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Stress in the brain: implications for treatment of depression

Published online by Cambridge University Press:  11 July 2016

Er de Kloet*
Affiliation:
Department of Medical Pharmacology, LACDR/LUMC, Leiden University, the Netherlands

Abstract

A fundamental question in stress research is when the glucocorticoid stress hormone (cortisol in man) stops being neuroprotective and becomes harmful to the brain with negative consequences for cognition and mood. To address this question Section 1 focuses on the action mechanism of glucocorticoids. These hormones act via high and low affinity nuclear receptors, which regulate gene transcription in a coordinate manner. The receptors are expressed abundantly in hippocampus, amygdala and frontal cortex involved in cognitive processes. In Section 2 hypercortisolism is considered a potential disease factor for about 50% of the patients suffering from major depression. Recent data show that these patients recover within a few days when excess cortisol action is blocked with high doses of an antiglucocorticoid. Section 3 concerns animal models with ‘depression-like’ features of hypercorticism generated by manipulation of gene X environment inputs. Using gene expression profiling technology in the hippocampal transcriptome of these animals we identified about 700 potential targets for antidepressants out of 30 000 detectable gene products. One of our models is based on early life programming of the stress system. Rats exposed as pups to maternal deprivation display at senescence an enhanced individual difference in cognitive performance. The maternally deprived senescent animals age either successfully or become senile, at the expense of the average performance of non-deprived controls. The essay is concluded with the notion that the new generation of antidepressants ameliorates specific psychic dysfunctions (e.g. cognitive performance) linked to aberrant stress hormone action in discrete brain regions.

