Altered expression of small-conductance Ca2+-activated K+ (SK3) channels modulates arterial tone and blood pressure

Mark S. Taylor, Adrian D. Bonev, Tobias P. Gross, Delrae M. Eckman, Joseph E. Brayden, Chris T. Bond, John Adelman, Mark T. Nelson

Research output: Contribution to journalArticle

203 Citations (Scopus)

Abstract

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, Ca2+-activated K+ 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 (SK3T/T) 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 SK3T/T 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 SK3T/T 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 SK3T/T 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.

Original languageEnglish (US)
Pages (from-to)124-131
Number of pages8
JournalCirculation Research
Volume93
Issue number2
DOIs
StatePublished - Jul 25 2003

Fingerprint

Calcium-Activated Potassium Channels
Doxycycline
Endothelium
Arterial Pressure
Apamin
Blood Vessels
Endothelial Cells
Arteries
Smooth Muscle
Blood Pressure
Mesenteric Arteries
Phenylephrine
Constriction
Vasodilation
Membrane Potentials
Transgenic Mice
Immunohistochemistry
Pathology
Pressure
Proteins

Keywords

  • Blood pressure
  • Endothelium
  • Potassium channels
  • Vascular tone

ASJC Scopus subject areas

  • Physiology
  • Cardiology and Cardiovascular Medicine

Cite this

Taylor, M. S., Bonev, A. D., Gross, T. P., Eckman, D. M., Brayden, J. E., Bond, C. T., ... Nelson, M. T. (2003). Altered expression of small-conductance Ca2+-activated K+ (SK3) channels modulates arterial tone and blood pressure. Circulation Research, 93(2), 124-131. https://doi.org/10.1161/01.RES.0000081980.63146.69

Altered expression of small-conductance Ca2+-activated K+ (SK3) channels modulates arterial tone and blood pressure. / Taylor, Mark S.; Bonev, Adrian D.; Gross, Tobias P.; Eckman, Delrae M.; Brayden, Joseph E.; Bond, Chris T.; Adelman, John; Nelson, Mark T.

In: Circulation Research, Vol. 93, No. 2, 25.07.2003, p. 124-131.

Research output: Contribution to journalArticle

Taylor, MS, Bonev, AD, Gross, TP, Eckman, DM, Brayden, JE, Bond, CT, Adelman, J & Nelson, MT 2003, 'Altered expression of small-conductance Ca2+-activated K+ (SK3) channels modulates arterial tone and blood pressure', Circulation Research, vol. 93, no. 2, pp. 124-131. https://doi.org/10.1161/01.RES.0000081980.63146.69
Taylor, Mark S. ; Bonev, Adrian D. ; Gross, Tobias P. ; Eckman, Delrae M. ; Brayden, Joseph E. ; Bond, Chris T. ; Adelman, John ; Nelson, Mark T. / Altered expression of small-conductance Ca2+-activated K+ (SK3) channels modulates arterial tone and blood pressure. In: Circulation Research. 2003 ; Vol. 93, No. 2. pp. 124-131.
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