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Mineralocorticoid receptors are indispensable for nongenomic modulation of hippocampal glutamate transmission by corticosterone

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Magnesium gates glutamate-activated channels in mouse central neurones

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NMDA and non-NMDA receptors are co-localized at individual excitatory synapses in cultured rat hippocampus

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Corticosteroid actions in hippocampus require DNA binding of glucocorticoid receptor homodimers

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Stress and the brain: from adaptation to disease

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Glucocorticoid receptor impairment alters CNS responses to a psychological stressor: an in vivo microdialysis study in transgenic mice

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Paired‐pulse facilitation and depression at unitary synapses in rat hippocampus: quantal fluctuation affects subsequent release.

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Dynamic Changes in Subcellular Localization of Mineralocorticoid Receptor in Living Cells: In Comparison with Glucocorticoid Receptor using Dual-Color Labeling with Green Fluorescent Protein Spectral Variants

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Corticosterone Peak is Responsible for Stress-Induced Elevation of Glutamate in the Hippocampus

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Time-Dependent Shifts in Neural Systems Supporting Decision-Making Under Stress

inferred← citeshttps://doi.org/10.1016/b978-0-12-809324-5.22064-6openalex-snapshot

Stress and Brain Aging: Role of Glucocorticoid and Mineralocorticoid Hormones

inferred← citeshttps://doi.org/10.1016/b978-0-12-811060-7.00012-7openalex-snapshot

Biological Embedding of Psychosocial Stress Over the Life Course

inferred← citeshttps://doi.org/10.1016/b978-0-12-813146-6.00004-7openalex-snapshot

Stress-Hyporesponsive Period

inferred← citeshttps://doi.org/10.1016/b978-0-12-813146-6.00008-4openalex-snapshot

Stress, Corticosterone, and Hippocampal Plasticity

inferred← citeshttps://doi.org/10.1016/b978-0-12-813146-6.00020-5openalex-snapshot

Stress and Glucocorticoids as Experience-Dependent Modulators of Huntington's Disease

inferred← citeshttps://doi.org/10.1016/b978-0-12-813156-5.00021-2openalex-snapshot

Mutations of the Human Mineralocorticoid Receptor and Targeted Deletion in Model Organisms

inferred← citeshttps://doi.org/10.1016/b978-0-12-813814-4.00028-6openalex-snapshot

Adrenal Cortex Hormones

inferred← citeshttps://doi.org/10.1016/b978-0-12-813983-7.00004-5openalex-snapshot

The brain mineralocorticoid receptor

inferred← citeshttps://doi.org/10.1016/b978-0-323-18907-1.00101-3openalex-snapshot

Aldosterone Secretion and Action

inferred← citeshttps://doi.org/10.1016/b978-0-443-13825-6.00219-3openalex-snapshot

Glucocorticoid receptor

inferred← citeshttps://doi.org/10.1016/b978-0-443-13825-6.00364-2openalex-snapshot

Effects of glucocorticoids on the brain

inferred← citeshttps://doi.org/10.1016/b978-008045046-9.00117-0openalex-snapshot

Neuroendocrine Aging: Pituitary-Adrenal Axis

inferred← citeshttps://doi.org/10.1016/b978-008088783-8.00041-3openalex-snapshot

Rapid Corticosteroid Actions on Behavior: Mechanisms and Implications

inferred← citeshttps://doi.org/10.1016/b978-008088783-8.00042-5openalex-snapshot

Corticosteroid Actions on Electrical Activity in the Limbic Brain

inferred← citeshttps://doi.org/10.1016/b978-008088783-8.00043-7openalex-snapshot

Molecular Genomics of Mineralocorticoid Action

inferred← citeshttps://doi.org/10.1016/b978-012370544-0.50016-1openalex-snapshot

Regulation of Bone Cell Function by Estrogens

inferred← citeshttps://doi.org/10.1016/b978-012373947-6.00097-0openalex-snapshot

Corticosteroid Receptors

inferred← citeshttps://doi.org/10.1016/b978-012373947-6.00658-9openalex-snapshot

Stress System Balance Hypothesis

inferred← citeshttps://doi.org/10.1016/b978-012373947-6.00701-7openalex-snapshot

Corticosteroid Receptor Genes: Functional Dissection in Mice

inferred← citeshttps://doi.org/10.1016/b978-1-4160-5583-9.00099-xopenalex-snapshot

