Hybrid assemblies of ATP-sensitive K+ channels determine their muscle-type-dependent biophysical and pharmacological properties

Proc Natl Acad Sci U S A. 2006 Jan 24;103(4):1118-23. doi: 10.1073/pnas.0505974103. Epub 2006 Jan 17.

Abstract

ATP-sensitive K(+) channels (K(ATP)) are an octameric complex of inwardly rectifying K(+) channels (Kir6.1 and Kir6.2) and sulfonylurea receptors (SUR1 and SUR2A/B), which are involved in several diseases. The tissue-selective expression of the subunits leads to different channels; however, the composition and role of the functional channel in native muscle fibers is not known. In this article, the properties of K(ATP) channels of fast-twitch and slow-twitch muscles were compared by combining patch-clamp experiments with measurements of gene expression. We found that the density of K(ATP) currents/area was muscle-type specific, being higher in fast-twitch muscles compared with the slow-twitch muscle. The density of K(ATP) currents/area was correlated with the level of Kir6.2 expression. SUR2A was the most abundant subunit expressed in all muscles, whereas the vascular SUR2B subunit was expressed but at lower levels. A significant expression of the pancreatic SUR1 was also found in fast-twitch muscles. Pharmacological experiments showed that the channel response to the SUR1 agonist diazoxide, SUR2A/B agonist cromakalim, SUR1 antagonist tolbutamide, and the SUR1/SUR2A/B-antagonist glibenclamide matched the SURs expression pattern. Muscle-specific K(ATP) subunit compositions contribute to the physiological performance of different muscle fiber types and determine the pharmacological actions of drugs modulating K(ATP) activity in muscle diseases.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • ATP-Binding Cassette Transporters / metabolism
  • Adenosine Triphosphate / chemistry*
  • Animals
  • Anti-Arrhythmia Agents / pharmacology
  • Antihypertensive Agents / pharmacology
  • Biophysics / methods*
  • Cromakalim / metabolism
  • Cromakalim / pharmacology
  • DNA Primers / chemistry
  • Diazoxide / pharmacology
  • Dose-Response Relationship, Drug
  • Gene Expression Regulation
  • Glyburide / pharmacology
  • Hypoglycemic Agents / pharmacology
  • KATP Channels
  • Kinetics
  • Male
  • Models, Statistical
  • Muscle Fibers, Skeletal / metabolism
  • Muscle, Skeletal / metabolism
  • Muscles / metabolism
  • Patch-Clamp Techniques
  • Phenotype
  • Potassium / chemistry
  • Potassium / metabolism
  • Potassium Channels / chemistry*
  • Potassium Channels / metabolism
  • Potassium Channels, Inwardly Rectifying / metabolism
  • Rats
  • Rats, Wistar
  • Receptors, Drug / metabolism
  • Recombinant Fusion Proteins / chemistry*
  • Reverse Transcriptase Polymerase Chain Reaction
  • Sulfonylurea Receptors
  • Tolbutamide / pharmacology

Substances

  • ATP-Binding Cassette Transporters
  • Abcc8 protein, rat
  • Anti-Arrhythmia Agents
  • Antihypertensive Agents
  • DNA Primers
  • Hypoglycemic Agents
  • KATP Channels
  • Kir6.2 channel
  • Potassium Channels
  • Potassium Channels, Inwardly Rectifying
  • Receptors, Drug
  • Recombinant Fusion Proteins
  • Sulfonylurea Receptors
  • uK-ATP-1 potassium channel
  • Cromakalim
  • Adenosine Triphosphate
  • Tolbutamide
  • Diazoxide
  • Potassium
  • Glyburide