The mineralocorticoid receptor agonist, fludrocortisone, differentially inhibits pituitary-adrenal activity in humans with psychotic major depression. (Q36787614)

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scientific article published on 21 June 2012

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English	The mineralocorticoid receptor agonist, fludrocortisone, differentially inhibits pituitary-adrenal activity in humans with psychotic major depression.	scientific article published on 21 June 2012

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5 February 2020

The mineralocorticoid receptor agonist, fludrocortisone, differentially inhibits pituitary-adrenal activity in humans with psychotic major depression (English)

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5 February 2020

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fludrocortisone

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Rowena Gomez

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5 February 2020

Lakshika Tenakoon

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5 February 2020

Jennifer Keller

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5 February 2020

Gregory Cohen

5

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5 February 2020

Gordon H Williams

6

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5 February 2020

Alan F Schatzberg

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5 February 2020

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21 June 2012

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5 February 2020

Psychoneuroendocrinology

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5 February 2020

38

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5 February 2020

1

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5 February 2020

115-121

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5 February 2020

Modulation of the mineralocorticoid receptor as add-on treatment in depression: a randomized, double-blind, placebo-controlled proof-of-concept study

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The HPA axis in major depression: classical theories and new developments

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Corticosteroid receptor polymorphisms: determinants of vulnerability and resilience.

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Central CRH system in depression and anxiety--evidence from clinical studies with CRH1 receptor antagonists

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Mifepristone versus placebo in the treatment of psychosis in patients with psychotic major depression

1 reference

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Stress and the brain: from adaptation to disease

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A rating scale for depression

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Mineralocorticoid receptor function in major depression

1 reference

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24-Hour monitoring of cortisol and corticotropin secretion in psychotic and nonpsychotic major depression

1 reference

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Pituitary-adrenal and autonomic responses to stress in women after sexual and physical abuse in childhood

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The rationale for corticotropin-releasing hormone receptor (CRH-R) antagonists to treat depression and anxiety

1 reference

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29 September 2017

DST studies in psychotic depression: a meta-analysis

1 reference

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Do antidepressants stabilize mood through actions on the hypothalamic-pituitary-adrenocortical system?

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The dexamethasone suppression test for melancholia

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Long-term antidepressant administration alters corticotropin-releasing hormone, tyrosine hydroxylase, and mineralocorticoid receptor gene expression in rat brain. Therapeutic implications

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29 September 2017

Antiglucocorticoid treatment of depression: double-blind ketoconazole

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27 June 2018

A.E. Bennett Research Award. Regulation of serotonin1A, glucocorticoid, and mineralocorticoid receptor in rat and human hippocampus: implications for the neurobiology of depression

1 reference

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Antidepressants increase glucocorticoid and mineralocorticoid receptor mRNA expression in rat hippocampus in vivo

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Physiological activity and receptor binding of 9 alpha fluorohydrocortisone.

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27 June 2018

A 6-week randomized, placebo-controlled trial of CP-316,311 (a selective CRH1 antagonist) in the treatment of major depression

1 reference

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5 September 2018

The acute effects of a mineralocorticoid receptor (MR) agonist on nocturnal hypothalamic-adrenal-pituitary (HPA) axis activity in healthy controls

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5 September 2018

The neuropsychological profile of psychotic major depression and its relation to cortisol

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Metyrapone as additive treatment in major depression: a double-blind and placebo-controlled trial

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5 September 2018

The mineralocorticoid receptor agonist, fludrocortisone, inhibits pituitary-adrenal activity in humans after pre-treatment with metyrapone

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3633490

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An open label trial of C-1073 (mifepristone) for psychotic major depression

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Effects of the high-affinity corticotropin-releasing hormone receptor 1 antagonist R121919 in major depression: the first 20 patients treated

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1 reference

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12 December 2020

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10.1016/J.PSYNEUEN.2012.05.006

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5 February 2020

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5 February 2020

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