Journal
INTERNATIONAL BRAZ J UROL
Volume 34, Issue 5, Pages 638-645Publisher
BRAZILIAN SOC UROL
DOI: 10.1590/S1677-55382008000500013
Keywords
nitric oxide; vascular endothelium; corpus cavernosum; nitrosil-ruthenium complex
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Introduction Endothelial dysfunction characterized by endogenous nitric oxide (NO) deficiency made 56% of patients affected with erectile dysfunction decline treatment with PDE-5 inhibitors. New forms of treatment are currently being developed for this group of patients. Materials and Methods. The study compared the effect of sodium nitroprusside (SNP) and two substances of the nitrosyl-ruthenium complex, cis-[Ru(bpy)2(SO3)(NO)]PF-6-9 (FONOI) and trans-[Ru(NH3)4(caffeine)(NO)]C13 (LLNOI) on relaxation of rabbit corpus cavernosum smooth muscle and aortic vascular endothelium The samples were immersed in isolated baths and precontracted with 0 1 mu M phenylephrine (PE) and the corresponding relaxation concentration/response curves were plotted. In order to investigate the relaxation mechanisms involved, 100 mu M ODQ (a soluble guanylate cyclase-specific inhibitor), 3 mu M or 10 mu M oxyhemoglobin (an extracellular NO scavenger) or 1 mM L-cysteine (a nitrosyl anion-specific scavenger) was added to the samples Results All the NO donors tested produced a significant level of relaxation in the vascular endothelium In corpus cavernosum samples, FONOI produced no significant effect, but LLNOI and SNP induced dose-dependent relaxation with comparable potency (pEC(50) = 6.14 +/- 0.08 and 6 4 +/- 0.14, respectively) and maximum effect (Emax = 82% vs. 100%, respectively). All NO donors were found to activate soluble guanylate cyclase, since the addition of the corresponding inhibitor (100 mu M ODQ) completely neutralized the relaxation effect observed. The addition of oxyhemoglobin reduced the relaxation effect, but did not inhibit it completely. In aortic vascular endothelium 3 mu M oxyhemoglobin decreased the relaxation effect by 26% on the average, while 10 mu M oxyhemoglobin reduced it by over 52% The addition of 100 pM L-cysteine produced no significant inhibiting effect Conclusions. These results suggest that LLNOI and FONO I are potent vasodilators. LLNOI was shown to induce a significant level of relaxation in rabbit corpus cavernosum The substances tested were shown to activate soluble guanylate cyclase and release intracellular NO.
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