Literature DB >> 28862266

Genomic and epigenomic mechanisms of glucocorticoids in the brain.

Jason D Gray1, Joshua F Kogan1, Jordan Marrocco1, Bruce S McEwen1.   

Abstract

Following the discovery of glucocorticoid receptors in the hippocampus and other brain regions, research has focused on understanding the effects of glucocorticoids in the brain and their role in regulating emotion and cognition. Glucocorticoids are essential for adaptation to stressors (allostasis) and in maladaptation resulting from allostatic load and overload. Allostatic overload, which can occur during chronic stress, can reshape the hypothalamic-pituitary-adrenal axis through epigenetic modification of genes in the hippocampus, hypothalamus and other stress-responsive brain regions. Glucocorticoids exert their effects on the brain through genomic mechanisms that involve both glucocorticoid receptors and mineralocorticoid receptors directly binding to DNA, as well as by non-genomic mechanisms. Furthermore, glucocorticoids synergize both genomically and non-genomically with neurotransmitters, neurotrophic factors, sex hormones and other stress mediators to shape an organism's present and future responses to a stressful environment. Here, we discuss the mechanisms of glucocorticoid action in the brain and review how glucocorticoids interact with stress mediators in the context of allostasis, allostatic load and stress-induced neuroplasticity.

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Year:  2017        PMID: 28862266     DOI: 10.1038/nrendo.2017.97

Source DB:  PubMed          Journal:  Nat Rev Endocrinol        ISSN: 1759-5029            Impact factor:   43.330


  193 in total

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Review 3.  Stress and the dynamic genome: Steroids, epigenetics, and the transposome.

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Review 4.  Mitochondrial allostatic load puts the 'gluc' back in glucocorticoids.

Authors:  Martin Picard; Robert-Paul Juster; Bruce S McEwen
Journal:  Nat Rev Endocrinol       Date:  2014-03-25       Impact factor: 43.330

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6.  GRKO mice express an aberrant dexamethasone-binding glucocorticoid receptor, but are profoundly glucocorticoid resistant.

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7.  Steroid receptor coactivator-1 splice variants differentially affect corticosteroid receptor signaling.

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2.  Sex-specific deficits in biochemical but not behavioral responses to delay fear conditioning in prenatal alcohol exposure mice.

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5.  Dual-release hydrocortisone and its benefits on cognitive function and quality of sleep.

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6.  Brain Differences in the Prefrontal Cortex, Amygdala, and Hippocampus in Youth with Congenital Adrenal Hyperplasia.

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Review 7.  Minimally-invasive methods for examining biological changes in response to chronic stress: A scoping review.

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Review 8.  The hypothalamic-pituitary-adrenal axis as a substrate for stress resilience: Interactions with the circadian clock.

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