ORIGINAL RESEARCH—BASIC SCIENCE: Heme Oxygenase vs. Nitric Oxide Synthase in Signaling Mediating Sildenafil Citrate Action
Article first published online: 10 JUL 2007
The Journal of Sexual Medicine
Volume 4, Issue 4ii, pages 1098–1107, July 2007
How to Cite
Abdel Aziz, M. T., El-Asmer, M. F., Mostafa, T., Mostafa, S., Atta, H., Abdel Aziz Wassef, M., Fouad, H., Rashed, L., Sabry, D. and Mahfouz, S. (2007), ORIGINAL RESEARCH—BASIC SCIENCE: Heme Oxygenase vs. Nitric Oxide Synthase in Signaling Mediating Sildenafil Citrate Action. Journal of Sexual Medicine, 4: 1098–1107. doi: 10.1111/j.1743-6109.2007.00533.x
- Issue published online: 10 JUL 2007
- Article first published online: 10 JUL 2007
- Erectile Dysfunction;
- Heme Oxygenase;
- Sildenafil Citrate;
- Corpus Cavernosum;
- Nitric Oxide;
- Carbon Monoxide
Introduction. Heme oxygenase (HO) enzyme catalyzes the rate limiting step in oxidative degradation of heme to biliverdin and carbon monoxide (CO). CO has been shown to share many properties with nitric oxide (NO), including activation of guanyl cyclase, signal transduction, and gene regulation.
Aim. To assess the signaling pathways mediating cavernous tissues response to sildenafil citrate intake experimentally.
Main Outcome Measures. In dissected cavernous tissues; detection of HO-1, HO-2 and nueronal nitric oxide synthase (nNOS) gene expressions by reverse transcriptase polymerase chain reaction (RT-PCR), HO enzyme activity assay, HO-1, HO-2 protein detection by Western blot, cyclic guanosine monophosphate (cGMP) tissue levels by enzyme linked immunosorbent assay (ELISA) and histopathology.
Methods. Two hundred forty Sprague-Dawley rats divided into five equal groups were investigated: group (Gr) 1, controls received regular diet; Gr 2, received sildenafil citrate 4 mg/kg orally; Gr 3, received the same dose of sildenafil added to HO inducer, diferuloylmethane; Gr 4, received sildenafil added to HO inhibitor, zinc protoporphyrin, and Gr 5, received sildenafil kg orally by gastric tube. Gr 3 received the same dose of sildenafil added to HO inducer, added to nitric oxide synthase inhibitor, L-Nitroarginine methylester. Twelve rats from each group were sacrificed by cervical dislocation successively after 1/2, 1, 2, and 3 hours from the intake.
Results. HO-2 gene expression was demonstrated in all groups. HO-1 was not expressed in controls, expressed in Gr 2, accentuated in Gr 3, and attenuated in Gr 4 and 5. These results were confirmed by Western blot. The nNOS was expressed in controls, increased in Gr 2 and 3, and decreased in Gr 4 and 5. HO enzyme activity and cGMP levels were significantly elevated in Gr 2, accentuated in Gr 3, and significantly decreased in Gr 4 and 5 compared to controls. Vasodilatations were observed in cavernous tissues of histopathologic sections of Gr 2 and increased in those of Gr 3.
Conclusion. Sildenafil citrate actions may be mediated by up-regulation of HO-1 gene expression. Abdel Aziz MT, El-Asmer MF, Mostafa T, Mostafa S, Atta H, Abdel Aziz Wassef M, Fouad H, Rashed L, Sabry D, and Mahfouz S. Heme oxygenase vs. nitric oxide synthase in signaling mediating sildenafil citrate action. J Sex Med 2007;4:1098–1107.