15 To assess this approach GRK2 inhibition was tested in rabbits in a study where adenovirus encoding for βARKct was administered into the coronaries at the time of myocardial infarction (MI). Three weeks post-gene transfer, GRK2 inhibition resulted in prevention of left ventricular (LV) adverse remodeling, improvement of cardiac contractility, and preservation of βAR signaling and function.16 Similarly, left ventricular remodeling Inhibitors,research,lifescience,medical was reversed by adeno-associated virus encoding for βARKct

gene therapy in a pig model of heart failure.17 This and other studies make the βARKct a promising candidate for future application in human heart failure (moreover Figure 1). Figure 1 Beyond G-protein-coupled receptor blockade. “FIXING” CALCIUM

HANDLING IN FAILING HEARTS sellectchem Impaired calcium homeostasis is a prominent feature of the remodeling process and heart Inhibitors,research,lifescience,medical failure, and it manifests clinically as contractile dysfunction and development of arrhythmias.18 When compared to normal myocytes, the failing heart myocytes exhibit typical changes in intracellular calcium Inhibitors,research,lifescience,medical handling, including impaired extrusion of cytosolic calcium, reduced calcium loading in the cardiac sarcoplasmic reticulum (SR), and defects in the SR calcium release.19 These changes in calcium handling are thought to contribute to the impairment of cardiac contractile functions (Figure 2).20 Figure 2 Correcting Inhibitors,research,lifescience,medical calcium handling in failing hearts. Relaxation of the myofilaments after contraction is facilitated by two mechanisms of calcium extrusion: the rapid re-sequestration of calcium into the SR and calcium efflux outside of the cells Inhibitors,research,lifescience,medical through the plasma membranes. The sarco-endoplasmic reticulum calcium ATPase 2 pump (SERCA2) is localized on the SR membrane

and is responsible for the re-uptake of calcium from the cytoplasm into the SR lumen. Since the amount of calcium released through the ryanodine receptors (RyR) during each cardiac cycle is proportional to the calcium content of the SR, the SERCA2 activity is a critical determinant of both relaxation (via calcium re-uptake into the SR) and contractility AV-951 (via controlling the amount of calcium in the SR) in the cardiomyocytes.21 Indeed, experimental studies in animal models of heart failure have shown that increasing the expression of SERCA2a in cardiomyocytes normalizes intracellular calcium cycling, restores both relaxation and contractile function, and results in significant improvement in survival.22 Following the success of these animal studies, the Calcium Upregulation by Percutaneous Administration of Gene Therapy in Cardiac Disease (CUPID) trial enrolled 39 patients to receive intracoronary adeno-associated virus type 1 encoding for SERCA2 or placebo.