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Characterization of cold sensitivity and thermal preference using an operant orofacial assay

BACKGROUND: A hallmark of many orofacial pain disorders is cold sensitivity, but relative to heat-related pain, mechanisms of cold perception and the development of cold allodynia are not clearly understood. Molecular mediators of cold sensation such as TRPM8 have been recently identified and charac...

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Autores principales: Rossi, Heather L, Vierck, Charles J, Caudle, Robert M, Neubert, John K
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1764875/
https://www.ncbi.nlm.nih.gov/pubmed/17166284
http://dx.doi.org/10.1186/1744-8069-2-37
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author Rossi, Heather L
Vierck, Charles J
Caudle, Robert M
Neubert, John K
author_facet Rossi, Heather L
Vierck, Charles J
Caudle, Robert M
Neubert, John K
author_sort Rossi, Heather L
collection PubMed
description BACKGROUND: A hallmark of many orofacial pain disorders is cold sensitivity, but relative to heat-related pain, mechanisms of cold perception and the development of cold allodynia are not clearly understood. Molecular mediators of cold sensation such as TRPM8 have been recently identified and characterized using in vitro studies. In this study we characterized operant behavior with respect to individually presented cold stimuli (24, 10, 2, and -4°C) and in a thermal preference task where rats chose between -4 and 48°C stimulation. We also evaluated the effects of menthol, a TRPM8 agonist, on operant responses to cold stimulation (24, 10, and -4°C). Male and female rats were trained to drink sweetened milk while pressing their shaved faces against a thermode. This presents a conflict paradigm between milk reward and thermal stimulation. RESULTS: We demonstrated that the cold stimulus response function was modest compared to heat. There was a significant effect of temperature on facial (stimulus) contacts, the ratio of licking contacts to stimulus contacts, and the stimulus duration/contact ratio. Males and females differed only in their facial contacts at 10°C. In the preference task, males preferred 48°C to -4°C, despite the fact that 48°C and -4°C were equally painful as based on their reward/stimulus and duration/contact ratios. We were able to induce hypersensitivity to cold using menthol at 10°C, but not at 24 or -4°C. CONCLUSION: Our results indicate a strong role for an affective component in processing of cold stimuli, more so than for heat, which is in concordance with human psychophysical findings. The induction of allodynia with menthol provides a model for cold allodynia. This study provides the basis for future studies involving orofacial pain and analgesics, and is translatable to the human experience.
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spelling pubmed-17648752007-01-10 Characterization of cold sensitivity and thermal preference using an operant orofacial assay Rossi, Heather L Vierck, Charles J Caudle, Robert M Neubert, John K Mol Pain Research BACKGROUND: A hallmark of many orofacial pain disorders is cold sensitivity, but relative to heat-related pain, mechanisms of cold perception and the development of cold allodynia are not clearly understood. Molecular mediators of cold sensation such as TRPM8 have been recently identified and characterized using in vitro studies. In this study we characterized operant behavior with respect to individually presented cold stimuli (24, 10, 2, and -4°C) and in a thermal preference task where rats chose between -4 and 48°C stimulation. We also evaluated the effects of menthol, a TRPM8 agonist, on operant responses to cold stimulation (24, 10, and -4°C). Male and female rats were trained to drink sweetened milk while pressing their shaved faces against a thermode. This presents a conflict paradigm between milk reward and thermal stimulation. RESULTS: We demonstrated that the cold stimulus response function was modest compared to heat. There was a significant effect of temperature on facial (stimulus) contacts, the ratio of licking contacts to stimulus contacts, and the stimulus duration/contact ratio. Males and females differed only in their facial contacts at 10°C. In the preference task, males preferred 48°C to -4°C, despite the fact that 48°C and -4°C were equally painful as based on their reward/stimulus and duration/contact ratios. We were able to induce hypersensitivity to cold using menthol at 10°C, but not at 24 or -4°C. CONCLUSION: Our results indicate a strong role for an affective component in processing of cold stimuli, more so than for heat, which is in concordance with human psychophysical findings. The induction of allodynia with menthol provides a model for cold allodynia. This study provides the basis for future studies involving orofacial pain and analgesics, and is translatable to the human experience. BioMed Central 2006-12-13 /pmc/articles/PMC1764875/ /pubmed/17166284 http://dx.doi.org/10.1186/1744-8069-2-37 Text en Copyright © 2006 Rossi et al; 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
Rossi, Heather L
Vierck, Charles J
Caudle, Robert M
Neubert, John K
Characterization of cold sensitivity and thermal preference using an operant orofacial assay
title Characterization of cold sensitivity and thermal preference using an operant orofacial assay
title_full Characterization of cold sensitivity and thermal preference using an operant orofacial assay
title_fullStr Characterization of cold sensitivity and thermal preference using an operant orofacial assay
title_full_unstemmed Characterization of cold sensitivity and thermal preference using an operant orofacial assay
title_short Characterization of cold sensitivity and thermal preference using an operant orofacial assay
title_sort characterization of cold sensitivity and thermal preference using an operant orofacial assay
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1764875/
https://www.ncbi.nlm.nih.gov/pubmed/17166284
http://dx.doi.org/10.1186/1744-8069-2-37
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