Fasting activated histaminergic neurons and enhanced arousal effect of caffeine in mice

Pharmacol Biochem Behav. 2015 Jun:133:164-73. doi: 10.1016/j.pbb.2015.04.003. Epub 2015 Apr 17.

Abstract

Caffeine, a popular psychoactive compound, promotes wakefulness via blocking adenosine A2A receptors in the shell of the nucleus accumbens, which projects to the arousal histaminergic tuberomammillary nucleus (TMN). The TMN controls several behaviors such as wakefulness and feeding. Fasting has been reported to activate the TMN histaminergic neurons to increase arousal. Therefore, we propose that caffeine may promote greater arousal under fasting rather than normal feeding conditions. In the current study, locomotor activity recording, electroencephalogram (EEG) and electromyogram recording and c-Fos expression were used in wild type (WT) and histamine H1 receptor (H1R) knockout (KO) mice to investigate the arousal effects of caffeine under fasting conditions. Caffeine (15mg/kg) enhanced locomotor activity in fasted mice for 5h, but only did so for 3h in normally fed animals. Pretreatment with the H1R antagonist pyrilamine abolished caffeine-induced stimulation on locomotor activity in fasted mice. EEG recordings confirmed that caffeine-induced wakefulness for 3h in fed WT mice, and for 5h in fasted ones. A stimulatory effect of caffeine was not observed in fasted H1R KO mice. Furthermore, c-Fos expression was increased in the TMN under fasting conditions. These results indicate that caffeine had greater wakefulness-promoting effects in fasted mice through the mediation of H1R.

Keywords: Caffeine; EEG; Fasted; H(1)R; Wakefulness.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Arousal / drug effects*
  • Caffeine / antagonists & inhibitors
  • Caffeine / pharmacology*
  • Fasting / physiology*
  • Histamine H1 Antagonists / pharmacology
  • Hypothalamic Area, Lateral / cytology
  • Hypothalamic Area, Lateral / drug effects
  • Hypothalamic Area, Lateral / metabolism
  • Male
  • Mice
  • Mice, Knockout
  • Motor Activity / drug effects
  • Neurons / drug effects
  • Neurons / metabolism*
  • Proto-Oncogene Proteins c-fos / metabolism
  • Pyrilamine / pharmacology
  • Receptors, Histamine H1 / deficiency
  • Receptors, Histamine H1 / genetics
  • Receptors, Histamine H1 / metabolism*
  • Sleep / drug effects
  • Wakefulness / drug effects

Substances

  • Histamine H1 Antagonists
  • Proto-Oncogene Proteins c-fos
  • Receptors, Histamine H1
  • Caffeine
  • Pyrilamine