Astrocyte-derived adenosine and A1 receptor activity contribute to sleep loss-induced deficits in hippocampal synaptic plasticity and memory in mice

J Neurosci. 2011 May 11;31(19):6956-62. doi: 10.1523/JNEUROSCI.5761-10.2011.

Abstract

Sleep deprivation (SD) can have a negative impact on cognitive function, but the mechanism(s) by which SD modulates memory remains unclear. We have previously shown that astrocyte-derived adenosine is a candidate molecule involved in the cognitive deficits following a brief period of SD (Halassa et al., 2009). In this study, we examined whether genetic disruption of soluble N-ethylmaleimide-sensitive factor attached protein (SNARE)-dependent exocytosis in astrocytes (dnSNARE mice) or pharmacological blockade of A1 receptor signaling using an adenosine A1 receptor (A1R) antagonist, 8-cyclopentyl-1,3-dimethylxanthine (CPT), could prevent the negative effects of 6 h of SD on hippocampal late-phase long-term potentiation (L-LTP) and hippocampus-dependent spatial object recognition memory. We found that SD impaired L-LTP in wild-type mice but not in dnSNARE mice. Similarly, this deficit in L-LTP resulting from SD was prevented by a chronic infusion of CPT. Consistent with these results, we found that hippocampus-dependent memory deficits produced by SD were rescued in dnSNARE mice and CPT-treated mice. These data provide the first evidence that astrocytic ATP and adenosine A1R activity contribute to the effects of SD on hippocampal synaptic plasticity and hippocampus-dependent memory, and suggest a new therapeutic target to reverse the hippocampus-related cognitive deficits induced by sleep loss.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Adenosine / metabolism*
  • Analysis of Variance
  • Animals
  • Astrocytes / drug effects
  • Astrocytes / metabolism*
  • Electrophysiology
  • Exocytosis / physiology
  • Female
  • Hippocampus / drug effects
  • Hippocampus / physiology*
  • Male
  • Memory / drug effects
  • Memory / physiology*
  • Mice
  • Mice, Transgenic
  • Neuronal Plasticity / drug effects
  • Neuronal Plasticity / physiology*
  • Receptor, Adenosine A1 / metabolism*
  • SNARE Proteins / genetics
  • SNARE Proteins / metabolism
  • Sleep Deprivation / metabolism*
  • Sleep Deprivation / physiopathology
  • Synapses / drug effects
  • Synapses / physiology*
  • Theophylline / analogs & derivatives
  • Theophylline / pharmacology

Substances

  • Receptor, Adenosine A1
  • SNARE Proteins
  • 8-cyclopentyl-1,3-dimethylxanthine
  • Theophylline
  • Adenosine