Aldosterone

inferred← citeshttps://doi.org/10.1016/bs.ircmb.2019.03.004openalex-snapshot

Nongenomic glucocorticoid effects and their mechanisms of action in vertebrates

inferred← citeshttps://doi.org/10.1016/bs.vh.2018.11.001openalex-snapshot

Brain Mineralocorticoid Receptors and Resilience to Stress

inferred← citeshttps://doi.org/10.1016/bs.vh.2020.04.007openalex-snapshot

Stress and remodeling of hippocampal spine synapses

inferred← citeshttps://doi.org/10.1016/bs.vh.2023.06.005openalex-snapshot

The human glucocorticoid receptor

inferred← citeshttps://doi.org/10.1016/j.abb.2016.06.021openalex-snapshot

Insight into cognitive decline from Zn 2+ dynamics through extracellular signaling of glutamate and glucocorticoids

inferred← citeshttps://doi.org/10.1016/j.actpsy.2007.08.002openalex-snapshot

The influence of stress hormones on emotional memory: Relevance for psychopathology

inferred← citeshttps://doi.org/10.1016/j.alcohol.2015.03.008openalex-snapshot

Activation of mGluR2/3 following stress hormone exposure restores sensitivity to alcohol in rats

inferred← citeshttps://doi.org/10.1016/j.ando.2009.02.011openalex-snapshot

Various actions of aldosterone: The kidney and beyond…

inferred← citeshttps://doi.org/10.1016/j.animal.2024.101343openalex-snapshot

Investigating the correlation between phenotypes, adrenal transcriptome, and serum metabolism in laying ducks exhibiting varying behaviours under the same stressor

inferred← citeshttps://doi.org/10.1016/j.aquatox.2017.01.001openalex-snapshot

Metabolomics for informing adverse outcome pathways: Androgen receptor activation and the pharmaceutical spironolactone

inferred← citeshttps://doi.org/10.1016/j.bandc.2009.06.003openalex-snapshot

Investigations of HPA function and the enduring consequences of stressors in adolescence in animal models

inferred← citeshttps://doi.org/10.1016/j.bandc.2014.01.010openalex-snapshot

Brief, pre-retrieval stress differentially influences long-term memory depending on sex and corticosteroid response

inferred← citeshttps://doi.org/10.1016/j.bandc.2018.05.012openalex-snapshot

Interactive influence of sex, stressor timing, and the BclI glucocorticoid receptor polymorphism on stress-induced alterations of long-term memory

inferred← citeshttps://doi.org/10.1016/j.bandc.2018.11.009openalex-snapshot

Enhancing memory with stress: Progress, challenges, and opportunities

inferred← citeshttps://doi.org/10.1016/j.bbadis.2020.165821openalex-snapshot

Interplay between hormones and exercise on hippocampal plasticity across the lifespan

inferred← citeshttps://doi.org/10.1016/j.bbi.2006.11.006openalex-snapshot

An inflammatory review of glucocorticoid actions in the CNS

inferred← citeshttps://doi.org/10.1016/j.bbr.2010.06.001openalex-snapshot

Translating rodent behavioral repertoire to zebrafish (Danio rerio): Relevance for stress research

inferred← citeshttps://doi.org/10.1016/j.bbr.2012.02.036openalex-snapshot

Low-dose neonatal domoic acid causes persistent changes in behavioural and molecular indicators of stress response in rats

