Keswani, Amit N.Peyton, Kelly J.Durante, WilliamSchafer, Andrew I.Tulis, David A.2011-04-132011-05-172011-04-132011-05-172009-06Journal of Cardiovascular Pharmacology and Therapeutics; 14:2 p. 116-124http://hdl.handle.net/10342/3312Guanosine-specific cyclic nucleotide signaling is suggested to serve protective actions in the vasculature; however, the influence of selective pharmacologic modulation of cyclic guanosine monophosphate (GMP)-synthesizing soluble guanylate cyclase (sGC) or cyclic GMP-degrading phosphodiesterase (PDE) on vessel remodeling has not been thoroughly examined. In this study, rat carotid artery balloon injury was performed and the growth-modulating effects of the sGC stimulator YC-1 or the cGMP-dependent PDE-V inhibitor zaprinast were examined. YC-1 or zaprinast elevated vessel cyclic GMP content, reduced medial wall and neointimal cell proliferation, stimulated medial and neointimal cellular apoptosis, and markedly attenuated neointimal remodeling in comparable fashion. Interestingly, sGC inhibition by ODQ failed to noticeably alter neointimal growth, and concomitant zaprinast with YC-1 did not modify any parameter compared to individual treatments. These results provide novel in vivo evidence that YC-1 and zaprinast inhibit injury-induced vascular remodeling through anti-mitogenic and pro-apoptotic actions and may offer promising therapeutic approaches against vasoproliferative disorders. Originally published J Cardiovasc Pharmacol Ther, Vol. 14, No. 2, June 2009en-USAuthor notified of opt-out rights by Cammie Jennings prior to upload of this article.ApoptosisCarotid artery balloon injuryProliferationYC-1ZaprinastArticlePMC270276210.1177/1074248409333266