Impact of acute psychosocial stress on peripheral blood gene expression pathways in healthy men

Urs M Nater, Toni Whistler, William Lonergan, Tanja Mletzko, Suzanne D Vernon, Christine Heim

Publications: Contribution to journalArticlePeer Reviewed

Abstract

We investigated peripheral blood mononuclear cell gene expression responses to acute psychosocial stress to identify molecular pathways relevant to the stress response. Blood samples were obtained from 10 healthy male subjects before, during and after (at 0, 30, and 60 min) a standardized psychosocial laboratory stressor. Ribonucleic acid (RNA) was extracted and gene expression measured by hybridization to a 20,000-gene microarray. Gene Set Expression Comparisons (GSEC) using defined pathways were used for the analysis. Forty-nine pathways were significantly changed from baseline to immediately after the stressor (p<0.05), implicating cell cycle, cell signaling, adhesion and immune responses. The comparison between stress and recovery (measured 30 min later) identified 36 pathways, several involving stress-responsive signaling cascades and cellular defense mechanisms. These results have relevance for understanding molecular mechanisms of the physiological stress response, and might be used to further study adverse health outcomes of psychosocial stress.

Original languageEnglish
Pages (from-to)125-132
Number of pages8
JournalBiological Psychology
Volume82
Issue number2
DOIs
Publication statusPublished - 2009
Externally publishedYes

Austrian Fields of Science 2012

  • 501010 Clinical psychology

Keywords

  • Adrenocorticotropic Hormone
  • Adult
  • Gene Expression
  • Gene Expression Profiling
  • Humans
  • Hydrocortisone
  • Interleukin-6
  • Leukocytes, Mononuclear
  • Male
  • Middle Aged
  • Norethandrolone
  • Oligonucleotide Array Sequence Analysis
  • Psychometrics
  • Signal Transduction
  • Stress, Psychological
  • Time Factors
  • Transcription Factors
  • Young Adult
  • Journal Article
  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

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