Evidence supporting the match/mismatch hypothesis of psychiatric disorders

Eur Neuropsychopharmacol. 2014 Jun;24(6):907-18. doi: 10.1016/j.euroneuro.2014.02.002. Epub 2014 Feb 15.

Abstract

Chronic stress is one of the predominant environmental risk factors for a number of psychiatric disorders, particularly for major depression. Different hypotheses have been formulated to address the interaction between early and adult chronic stress in psychiatric disease vulnerability. The match/mismatch hypothesis of psychiatric disease states that the early life environment shapes coping strategies in a manner that enables individuals to optimally face similar environments later in life. We tested this hypothesis in female Balb/c mice that underwent either stress or enrichment early in life and were in adulthood further subdivided in single or group housed, in order to provide aversive or positive adult environments, respectively. We studied the effects of the environmental manipulation on anxiety-like, depressive-like and sociability behaviors and gene expression profiles. We show that continuous exposure to adverse environments (matched condition) is not necessarily resulting in an opposite phenotype compared to a continuous supportive environment (matched condition). Rather, animals with mismatched environmental conditions behaved differently from animals with matched environments on anxious, social and depressive like phenotypes. These results further support the match/mismatch hypothesis and illustrate how mild or moderate aversive conditions during development can shape an individual to be optimally adapted to similar conditions later in life.

Keywords: Behavior; Cumulative stress hypothesis; Depression; Match/mismatch hypothesis; Mouse; Stress vulnerability.

MeSH terms

  • Adaptation, Psychological
  • Adrenal Glands / physiopathology
  • Amino Acid Transport Systems, Neutral / metabolism
  • Animals
  • Anxiety Disorders / etiology*
  • Anxiety Disorders / physiopathology
  • Anxiety Disorders / psychology
  • Brain-Derived Neurotrophic Factor / metabolism
  • Corticosterone / blood
  • Depressive Disorder / etiology*
  • Depressive Disorder / physiopathology
  • Depressive Disorder / psychology
  • Disease Models, Animal
  • Environment*
  • Estrous Cycle / physiology
  • Female
  • Hippocampus / physiopathology
  • Housing, Animal
  • Mice, Inbred BALB C
  • Models, Psychological*
  • Neuropsychological Tests
  • Phenotype
  • Social Behavior*
  • Social Isolation / psychology
  • Stress, Psychological / complications*
  • Stress, Psychological / physiopathology
  • Stress, Psychological / psychology
  • Thymus Gland / physiopathology

Substances

  • Amino Acid Transport Systems, Neutral
  • Brain-Derived Neurotrophic Factor
  • Slc6a15 protein, mouse
  • Corticosterone