inferred← citeshttps://doi.org/10.1016/j.bbr.2018.04.027openalex-snapshot

Acute stress, but not corticosterone, facilitates acquisition of paired associates learning in rats using touchscreen-equipped operant conditioning chambers

inferred← citeshttps://doi.org/10.1016/j.bbr.2019.02.005openalex-snapshot

Coping with the forced swim stressor: Current state-of-the-art

inferred← citeshttps://doi.org/10.1016/j.bbr.2019.111980openalex-snapshot

Immediate pre-learning stress enhances baseline startle response and fear acquisition in a fear-potentiated startle paradigm

inferred← citeshttps://doi.org/10.1016/j.bbr.2021.113410openalex-snapshot

Stress, memory, and implications for major depression

inferred← citeshttps://doi.org/10.1016/j.biopsych.2006.07.007openalex-snapshot

Enhanced Long-Term Synaptic Depression in an Animal Model of Depression

inferred← citeshttps://doi.org/10.1016/j.biopsych.2010.02.013openalex-snapshot

Loss of Limbic System-Associated Membrane Protein Leads to Reduced Hippocampal Mineralocorticoid Receptor Expression, Impaired Synaptic Plasticity, and Spatial Memory Deficit

inferred← citeshttps://doi.org/10.1016/j.biopsych.2012.03.016openalex-snapshot

Maternal Care Influences Hippocampal N-Methyl-D-Aspartate Receptor Function and Dynamic Regulation by Corticosterone in Adulthood

inferred← citeshttps://doi.org/10.1016/j.biopsych.2012.11.009openalex-snapshot

The Action of Antidepressants on the Glutamate System: Regulation of Glutamate Release and Glutamate Receptors

inferred← citeshttps://doi.org/10.1016/j.biopsych.2013.06.022openalex-snapshot

Time-Dependent Effects of Cortisol on the Contextualization of Emotional Memories

inferred← citeshttps://doi.org/10.1016/j.biopsych.2021.04.010openalex-snapshot

Glucocorticoids Promote Fear Generalization by Increasing the Size of a Dentate Gyrus Engram Cell Population

inferred← citeshttps://doi.org/10.1016/j.biopsych.2023.08.026openalex-snapshot

LHPP in Glutamatergic Neurons of the Ventral Hippocampus Mediates Depression-like Behavior by Dephosphorylating CaMKIIα and ERK

inferred← citeshttps://doi.org/10.1016/j.biopsych.2023.11.008openalex-snapshot

Shaping Memories via Stress: A Synaptic Engram Perspective

inferred← citeshttps://doi.org/10.1016/j.biopsych.2024.02.005openalex-snapshot

Acute Stress Increases Striatal Connectivity With Cortical Regions Enriched for μ and κ Opioid Receptors

inferred← citeshttps://doi.org/10.1016/j.bpsc.2024.12.015openalex-snapshot

Multiscale Analysis Reveals Hippocampal Subfield Vulnerabilities to Chronic Cortisol Overexposure: Evidence From Cushing’s Disease

inferred← citeshttps://doi.org/10.1016/j.bpsgos.2025.100651openalex-snapshot

Mineralocorticoid Receptor in Glutamatergic Neurons Modulates Anxiety Exclusively in Male Mice Via Regulation of the Actin-Bundling Factor Fam107a

inferred← citeshttps://doi.org/10.1016/j.brainres.2009.02.017openalex-snapshot

The role of glucocorticoids for spiral ganglion neuron survival

inferred← citeshttps://doi.org/10.1016/j.brainres.2009.03.036openalex-snapshot

Corticosteroid effects on cellular physiology of limbic cells

inferred← citeshttps://doi.org/10.1016/j.brainres.2009.03.039openalex-snapshot

Glucocorticoid signaling and stress-related limbic susceptibility pathway: About receptors, transcription machinery and microRNA

inferred← citeshttps://doi.org/10.1016/j.brainres.2010.01.031openalex-snapshot

Repeated restraint-induced modulation of long-term potentiation in the dentate gyrus of the mouse

