Interleukin-1β and interleukin-6 affect electrophysiological properties of thalamic relay cells

Neurosci Res. 2014 Oct:87:16-25. doi: 10.1016/j.neures.2014.06.011. Epub 2014 Aug 1.

Abstract

By acknowledging the relation between brain and body in health and disease, inflammatory processes may play a key role in this reciprocal relation. Pro-inflammatory cytokines such as interleukin-1β (IL-1β) and interleukin-6 (IL-6) are some of the agents involved in those processes. What exactly is their role in the CNS however is not that clear so far. To address the question of how pro-inflammatory cytokines may affect information processing at the cellular and molecular levels, relay neurons in the thalamic dorsal lateral geniculate nucleus in mouse brain slices were exposed to those cytokines and studied with the patch-clamp technique. IL-1β promoted hyperpolarization of the resting membrane potential (Vrest), decrease of input resistance (Rin), decrease of Ih rectification, decrease in action potential (AP) threshold and decrease in the number of APs in low threshold calcium spike (LTS) bursts, while IL-6 promoted decrease of Rin and decrease in the number of APs in LTS bursts. Computer simulations provided candidates for ionic conductance affected by those cytokines. Collectively, these findings demonstrate that IL-1β and IL-6 have modulatory effects on electrophysiological properties of thalamic neurons, implying that the thalamic functions may be affected by systemic disorders that present with high levels of those cytokines.

Keywords: IL-1β; IL-6; Interleukin; Patch-clamp; Thalamic relay cell.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Action Potentials / drug effects
  • Animals
  • Computer Simulation
  • Female
  • Geniculate Bodies / cytology
  • Geniculate Bodies / drug effects
  • Geniculate Bodies / physiology*
  • Interleukin-1beta / pharmacology
  • Interleukin-1beta / physiology*
  • Interleukin-6 / pharmacology
  • Interleukin-6 / physiology*
  • Male
  • Membrane Potentials* / drug effects
  • Mice
  • Mice, Inbred C57BL
  • Neurons / drug effects
  • Neurons / physiology*

Substances

  • Interleukin-1beta
  • Interleukin-6