Zeneca ZD6169 activates ATP-sensitive K+ channels in the urinary bladder of the guinea pig

Pharmacology. 1996 Sep;53(3):170-9. doi: 10.1159/000139428.

Abstract

The effects of Zeneca ZD6169, a tertiary carbinol, and levcromakalim were examined on the membrane potential of intact smooth muscle cells, and on ATP-sensitive K+ (KATP) channel currents in isolated smooth muscle cells from the guinea pig urinary bladder. ZD6169 and levcromakalim induced a glibenclamide-sensitive hyperpolarization of the membrane potential. The ZD6169- and levcromakalim-induced KATP currents were half-maximal at 1.02 and 2.63 mumol/l, respectively, with Hill coefficients of 1.46 and 1.62, respectively. The ZD6169-induced KATP currents were inhibited by internal ATP (3.0 mmol/l), reduced 34% by activators of protein kinase C, and decreased 35% when the external pH was lowered to 6.4. This study provides the first characterization of ZD6169 on KATP currents and indicates that ZD6169 is a potent opener of KATP channels in the smooth muscle from the urinary bladder.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adenosine Triphosphate / pharmacology*
  • Amides / pharmacology*
  • Animals
  • Benzophenones / pharmacology*
  • Benzopyrans / pharmacology
  • Cromakalim
  • Dose-Response Relationship, Drug
  • Enzyme Activation
  • Glyburide / pharmacology
  • Guinea Pigs
  • Hydrogen-Ion Concentration
  • In Vitro Techniques
  • Ion Channel Gating
  • Membrane Potentials / drug effects
  • Muscle, Smooth / drug effects*
  • Muscle, Smooth / physiology
  • Potassium Channels / drug effects*
  • Protein Kinase C / metabolism
  • Pyrroles / pharmacology
  • Urinary Bladder / drug effects*
  • Urinary Bladder / physiology

Substances

  • Amides
  • Benzophenones
  • Benzopyrans
  • Potassium Channels
  • Pyrroles
  • Zeneca ZD 6169
  • Cromakalim
  • Adenosine Triphosphate
  • Protein Kinase C
  • Glyburide