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Offset analgesia and onset hyperalgesia with different stimulus ranges

INTRODUCTION: Offset analgesia (OA), a large reduction in pain after a brief increase in intensity of an otherwise stable painful stimulus, has been established by a large body of research. But the opposite effect, onset hyperalgesia (OH), a disproportional hyperalgesic response after a briefly decr...

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Detalles Bibliográficos
Autores principales: Fust, Jens, Lalouni, Maria, Vadenmark Lundqvist, Viktor, Wärnberg, Emil, Jensen, Karin B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7997128/
https://www.ncbi.nlm.nih.gov/pubmed/33786407
http://dx.doi.org/10.1097/PR9.0000000000000914
Descripción
Sumario:INTRODUCTION: Offset analgesia (OA), a large reduction in pain after a brief increase in intensity of an otherwise stable painful stimulus, has been established by a large body of research. But the opposite effect, onset hyperalgesia (OH), a disproportional hyperalgesic response after a briefly decreased intensity of a painful stimulus, has only been investigated in one previous study. OBJECTIVES: The aim of this study was to induce OA and OH in healthy participants and explore the effects of different stimulus ranges (increase/decrease of temperature) on OA and OH. METHODS: A total of 62 participants were tested in 2 identical experiments. Offset analgesia and OH conditions included 2 different temperature deviations (±1°C/±2°C) from initial temperature and were compared with a constant temperature (control). RESULTS: Offset analgesia was successfully elicited in OA(1°C) in experiment 1, and in OA(1°C) and OA(2°C) in experiment 2. Results indicate a continuous stimulus–response relationship between the stimulus range and the resulting hypoalgesic response. Onset hyperalgesia was only elicited in OH(2°C) in experiment 1. Exploratory analysis showed that the lack of OH response in experiment 2 could be explained by sex differences, and that OA and OH responses were only weakly correlated. CONCLUSIONS: The asymmetry between pain responses after a brief temperature increase and decrease suggests that different mechanisms are involved in the pain responses to increasing and decreasing temperature. This asymmetry may also be explained by high temperatures in OA condition (+1°C/+2°C above baseline) that could be seen as salient “learning signals,” which augment the response to following changes in temperature.