4.6 Article

Altered acoustic startle, prepulse facilitation, and object recognition memory produced by corticosterone withdrawal in male rats

期刊

BEHAVIOURAL BRAIN RESEARCH
卷 408, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.bbr.2021.113291

关键词

Depression; Stress; Cognition; Startle; Sensorimotor gating; Forced swim test

资金

  1. Natural Sciences and Engineering Research Council of Canada (NSERC)
  2. NSERC Doctoral Canada Graduate Scholarship

向作者/读者索取更多资源

Repeated corticosterone injections in rats lead to cognitive deficits and depression-like behavior, highlighting the importance of considering cognitive impairments in assessing depression. Corticosterone significantly affects body weight, immobility in the forced swim test, startle amplitudes, and object recognition memory, suggesting a complex phenotype induced by chronic stress.
The symptoms of human depression often include cognitive deficits. However, cognition is not frequently included in the behavioral assessments conducted in preclinical models of depression. For example, it is well known that repeated corticosterone (CORT) injections in rodents produce depression-like behavior as measured by the forced swim test, sucrose preference test, and tail suspension test, but the cognitive impairments produced by repeated CORT have not been thoroughly examined. The purpose of this experiment was to assess the effect of repeated CORT injections on several versions of object recognition memory and modulation of the acoustic startle response by relatively low intensity prepulses, along with the more traditional assessment of depressionlike behavior using the forced swim test. Rats received 21 days of CORT (40 mg/kg) or vehicle injections followed by a battery of behavioral tests. Importantly, during behavioral testing CORT treatment did not occur (CORT withdrawal). Corticosterone decreased body weight, increased immobility in the forced swim test, lowered startle amplitudes, and facilitated responding to trials with a short interval (30 ms) between the prepulse and pulse. Corticosterone also impaired both object location and object-in-place recognition memory, while sparing performance on object recognition memory. Collectively, our data suggest that CORT produces selective disruptions in prepulse facilitation, object location, and object-in-place recognition memory, and that these impairments should be considered as part of the phenotype produced by repeated CORT, and perhaps chronic stress.

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