4.7 Article

Preliminary evidence that hippocampal volumes in monkeys predict stress levels of adrenocorticotropic hormone

Journal

BIOLOGICAL PSYCHIATRY
Volume 62, Issue 10, Pages 1171-1174

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.biopsych.2007.03.012

Keywords

ACTH; glucocorticoid feedback; hippocampus; HPA axis; stress

Funding

  1. NIDA NIH HHS [R01 DA016902-03, DA16902, R01 DA016902] Funding Source: Medline
  2. NIMH NIH HHS [MH47573, MH50604, R01 MH050604, R01 MH047573, R01 MH047573-16, R01 MH050604-12] Funding Source: Medline

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Background: Hippocampal volumes previously determined in monkeys by magnetic resonance imaging are used to test the hypothesis that small hippocampi predict increased stress levels of adrenocorticotropic hormone (ACTH). Methods: Plasma ACTH levels were measured after restraint stress in 19 male monkeys pretreated with saline or hydrocortisone. Monkeys were then randomized to an undisturbed control condition or intermittent social separations followed by new pair formations. After 17 months of exposure to the intermittent social manipulations, restraint stress tests were repeated to determine test/retest correlations. Results: Individual differences in postrestraint stress ACTH levels over the 17-month test/retest interval were remarkably consistent for the saline (r(s) = .82,p = .0004) and hydrocortisone (r(s) = .78, p = .001) pretreatments. Social manipulations did not affect postrestraint stress ACTH levels, but monkeys with smaller hippocampal volumes responded to restraint after saline pretreatment with greater increases in ACTH levels with total brain volume variation controlled as a statistical covariate (beta = -.58,p = .031). Monkeys with smaller hippocampal volumes also responded with diminished sensitivity to glucocorticoid feedback determined by greater postrestraint ACTH levels after pretreatment with hydrocortisone (beta = -.68, p = .010). Conclusions: These findings support clinical reports that small hippocampi may be a risk factor for impaired regulation of the hypothalamic-pituitary-adrenal axis in humans with stress-related psychiatric disorders.

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