Thalamic control of visceral nociception mediated by T-type Ca2+ channels

Science. 2003 Oct 3;302(5642):117-9. doi: 10.1126/science.1088886.

Abstract

Sensations from viscera, like fullness, easily become painful if the stimulus persists. Mice lacking alpha1G T-type Ca2+ channels show hyperalgesia to visceral pain. Thalamic infusion of a T-type blocker induced similar hyperalgesia in wild-type mice. In response to visceral pain, the ventroposterolateral thalamic neurons evokeda surge of single spikes, which then slowly decayed as T type-dependent burst spikes gradually increased. In alpha1G-deficient neurons, the single-spike response persisted without burst spikes. These results indicate that T-type Ca2+ channels underlie an antinociceptive mechanism operating in the thalamus andsupport the idea that burst firing plays a critical role in sensory gating in the thalamus.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Abdominal Pain / physiopathology
  • Acetic Acid / pharmacology
  • Action Potentials
  • Analysis of Variance
  • Animals
  • Calcium Channel Blockers / pharmacology
  • Calcium Channels, T-Type / genetics
  • Calcium Channels, T-Type / physiology*
  • Female
  • Magnesium Sulfate / pharmacology
  • Male
  • Mibefradil / pharmacology
  • Mice
  • Mice, Inbred C57BL
  • Mutation
  • Neurons / physiology
  • Pain / physiopathology*
  • Pain Measurement
  • Ventral Thalamic Nuclei / physiology*
  • Viscera

Substances

  • Cacna1g protein, mouse
  • Calcium Channel Blockers
  • Calcium Channels, T-Type
  • Mibefradil
  • Magnesium Sulfate
  • Acetic Acid