Application of single prolonged stress induces post-traumatic stress disorder-like characteristics in mice

Ken Ichi Tanaka, Takao Yagi, Takeshi Nanba, Masato Asanuma

Research output: Contribution to journalArticle

1 Citation (Scopus)

Abstract

We tried to clarify the applicability of a single prolonged stress (SPS) protocol as post-traumatic stress disorder (PTSD) model in mice. To investigate PTSD pathophysiology, we conducted hypothalamo-pituitary-adrenal (HPA) negative feedback testing at 1, 4, 8 and 12 weeks after the SPS by administrating a dexamethasone (DEX) suppression test. The SPS induced over-suppression of the HPA system by DEX treatment at 8 and 12 weeks. To investigate PTSD-like behavioral characteristics, we subjected mice to testing in a light/dark box (to assess anxiety), a Y-maze (working memory), a cliff avoidance (visual cognition), and an open field (locomotor activity) at 1, 4, 8 and 12 weeks after the SPS. In the light/dark box test, the SPS-applied mice spent significantly less time in the light box at 8 or 12 weeks. In the cliff avoidance test, the SPS-applied mice spent significantly less time in the open area at 1 week. However, in both the Y-maze test and the open field test, SPS-applied mice tended toward slight decreases in a time-dependent manner until 12 weeks. Therefore, SPS-applied mice may thus be useful for assessing characteristics relevant to PTSD that coincide with changes in the HPA axis.

Original languageEnglish
Pages (from-to)479-486
Number of pages8
JournalActa Medica Okayama
Volume72
Issue number5
Publication statusPublished - Jan 1 2018

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Post-Traumatic Stress Disorders
Light
Dexamethasone
Pituitary-Adrenal System
Locomotion
Short-Term Memory
Cognition
Testing
Anxiety
Feedback
Data storage equipment

Keywords

  • Corticosterone
  • Mouse
  • PTSD
  • Single prolonged stress

ASJC Scopus subject areas

  • Biochemistry, Genetics and Molecular Biology(all)

Cite this

Application of single prolonged stress induces post-traumatic stress disorder-like characteristics in mice. / Tanaka, Ken Ichi; Yagi, Takao; Nanba, Takeshi; Asanuma, Masato.

In: Acta Medica Okayama, Vol. 72, No. 5, 01.01.2018, p. 479-486.

Research output: Contribution to journalArticle

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