Altered Expression of Small-Conductance Ca <sup>2+</sup> -Activated K <sup>+</sup> (SK3) Channels Modulates Arterial Tone and Blood Pressure

  • Mark S. Taylor
    From the Department of Pharmacology (M.S.T., A.D.B., T.P.G., D.M.E., J.E.B., M.T.N.), University of Vermont, Burlington, Vt, and Oregon Health Sciences University (C.T.B., J.P.A.), Portland, Ore.
  • Adrian D. Bonev
    From the Department of Pharmacology (M.S.T., A.D.B., T.P.G., D.M.E., J.E.B., M.T.N.), University of Vermont, Burlington, Vt, and Oregon Health Sciences University (C.T.B., J.P.A.), Portland, Ore.
  • Tobias P. Gross
    From the Department of Pharmacology (M.S.T., A.D.B., T.P.G., D.M.E., J.E.B., M.T.N.), University of Vermont, Burlington, Vt, and Oregon Health Sciences University (C.T.B., J.P.A.), Portland, Ore.
  • Delrae M. Eckman
    From the Department of Pharmacology (M.S.T., A.D.B., T.P.G., D.M.E., J.E.B., M.T.N.), University of Vermont, Burlington, Vt, and Oregon Health Sciences University (C.T.B., J.P.A.), Portland, Ore.
  • Joseph E. Brayden
    From the Department of Pharmacology (M.S.T., A.D.B., T.P.G., D.M.E., J.E.B., M.T.N.), University of Vermont, Burlington, Vt, and Oregon Health Sciences University (C.T.B., J.P.A.), Portland, Ore.
  • Chris T. Bond
    From the Department of Pharmacology (M.S.T., A.D.B., T.P.G., D.M.E., J.E.B., M.T.N.), University of Vermont, Burlington, Vt, and Oregon Health Sciences University (C.T.B., J.P.A.), Portland, Ore.
  • John P. Adelman
    From the Department of Pharmacology (M.S.T., A.D.B., T.P.G., D.M.E., J.E.B., M.T.N.), University of Vermont, Burlington, Vt, and Oregon Health Sciences University (C.T.B., J.P.A.), Portland, Ore.
  • Mark T. Nelson
    From the Department of Pharmacology (M.S.T., A.D.B., T.P.G., D.M.E., J.E.B., M.T.N.), University of Vermont, Burlington, Vt, and Oregon Health Sciences University (C.T.B., J.P.A.), Portland, Ore.

説明

<jats:p> The endothelium is a critical regulator of vascular tone, and dysfunction of the endothelium contributes to numerous cardiovascular pathologies. Recent studies suggest that apamin-sensitive, small-conductance, Ca <jats:sup>2+</jats:sup> -activated K <jats:sup>+</jats:sup> channels may play an important role in active endothelium-dependent vasodilations, and expression of these channels may be altered in disease states characterized by vascular dysfunction. Here, we used a transgenic mouse (SK3 <jats:sup>T/T</jats:sup> ) in which SK3 expression levels can be manipulated with dietary doxycycline (DOX) to test the hypothesis that the level of expression of the SK subunit, SK3, in endothelial cells alters arterial function and blood pressure. SK3 protein was elevated in small mesenteric arteries from SK3 <jats:sup>T/T</jats:sup> mice compared with wild-type mice and was greatly suppressed by dietary DOX. SK3 was detected in the endothelium and not in the smooth muscle by immunohistochemistry. In whole-cell patch-clamp experiments, SK currents in endothelial cells from SK3 <jats:sup>T/T</jats:sup> mice were almost completely suppressed by dietary DOX. In intact arteries, SK3 channels contributed to sustained hyperpolarization of the endothelial membrane potential, which was communicated to the arterial smooth muscle. Pressure- and phenylephrine-induced constrictions of SK3 <jats:sup>T/T</jats:sup> arteries were substantially enhanced by treatment with apamin, suppression of SK3 expression with DOX, or removal of the endothelium. In addition, suppression of SK3 expression caused a pronounced and reversible elevation of blood pressure. These results indicate that endothelial SK3 channels exert a profound, tonic, hyperpolarizing influence in resistance arteries and suggest that the level of SK3 channel expression in endothelial cells is a fundamental determinant of vascular tone and blood pressure. </jats:p>

収録刊行物

  • Circulation Research

    Circulation Research 93 (2), 124-131, 2003-07-25

    Ovid Technologies (Wolters Kluwer Health)

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