@article {Abdel Aziz:April 2007:0303-4569:66, author = "Abdel Aziz, M. T.", author = "Mostafa, T.", author = "Atta, H.", author = "Rashed, L.", author = "Marzouk, S. A.", author = "Obaia, E. M.", author = "Sabry, D.", author = "Hassouna, A. A.", author = "El-Shehaby, A. M.", author = "Abdel Aziz, A.T.", title = "Oral phosphodiesterase-5 inhibitors: effect of heme oxygenase inhibition on cGMP signalling in rat cavernous tissue", journal = "Andrologia", volume = "39", year = "April 2007", abstract = "Summary

This work postulated that heme oxygenase (HO) is partly responsible for controlling phosphodiesterase-5 inhibitor actions by modulating cyclic guanosine monophosphate (cGMP) cavernous tissue levels. Five hundred and four male Sprague-Dawley rats, divided into five groups, were investigated. Group 1 (n = 72) included controls, group 2 (n = 72) received sildenafil citrate (ViagraR) orally, group 3 (n = 72) received vardenafil hydrochloride (LevitraR), group 4 (n = 72) received tadalafil (CialisR). Group 5 (n = 216), subdivided into three subgroups (A, B and C, 72 each), received the same dose of each drug with the HO inhibitor, Zn protoporphyrin. Eight rats from each group/subgroup were killed at 0.5, 1, 2, 3, 4, 6, 18, 24 and 36 h when cGMP levels in the cavernous tissues were estimated. Cavernous tissue cGMP levels increased significantly in sildenafil, vardenafil and tadalafil-treated rats compared to the controls with significant decreases after HO inhibition. It is concluded that the effects of these PDE-5 inhibitors in rat cavernous tissue are partly mediated through HO activity via the cGMP signalling pathway.", pages = "66-70(5)", url = "http://www.ingentaconnect.com/content/bsc/and/2007/00000039/00000002/art00005" doi = "doi:10.1111/j.1439-0272.2007.00765.x" }