Plasticity of the Hippocampus: Adaptation to Chronic Stress and Allostatic Load

Abstract: The hippocampus is an important structure for declarative, spatial, and contextual memory and is implicated in the perception of chronic pain. The hippocampal formation is vulnerable to damage from seizures, ischemia, and head trauma and is particularly sensitive to the effects of adrenal glucocorticoids secreted during the diurnal rhythm and chronic stress. Adrenal steroids typically have adaptive effects in the short run, but promote pathophysiology when there is either repeated stress or dysregulation of the HPA axis. The damaging actions of glucocorticoids under such conditions have been termed “allostatic load”, referring to the cost to the body of adaptation to adverse conditions. Adrenal steroids display both protective and damaging effects in the hippocampus. They biphasically modulate excitability of hippocampal neurons, and high glucocorticoid levels and severe acute stress impair declarative memory in a reversible manner. The hippocampus also displays structural plasticity, involving ongoing neurogenesis of the dentate gyrus, synaptogenesis under control of estrogens in the CA1 region, and dendritic remodeling caused by repeated stress or elevated levels of exogenous glucocorticoids in the CA3 region. In all three forms of structural plasticity, excitatory amino acids participate along with circulating steroid hormones. Glucocorticoids and stressors suppress neurogenesis in the dentate gyrus. They also potentiate the damage produced by ischemia and seizures. Moreover, the aging rat hippocampus displays elevated and prolonged levels of excitatory amino acids released during acute stress. Our working hypothesis is that structural plasticity in response to repeated stress starts out as an adaptive and protective response, but ends up as damage if the imbalance in the regulation of the key mediators is not resolved. It is likely that morphological rearrangements in the hippocampus brought on by various types of allostatic load alter the manner in which the hippocampus participates in memory functions and it is conceivable that these may also have a role in chronic pain perception.

[1]  Schwartz,et al.  Basal cortisol levels and cognitive deficits in human aging , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[2]  Bruce S. McEwen,et al.  Stress induces atrophy of apical dendrites of hippocampal CA3 pyramidal neurons , 1992, Brain Research.

[3]  A. Convit,et al.  Cortisol levels during human aging predict hippocampal atrophy and memory deficits , 1998, Nature Neuroscience.

[4]  C. Pavlides,et al.  Genetic Inactivation of the Serotonin1A Receptor in Mice Results in Downregulation of Major GABAA Receptor α Subunits, Reduction of GABAA Receptor Binding, and Benzodiazepine-Resistant Anxiety , 2000, The Journal of Neuroscience.

[5]  D. Jezova,et al.  Stress-induced changes in messenger RNA levels of N-methyl-d-aspartate and AMPA receptor subunits in selected regions of the rat hippocampus and hypothalamus , 1995, Neuroscience.

[6]  B. McEwen,et al.  Stress-induced atrophy of apical dendrites of hippocampal CA3c neurons: Comparison of stressors , 1995, Neuroscience.

[7]  R. Sapolsky,et al.  Glucocortcoids mediate the stress-induced extracellular accumulation of glutamate , 1994, Brain Research.

[8]  J. McCord,et al.  Oxygen-derived free radicals in postischemic tissue injury. , 1985, The New England journal of medicine.

[9]  D C Blanchard,et al.  Chronic social stress reduces dendritic arbors in CA3 of hippocampus and decreases binding to serotonin transporter sites , 2000, Synapse.

[10]  B. Roth,et al.  Morphometric evidence for neuronal and glial prefrontal cell pathology in major depression∗ ∗ See accompanying Editorial, in this issue. , 1999, Biological Psychiatry.

[11]  S. Berent,et al.  Hippocampal formation volume, memory dysfunction, and cortisol levels in patients with Cushing's syndrome , 1992, Biological Psychiatry.

[12]  M. Raichle,et al.  Subgenual prefrontal cortex abnormalities in mood disorders , 1997, Nature.

[13]  M. Marinelli,et al.  Inhibition of corticosterone synthesis by Metyrapone decreases cocaine-induced locomotion and relapse of cocaine self-administration , 1994, Brain Research.

[14]  H. Fukuzako,et al.  Reduction in hippocampal formation volume is caused mainly by its shortening in chronic schizophrenia: Assessment by MRI , 1996, Biological Psychiatry.

