Natural steroids counteracting some actions of putative depressogenic steroids on the central nervous system: potential therapeutic benefits
- PMID: 9247908
- DOI: 10.1016/s0306-9877(97)90252-8
Natural steroids counteracting some actions of putative depressogenic steroids on the central nervous system: potential therapeutic benefits
Abstract
Psychological similarities in the symptomatology of Cushing's and depressive diseases led to repeated attempts of treatment of the affective disease by suppression of adrenocortical secretion. While successful in many patients, all drugs employed-metyrapone, ketoconazole and aminoglutethimide-carry the danger of inducing adrenal insufficiency. In addition, their undesirable side effects were also a main reason for treatment suspension. In our 1990 proposal for the treatment of depression through control of adrenal steroid levels, we set as one of the goals the identification of steroids which can antagonize each other on their effects on the central nervous system. Specifically, we looked first at steroids that could counter each other's effects on long-term potentiation, a putative memory mechanism in the central nervous system. One reason for this was the consensus that memory mechanisms are affected in both Cushing's and depressive patients. Another was the fact that cortisol-type hormones which underlie, at least in part, the depressogenic actions of adrenal steroids also have inhibitory effects on LTP. We conjectured, then, that a steroid with opposite effects, one that could enhance long-term potentiation and, further, that could counter the depressant effects of corticosterone on long-term potentiation, could be of use in the treatment of depression. Dehydroepiandrosterone sulfate increases long-term potentiation in a dose-related manner, and preliminary data suggest that it also counteracts the depressant effects of corticosterone on long-term potentiation when injected simultaneously on experimental animals. Potentially at least, rather than resort to total suppression of adrenocortical activity, it may be possible to treat depression just by counteracting some of the effects of cortisol-like hormone actions in the central nervous system. Further, both in clinical trials as well as in experimental animals, dehydroepiandro-sterone sulfate has been shown to enhance performance in memory-requiring tasks.
Similar articles
-
Adrenal steroids and the physiopathology of a subset of depressive disorders.Med Hypotheses. 1991 Nov;36(3):300-5. doi: 10.1016/0306-9877(91)90153-p. Med Hypotheses. 1991. PMID: 1787828
-
Effects of adrenal cortex hormones on limbic structures: some experimental and clinical correlations related to depression.J Psychiatry Neurosci. 1993 Jan;18(1):4-16. J Psychiatry Neurosci. 1993. PMID: 8461280 Free PMC article. Review.
-
Treatment of Cushing's syndrome with trilostane (WIN 24,540), an inhibitor of adrenal steroid biosynthesis.J Clin Endocrinol Metab. 1978 Nov;47(5):1042-51. doi: 10.1210/jcem-47-5-1042. J Clin Endocrinol Metab. 1978. PMID: 233687
-
Short and long-term responses to metyrapone in the medical management of 91 patients with Cushing's syndrome.Clin Endocrinol (Oxf). 1991 Aug;35(2):169-78. doi: 10.1111/j.1365-2265.1991.tb03517.x. Clin Endocrinol (Oxf). 1991. PMID: 1657460
-
Drugs in the medical treatment of Cushing's syndrome.Expert Opin Emerg Drugs. 2009 Dec;14(4):661-71. doi: 10.1517/14728210903413522. Expert Opin Emerg Drugs. 2009. PMID: 19939210 Review.
Cited by
-
Neurobiological and neuropsychiatric effects of dehydroepiandrosterone (DHEA) and DHEA sulfate (DHEAS).Front Neuroendocrinol. 2009 Jan;30(1):65-91. doi: 10.1016/j.yfrne.2008.11.002. Epub 2008 Dec 3. Front Neuroendocrinol. 2009. PMID: 19063914 Free PMC article. Review.
-
Randomised controlled trial of the effects of L-ornithine on stress markers and sleep quality in healthy workers.Nutr J. 2014 Jun 3;13:53. doi: 10.1186/1475-2891-13-53. Nutr J. 2014. PMID: 24889392 Free PMC article. Clinical Trial.
-
Cortisol and DHEA-S are associated with startle potentiation during aversive conditioning in humans.Psychopharmacology (Berl). 2006 Jun;186(3):434-41. doi: 10.1007/s00213-005-0124-2. Epub 2005 Jul 29. Psychopharmacology (Berl). 2006. PMID: 16052364 Free PMC article. Clinical Trial.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources