Relationships among plasma dehydroepiandrosterone sulfate and cortisol levels, symptoms of dissociation, and objective performance in humans exposed to acute stress.

CONTEXT Recently, a growing body of research has provided evidence that dehydroepiandrosterone sulfate (DHEA-S) is involved in an organism's response to stress and that it may provide beneficial behavioral and neurotrophic effects. OBJECTIVE To investigate plasma DHEA-S and cortisol levels, psychological symptoms of dissociation, and military performance. DESIGN Prospective study. SETTING AND PARTICIPANTS Twenty-five healthy subjects enrolled in military survival school. RESULTS The DHEA-S-cortisol ratios during stress were significantly higher in subjects who reported fewer symptoms of dissociation and exhibited superior military performance. CONCLUSIONS These data provide prospective, empirical evidence that the DHEA-S level is increased by acute stress in healthy humans and that the DHEA-S-cortisol ratio may index the degree to which an individual is buffered against the negative effects of stress.

[1]  J. Harris,et al.  Dehydroepiandrosterone sulfate (DHEAS) counteracts decremental effects of corticosterone on dentate gyrus LTP. implications for depression , 2000, Brain Research Bulletin.

[2]  E. London,et al.  Receptor binding and electrophysiological effects of Dehydroepiandrosterone sulfate, an antagonist of the GABAA receptor , 1991, Neuroscience.

[3]  I. Goodyer,et al.  Adrenal steroid secretion and major depression in 8- to 16-year-olds, III. Influence of cortisol/DHEA ratio at presentation on subsequent rates of disappointing life events and persistent major depression , 1998, Psychological Medicine.

[4]  J. Fawcett,et al.  Dehydroepiandrosterone antagonizes the neurotoxic effects of corticosterone and translocation of stress-activated protein kinase 3 in hippocampal primary cultures , 1999, Neuroscience.

[5]  C. A. Morgan,et al.  Plasma neuropeptide-Y concentrations in humans exposed to military survival training , 2000, Biological Psychiatry.

[6]  R. Ritzmann,et al.  Dehydroepiandrosterone is an anxiolytic in mice on the plus maze. , 1994, Pharmacology, biochemistry, and behavior.

[7]  M. Hill,et al.  Age and sex related differences in serum levels of unconjugated dehydroepiandrosterone and its sulphate in normal subjects. , 1997, The Journal of endocrinology.

[8]  Charles A Morgan,et al.  Hormone profiles in humans experiencing military survival training , 2000, Biological Psychiatry.

[9]  T. Dinan,et al.  Differences in adrenal steroid profile in chronic fatigue syndrome, in depression and in health. , 1999, Journal of affective disorders.

[10]  R. D. Schwartz,et al.  Pregnenolone-sulfate: an endogenous antagonist of the γ-aminobutyric acid receptor complex in brain? , 1987, Brain Research.

[11]  R. Oades,et al.  Serum gonadal steroid hormones in young schizophrenic patients , 1994, Psychoneuroendocrinology.

[12]  R. Lathe,et al.  Cyp7b, a novel brain cytochrome P450, catalyzes the synthesis of neurosteroids 7α-hydroxy dehydroepiandrosterone and 7α-hydroxy pregnenolone , 1997 .

[13]  N. Orentreich,et al.  Age changes and sex differences in serum dehydroepiandrosterone sulfate concentrations throughout adulthood. , 1984, The Journal of clinical endocrinology and metabolism.

[14]  I. Goodyer,et al.  Adrenal secretion during major depression in 8- to 16-year-olds, I. Altered diurnal rhythms in salivary cortisol and dehydroepiandrosterone (DHEA) at presentation , 1996, Psychological Medicine.

[15]  J. Poirier,et al.  Dehydroepiandrosterone (DHEA) protects hippocampal cells from oxidative stress-induced damage. , 1999, Brain research. Molecular brain research.

[16]  E. Bernton,et al.  Dehydroepiandrosterone antagonizes the suppressive effects of dexamethasone on lymphocyte proliferation. , 1991, Endocrinology.

