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Helplessness and perceived pain intensity: relations to cortisol concentrations after electrocutaneous stimulation in healthy young men

BACKGROUND: Uncontrollable aversive events are associated with feelings of helplessness and cortisol elevation and are suitable as a model of depression. The high comorbidity of depression and pain symptoms and the importance of controllability in both conditions are clinically well-known but empiri...

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Autor principal: Müller, Matthias J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3141369/
https://www.ncbi.nlm.nih.gov/pubmed/21718526
http://dx.doi.org/10.1186/1751-0759-5-8
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author Müller, Matthias J
author_facet Müller, Matthias J
author_sort Müller, Matthias J
collection PubMed
description BACKGROUND: Uncontrollable aversive events are associated with feelings of helplessness and cortisol elevation and are suitable as a model of depression. The high comorbidity of depression and pain symptoms and the importance of controllability in both conditions are clinically well-known but empirical studies are scarce. The study investigated the relationship of pain experience, helplessness, and cortisol secretion after controllable vs. uncontrollable electric skin stimulation in healthy male individuals. METHODS: Sixty-four male volunteers were randomly assigned to receive 30 controllable (self-administered) or uncontrollable (experimenter-administered) painful electric skin stimuli. Perceived pain intensity (PPI), subjective helplessness ratings, and salivary cortisol concentrations were assessed. PPI was assessed after stress exposure. For salivary cortisol concentrations and subjective helplessness ratings, areas under the response curve (AUC) were calculated. RESULTS: After uncontrollable vs. controllable stress exposure significantly higher PPI ratings (P = 0.023), higher subjective helplessness AUC (P < 0.0005) and higher salivary cortisol AUC (P = 0.004, t-tests) were found. Correlation analyses revealed a significant correlation between subjective helplessness AUC and PPI (r = 0.500, P < 0.0005), subjective helplessness AUC and salivary cortisol AUC (r = 0.304, P = 0.015) and between PPI and salivary cortisol AUC (r = 0.298, P = 0.017). CONCLUSIONS: The results confirm the impact of uncontrollability on stress responses in humans; the relationship of PPI with subjective helplessness and salivary cortisol suggests a cognitive-affective sensitization of pain perception, particularly under uncontrollable conditions.
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spelling pubmed-31413692011-07-23 Helplessness and perceived pain intensity: relations to cortisol concentrations after electrocutaneous stimulation in healthy young men Müller, Matthias J Biopsychosoc Med Research BACKGROUND: Uncontrollable aversive events are associated with feelings of helplessness and cortisol elevation and are suitable as a model of depression. The high comorbidity of depression and pain symptoms and the importance of controllability in both conditions are clinically well-known but empirical studies are scarce. The study investigated the relationship of pain experience, helplessness, and cortisol secretion after controllable vs. uncontrollable electric skin stimulation in healthy male individuals. METHODS: Sixty-four male volunteers were randomly assigned to receive 30 controllable (self-administered) or uncontrollable (experimenter-administered) painful electric skin stimuli. Perceived pain intensity (PPI), subjective helplessness ratings, and salivary cortisol concentrations were assessed. PPI was assessed after stress exposure. For salivary cortisol concentrations and subjective helplessness ratings, areas under the response curve (AUC) were calculated. RESULTS: After uncontrollable vs. controllable stress exposure significantly higher PPI ratings (P = 0.023), higher subjective helplessness AUC (P < 0.0005) and higher salivary cortisol AUC (P = 0.004, t-tests) were found. Correlation analyses revealed a significant correlation between subjective helplessness AUC and PPI (r = 0.500, P < 0.0005), subjective helplessness AUC and salivary cortisol AUC (r = 0.304, P = 0.015) and between PPI and salivary cortisol AUC (r = 0.298, P = 0.017). CONCLUSIONS: The results confirm the impact of uncontrollability on stress responses in humans; the relationship of PPI with subjective helplessness and salivary cortisol suggests a cognitive-affective sensitization of pain perception, particularly under uncontrollable conditions. BioMed Central 2011-06-30 /pmc/articles/PMC3141369/ /pubmed/21718526 http://dx.doi.org/10.1186/1751-0759-5-8 Text en Copyright ©2011 Müller; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Müller, Matthias J
Helplessness and perceived pain intensity: relations to cortisol concentrations after electrocutaneous stimulation in healthy young men
title Helplessness and perceived pain intensity: relations to cortisol concentrations after electrocutaneous stimulation in healthy young men
title_full Helplessness and perceived pain intensity: relations to cortisol concentrations after electrocutaneous stimulation in healthy young men
title_fullStr Helplessness and perceived pain intensity: relations to cortisol concentrations after electrocutaneous stimulation in healthy young men
title_full_unstemmed Helplessness and perceived pain intensity: relations to cortisol concentrations after electrocutaneous stimulation in healthy young men
title_short Helplessness and perceived pain intensity: relations to cortisol concentrations after electrocutaneous stimulation in healthy young men
title_sort helplessness and perceived pain intensity: relations to cortisol concentrations after electrocutaneous stimulation in healthy young men
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3141369/
https://www.ncbi.nlm.nih.gov/pubmed/21718526
http://dx.doi.org/10.1186/1751-0759-5-8
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