Anxiolytic-like effects of restraint during the dark cycle in adolescent mice

Behav Brain Res. 2015 May 1:284:103-11. doi: 10.1016/j.bbr.2015.02.010. Epub 2015 Feb 14.

Abstract

Stress during developmental stage may cause psychological morbidities, and then the studies on stress are important in adolescent rodents. Restraint is used as a common stressor in rodents and the effects of restraint during the light cycle have been studied, but those of restraint during the dark cycle have not. The present study examined the effects of restraint during the light and dark cycles on anxiety behaviors in adolescent mice. Restraint for 3h during either the light or dark cycle impaired memory function in the fear conditioning test, but did not affect locomotor activity. In the elevated plus-maze test, restraint during the dark cycle reduced anxiety-like behaviors in mice. Repeated exposure to a 3-h period dark cycle restraint for 2 weeks had a similar anxiolytic-like effect. In contrast, restraint for 3h during the light cycle produced anxiety behavior in adolescent, but not adult, mice. The light cycle stress increased plasma corticosterone levels, and elevated c-Fos expression in the prefrontal cortex, paraventricular hypothalamic nucleus, basolateral amygdala and dentate gyrus, and enhanced serotonin turnover in the hippocampus and striatum, while the dark cycle stress did not. There was no difference in the stress-mediated reduction in pentobarbital-induced sleeping time between dark and light cycle restraint. These findings suggest that the anxiolytic effect of dark cycle restraint is mediated by corticosterone, serotonin or γ-aminobutyric acid-independent mechanisms, although the anxiogenic effect of light cycle restraint is associated with changes in plasma corticosterone levels and serotonin turnover in specific brain regions.

Keywords: Anxiety behavior; Dark cycle; Light cycle; Restraint.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aging / physiology*
  • Aging / psychology*
  • Animals
  • Anxiety / physiopathology*
  • Anxiety / therapy
  • Brain / metabolism
  • Conditioning, Psychological / physiology
  • Corticosterone / blood
  • Darkness*
  • Exploratory Behavior / physiology
  • Fear / physiology
  • Hypnotics and Sedatives / pharmacology
  • Light
  • Male
  • Mice
  • Motor Activity / physiology
  • Pentobarbital / pharmacology
  • Photoperiod
  • Proto-Oncogene Proteins c-fos / metabolism
  • Restraint, Physical / physiology*
  • Restraint, Physical / psychology*
  • Serotonin / metabolism
  • Sleep / drug effects
  • Sleep / physiology

Substances

  • Hypnotics and Sedatives
  • Proto-Oncogene Proteins c-fos
  • Serotonin
  • Pentobarbital
  • Corticosterone