Cargando…
Modeling homeostatic and circadian modulation of human pain sensitivity
INTRODUCTION: Mathematical modeling has played a significant role in understanding how homeostatic sleep pressure and the circadian rhythm interact to influence sleep-wake behavior. Pain sensitivity is also affected by these processes, and recent experimental results have measured the circadian and...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10285085/ https://www.ncbi.nlm.nih.gov/pubmed/37360178 http://dx.doi.org/10.3389/fnins.2023.1166203 |
_version_ | 1785061534199709696 |
---|---|
author | Crodelle, Jennifer Vanty, Carolyn Booth, Victoria |
author_facet | Crodelle, Jennifer Vanty, Carolyn Booth, Victoria |
author_sort | Crodelle, Jennifer |
collection | PubMed |
description | INTRODUCTION: Mathematical modeling has played a significant role in understanding how homeostatic sleep pressure and the circadian rhythm interact to influence sleep-wake behavior. Pain sensitivity is also affected by these processes, and recent experimental results have measured the circadian and homeostatic components of the 24 h rhythm of thermal pain sensitivity in humans. To analyze how rhythms in pain sensitivity are affected by disruptions in sleep behavior and shifts in circadian rhythms, we introduce a dynamic mathematical model for circadian and homeostatic regulation of sleep-wake states and pain intensity. METHODS: The model consists of a biophysically based, sleep-wake regulation network model coupled to data-driven functions for the circadian and homeostatic modulation of pain sensitivity. This coupled sleep-wake-pain sensitivity model is validated by comparison to thermal pain intensities in adult humans measured across a 34 h sleep deprivation protocol. RESULTS: We use the model to predict dysregulation of pain sensitivity rhythms across different scenarios of sleep deprivation and circadian rhythm shifts, including entrainment to new environmental light and activity timing as occurs with jet lag and chronic sleep restriction. Model results show that increases in pain sensitivity occur under conditions of increased homeostatic sleep drive with nonlinear modulation by the circadian rhythm, leading to unexpected decreased pain sensitivity in some scenarios. DISCUSSION: This model provides a useful tool for pain management by predicting alterations in pain sensitivity due to varying or disrupted sleep schedules. |
format | Online Article Text |
id | pubmed-10285085 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-102850852023-06-23 Modeling homeostatic and circadian modulation of human pain sensitivity Crodelle, Jennifer Vanty, Carolyn Booth, Victoria Front Neurosci Neuroscience INTRODUCTION: Mathematical modeling has played a significant role in understanding how homeostatic sleep pressure and the circadian rhythm interact to influence sleep-wake behavior. Pain sensitivity is also affected by these processes, and recent experimental results have measured the circadian and homeostatic components of the 24 h rhythm of thermal pain sensitivity in humans. To analyze how rhythms in pain sensitivity are affected by disruptions in sleep behavior and shifts in circadian rhythms, we introduce a dynamic mathematical model for circadian and homeostatic regulation of sleep-wake states and pain intensity. METHODS: The model consists of a biophysically based, sleep-wake regulation network model coupled to data-driven functions for the circadian and homeostatic modulation of pain sensitivity. This coupled sleep-wake-pain sensitivity model is validated by comparison to thermal pain intensities in adult humans measured across a 34 h sleep deprivation protocol. RESULTS: We use the model to predict dysregulation of pain sensitivity rhythms across different scenarios of sleep deprivation and circadian rhythm shifts, including entrainment to new environmental light and activity timing as occurs with jet lag and chronic sleep restriction. Model results show that increases in pain sensitivity occur under conditions of increased homeostatic sleep drive with nonlinear modulation by the circadian rhythm, leading to unexpected decreased pain sensitivity in some scenarios. DISCUSSION: This model provides a useful tool for pain management by predicting alterations in pain sensitivity due to varying or disrupted sleep schedules. Frontiers Media S.A. 2023-06-08 /pmc/articles/PMC10285085/ /pubmed/37360178 http://dx.doi.org/10.3389/fnins.2023.1166203 Text en Copyright © 2023 Crodelle, Vanty and Booth. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Crodelle, Jennifer Vanty, Carolyn Booth, Victoria Modeling homeostatic and circadian modulation of human pain sensitivity |
title | Modeling homeostatic and circadian modulation of human pain sensitivity |
title_full | Modeling homeostatic and circadian modulation of human pain sensitivity |
title_fullStr | Modeling homeostatic and circadian modulation of human pain sensitivity |
title_full_unstemmed | Modeling homeostatic and circadian modulation of human pain sensitivity |
title_short | Modeling homeostatic and circadian modulation of human pain sensitivity |
title_sort | modeling homeostatic and circadian modulation of human pain sensitivity |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10285085/ https://www.ncbi.nlm.nih.gov/pubmed/37360178 http://dx.doi.org/10.3389/fnins.2023.1166203 |
work_keys_str_mv | AT crodellejennifer modelinghomeostaticandcircadianmodulationofhumanpainsensitivity AT vantycarolyn modelinghomeostaticandcircadianmodulationofhumanpainsensitivity AT boothvictoria modelinghomeostaticandcircadianmodulationofhumanpainsensitivity |