Dopamine and opioids interactions in sleep deprivation

Prog Neuropsychopharmacol Biol Psychiatry. 1993 Mar;17(2):269-78. doi: 10.1016/0278-5846(93)90047-v.

Abstract

1. Sleep deprivation induced by the platform technique is considered to be a heavy stressful situation in rats. At the end of the sleep deprivation period (72 hrs) the rat displayed particular behavior characterized by wakefulness, a high degree of motor and exploratory activity, increased alertness and reactivity to environmental stimuli. 2. Our results indicate that this behavior is potently antagonized by the administration of D1 antagonist SCH 23390 and by the opioid antagonist naloxone. 3. We also show that concomitantly to this behavior, an increased number of D1 receptors associated with an increased dopamine-stimulated adenylate cyclase activity is present in the limbic system but not in the striatum of these animals. On the contrary, a decreased Bmax of mu and delta opioid receptors was found in the same brain areas. 4. These data suggest an active role of limbic dopamine and opioid system in the generation of arousal and insomnia related to sleep deprivation-induced stress.

MeSH terms

  • Adenylyl Cyclases / metabolism
  • Animals
  • Benzazepines / metabolism
  • Corpus Striatum / drug effects
  • Corpus Striatum / metabolism
  • Dopamine / physiology*
  • Dopamine Agents / pharmacology
  • Dopamine Antagonists
  • Endorphins / pharmacology
  • Endorphins / physiology*
  • Limbic System / drug effects
  • Limbic System / metabolism
  • Male
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, Dopamine D1 / antagonists & inhibitors
  • Receptors, Dopamine D1 / metabolism
  • Sleep Deprivation / physiology*

Substances

  • Benzazepines
  • Dopamine Agents
  • Dopamine Antagonists
  • Endorphins
  • Receptors, Dopamine D1
  • Adenylyl Cyclases
  • Dopamine