteinChip technology.
Results. Significantly lower intracavernous pressures were demonstrated in animals subjected to UIIAL surgery, which correlated to the extent of artery ligation. The intensity and quantity of immunohistochemical staining for neuronal nitric oxide synthase, endothelial cell integrity, smooth muscle cell α-actin, and vascular endothelial growth factor (VEGF) receptor flk1 were decreased in the BIIAL group compared to sham controls. SELDI-TOF-MS analysis revealed changes in molecular expression of a ∼6,560 Da protein relative to a 7,720 Da protein (peak ratio = 1.34 ± 0.3, BIIAL; 0.36 ± 0.1 controls, P < 0.05).
Conclusions. In this report, an animal model of vascular penile insufficiency demonstrates altered protein expression associated with cavernosal tissue injury and reduced erectile function. Although the clinical significance of these observations is currently undefined, this model may allow greater insight into the complex biologic changes associated with arteriogenic ED in man.