[HTML][HTML] PKA-dependent activation of the vascular smooth muscle isoform of KATP channels by vasoactive intestinal polypeptide and its effect on relaxation of the …

Y Yang, Y Shi, S Guo, S Zhang, N Cui, W Shi… - … et Biophysica Acta (BBA …, 2008 - Elsevier
Y Yang, Y Shi, S Guo, S Zhang, N Cui, W Shi, D Zhu, C Jiang
Biochimica et Biophysica Acta (BBA)-Biomembranes, 2008Elsevier
Vasoactive intestinal polypeptide (VIP) is a potent vasodilator and has been successfully
used to alleviate hypertension. Consistently, disruption of VIP gene in mice leads to
hypertension. However, its downstream targets in the vascular regulation are still not well
demonstrated. To test the hypothesis that the vascular smooth muscle isoform of KATP
channels is a downstream target of the VIP signaling, we performed the studies on the Kir6.
1/SUR2B channel expressed in HEK293 cells. We found that the channel was strongly …
Vasoactive intestinal polypeptide (VIP) is a potent vasodilator and has been successfully used to alleviate hypertension. Consistently, disruption of VIP gene in mice leads to hypertension. However, its downstream targets in the vascular regulation are still not well demonstrated. To test the hypothesis that the vascular smooth muscle isoform of KATP channels is a downstream target of the VIP signaling, we performed the studies on the Kir6.1/SUR2B channel expressed in HEK293 cells. We found that the channel was strongly activated by VIP. Through endogenous VIP receptors, the channel activation was reversible and dependent on VIP concentrations with the midpoint-activation concentration ∼10 nM. The channel activation was voltage-independent and could be blocked by KATP channel blocker glibenclamide. In cell-attached patches, VIP augmented the channel open-state probability with modest suppression of the single channel conductance. The VIP-induced Kir6.1/SUR2B channel activation was blocked by PKA inhibitor RP-cAMP. Forskolin, an adenylyl cyclase activator, activated the channel similarly as VIP. The effect of VIP was further evident in the native tissues. In acutely dissociated mesenteric vascular smooth myocytes, VIP activated the KATP currents in a similar manner as in HEK293 cells. In endothelium-free mesenteric artery rings, VIP produced concentration-dependent vasorelaxation that was attenuated by glibenclamide. These results therefore indicate that the vascular isoform (Kir6.1/SUR2B) of KATP channels is a target of VIP. The channel activation relies on the PKA pathway and produces mesenteric arterial relaxation.
Elsevier