Schaftoside improves HFpEF through regulation the autophagy-lysosome pathway by allosterically targeting CaMKII-δ

Abstract

Heart failure with preserved ejection fraction (HFpEF) presents a significant challenge to global healthcare systems due to its complex presentation. HFpEF presents with a normal or near-normal left ventricular ejection fraction, cardiac diastolic dysfunction, and a metabolic profile characterized by impaired inflammation and oxidative stress. There have been few valuable drug targets reported for HFpEF to date. Here, we discovered that schaftoside, an active component from licorice, has a significant protective effect on the cardiac remodeling induced by continuous infusion of angiotensin II (AngII), which leads to the HFpEF phenotype. Mechanistically, schaftoside has demonstrated the ability to ameliorate lysosomal dysfunction in both in vitro and in vivo models, thereby activating autophagy. Bioinformatic analyses based on proteome and phosphoproteome suggested that Ca 2+ /calmodulin-dependent protein kinase II (CaMKII) was a potential target for schaftoside. It was confirmed that schaftoside allosterically mediated CaMKII-δ conformation via targeting a unique active pocket near the ATP-binding site to inhibit protein phosphorylation and regulate the lysosomal autophagy pathway. Therefore, schaftoside represents the first small molecule identified to inhibit CaMKII-δ activity through allosteric inhibition, providing a novel candidate for alleviating cardiac metabolic imbalance in HFpEF. Schaftoside allosterically modulates the conformation of CaMKII-δ to inhibit protein phosphorylation, alleviating cardiomyocyte hypertrophy and lysosomal dysfunction in the HFpEF mouse model, promoting autophagy, and improving the left ventricular diastolic dysfunction associated with HFpEF. • Autophagic activity inhibited by lysosomal dysfunction is responsible for cardiac remodeling in HFpEF mice. • Schaftoside promotes lysosomal autophagy in the hearts of HFpEF mice by direct binding to CaMKII-δ. • Schaftoside target a unique active pocket near the ATP-binding site to inhibit CaMKII-δ protein phosphorylation. • Schaftoside identified as a key compound for improving HFpEF.