[15]  E. Gould,et al.  Neurogenesis in the Dentate Gyrus of the Adult Tree Shrew Is Regulated by Psychosocial Stress and NMDA Receptor Activation , 1997, The Journal of Neuroscience.

[16]  Y. Ikegaya,et al.  The Basomedial and Basolateral Amygdaloid Nuclei Contribute to the Induction of Long‐term Potentiation in the Dentate Gyrus In Vivo , 1996, The European journal of neuroscience.

[17]  T. Yaksh,et al.  Concurrent mapping of brain sites for sensitivity to the direct application of morphine and focal electrical stimulation in the production of antinociception in the rat , 1977, Pain.

[18]  R. Kikinis,et al.  Magnetic resonance imaging study of hippocampal volume in chronic, combat-related posttraumatic stress disorder , 1996, Biological Psychiatry.

[19]  C. McKittrick,et al.  Serotonin receptor binding in a colony model of chronic social stress , 1995, Biological Psychiatry.

[20]  M. Meaney,et al.  Early environmental programming hypothalamic-pituitary-adrenal responses to stress , 1994 .

[21]  S. Khanna,et al.  Noxious stimuli produce prolonged changes in the CA1 region of the rat hippocampus , 1989, Pain.

[22]  Yvette I. Sheline,et al.  Depression Duration But Not Age Predicts Hippocampal Volume Loss in Medically Healthy Women with Recurrent Major Depression , 1999, The Journal of Neuroscience.

[23]  R. Spengler,et al.  Brain-derived TNFα: involvement in neuroplastic changes implicated in the conscious perception of persistent pain , 2000, Brain Research.

[24]  B. McEwen,et al.  Selective Retention of Corticosterone by Limbic Structures in Rat Brain , 1968, Nature.

[25]  C. McKittrick,et al.  Chronic Social Stress Alters Levels of Corticotropin-Releasing Factor and Arginine Vasopressin mRNA in Rat Brain , 1997, The Journal of Neuroscience.

[26]  M. Joëls,et al.  Brain corticosteroid receptor balance in health and disease. , 1998, Endocrine reviews.

[27]  F. Gage,et al.  [New nerve cells for the adult brain. Adult neurogenesis and stem cell concepts in neurologic research]. , 1998, Der Nervenarzt.

[28]  B. McEwen Stress and hippocampal plasticity. , 1999, Annual review of neuroscience.

[29]  H Eichenbaum,et al.  How Does the Brain Organize Memories? , 1997, Science.

[30]  J. Price,et al.  Neuroimaging abnormalities in the subgenual prefrontal cortex: implications for the pathophysiology of familial mood disorders , 1998, Molecular Psychiatry.

[31]  R Hen,et al.  Serotonin receptor 1A knockout: an animal model of anxiety-related disorder. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[32]  Bruce S. McEwen,et al.  Repeated stress causes reversible impairments of spatial memory performance , 1994, Brain Research.

[33]  M. Zigmond,et al.  Prior exposure to chronic stress results in enhanced synthesis and release of hippocampal norepinephrine in response to a novel stressor , 1991, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[34]  S. Ogawa,et al.  Role of adrenal steroid mineralocorticoid and glucocorticoid receptors in long-term potentiation in the CA1 field of hippocampal slices , 1996, Brain Research.

[35]  J. Korf,et al.  Mild stress stimulates rat hippocampal glucose utilization transiently via NMDA receptors, as assessed by lactography , 1988, Brain Research.

[36]  P. Tanapat,et al.  Chronic corticosterone treatment induces parallel changes in N-methyl-d-aspartate receptor subunit messenger RNA levels and antagonist binding sites in the hippocampus , 1997, Neuroscience.

[37]  Richard S. J. Frackowiak,et al.  Navigation-related structural change in the hippocampi of taxi drivers. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[38]  P. Sterling,et al.  Allostasis: A new paradigm to explain arousal pathology. , 1988 .

[39]  R. Blanchard,et al.  Effects of limbic lesions on passive avoidance and reactivity to shock. , 1968, Journal of comparative and physiological psychology.

[40]  D. Diamond,et al.  Psychological stress repeatedly blocks hippocampal primed burst potentiation in behaving rats , 1994, Behavioural Brain Research.

[41]  D. Men,et al.  Effect of prenatal stress on plasma corticosterone and catecholamines in response to footshock in rats , 1998, Physiology & Behavior.