inferred← citeshttps://doi.org/10.1016/j.brainres.2011.12.049openalex-snapshot

Stress, neurotransmitters, corticosterone and body–brain integration

inferred← citeshttps://doi.org/10.1016/j.brainres.2012.03.053openalex-snapshot

Dysfunctional hippocampal activity affects emotion and cognition in mood disorders

inferred← citeshttps://doi.org/10.1016/j.brainres.2015.04.010openalex-snapshot

Tuning hippocampal synapses by stress-hormones: Relevance for emotional memory formation

inferred← citeshttps://doi.org/10.1016/j.brainres.2015.07.040openalex-snapshot

Exposure to prenatal stress has deleterious effects on hippocampal function in a febrile seizure rat model

inferred← citeshttps://doi.org/10.1016/j.brainres.2017.06.007openalex-snapshot

Methylprednisolone as a memory enhancer in rats: Effects on aversive memory, long-term potentiation and calcium influx

inferred← citeshttps://doi.org/10.1016/j.brainres.2019.146551openalex-snapshot

Long-term effects of the glucocorticoid receptor modulator CORT113176 in murine motoneuron degeneration

inferred← citeshttps://doi.org/10.1016/j.brainresbull.2011.05.008openalex-snapshot

Brief neck restraint stress enhances long-term potentiation and suppresses long-term depression in the dentate gyrus of the mouse

inferred← citeshttps://doi.org/10.1016/j.brainresbull.2020.06.001openalex-snapshot

Hippocampal mRNA expression profiling in mice exposed to chronic unpredictable mild stress

inferred← citeshttps://doi.org/10.1016/j.brainresrev.2007.02.006openalex-snapshot

Hippocampal formation: Shedding light on the influence of sex and stress on the brain

inferred← citeshttps://doi.org/10.1016/j.brainresrev.2007.08.005openalex-snapshot

Postnatal ontogeny of expression of the corticosteroid receptor genes in mammalian brains: Inter-species and intra-species differences

inferred← citeshttps://doi.org/10.1016/j.cell.2020.02.018openalex-snapshot

Long-Term Programming of CD8 T Cell Immunity by Perinatal Exposure to Glucocorticoids

inferred← citeshttps://doi.org/10.1016/j.coemr.2022.100380openalex-snapshot

Analysis of wearable time series data in endocrine and metabolic research

inferred← citeshttps://doi.org/10.1016/j.cub.2014.11.028openalex-snapshot

Reducing Social Stress Elicits Emotional Contagion of Pain in Mouse and Human Strangers

inferred← citeshttps://doi.org/10.1016/j.ejphar.2007.10.045openalex-snapshot

An anti-immobility effect of exogenous corticosterone in mice

inferred← citeshttps://doi.org/10.1016/j.ejphar.2007.11.064openalex-snapshot

Functional actions of corticosteroids in the hippocampus

inferred← citeshttps://doi.org/10.1016/j.ejphar.2007.11.070openalex-snapshot

Central corticosteroid actions: Search for gene targets

inferred← citeshttps://doi.org/10.1016/j.ejphar.2007.11.071openalex-snapshot

Central effects of stress hormones in health and disease: Understanding the protective and damaging effects of stress and stress mediators

inferred← citeshttps://doi.org/10.1016/j.ejphar.2007.11.072openalex-snapshot

Corticosteroid receptor polymorphisms: Determinants of vulnerability and resilience

inferred← citeshttps://doi.org/10.1016/j.ejphar.2007.11.073openalex-snapshot

The significance of glucocorticoid pulsatility

inferred← citeshttps://doi.org/10.1016/j.ejphar.2007.11.076openalex-snapshot

Selective transrepression versus transactivation mechanisms by glucocorticoid receptor modulators in stress and immune systems

inferred← citeshttps://doi.org/10.1016/j.ejphar.2008.01.060openalex-snapshot

Pharmacology of glucocorticoids: Beyond receptors

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