Abstract
The potential of ATP-sensitive potassium channel openers (KCOs) for the treatment of male erectile dysfunction has recently been suggested based on positive clinical outcomes following intra-cavernosal administration of pinacidil. Agents that increase the levels of cGMP via elevation of nitric oxide (NO) nitroglycerin, for example, are also effective in improving erectile function preclinically and clinically. The aim of the present study was to determine the effects and mechanism of the action of nicorandil on rabbit corpus cavernosum. The in vitro regulation of smooth muscle tone was assessed in isolated cavernosal tissues pre-contracted with phenyl-ephrine. Nicorandil, but not its major metabolite, relaxed phenylephrine-precontracted cavernosum smooth muscle with an EC50 of 15 μM. The effects of nicorandil were only partially reversed by the KATP channel blocker glyburide (10 μM) or by a soluble guanylate cyclase (sGC) inhibitor 1H-[1,2,4] oxadiazole [4,3-a] quinoxalin-1-one (ODQ, 3 μM). However, a combination of ODQ and glyburide completely blocked the relaxant effects of nicorandil. The results of the present study indicate that nicorandil can relax rabbit cavernosal tissue in vitro via a mechanism that involves activation of KATP channels and stimulation of soluble guanylate cyclase.
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The authors are grateful to Dr Robert B Moreland for his valuable comments on the manuscript.
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Hsieh, G., Kolasa, T., Sullivan, J. et al. Dual mechanism of action of nicorandil on rabbit corpus cavernosal smooth muscle tone. Int J Impot Res 13, 240–246 (2001). https://doi.org/10.1038/sj.ijir.3900702
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DOI: https://doi.org/10.1038/sj.ijir.3900702
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