Korean J Physiol Pharmacol.  2014 Jun;18(3):263-268. 10.4196/kjpp.2014.18.3.263.

Chronic Non-Social Stress Affects Depressive Behaviors But Not Anxiety in Mice

Affiliations
  • 1Department of Physiology, Seoul National University College of Medicine, Seoul 110-799, Korea. kmhwany@snu.ac.kr
  • 2Neuroscience Research Institute, Seoul National University Medical Research Center, Seoul 110-799, Korea.
  • 3Department of Pharmacology, Seoul National University College of Medicine, Seoul 110-799, Korea.
  • 4Seoul National University Bundang Hospital, Seongnam 463-707, Korea.

Abstract

The etiology of most psychiatric disorders is still incompletely understood. However, growing evidence suggests that stress is a potent environmental risk factor for depression and anxiety. In rodents, various stress paradigms have been developed, but psychosocial stress paradigms have received more attention than non-social stress paradigms because psychosocial stress is more prevalent in humans. Interestingly, some recent studies suggest that chronic psychosocial stress and social isolation affects mainly anxiety-related behaviors in mice. However, it is unclear whether chronic non-social stress induces both depression- and anxiety-related phenotypes or induces one specific phenotype in mice. In the present study, we examined the behavioral consequences of three chronic non-social stress paradigms: chronic predictable (restraint) stress (CPS), chronic unpredictable stress (CUS), and repeated corticosterone-HBC complex injection (RCI). Each of the three paradigms induced mild to severe depression/despair-like behaviors in mice and resulted in increased immobility in a tail suspension test. However, anxiety-related phenotypes, thigmotaxis and explorative behaviors, were not changed by the three paradigms. These results suggest that depression- and anxiety-related phenotypes can be dissociated in mouse stress models and that social and non-social stressors might affect brain circuits and behaviors differently.

Keyword

Anxiety; Chronic non-social stress; Depression; Open field test; Tail suspension test

MeSH Terms

Animals
Anxiety*
Brain
Depression
Hindlimb Suspension
Humans
Mice*
Phenotype
Risk Factors
Rodentia
Social Isolation

Figure

  • Fig. 1 Schematic representation of the experimental design. Experimental groups were exposed to chronic predictable (restraint) stress (CPS), chronic unpredictable stress (CUS), or repeated corticosterone-HBC complex injection (RCI).

  • Fig. 2 Effect of 3-week non-social stress on body weight. The body weight of mice during the period of CPS (A), CUS (B), and RCI (C). (D) Body weights of the stressed groups after the stress phase. Data were normalized to each control group (dashed line).

  • Fig. 3 Chronic non-social stress increases depression-like behaviors. Minute-by-minute analysis of the time spent immobile during the tail suspension test in mice exposed to CPS (A), CUS (B), and RCI (C). (D) The total time spent immobile during the 6-minute test in each stress group was normalized to each control group (dashed line).

  • Fig. 4 Normal locomotor activity and thigmotaxic behaviors in mice with chronic non-social stress. Examples of exploratory paths (A), distance moved (B), and thigmotaxis (C) from the CPS and control groups are shown. Thigmotaxis levels are expressed as the percent time spent in the periphery. Exploratory paths, distance moved, and thigmotaxis from the CUS (D-F) and RCI (G-I) groups are compared with each control. Total distance moved (J) and thigmotaxis (K) during the 30-minute test were normalized to the control group (dashed line) and summarized.


Cited by  1 articles

Alterations of Amino Acid Level in Depressed Rat Brain
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Korean J Physiol Pharmacol. 2014;18(5):371-376.    doi: 10.4196/kjpp.2014.18.5.371.


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