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Glucocorticoid ultradian rhythmicity differentially regulates mood and resting state networks in the human brain: A randomised controlled clinical trial

Adrenal glucocorticoid secretion into the systematic circulation is characterised by a complex rhythm, composed of the diurnal variation, formed by changes in pulse amplitude of an underlying ultradian rhythm of short duration hormonal pulses. To elucidate the potential neurobiological significance...

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Autores principales: Kalafatakis, Konstantinos, Russell, Georgina M., Ferguson, Stuart G., Grabski, Meryem, Harmer, Catherine J., Munafò, Marcus R., Marchant, Nicola, Wilson, Aileen, Brooks, Jonathan C., Thakrar, Jamini, Murphy, Patrick, Thai, Ngoc J., Lightman, Stafford L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Pergamon Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7895801/
https://www.ncbi.nlm.nih.gov/pubmed/33296841
http://dx.doi.org/10.1016/j.psyneuen.2020.105096
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author Kalafatakis, Konstantinos
Russell, Georgina M.
Ferguson, Stuart G.
Grabski, Meryem
Harmer, Catherine J.
Munafò, Marcus R.
Marchant, Nicola
Wilson, Aileen
Brooks, Jonathan C.
Thakrar, Jamini
Murphy, Patrick
Thai, Ngoc J.
Lightman, Stafford L.
author_facet Kalafatakis, Konstantinos
Russell, Georgina M.
Ferguson, Stuart G.
Grabski, Meryem
Harmer, Catherine J.
Munafò, Marcus R.
Marchant, Nicola
Wilson, Aileen
Brooks, Jonathan C.
Thakrar, Jamini
Murphy, Patrick
Thai, Ngoc J.
Lightman, Stafford L.
author_sort Kalafatakis, Konstantinos
collection PubMed
description Adrenal glucocorticoid secretion into the systematic circulation is characterised by a complex rhythm, composed of the diurnal variation, formed by changes in pulse amplitude of an underlying ultradian rhythm of short duration hormonal pulses. To elucidate the potential neurobiological significance of glucocorticoid pulsatility in man, we have conducted a randomised, double-blind, placebo-controlled, three-way crossover clinical trial on 15 healthy volunteers, investigating the impact of different glucocorticoid rhythms on measures of mood and neural activity under resting conditions by recruiting functional neuroimaging, computerised behavioural tests and ecological momentary assessments. Endogenous glucocorticoid biosynthesis was pharmacologically suppressed, and plasma levels of corticosteroid restored by hydrocortisone replacement in three different regimes, either mimicking the normal ultradian and circadian profile of the hormone, or retaining the normal circadian but abolishing the ultradian rhythm of the hormone, or by our current best oral replacement regime which results in a suboptimal circadian and ultradian rhythm. Our results indicate that changes in the temporal mode of glucocorticoid replacement impact (i) the morning levels of self-perceived vigour, fatigue and concentration, (ii) the diurnal pattern of mood variation, (iii) the within-network functional connectivity of various large-scale resting state networks of the human brain, (iv) the functional connectivity of the default-mode, salience and executive control networks with glucocorticoid-sensitive nodes of the corticolimbic system, and (v) the functional relationship between mood variation and underlying neural networks. The findings indicate that the pattern of the ultradian glucocorticoid rhythm could affect cognitive psychophysiology under non-stressful conditions and opens new pathways for our understanding on the neuropsychological effects of cortisol pulsatility with relevance to the goal of optimising glucocorticoid replacement strategies.
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spelling pubmed-78958012021-03-02 Glucocorticoid ultradian rhythmicity differentially regulates mood and resting state networks in the human brain: A randomised controlled clinical trial Kalafatakis, Konstantinos Russell, Georgina M. Ferguson, Stuart G. Grabski, Meryem Harmer, Catherine J. Munafò, Marcus R. Marchant, Nicola Wilson, Aileen Brooks, Jonathan C. Thakrar, Jamini Murphy, Patrick Thai, Ngoc J. Lightman, Stafford L. Psychoneuroendocrinology Article Adrenal glucocorticoid secretion into the systematic circulation is characterised by a complex rhythm, composed of the diurnal variation, formed by changes in pulse amplitude of an underlying ultradian rhythm of short duration hormonal pulses. To elucidate the potential neurobiological significance of glucocorticoid pulsatility in man, we have conducted a randomised, double-blind, placebo-controlled, three-way crossover clinical trial on 15 healthy volunteers, investigating the impact of different glucocorticoid rhythms on measures of mood and neural activity under resting conditions by recruiting functional neuroimaging, computerised behavioural tests and ecological momentary assessments. Endogenous glucocorticoid biosynthesis was pharmacologically suppressed, and plasma levels of corticosteroid restored by hydrocortisone replacement in three different regimes, either mimicking the normal ultradian and circadian profile of the hormone, or retaining the normal circadian but abolishing the ultradian rhythm of the hormone, or by our current best oral replacement regime which results in a suboptimal circadian and ultradian rhythm. Our results indicate that changes in the temporal mode of glucocorticoid replacement impact (i) the morning levels of self-perceived vigour, fatigue and concentration, (ii) the diurnal pattern of mood variation, (iii) the within-network functional connectivity of various large-scale resting state networks of the human brain, (iv) the functional connectivity of the default-mode, salience and executive control networks with glucocorticoid-sensitive nodes of the corticolimbic system, and (v) the functional relationship between mood variation and underlying neural networks. The findings indicate that the pattern of the ultradian glucocorticoid rhythm could affect cognitive psychophysiology under non-stressful conditions and opens new pathways for our understanding on the neuropsychological effects of cortisol pulsatility with relevance to the goal of optimising glucocorticoid replacement strategies. Pergamon Press 2021-02 /pmc/articles/PMC7895801/ /pubmed/33296841 http://dx.doi.org/10.1016/j.psyneuen.2020.105096 Text en © 2020 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kalafatakis, Konstantinos
Russell, Georgina M.
Ferguson, Stuart G.
Grabski, Meryem
Harmer, Catherine J.
Munafò, Marcus R.
Marchant, Nicola
Wilson, Aileen
Brooks, Jonathan C.
Thakrar, Jamini
Murphy, Patrick
Thai, Ngoc J.
Lightman, Stafford L.
Glucocorticoid ultradian rhythmicity differentially regulates mood and resting state networks in the human brain: A randomised controlled clinical trial
title Glucocorticoid ultradian rhythmicity differentially regulates mood and resting state networks in the human brain: A randomised controlled clinical trial
title_full Glucocorticoid ultradian rhythmicity differentially regulates mood and resting state networks in the human brain: A randomised controlled clinical trial
title_fullStr Glucocorticoid ultradian rhythmicity differentially regulates mood and resting state networks in the human brain: A randomised controlled clinical trial
title_full_unstemmed Glucocorticoid ultradian rhythmicity differentially regulates mood and resting state networks in the human brain: A randomised controlled clinical trial
title_short Glucocorticoid ultradian rhythmicity differentially regulates mood and resting state networks in the human brain: A randomised controlled clinical trial
title_sort glucocorticoid ultradian rhythmicity differentially regulates mood and resting state networks in the human brain: a randomised controlled clinical trial
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7895801/
https://www.ncbi.nlm.nih.gov/pubmed/33296841
http://dx.doi.org/10.1016/j.psyneuen.2020.105096
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