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Integrative Physiology |
From the Departments of Nephrology (R.K., S.B., M.K., C.B., C.D., J.H.) and Clinical Pharmacology (R.R., H.-D.O., M.P.), Benjamin Franklin Medical Center, and the Institute for Physiology (A.R.P.), Freie Universität, Berlin, Germany.
Correspondence to R. Köhler, Benjamin Franklin Medical Center, Hindenburgdamm 30, 12200 Berlin, Germany. E-mail koe{at}zedat.fu-berlin.de
Abstract Ca2+-activated K+ (KCa) channels control endothelial Ca2+ homeostasis and the formation of vasodilators. After angioplasty, dysfunction of the regenerated endothelium leads to abnormal vasoregulation. In this study, we tested the expression and function of KCa channels in regenerated endothelium at 6 weeks after balloon catheter injury of rat carotid arteries (CAs) by using single-cell reverse transcriptionpolymerase chain reaction, patch-clamp techniques, and analysis of vasoreactivity. In single regenerated endothelial cells (ECs), the percentage of ECs expressing the KCa genes, rSK3 (12±8%) and rIK1 (22±9%), was significantly lower compared with the percentage of native ECs expressing these genes (rSK3 58±8%, rIK1 64±10%). In patch-clamp experiments, KCa currents and acetylcholine-induced hyperpolarization were markedly reduced in regenerated ECs (shift of membrane potential -6±3 mV) compared with those in native ECs (shift of membrane potential -21±5 mV). In pressure myograph experiments, acetylcholine-induced dilation was impaired in reendothelialized CAs compared with normal CAs. Intraluminal application of the KCa blocker apamin and charybdotoxin inhibited dilation by 30% in normal CAs but was without effect in reendothelialized CAs. Intraluminal application of 1-ethyl-2-benzimidazolinone (100 µmol/L), an opener of KCa channels, evoked dilation by 29% in normal CAs but had no effect in reendothelialized CAs. In conclusion, the impaired expression of KCa channels in regenerated endothelium results in defective hyperpolarization and impaired dilation. Thus, the impaired KCa channel function contributes to functional alterations of regenerated endothelium after angioplasty.
Key Words: angioplasty neointima endothelium Ca2+-activated K+ channels endothelium-dependent vasodilation
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