[17]  J. Krystal,et al.  Attenuation of the neuropsychiatric effects of ketamine with lamotrigine: support for hyperglutamatergic effects of N-methyl-D-aspartate receptor antagonists. , 2000, Archives of general psychiatry.

[18]  C. Frye,et al.  The Neurosteroids DHEA and DHEAS May Influence Cognitive Performance by Altering Affective State , 1999, Physiology & Behavior.

[19]  J. Strain,et al.  Subnormal plasma adrenal androgen levels in men with uremia. , 1980, The Journal of clinical endocrinology and metabolism.

[20]  D. Jakubowicz,et al.  Disparate effects of weight reduction by diet on serum dehydroepiandrosterone-sulfate levels in obese men and women. , 1995, The Journal of clinical endocrinology and metabolism.

[21]  N. Orentreich,et al.  Long-term longitudinal measurements of plasma dehydroepiandrosterone sulfate in normal men. , 1992, The Journal of clinical endocrinology and metabolism.

[22]  M. Fava,et al.  Dehydroepiandrosterone-sulfate/cortisol ratio in panic disorder , 1989, Psychiatry Research.

[23]  Dehydroepiandrosterone (DHEA) treatment of depression , 1997, Biological Psychiatry.

[24]  A. Masi,et al.  Sex hormones and rheumatoid arthritis: cause or effect relationships in a complex pathophysiology? , 1995, Clinical and experimental rheumatology.

[25]  T. Theorell,et al.  A Longitudinal Study of Hormonal Reactions Accompanying Life Events in Recently Resettled Refugees , 2002, Psychotherapy and Psychosomatics.

[26]  L. Havelec,et al.  Role of glucocorticoids in the cholinergic degeneration in rat hippocampus induced by ethylcholine aziridinium (AF64A) , 1993, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[27]  D. Weiss,et al.  Longitudinal course and predictors of continuing distress following critical incident exposure in emergency services personnel. , 1999, The Journal of nervous and mental disease.

[28]  E. Baulieu,et al.  Dehydroepiandrosterone (DHEA) Is a Neuroactive Neurosteroid , 1995, Annals of the New York Academy of Sciences.

[29]  E. Paykel,et al.  Altered salivary dehydroepiandrosterone levels in major depression in adults , 2000, Biological Psychiatry.

[30]  H. Weisman,et al.  Plasma dehydroepiandrosterone and dehydroepiandrosterone sulfate in patients undergoing diagnostic coronary angiography. , 1990, Journal of the American College of Cardiology.

[31]  A. Floreani,et al.  Sex hormone changes in post-menopausal women with primary biliary cirrhosis (PBC) and with cryptogenic chronic liver disease. , 1991, Clinical and experimental obstetrics & gynecology.

[32]  L. Hansson,et al.  Elevated Blood Levels of Dehydroepiandrosterone Sulphate Vary with Symptom Load in Posttraumatic Stress Disorder: Findings from a Longitudinal Study of Refugees in Sweden , 2002, Psychotherapy and Psychosomatics.

[33]  R. Ritzmann,et al.  Dehydroepiandrosterone is an anxiolytic in mice mice on the plus maze , 1994, Pharmacology Biochemistry and Behavior.

[34]  E. Browne,et al.  Dehydroepiandrosterone: antiglucocorticoid action in mice. , 1992, The American journal of the medical sciences.

[35]  P. Cowen Back to the future: the neurobiology of major depression , 1998, Psychological Medicine.

[36]  E. Roberts DEHYDROEPIANDROSTERONE (DHEA) AND ITS SULFATE (DHEAS) AS NEURAL FACILITATORS: EFFECTS ON BRAIN TISSUE IN CULTURE AND ON MEMORY IN YOUNG AND OLD MICE. A CYCLIC GMP HYPOTHESIS OF ACTION OF DHEA AND DHEAS IN NERVOUS SYSTEM AND OTHER TISSUES , 1990 .

[37]  I. R. Zucker,et al.  The secretion of dehydroepiandrosterone and dehydroepiandrosterone sulphate in man. , 1973, The Journal of endocrinology.