Type
Original Article
Copyright
Copyright © Blackwell Munksgaard 2002

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References

De Kloet, ER. Brain corticosteroid receptor balance and homeostatic control. Front Neuroendocrinol 1991;12: 95164. Google Scholar
McEwen, BS. Allostasis and allostatic load: implications for neuropsychopharmacology. Neuropsychopharmacology 2000;22: 108124.CrossRefGoogle ScholarPubMed
Sapolsky, R, Romero, LM, Munck, AU. How do glucocorticoids influence stress responses? Integrating permissive, suppressive, stimulatory and preparative actions. Endocr Rev 2000;21: 5589.Google ScholarPubMed
Seckl, JR. 11beta-hydroxysteroid dehydrogenase in the brain. a novel regulator of glucocorticoid action? Front Neuroendocrinol 1997;18: 4999.CrossRefGoogle Scholar
Reul, JMHM, De Kloet, ER. Two receptor systems for corticosterone in rat brain: microdistribution and differential occupation. Endocrinology 1985;117: 25022511. CrossRefGoogle ScholarPubMed
De Kloet, ER. Brain corticosteroid balance and homeostatic control. Front Neuroendocrinol 1991;12: 95164. Google Scholar
Hsu, SY, Hsueh, AJ. Human stresscopin and stresscopin-related peptide are selective ligands for the type 2 corticotropin-releasing hormone receptor. Nature Med 2001;7: 605611.CrossRefGoogle ScholarPubMed
Holsboer, F, Barden, N. Antidepressants and hypothalamic–pituitary–adrenocortical regulation. Endocr Rev 1996;17: 187205.CrossRefGoogle ScholarPubMed
Meijer, OC, Steenbergen, PJ, De Kloet, ER. Differential expression and regional distribution of steroid receptor co-activators SRC-1 and SRC-2 in brain and pituitary. Endocrinology 2000;141: 21922198.CrossRefGoogle Scholar
Wolkowitz, OM. Prospective controlled studies of the behavioural and biological effects of exogenous corticosteroids. Psychoneuroendocrinology 1994;19: 233255.CrossRefGoogle Scholar
Joëls, M, De Kloet, ER. Mineralocorticoid and glucocorticoid receptors in the brain: implications for ion permeability and transmitter systems. Prog Neurobiol 1994;43: 136.CrossRefGoogle ScholarPubMed
Karten, YJ, Nair, SM, Van Essen, I, Sibug, R, Joëls, M. Long-term exposure to high corticosterone levels attenuates serotonin responses in rat hippocampal CA1 neurones. Proc Natl Acad Sci USA 1999;96: 1345613461.CrossRefGoogle Scholar
Herman, JP, Cullinan, WE. Neurocircuitry of stress: central control of hypothalamo–pituitary–adrenocortical axis. Trends Neurosci 1997;20: 7884.CrossRefGoogle ScholarPubMed
Oitzl, MS, Fluttert, M, De Kloet, ER. The effect of corticosterone on reactivity to spatial novelty is mediated by central mineralocorticoisteroid receptors. Eur J Neurosci 1994;6: 10721079.CrossRefGoogle Scholar
Oitzl, MS, De Kloet, ER. Selective corticosteroid antagonists modulate specific aspects of spatial orientation learning. Behav Neurosci 1992;106: 6271.CrossRefGoogle ScholarPubMed
Oitzl, MS, Reichardt, HM, Joëls, M, De Kloet, ER. Point mutation in the mouse glucocorticoid receptor preventing DNA binding impairs spatial memory. Proc Natl Acad Sci USA 2001;98: 1279012795.CrossRefGoogle ScholarPubMed
De Kloet, ER, Oitzl, MS, Joëls, M. Stress and cognition. are corticosteroids good or bad guys? Trends Neurosci 1999;22: 422426.CrossRefGoogle ScholarPubMed
Holsboer, F, Lauer, CJ, Schreiber, W, Krieg, JC. Altered hypothalamic–pituitary–adrenocortical regulation in healthy subjects at high familial risk for depression. Neuroendocrinology 1995;62: 340347.CrossRefGoogle Scholar
Raadsheer, FC, Hoogendijk, WJG, Stam, FC, Tilders, FJH, Swaab, DF. Increased numbers of corticotrophin releasing expressing neurones in the paraventricular nucleus of depressed patients. Neuroendocrinology 1994;60: 436444.CrossRefGoogle Scholar
De Kloet, ER, Vreugdenhil, E, Oitzl, MS, Joëls, M. Glucocorticoid feedback resistance. Trends Endocrinol Metabol 1997;8: 2633. CrossRefGoogle ScholarPubMed
Meijer, OC, De Lange, ECM, Breimer, DD, De Boer, AG, Workel, JO, De Kloet, ER. Penetration of dexamethasone into brain glucocorticoid targets is enhanced in mdr1A P-glycoprotein knockout mice. Endocrinology 1998;139: 17891793.CrossRefGoogle ScholarPubMed
Rubin, RT, Phillips, JJ, Sadow, TF, McCracken, JT. Adrenal gland volume in major depression. Arch Gen Psychiatry 1995;52: 213218.CrossRefGoogle ScholarPubMed
Wolkowitz, OM, Epel, ES, Reus, VI. Stress hormone-related psychopathology: pathophysiological and treatment implications. World J Biol Psych 2001;2: 115144. CrossRefGoogle ScholarPubMed
Lupien, SJ, Lecours, A, Lussier, I, Schwartz, G, Nair, N, Meaney, M. Basal cortisol levels and cognitive deficits in human aging. J Neurosci 1994;14: 28932903.Google ScholarPubMed
Lupien, SJ, McEwen, BS. The acute effects of corticosteroids on cognition: integration of animal and human studies. Brain Res Rev 1997;24: 127.CrossRefGoogle Scholar
Reul, JM, Stec, I, Soder, M, Holsboer, F. Chronic treatment of rats with the anti-depressant amitryptiline attenuates the activity of the hypothalamic–pituitary–adrenal activity. Endocrinology 1993;133: 312320.CrossRefGoogle Scholar
Thakore, JH, Dinan, TG. Cortisol synthesis inhibition: a new treatment strategy for the clinical and endocrine manifestations of depression. Biol Psychiatry 1995;37: 364368.CrossRefGoogle Scholar
Belanoff, JK, Flores, B, Kalezhan, M, Sund, B, Schatzberg, AF. Rapid reversal of psychotic depression using mifepristone. J Clin Psychopharmacol 2001;21: 516521.CrossRefGoogle ScholarPubMed