[42]  Yvette I. Sheline,et al.  Amygdala core nuclei volumes are decreased in recurrent major depression , 1998, Neuroreport.

[43]  B. McEwen,et al.  Stress and the individual. Mechanisms leading to disease. , 1993, Archives of internal medicine.

[44]  E. Abercrombie,et al.  Characterization of hippocampal norepinephrine release as measured by microdialysis perfusion: Pharmacological and behavioral studies , 1988, Neuroscience.

[45]  Victor H. Denenberg,et al.  Physiological and behavioral effects of infantile stimulation , 1967 .

[46]  T. J. Nickola,et al.  Brain-derived TNFα mediates neuropathic pain , 1999, Brain Research.

[47]  Y. Watanabe,et al.  Tianeptine attenuates stress-induced morphological changes in the hippocampus. , 1992, European journal of pharmacology.

[48]  B. McEwen,et al.  Stress-induced atrophy of apical dendrites of hippocampal CA3c neurons: Involvement of glucocorticoid secretion and excitatory amino acid receptors , 1995, Neuroscience.

[49]  Jeffrey A. Lieberman,et al.  Hippocampus-amygdala volumes and psychopathology in chronic schizophrenia , 1993, Biological Psychiatry.

[50]  R. Melzack,et al.  Analgesia produced by lidocaine microinjection into the dentate gyms , 1992, Pain.

[51]  M. Albert,et al.  Journal of Clinical Endocrinology and Metabolism Printed in U.S.A. Copyright © 1997 by The Endocrine Society Increase in Urinary Cortisol Excretion and Memory Declines: MacArthur Studies of Successful Aging* , 2022 .

[52]  B. McEwen,et al.  The neuroendocrinology of stress and aging: the glucocorticoid cascade hypothesis. , 1986, Endocrine reviews.

[53]  P. Landfield,et al.  Evolving aspects of the glucocorticoid hypothesis of brain aging: Hormonal modulation of neuronal calcium homeostasis , 1994, Neurobiology of Aging.

[54]  Elizabeth Gould,et al.  Regulation of hippocampal neurogenesis in adulthood , 2000, Biological Psychiatry.

[55]  D. Williamson,et al.  Relationship of childhood abuse and household dysfunction to many of the leading causes of death in adults. The Adverse Childhood Experiences (ACE) Study. , 1998, American journal of preventive medicine.

[56]  G M Rose,et al.  Psychological stress impairs spatial working memory: relevance to electrophysiological studies of hippocampal function. , 1996, Behavioral neuroscience.

[57]  J. L. Hess,et al.  Modification of the corticosterone response curve as a function of handling in infancy , 1969 .

[58]  W. A. Prado,et al.  An assessment of the antinociceptive and aversive effects of stimulating identified sites in the rat brain , 1985, Brain Research.

[59]  B. Yamamoto,et al.  Effect of Acute Stress on Hippocampal Glutamate Levels and Spectrin Proteolysis in Young and Aged Rats , 1995, Journal of neurochemistry.

[60]  J. Csernansky,et al.  Hippocampal atrophy in recurrent major depression. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[61]  G. Buzsáki,et al.  Hippocampal responses evoked by tooth pulp and acoustic stimulation: Depth profiles and effect of behavior , 1986, Brain Research.

[62]  M. Mattson,et al.  Roles of Lipid Peroxidation in Modulation of Cellular Signaling Pathways, Cell Dysfunction, and Death in the Nervous System , 1998, Reviews in the neurosciences.

[63]  Clemens Kirschbaum,et al.  Persistent High Cortisol Responses to Repeated Psychological Stress in a Subpopulation of Healthy Men , 1995, Psychosomatic medicine.

[64]  R. Ader Effects of early experiences on emotional and physiological reactivity in the rat. , 1968, Journal of comparative and physiological psychology.

[65]  Stephen Maren,et al.  Long-term potentiation in the amygdala: a mechanism for emotional learning and memory , 1999, Trends in Neurosciences.

[66]  B. McEwen,et al.  Chronic Psychosocial Stress Causes Apical Dendritic Atrophy of Hippocampal CA3 Pyramidal Neurons in Subordinate Tree Shrews , 1996, The Journal of Neuroscience.

[67]  B. McEwen,et al.  Estrogen actions in the central nervous system. , 1999, Endocrine reviews.

