Dilatation of cerebral arterioles in response to activation of adenylate cyclase is dependent on activation of Ca2+-dependent K+ channels

H. Taguchi, D. D. Heistad, T. Kitazono, F. M. Faraci

Research output: Contribution to journalArticle

70 Citations (Scopus)

Abstract

The role of Ca2+-dependent potassium channels in mediating vascular responses to activation of adenylate cyclase in vivo is not known. The goal of this study was to examine the hypothesis that dilatation of cerebral arterioles in response to activation of adenylate cyclase is mediated by activation of Ca2+-dependent potassium channels. Diameters of cerebral arterioles were measured in vivo in anesthetized rabbits. Topical application of forskolin (1 and 10 μmol/L), a direct activator of adenylate cyclase, dilated cerebral arterioles by 40±8% (mean±SEM) and 71±9%, respectively, from a control diameter of 85±4 μm. Iberiotoxin (50 and 100 nmol/L), a selective inhibitor of Ca2+-dependent potassium channels, inhibited dilatation in response to both concentrations of forskolin by 45% to 60%. We obtained similar results by using charybdotoxin (50 nmol/L), another inhibitor of Ca2+-dependent potassium channels. Vasodilatation in response to dibutyryl cAMP (a cell-permeable cAMP analogue) was also inhibited by iberiotoxin. In contrast, dilation of cerebral arterioles in response to sodium nitroprusside and acetylcholine (activators of guanylate cyclase) and aprikalim (activator of ATP-sensitive potassium channels) was not inhibited by iberiotoxin. These findings suggest that dilatation of cerebral arterioles in response to forskolin and increases in intracellular concentrations of cAMP are mediated by activation of Ca2+-dependent potassium channels. Thus, activation of Ca2+-dependent potassium channels may be a major mechanism of cerebral vasodilatation in response to activation of adenylate cyclase in vivo.

Original languageEnglish
Pages (from-to)1057-1062
Number of pages6
JournalCirculation research
Volume76
Issue number6
DOIs
Publication statusPublished - 1995

All Science Journal Classification (ASJC) codes

  • Physiology
  • Cardiology and Cardiovascular Medicine

Fingerprint Dive into the research topics of 'Dilatation of cerebral arterioles in response to activation of adenylate cyclase is dependent on activation of Ca<sup>2+</sup>-dependent K<sup>+</sup> channels'. Together they form a unique fingerprint.

Cite this