Literature DB >> 19330152

Enhancement of Cognitive and Electrophysiological Measures of Hippocampal Functioning in Rats by a Low, But Not High, Dose of Dehydroepiandrosterone Sulfate (DHEAS).

David M Diamond1.   

Abstract

Dehydroepiandrosterone sulfate (DHEAS) is a steroid hornone that is synthesized, de novo, in the brain. Endogenous DHEAS levels correlate with the quality of mental and physical health, where the highest levels of DHEAS occur in healthy young adults and reduced levels of DHEAS are found with advanced age, disease, or extreme stress. DHEAS supplementation, therefore, may serve as a therapeutic agent against a broad range of maladies. This paper summarizes laboratory findings on dose-response relationships between DHEAS and cognitive and electrophysiological measures of hippocampal functioning. It was found that a low, but not a high, dose of DHEAS enhanced hippocampal primed burst potentiation (a physiological model of memory) as well as spatial (hippocampal-dependent) memory in rats. This complex dose-response function of DHEAS effects on the brain and memory may contribute toward the inconsistent findings that have been obtained by other investigators in studies on DHEAS administration in people.

Entities:  

Keywords:  DHEA; dehydroepiandrosterone; hippocampus; long-term potentiation; memory; neurosteroid

Year:  2004        PMID: 19330152      PMCID: PMC2657507          DOI: 10.1080/15401420490900290

Source DB:  PubMed          Journal:  Nonlinearity Biol Toxicol Med        ISSN: 1540-1421


  42 in total

1.  The enhancement of hippocampal primed burst potentiation by dehydroepiandrosterone sulfate (DHEAS) is blocked by psychological stress.

Authors:  D M Diamond; M Fleshner; G M Rose
Journal:  Stress       Date:  1999-12       Impact factor: 3.493

Review 2.  Is there a case for DHEA replacement?

Authors:  T B Nippoldt; K S Nair
Journal:  Baillieres Clin Endocrinol Metab       Date:  1998-10

3.  Treatment with dehydroepiandrosterone sulfate increases NMDA receptors in hippocampus and cortex.

Authors:  S Wen; K Dong; J P Onolfo; M Vincens
Journal:  Eur J Pharmacol       Date:  2001-11-02       Impact factor: 4.432

4.  Dehydroepiandrosterone sulfate: a biomarker of primate aging slowed by calorie restriction.

Authors:  M A Lane; D K Ingram; S S Ball; G S Roth
Journal:  J Clin Endocrinol Metab       Date:  1997-07       Impact factor: 5.958

Review 5.  Neurosteroids in depression: a review.

Authors:  Frank van Broekhoven; Robbert J Verkes
Journal:  Psychopharmacology (Berl)       Date:  2002-11-06       Impact factor: 4.530

Review 6.  Actions of dehydroepiandrosterone and its sulfate in the central nervous system: effects on cognition and emotion in animals and humans.

Authors:  O T Wolf; C Kirschbaum
Journal:  Brain Res Brain Res Rev       Date:  1999-11

Review 7.  Antiglucocorticoid treatments in psychiatry.

Authors:  V I Reus; O M Wolkowitz; S Frederick
Journal:  Psychoneuroendocrinology       Date:  1997       Impact factor: 4.905

8.  Potentiation of neuronal NMDA response induced by dehydroepiandrosterone and its suppression by progesterone: effects mediated via sigma receptors.

Authors:  R Bergeron; C de Montigny; G Debonnel
Journal:  J Neurosci       Date:  1996-02-01       Impact factor: 6.167

9.  Dehydroepiandrosterone (DHEA) sulfate prevents reduction in tissue vitamin E and increased lipid peroxidation due to murine retrovirus infection of aged mice.

Authors:  M Araghi-Niknam; S K Ardestani; M Molitor; P Inserra; C D Eskelson; R R Watson
Journal:  Proc Soc Exp Biol Med       Date:  1998-07

10.  Effects of syphilis infection on adrenocortical function in men.

Authors:  C R Parker; M W Schuster
Journal:  Proc Soc Exp Biol Med       Date:  1991-06
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  1 in total

Review 1.  The Potential Role of Inflammation in Modulating Endogenous Hippocampal Neurogenesis After Spinal Cord Injury.

Authors:  Arthur Sefiani; Cédric G Geoffroy
Journal:  Front Neurosci       Date:  2021-06-18       Impact factor: 4.677

  1 in total

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