Holsboer, F. Anti-depressant drug discovery in the postgenomic era. World J Biol Psych 2001;2: 165178. CrossRefGoogle Scholar
De Kloet, ER, Wallach, G, McEwen, BS. Difference in binding of corticosterone and dexamethasone to rat brain and pituitary. Endocrinology 1975;96: 598611.CrossRefGoogle Scholar
Ratka, A, Sutanto, W, Bloemers, M, De Kloet, ER. On the role of mineralocorticoid (type 1) and glucocorticoid (type 2) receptors in neuroendocrine regulation. Neuroendocrinologyn 1989;50: 117123. CrossRefGoogle ScholarPubMed
Checkley, S. The neuroendocrinology of depression and chronic stress. Br Med Bull 1996;52: 597617.CrossRefGoogle ScholarPubMed
Grootendorst, J, De Kloet, ER, Vossen, C, Dalm, S, Oitzl, MS. Reversal of cognitive deficit of apolipoprotein E knockout mice after repeated exposure to a common environmental experience. Neuroscience 2001;108: 237247.CrossRefGoogle ScholarPubMed
Gesing, A, Bilang-Bleuel, A, Droste, SK, Linthorst, AC, Holsboer, F, Reul, JM. Psychological stress increases hippocampal mineralocorticoid receptor levels: involvement of corticotropin releasing hormone. J Neurosci 2001;21: 48224829.Google ScholarPubMed
Van Haarst, AD, Oitzl, MS, Workel, JO, De Kloet, ER. Chronic brain glucocorticoid receptor blockade enhances the rise in circadian and stress-induced pituitary–adrenal activity. Endocrinology 1996;137: 49354943.CrossRefGoogle ScholarPubMed
Oitzl, MS, Van Haarst, AD, Sutanto, W, De Kloet, ER. Corticosterone, brain mineralocorticoid receptors (MRs) and the activity of the hypothalamic–pituitary–adrenal (HPA) axis: the Lewis rat as an example of increased central MR capacity and a hyporesponsive HPA axis. Psychoneuroendocrinology 1995;20: 655677.CrossRefGoogle Scholar
Rots, NY, Cools, AR, Oitzl, MS, De Jong, J, Sutanto, W, De Kloet, ER. Divergent prolactin and pituitary–adrenal activity in rats selectively bred for different dopamine responsiveness. Endocrinology 1996;137: 16781686.CrossRefGoogle ScholarPubMed
Benus, RF, Bohus, B, Koolhaas, JM, Van Oortmerssen, GA. Behavioural differences between artificially selected aggressive and non-aggressive mice: response to apomorphine. Behav Brain Res 1991;43: 203208.CrossRefGoogle ScholarPubMed
Veenema, AH, Meijer, OC, De Kloet, ER, Koolhaas, JM. Differences in basal and stress-induced HPA regulation of wild house mice selected for high and low aggression. Horm Behav, in press.Google Scholar
Levine, S, Dent, G, De Kloet, ER. Stress-hyporesponsive period. In: Fink, G, ed. Encyclopedia of stress, vol. 3. New York: Academic Press, 2000, 518526. Google Scholar
Hofer, M. On the relationship between attachment and separation processes in infancy. In: Plutnik, R, Emtion, B, eds. Early development. New York: Academic Press, 1993, 199219. Google ScholarPubMed
Van Oers, HJJ, De Kloet, ER, Whelan, T, Levine, S. Maternal deprivation effect on the infants neural stress markers is reversed by tactile stimulation and feeding but not by suppressing corticosterone. J Neurosci 1998;18: 1017110179.Google Scholar
Rots, NY, De Jong, J, Workel, JO, Levine, S, Cools, AR, De Kloet, ER. Neonatal maternally deprived rats have as adults elevated basal pituitary-adrenal activity and enhanced susceptibility to apomorphine. J Neuroendocrinol 1996;8: 501506.CrossRefGoogle Scholar
Meaney, MJ, Aitken, DH, Van Berkel, C, Sapolsky, RM. Effect of neonatal handling on age-related impairments associated with the hippocampus. Science 1988;239: 766768.CrossRefGoogle ScholarPubMed
Oitzl, MS, Workel, JO, Fluttert, M, Frösch, F, De Kloet, ER. Maternal deprivation affects behaviour from youth to senescence: amplification of individual differences in spatial learning and memory in senescent brown Norway rats. Eur J Neuroscience 2000;34: 372378. Google Scholar
Workel, JO, Oitzl, MS, Fluttert, M, Lesscher, H, Karssen, A, De Kloet, ER. Differential and age-dependent effects of maternal deprivation on the hypothalamic–pituitary–adrenal axis of brown norway rats from youth to senescence. J Neuroendocrinol 2001;13: 113.CrossRefGoogle Scholar
Rinne, TH, De Kloet, ER, Goekoop, J, De Rijk, R, Van Den Brink, W. Persistent effect of severe childhood abuse on the hypothalamus–pituitary–adrenal axis of adult female borderline patients. Biol Psychiatry in press. Google Scholar
Van Praag, HM, Van Os, J, Leonard, BE, De Kloet, ER. Stress and Depression,in press. Google Scholar
Datson, NA, Van Der Perk, J, De Kloet, ER, Vreugdenhil, E. Expression profile of 30,000 genes in rat hippocampus using SAGE. Hippocampus 2001;11: 430444.CrossRefGoogle ScholarPubMed
Datson, NA, Van Der Perk, J, De Kloet, ER, Vreugdenhil, E. Identification of corticosteroid responsive genes in rat hippocampus using serial analysis of gene expression. Eur J Neuroscience 2001;14: 117. CrossRefGoogle ScholarPubMed
Karssen, AM, Meijer, OC, Van Der Sandt, ICJ, Lucassen, PJ, De Lange, ECM, De Boer, AG, De Kloet, ER. Multidrug resistance P-glycoprotein hampers the access of cortisol but not of corticosterone to mouse and human brain. Endocrinology 2001;142: 26862694.CrossRefGoogle Scholar
Joëls, M, De Kloet, ER. Effects of glucocorticoids and norepinephrine in the excitability in the hippocampus. Science 1989;245: 15021505.CrossRefGoogle ScholarPubMed
Joëls, M, Hesen, W, De Kloet, ER. Mineralcorticoid hormones suppress serotonin-induced hyperpolarization of rat hippocampal CA1 neurons. J Neuroscience 1991;11: 22852294. Google Scholar