Regulator of G protein signaling 2 mediates cardiac compensation to pressure overload and antihypertrophic effects of PDE5 inhibition in mice

The heart initially compensates for hypertension-mediated pressure overload by enhancing its contractile force and developing hypertrophy without dilation. G(q) protein-coupled receptor pathways become activated and can depress function, leading to cardiac failure. Initial adaptation mechanisms to reduce cardiac damage during such stimulation remain largely unknown. Here we have shown that this initial adaptation requires regulator of G protein signaling 2 (RGS2). Mice lacking RGS2 had a normal basal cardiac phenotype, yet responded rapidly to pressure overload, with increased myocardial G. signaling, marked cardiac hypertrophy and failure, and early mortality. Swimming exercise, which is not accompanied by Gq activation, induced a normal cardiac response, while Rgs2 deletion in G(alpha q)-overexpressing hearts exacerbated hypertrophy and dilation. In vascular smooth muscle, RGS2 is activated by cGMP-dependent protein kinase (PKG), suppressing G(q)-stimulated vascular contraction. In normal mice, but not Rgs2(-/-) mice, PKG activation by the chronic inhibition of cGMP-selective phosphodiesterase S (PDES) suppressed maladaptive cardiac hypertrophy, inhibiting G(q)-coupled stimuli. Importantly, PKG was similarly activated by PDES inhibition in myocardium. from both genotypes, but PKG plasma membrane translocation was more transient in Rgs2(-/-) myocytes than in controls and was unaffected by PDES inhibition. Thus, RGS2 is required for early myocardial compensation to pressure overload and mediates the initial antihypertrophic and cardioprotective effects of RDE5 inhibitors.