Endothelial K(Ca)1.1 And K(Ca)3.1 Channels Mediate Rat Intrarenal Artery Endothelium-Derived Hyperpolarization Response

Aim Endothelium-derived hyperpolarization (EDH)-mediated response plays an essential role in the control of kidney preglomerular circulation, but the identity of the K+ channels involved in this response is still controversial. We hypothesized that large- (K(Ca)1.1), intermediate- (K(Ca)3.1) and small (K(Ca)2.3) -conductance Ca2+-activated K+ (K-Ca) channels are expressed in the endothelium of the preglomerular circulation and participate in the EDH-mediated response.Methods We study the functional expression of different K+ channels in non-cultured, freshly isolated native endothelial cells (ECs) of rat intrarenal arteries using immunofluorescence and the patch-clamp technique. We correlate this with vasorelaxant responses ex vivo using wire myography.Results Immunofluorescence revealed the expression of K(Ca)1.1, K(Ca)3.1 and K(Ca)2.3 channels in ECs. Under voltage-clamp conditions, acetylcholine induced a marked increase in the outward currents in these cells, sensitive to the blockade of K(Ca)1.1, K(Ca)3.1 and K(Ca)2.3 channels respectively. Isometric myography experiments, under conditions of endothelial nitric oxide synthase and cyclooxygenase inhibition, showed that blockade either of K(Ca)1.1 or K(Ca)3.1 channels was able to reduce the endothelium-derived vasorelaxation of isolated interlobar arteries, while their combined blockade completely abolished it. In contrast, blockade of K(Ca)2.3 channels did not reduce this vasorelaxant response, despite being functionally expressed in the endothelial cells.Conclusion This study shows that K(Ca)1.1 and K(Ca)3.1 channels are functionally expressed at the renal vascular endothelium and play a central role in the EDH-mediated relaxation of kidney preglomerular arteries, which is important in the control of renal blood flow and glomerular filtration rate.