Conditioning cortisol in humans: design and pilot study of a randomized controlled trial
Abstract Background Conditioning of physiological responses can be achieved by repeatedly pairing a previously neutral conditioned stimulus with the administration of a pharmacologically salient unconditioned stimulus. This type of conditioning has been effective for specific immune and endocrine re...
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doaj-678b710f11424630ad91bd21ef6093d82020-11-25T01:06:36ZengBMCPilot and Feasibility Studies2055-57842019-01-015111010.1186/s40814-018-0382-5Conditioning cortisol in humans: design and pilot study of a randomized controlled trialJ. Tekampe0H. van Middendorp1F. C. G. J. Sweep2S. H. P. P. Roerink3A. R. M. M. Hermus4A. W. M. Evers5Health, Medical and Neuropsychology Unit, Faculty of Social and Behavioural Sciences, Institute of Psychology, Leiden UniversityHealth, Medical and Neuropsychology Unit, Faculty of Social and Behavioural Sciences, Institute of Psychology, Leiden UniversityDepartment of Laboratory Medicine, Radboud university medical centerDivision of Endocrinology, Department of Internal Medicine, Radboud university medical centerDivision of Endocrinology, Department of Internal Medicine, Radboud university medical centerHealth, Medical and Neuropsychology Unit, Faculty of Social and Behavioural Sciences, Institute of Psychology, Leiden UniversityAbstract Background Conditioning of physiological responses can be achieved by repeatedly pairing a previously neutral conditioned stimulus with the administration of a pharmacologically salient unconditioned stimulus. This type of conditioning has been effective for specific immune and endocrine responses, but results with regard to conditioning of cortisol, a key stress-regulatory parameter, are currently unclear. This paper describes a pharmacological conditioning design, optimized for the examination of effects of cortisol conditioning under both basal conditions and in response to stress. Methods A double-blind randomized controlled conditioning paradigm aimed at conditioning of cortisol is conducted in 48 healthy female volunteers. During the acquisition phase, a gustatory stimulus (conditioned stimulus) is paired with hydrocortisone (100 mg, capsulated, unconditioned stimulus) three times before being administered together with placebo during three evocation sessions. To investigate possible effects of cortisol conditioning in response to stress, participants are exposed to the Trier Social Stress Test during the third evocation session. Primary outcome measure of this study is the mean area under the curve of salivary cortisol during the first two evocation sessions. As secondary outcomes, self-reported affect and stress as well as alpha-amylase are investigated. A pilot study was conducted to ensure that this design is feasible to be used in a larger study. Discussion This study design provides an innovative opportunity to examine the conditioning of cortisol under basal conditions and in response to stress. Also, the possible effect of cortisol conditioning on secondary outcomes of self-reported affect and alpha-amylase can be investigated. If cortisol could successfully be conditioned, this would be of conceptual relevance, showing that hypothalamic pituitary adrenal (HPA) axis regulation can be influenced by associative learning processes. Eventually, this could also have important clinical implications for understanding and treating stress-related disorders in which HPA axis dysregulation might play a role. Trial registration Nederlands Trial Register, NTR4651. Registered on 29 July 2014http://link.springer.com/article/10.1186/s40814-018-0382-5Endocrine conditioningCortisolPlacebo effectStressHPA axisAssociative learning |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
J. Tekampe H. van Middendorp F. C. G. J. Sweep S. H. P. P. Roerink A. R. M. M. Hermus A. W. M. Evers |
spellingShingle |
J. Tekampe H. van Middendorp F. C. G. J. Sweep S. H. P. P. Roerink A. R. M. M. Hermus A. W. M. Evers Conditioning cortisol in humans: design and pilot study of a randomized controlled trial Pilot and Feasibility Studies Endocrine conditioning Cortisol Placebo effect Stress HPA axis Associative learning |
author_facet |
J. Tekampe H. van Middendorp F. C. G. J. Sweep S. H. P. P. Roerink A. R. M. M. Hermus A. W. M. Evers |
author_sort |
J. Tekampe |
title |
Conditioning cortisol in humans: design and pilot study of a randomized controlled trial |
title_short |
Conditioning cortisol in humans: design and pilot study of a randomized controlled trial |
title_full |
Conditioning cortisol in humans: design and pilot study of a randomized controlled trial |
title_fullStr |
Conditioning cortisol in humans: design and pilot study of a randomized controlled trial |
title_full_unstemmed |
Conditioning cortisol in humans: design and pilot study of a randomized controlled trial |
title_sort |
conditioning cortisol in humans: design and pilot study of a randomized controlled trial |
publisher |
BMC |
series |
Pilot and Feasibility Studies |
issn |
2055-5784 |
publishDate |
2019-01-01 |
description |
Abstract Background Conditioning of physiological responses can be achieved by repeatedly pairing a previously neutral conditioned stimulus with the administration of a pharmacologically salient unconditioned stimulus. This type of conditioning has been effective for specific immune and endocrine responses, but results with regard to conditioning of cortisol, a key stress-regulatory parameter, are currently unclear. This paper describes a pharmacological conditioning design, optimized for the examination of effects of cortisol conditioning under both basal conditions and in response to stress. Methods A double-blind randomized controlled conditioning paradigm aimed at conditioning of cortisol is conducted in 48 healthy female volunteers. During the acquisition phase, a gustatory stimulus (conditioned stimulus) is paired with hydrocortisone (100 mg, capsulated, unconditioned stimulus) three times before being administered together with placebo during three evocation sessions. To investigate possible effects of cortisol conditioning in response to stress, participants are exposed to the Trier Social Stress Test during the third evocation session. Primary outcome measure of this study is the mean area under the curve of salivary cortisol during the first two evocation sessions. As secondary outcomes, self-reported affect and stress as well as alpha-amylase are investigated. A pilot study was conducted to ensure that this design is feasible to be used in a larger study. Discussion This study design provides an innovative opportunity to examine the conditioning of cortisol under basal conditions and in response to stress. Also, the possible effect of cortisol conditioning on secondary outcomes of self-reported affect and alpha-amylase can be investigated. If cortisol could successfully be conditioned, this would be of conceptual relevance, showing that hypothalamic pituitary adrenal (HPA) axis regulation can be influenced by associative learning processes. Eventually, this could also have important clinical implications for understanding and treating stress-related disorders in which HPA axis dysregulation might play a role. Trial registration Nederlands Trial Register, NTR4651. Registered on 29 July 2014 |
topic |
Endocrine conditioning Cortisol Placebo effect Stress HPA axis Associative learning |
url |
http://link.springer.com/article/10.1186/s40814-018-0382-5 |
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