Inhibition of NMDA-type glutamate receptors induces arousal from torpor in hibernating arctic ground squirrels (Urocitellus parryii)

J Neurochem. 2012 Sep;122(5):934-40. doi: 10.1111/j.1471-4159.2012.07832.x. Epub 2012 Jul 11.

Abstract

Hibernation is an adaptation to overcome periods of resource limitation often associated with extreme climatic conditions. The hibernation season consists of prolonged bouts of torpor that are interrupted by brief interbout arousals. Physiological mechanisms regulating spontaneous arousals are poorly understood, but may be related to a need for gluconeogenesis or elimination of metabolic wastes. Glutamate is derived from glutamine through the glutamate-glutamine cycle and from glucose via the pyruvate carboxylase pathway when nitrogen balance favors formation of glutamine. This study tests the hypothesis that activation of NMDA-type glutamate receptors (NMDAR) maintains torpor in arctic ground squirrel (arctic ground squirrel (AGS); Urocitellus parryii). Administration of NMDAR antagonists MK-801 (5 mg/kg, i.p.) that crosses the blood-brain barrier and AP5 (5 mg/kg, i.p.) that does not cross the blood-brain barrier induced arousal in AGS. Central administration of MK-801 (0.2, 2, 20 or 200 μg; icv) to hibernating AGS failed to induce arousal. Results suggest that activation of NMDAR at a peripheral or circumventricular site is necessary to maintain prolonged torpor and that a decrease in glutamate at these sites may contribute to spontaneous arousal in AGS.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Analysis of Variance
  • Animals
  • Arctic Regions
  • Arousal / drug effects
  • Arousal / physiology*
  • Body Temperature / drug effects
  • Dizocilpine Maleate / pharmacology
  • Dose-Response Relationship, Drug
  • Drug Administration Routes
  • Excitatory Amino Acid Antagonists / pharmacology
  • Hibernation / drug effects
  • Hibernation / physiology*
  • Injections, Intraventricular
  • Oxygen Consumption / drug effects
  • Oxygen Consumption / physiology
  • Receptors, N-Methyl-D-Aspartate / metabolism*
  • Sciuridae / physiology*
  • Serotonin Antagonists / pharmacology
  • Tropanes / pharmacology
  • Valine / analogs & derivatives
  • Valine / pharmacology

Substances

  • Excitatory Amino Acid Antagonists
  • Receptors, N-Methyl-D-Aspartate
  • Serotonin Antagonists
  • Tropanes
  • Dizocilpine Maleate
  • 2-amino-5-phosphopentanoic acid
  • Valine
  • bemesetron