| Literature DB >> 29268036 |
Karin P Potoka1,2, Katherine C Wood2,3, Jeffrey J Baust2, Marta Bueno2,4, Scott A Hahn2, Rebecca R Vanderpool2, Tim Bachman2, Grace M Mallampalli2,3, David O Osei-Hwedieh2, Valerie Schrott2, Bin Sun2, Grant C Bullock2, Eva-Maria Becker-Pelster5,6, Matthias Wittwer5, Jan Stampfuss5, Ilka Mathar5, Johannes-Peter Stasch5,7, Hubert Truebel5,6, Peter Sandner5,8, Ana L Mora2,4, Adam C Straub2,9, Mark T Gladwin2,4.
Abstract
Sickle cell disease (SCD) is associated with intravascular hemolysis and oxidative inhibition of nitric oxide (NO) signaling. BAY 54-6544 is a small-molecule activator of oxidized soluble guanylate cyclase (sGC), which, unlike endogenous NO and the sGC stimulator, BAY 41-8543, preferentially binds and activates heme-free, NO-insensitive sGC to restore enzymatic cGMP production. We tested orally delivered sGC activator, BAY 54-6544 (17 mg/kg/d), sGC stimulator, BAY 41-8543, sildenafil, and placebo for 4-12 weeks in the Berkeley transgenic mouse model of SCD (BERK-SCD) and their hemizygous (Hemi) littermate controls (BERK-Hemi). Right ventricular (RV) maximum systolic pressure (RVmaxSP) was measured using micro right-heart catheterization. RV hypertrophy (RVH) was determined using Fulton's index and RV corrected weight (ratio of RV to tibia). Pulmonary artery vasoreactivity was tested for endothelium-dependent and -independent vessel relaxation. Right-heart catheterization revealed higher RVmaxSP and RVH in BERK-SCD versus BERK-Hemi, which worsened with age. Treatment with the sGC activator more effectively lowered RVmaxSP and RVH, with 90-day treatment delivering superior results, when compared with other treatments and placebo groups. In myography experiments, acetylcholine-induced (endothelium-dependent) and sodium-nitroprusside-induced (endothelium-independent NO donor) relaxation of the pulmonary artery harvested from placebo-treated BERK-SCD was impaired relative to BERK-Hemi but improved after therapy with sGC activator. By contrast, no significant effect for sGC stimulator or sildenafil was observed in BERK-SCD. These findings suggest that sGC is oxidized in the pulmonary arteries of transgenic SCD mice, leading to blunted responses to NO, and that the sGC activator, BAY 54-6544, may represent a novel therapy for SCD-associated pulmonary arterial hypertension and cardiac remodeling.Entities:
Keywords: pulmonary hypertension; sickle cell disease; soluble guanylate cyclase
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Year: 2018 PMID: 29268036 PMCID: PMC5946331 DOI: 10.1165/rcmb.2017-0292OC
Source DB: PubMed Journal: Am J Respir Cell Mol Biol ISSN: 1044-1549 Impact factor: 6.914