[68]  B. McEwen Protective and damaging effects of stress mediators. , 1998, The New England journal of medicine.

[69]  C. McKittrick,et al.  Chronic social stress: Changes in behavioral and physiological indices of emotion , 1998 .

[70]  T. Shors,et al.  Effect of adrenalectomy and demedullation on the stress-induced impairment of long-term potentiation. , 1990, Neuroendocrinology.

[71]  R. McKay,et al.  Restoring production of hippocampal neurons in old age , 1999, Nature Neuroscience.

[72]  C. McKittrick,et al.  Stress and the Brain: A Paradoxical Role for Adrenal Steroids , 1995 .

[73]  B. McEwen,et al.  Effects of antidepressants and benzodiazepine treatments on the dendritic structure of CA3 pyramidal neurons after chronic stress. , 1999, European journal of pharmacology.

[74]  Joseph E LeDoux,et al.  Repeated restraint stress facilitates fear conditioning independently of causing hippocampal CA3 dendritic atrophy. , 1999, Behavioral neuroscience.

[75]  B. Mcewen,et al.  Proliferation of granule cell precursors in the dentate gyrus of adult monkeys is diminished by stress. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[76]  B. McEwen,et al.  Controversies surrounding glucocorticoid-mediated cell death in the hippocampus , 1997, Journal of Chemical Neuroanatomy.

[77]  Robert M. Sapolsky,et al.  Stress, the Aging Brain, and the Mechanisms of Neuron Death , 1992 .

[78]  W. Abraham,et al.  Modulation of hippocampal long-term potentiation and long-term depression by corticosteroid receptor activation , 1994, Psychobiology.

[79]  D. Choi Calcium-mediated neurotoxicity: relationship to specific channel types and role in ischemic damage , 1988, Trends in Neurosciences.

[80]  Richard F. Thompson,et al.  Inescapable versus escapable shock modulates long-term potentiation in the rat hippocampus. , 1989, Science.

[81]  Bruno Giordani,et al.  Decrease in cortisol reverses human hippocampal atrophy following treatment of Cushing’s disease , 1999, Biological Psychiatry.

[82]  R. Sapolsky,et al.  Effect of neonatal handling on age-related impairments associated with the hippocampus. , 1988, Science.

[83]  Joseph E. LeDoux,et al.  In search of an emotional system in the brain: Leaping from fear to emotion and consciousness. , 1995 .

[84]  C. McKittrick,et al.  Effects of chronic social stress on tyrosine hydroxylase mRNA and protein levels. , 1995, Brain research. Molecular brain research.

[85]  M. Marinelli,et al.  Progeny of mothers drinking corticosterone during lactation has lower stress-induced corticosterone secretion and better cognitive performance , 1993, Brain Research.

[86]  B. Yamamoto,et al.  Rapid Communication: Adrenalectomy Attenuates Stress‐Induced Elevations in Extracellular Glutamate Concentrations in the Hippocampus , 1993, Journal of neurochemistry.

[87]  S. Southwick,et al.  MRI-based measurement of hippocampal volume in patients with combat-related posttraumatic stress disorder. , 1995, The American journal of psychiatry.

[88]  F. Gage,et al.  New nerve cells for the adult brain. , 1999, Scientific American.

[89]  T. Bliss,et al.  A synaptic model of memory: long-term potentiation in the hippocampus , 1993, Nature.

[90]  B L McNaughton,et al.  Circadian rhythm of synaptic excitability in rat and monkey central nervous system. , 1977, Science.

[91]  B. McEwen,et al.  Chronic stress impairs rat spatial memory on the Y maze, and this effect is blocked by tianeptine pretreatment. , 1996, Behavioral neuroscience.

[92]  J. Korf,et al.  Effects of stress and exercise on rat hippocampus and striatum extracellular lactate. , 1990, The American journal of physiology.

[93]  P. Piazza,et al.  Individual differences in the psychomotor effects of morphine are predicted by reactivity to novelty and influenced by corticosterone secretion , 1993, Brain Research.

[94]  H. Simon,et al.  Reactivity to novelty during youth as a predictive factor of cognitive impairment in the elderly: a longitudinal study in rats , 1994, Brain Research.

[95]  E. Gould,et al.  Learning enhances adult neurogenesis in the hippocampal formation , 1999, Nature Neuroscience.