Literature DB >> 14596810

Central mechanisms of stress integration: hierarchical circuitry controlling hypothalamo-pituitary-adrenocortical responsiveness.

James P Herman1, Helmer Figueiredo, Nancy K Mueller, Yvonne Ulrich-Lai, Michelle M Ostrander, Dennis C Choi, William E Cullinan.   

Abstract

Appropriate regulatory control of the hypothalamo-pituitary-adrenocortical stress axis is essential to health and survival. The following review documents the principle extrinsic and intrinsic mechanisms responsible for regulating stress-responsive CRH neurons of the hypothalamic paraventricular nucleus, which summate excitatory and inhibitory inputs into a net secretory signal at the pituitary gland. Regions that directly innervate these neurons are primed to relay sensory information, including visceral afferents, nociceptors and circumventricular organs, thereby promoting 'reactive' corticosteroid responses to emergent homeostatic challenges. Indirect inputs from the limbic-associated structures are capable of activating these same cells in the absence of frank physiological challenges; such 'anticipatory' signals regulate glucocorticoid release under conditions in which physical challenges may be predicted, either by innate programs or conditioned stimuli. Importantly, 'anticipatory' circuits are integrated with neural pathways subserving 'reactive' responses at multiple levels. The resultant hierarchical organization of stress-responsive neurocircuitries is capable of comparing information from multiple limbic sources with internally generated and peripherally sensed information, thereby tuning the relative activity of the adrenal cortex. Imbalances among these limbic pathways and homeostatic sensors are likely to underlie hypothalamo-pituitary-adrenocortical dysfunction associated with numerous disease processes.

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Year:  2003        PMID: 14596810     DOI: 10.1016/j.yfrne.2003.07.001

Source DB:  PubMed          Journal:  Front Neuroendocrinol        ISSN: 0091-3022            Impact factor:   8.606


  441 in total

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2.  Effects of developmental stress and lead (Pb) on corticosterone after chronic and acute stress, brain monoamines, and blood Pb levels in rats.

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Journal:  J Neurosci       Date:  2014-11-12       Impact factor: 6.167

4.  Elevated glucocorticoid levels are responsible for induction of tyrosine hydroxylase mRNA expression, phosphorylation, and enzyme activity in the nucleus of the solitary tract during morphine withdrawal.

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Review 5.  Genomic and epigenomic mechanisms of glucocorticoids in the brain.

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6.  Sex-dependent role of the amygdala in the development of emotional and neuroendocrine reactivity to threatening stimuli in infant and juvenile rhesus monkeys.

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Journal:  Horm Behav       Date:  2013-02-01       Impact factor: 3.587

7.  Brain organic cation transporter 2 controls response and vulnerability to stress and GSK3β signaling.

Authors:  T Couroussé; A Bacq; C Belzung; B Guiard; L Balasse; F Louis; A-M Le Guisquet; A M Gardier; A H Schinkel; B Giros; S Gautron
Journal:  Mol Psychiatry       Date:  2014-08-05       Impact factor: 15.992

Review 8.  Anteroventral bed nuclei of the stria terminalis neurocircuitry: Towards an integration of HPA axis modulation with coping behaviors - Curt Richter Award Paper 2017.

Authors:  Jason J Radley; Shane B Johnson
Journal:  Psychoneuroendocrinology       Date:  2017-12-24       Impact factor: 4.905

Review 9.  Stress reactivity after traumatic brain injury: implications for comorbid post-traumatic stress disorder.

Authors:  Ann N Hoffman; Anna N Taylor
Journal:  Behav Pharmacol       Date:  2019-04       Impact factor: 2.293

10.  Age-related dendritic hypertrophy and sexual dimorphism in rat basolateral amygdala.

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Journal:  Neurobiol Aging       Date:  2007-06-14       Impact factor: 4.673

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