Discovery of a Novel COS/H2S-Donor Hybridized sGC Stimulator for Alleviating Isoproterenol-Induced Myocardial Fibrosis.

Myocardial fibrosis contributes to heart failure (HF) progression, which is associated with impaired nitric oxide (NO)-soluble guanylyl cyclase (sGC)-cyclic guanosine monophosphate (cGMP) signaling. Hydrogen sulfide (H2S), a cardioprotective gasotransmitter, is reduced in patients with HF. Therapeutic options targeting both sGC activation and H2S enhancement remain limited. We have developed a novel carbonyl sulfide (COS)/H2S-donor hybrid sGC stimulator, COS-A, which exhibits a well-characterized H2S-releasing property. Compound COS-A outperformed vericiguat in sGC activation in vitro and reduced fibrosis in transforming growth factor-beta 1 (TGF-β1)-treated cardiac fibroblasts by increasing cGMP and H2S levels. In isoproterenol (ISO)-induced HF mice, COS-A improved cardiac function comparably to vericiguat. Histological findings revealed its antifibrotic effects through sGC activation and elevation of H2S. Our findings indicate that this COS/H2S-donor hybridized sGC stimulator holds therapeutic promise for HF treatment.