Do different types of stress differentially alter behavioural and neurobiological outcomes associated with depression in rodent models? A systematic review

Front Neuroendocrinol. 2021 Apr:61:100896. doi: 10.1016/j.yfrne.2020.100896. Epub 2020 Dec 24.

Abstract

Cataloguing the effects of different types of stress on behaviour and physiology in rodent models has not been comprehensively attempted. Here, we systematically review whether chronic exposure to physical stress, psychosocial stress, or both types of stress can induce different behavioural and neurobiological outcomes in male and female rodents. We found that physical stress consistently increased depressive-like behaviour, impaired social interaction and decreased body weight, while psychosocial stress consistently increased both anxiety- and depressive-like behaviour, impaired social interaction and learning and memory, increased HPA axis activity, peripheral inflammation and microglial activation, and decreased hippocampal neurogenesis in male rodents. Moreover, we found that the combined effect of both stress types resulted in a more severe pathological state defined by increased anxiety- and depressive-like behaviour, impaired social interaction and learning and memory, increased HPA axis activity and central inflammation, and reduced hippocampal neurogenesis and neural plasticity in male rodents. Phenotypes for females were less consistent, irrespective of the type of stress exposure, on account of the limited number of studies using females. This review highlights that the type of stress may indeed matter and will help animal researchers to more appropriately choose a stress/depression model that fits their research purposes.

Keywords: Anxiety; Chronic stress; Depression; Hippocampal neurogenesis; Hypothalamic pituitary adrenal (HPA) axis activity; Inflammation; Neural plasticity; Neuroinflammation; Stressor type.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review
  • Systematic Review

MeSH terms

  • Animals
  • Depression*
  • Female
  • Hippocampus
  • Hypothalamo-Hypophyseal System*
  • Male
  • Pituitary-Adrenal System
  • Rodentia
  • Stress, Psychological