[38]  M. Gavish,et al.  Altered Platelet Peripheral-Type Benzodiazepine Receptor in Posttraumatic Stress Disorder , 1996, Neuropsychopharmacology.

[39]  J W Rudy,et al.  DHEA-S selectively impairs contextual-fear conditioning: support for the antiglucocorticoid hypothesis. , 1997, Behavioral neuroscience.

[40]  D. Rubinow,et al.  Dehydroepiandrosterone (DHEA) and its sulfated derivative (DHEAS) regulate apoptosis during neurogenesis by triggering the Akt signaling pathway in opposing ways. , 2002, Brain research. Molecular brain research.

[41]  S. Vicini,et al.  Neurosteroid pregnenolone sulfate antagonizes electrophysiological responses to GABA in neurons , 1988, Neuroscience Letters.

[42]  C. A. Morgan,et al.  Symptoms of dissociation in humans experiencing acute, uncontrollable stress: a prospective investigation. , 2001, The American journal of psychiatry.

[43]  Y. Kishimoto,et al.  DEHYDROEPIANDROSTERONE SULPHATE IN RAT BRAIN: INCORPORATION FROM BLOOD AND METABOLISM IN VIVO 1 2 , 1972, Journal of neurochemistry.

[44]  Dirk H. Hellhammer,et al.  OPPOSING EFFECTS OF DHEA REPLACEMENT IN ELDERLY SUBJECTS ON DECLARATIVE MEMORY AND ATTENTION AFTER EXPOSURE TO A LABORATORY STRESSOR , 1998, Psychoneuroendocrinology.

[45]  R. Daynes,et al.  Regulation of murine lymphokine production in vivo II. Dehydroepiandrosterone is a natural enhancer of interleukin 2 synthesis by helper T cells , 1990, European journal of immunology.

[46]  Ľ. Stárka,et al.  Neurosteroid 7-hydroxylation products in the brain. , 2001, International review of neurobiology.

[47]  J. Goméz,et al.  Marked decline in serum concentrations of adrenal C19 sex steroid precursors and conjugated androgen metabolites during aging. , 1997, The Journal of clinical endocrinology and metabolism.

[48]  J. Herbert,et al.  Dehydroepiandrosterone (DHEA) stimulates neurogenesis in the hippocampus of the rat, promotes survival of newly formed neurons and prevents corticosterone‐induced suppression , 2002, The European journal of neuroscience.

[49]  S. Mellon,et al.  Neurosteroids: Biosynthesis and Function of These Novel Neuromodulators , 2000, Frontiers in Neuroendocrinology.

[50]  S. Southwick,et al.  Measurement of Dissociative States with the Clinician-Administered Dissociative States Scale (CADSS) , 1998, Journal of traumatic stress.

[51]  C. A. Morgan,et al.  Relationship Among Plasma Cortisol, Catecholamines, Neuropeptide Y, and Human Performance During Exposure to Uncontrollable Stress , 2001, Psychosomatic medicine.

[52]  E. London,et al.  The neurosteroid dehydroepiandrosterone sulfate is an allosteric antagonist of the GABAA receptor , 1990, Brain Research.

[53]  N. Schneiderman,et al.  Cognitive-behavioral stress management buffers decreases in dehydroepiandrosterone sulfate (DHEA-S) and increases in the cortisol/DHEA-S ratio and reduces mood disturbance and perceived stress among HIV-seropositive men , 1999, Psychoneuroendocrinology.

[54]  J Levin,et al.  Subnormal plasma dehydroisoandrosterone to cortisol ratio in anorexia nervosa: a second hormonal parameter of ontogenic regression. , 1983, The Journal of clinical endocrinology and metabolism.

[55]  M. Sofroniew,et al.  Dehydroepiandrosterone (DHEA) and DHEA-sulfate (DHEAS) protect hippocampal neurons against excitatory amino acid-induced neurotoxicity. , 1998, Proceedings of the National Academy of Sciences of the United States of America.