NO-donors induce cross talk between cGMP and cAMP in signalling to human atrial L-type Ca2+ current

Abstract

Results Application of SNAP (100μM) increased basal ICa,L from 5.93±0.23 pA/pF to 9.10±0.45pA/pF (p<0.001, n/N=117/ 62). The effect was abolished by inhibition of soluble guanylate cyclase (sGC) with ODQ (30μM), suggesting involvement of cGMP. Stimulator of sGC (BAY 41-2272, 10nM–10μM) also increased ICa,L and this effect was potentiated in the presence of SNAP. Direct activation of protein kinase G (PKG) with 8-Br-cGMP (100 μM, intracellular application) increased basal ICa,L. However, not only cGMP but also cAMP was involved, because, the effect of SNAP on ICa,L was prevented with the protein kinase A blocker (Rp-8-Br-cAMP 1 mM, intracellular). Thus, cGMP may activate ICa,L via direct activation of PKG and indirect activation of PKA at the same time. It is known, that cAMP-mediated activation of PKA is regulated by cGMP via modulation of phosphodiesterases (PDEs). The selective PDE2 inhibitor EHNA (10μM) did not affect basal or SNAP-stimulated ICa,L, therefore PDE2 does not regulate basal cAMP level. In contrast, PDE3 inhibition with cilostamide (1μM) increased basal ICa,L, suggesting that PDE3 is involved in basal cAMP level regulation. Interestingly, the cilostamide-induced increase in ICa,L is blunted upon addition of SNAP, most probably via activation of PDE2 by SNAP-mediated cGMP increase (Figure 1). Similarly, SNAP blunted enhancement of ICa,L by PKA activation with isoprenalin (1μM; 18.07 ± 1.12 pA/pF vs 23.06 ± 1.36 pA/pF, p<0.001, n/N=21-39/18), however, this effect was prevented by PDE2 inhibition with EHNA.