Pharmacological and physiological stimuli do not promote Ca(2+)-sensitive K+ channel activity in isolated heart mitochondria

Cardiovasc Res. 2007 Mar 1;73(4):720-8. doi: 10.1016/j.cardiores.2006.11.035. Epub 2006 Nov 30.

Abstract

Objective: Mitochondrial calcium-activated K(+) (mitoK(Ca)) channels have been described as channels that are activated by Ca(2+), inner mitochondrial membrane depolarization and drugs such as NS-1619. NS-1619 is cardioprotective, leading to the assumption that this effect is related to the opening of mitoK(Ca) channels. Here, we show several weaknesses in this hypothesis.

Methods: Isolated mitochondria from rat hearts were tested for evidence of mitoK(Ca) activity by analyzing functional parameters in K(+)-rich and K(+)-free media.

Results: NS-1619 promoted mitochondrial depolarization both in K(+)-rich and K(+)-free media. Respiratory rate increments were also seen in the presence of NS-1619 for both media. In parallel, NS-1619 promoted respiratory inhibition, as evidenced by respiratory measurements in state 3. Mitochondrial volume measurements conducted using light scattering showed that NS-1619 led to swelling, in a manner unaltered by inhibitors of mitoK(Ca) channels, antagonists of adenosine triphosphate-sensitive potassium channels or inhibitors of the permeability transition. Swelling was also maintained when K(+) in the media was substituted with tetraethylammonium (TEA(+)), which is not transported by any known K(+) carrier. Electron microscopy experiments gave support to the idea that NS-1619-induced mitochondrial swelling took place in the absence of K(+). In addition to testing the pharmacological effects of NS-1619, we attempted, unsuccessfully, to promote mitoK(Ca) activity by altering Ca(2+) concentrations in the medium and inducing mitochondrial uncoupling.

Conclusion: Our data indicate that NS-1619 promotes non-selective permeabilization of the inner mitochondrial membrane to ions, in addition to partial respiratory inhibition. Furthermore, we found no specific K(+) transport in isolated heart mitochondria compatible with mitoK(Ca) opening, whether by pharmacological or physiological stimuli. Our results indicate that NS-1619 has extensive mitochondrial effects unrelated to mitoK(Ca) and suggest that tissue protection mediated by NS-1619 may occur through mechanisms other than activation of these channels.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Benzimidazoles / pharmacology*
  • Calcium / metabolism
  • Calcium / pharmacology
  • Culture Media
  • Glutamic Acid / pharmacology
  • Ion Channel Gating / drug effects*
  • Malates / pharmacology
  • Membrane Potentials / drug effects
  • Microscopy, Electron, Transmission
  • Microscopy, Fluorescence
  • Mitochondria, Heart / drug effects
  • Mitochondria, Heart / metabolism*
  • Mitochondria, Heart / ultrastructure
  • Mitochondrial Membranes / drug effects
  • Mitochondrial Membranes / metabolism
  • Mitochondrial Swelling / drug effects
  • NADP / metabolism
  • Oligomycins / pharmacology
  • Oxidation-Reduction
  • Oxygen Consumption
  • Phenazines / pharmacology
  • Potassium / metabolism
  • Potassium / pharmacology
  • Potassium Channels, Calcium-Activated / drug effects*
  • Potassium Channels, Calcium-Activated / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Rotenone / pharmacology
  • Sodium / metabolism
  • Succinic Acid / pharmacology
  • Tetraethylammonium / metabolism
  • Tetraethylammonium / pharmacology
  • Tissue Culture Techniques
  • Uncoupling Agents / pharmacology

Substances

  • Benzimidazoles
  • Culture Media
  • Malates
  • Oligomycins
  • Phenazines
  • Potassium Channels, Calcium-Activated
  • Uncoupling Agents
  • Rotenone
  • NS 1619
  • Glutamic Acid
  • NADP
  • Tetraethylammonium
  • malic acid
  • Sodium
  • Succinic Acid
  • Potassium
  • Calcium
  • safranine T