Inflammation inhibits GABA transmission in multiple sclerosis

Mult Scler. 2012 Nov;18(11):1633-5. doi: 10.1177/1352458512440207. Epub 2012 Mar 14.

Abstract

Abnormal glutamate-dependent synaptic excitation contributes to neuronal damage in multiple sclerosis (MS). Little is known about the involvement of the GABA system in this disorder. Here we found that cerebrospinal fluid (CSF) from MS patients with enhanced brain lesions on magnetic resonance imaging inhibited GABA transmission in mouse brain slices. Enhanced IL-1β neuronal action was responsible for this effect, because IL-1β receptor antagonist blocked, and exogenous IL-1β mimicked the synaptic effect of inflamed CSF. Our results provide evidence that focal inflammation in MS perturbs the cytokine milieu within the circulating CSF, resulting in diffuse GABAergic alteration in neurons.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Animals
  • Anti-Inflammatory Agents / pharmacology
  • Brain / drug effects
  • Brain / immunology
  • Brain / metabolism*
  • Brain / pathology
  • Case-Control Studies
  • Cytokines / cerebrospinal fluid
  • Cytokines / metabolism*
  • Female
  • Humans
  • In Vitro Techniques
  • Inflammation Mediators / cerebrospinal fluid
  • Inflammation Mediators / metabolism*
  • Inhibitory Postsynaptic Potentials
  • Interleukin-1beta / metabolism
  • Magnetic Resonance Imaging
  • Male
  • Mice
  • Middle Aged
  • Multiple Sclerosis / cerebrospinal fluid
  • Multiple Sclerosis / immunology
  • Multiple Sclerosis / metabolism*
  • Multiple Sclerosis / pathology
  • Neural Inhibition* / drug effects
  • Neurons / drug effects
  • Neurons / metabolism*
  • Neurons / pathology
  • Synaptic Transmission* / drug effects
  • Young Adult
  • gamma-Aminobutyric Acid / metabolism*

Substances

  • Anti-Inflammatory Agents
  • Cytokines
  • Inflammation Mediators
  • Interleukin-1beta
  • gamma-Aminobutyric Acid