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Selective nociceptor activation in volunteers by infrared diode laser

BACKGROUND: Two main classes of peripheral sensory neurons contribute to thermal pain sensitivity: the unmyelinated C fibers and thinly myelinated Aδ fibers. These two fiber types may differentially underlie different clinical pain states and distinctions in the efficacy of analgesic treatments. Met...

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Autores principales: Tzabazis, Alexander Z, Klukinov, Michael, Crottaz-Herbette, Sonia, Nemenov, Mikhail I, Angst, Martin S, Yeomans, David C
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3070669/
https://www.ncbi.nlm.nih.gov/pubmed/21426575
http://dx.doi.org/10.1186/1744-8069-7-18
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author Tzabazis, Alexander Z
Klukinov, Michael
Crottaz-Herbette, Sonia
Nemenov, Mikhail I
Angst, Martin S
Yeomans, David C
author_facet Tzabazis, Alexander Z
Klukinov, Michael
Crottaz-Herbette, Sonia
Nemenov, Mikhail I
Angst, Martin S
Yeomans, David C
author_sort Tzabazis, Alexander Z
collection PubMed
description BACKGROUND: Two main classes of peripheral sensory neurons contribute to thermal pain sensitivity: the unmyelinated C fibers and thinly myelinated Aδ fibers. These two fiber types may differentially underlie different clinical pain states and distinctions in the efficacy of analgesic treatments. Methods of differentially testing C and Aδ thermal pain are widely used in animal experimentation, but these methods are not optimal for human volunteer and patient use. Thus, this project aimed to provide psychophysical and electrophysiological evidence that whether different protocols of infrared diode laser stimulation, which allows for direct activation of nociceptive terminals deep in the skin, could differentially activate Aδ or C fiber thermonociceptors in volunteers. RESULTS: Short (60 ms), high intensity laser pulses (SP) evoked monomodal "pricking" pain which was not enhanced by topical capsaicin, whereas longer, lower power pulses (LP) evoked monomodal "burning" pain which was enhanced by topical capsaicin. SP also produced cortical evoked EEG potentials consistent with Aδ mediation, the amplitude of which was directly correlated with pain intensity but was not affected by topical capsaicin. LP also produced a distinct evoked potential pattern the amplitude of which was also correlated with pain intensity, which was enhanced by topical capsaicin, and the latency of which could be used to estimate the conduction velocity of the mediating nociceptive fibers. CONCLUSIONS: Psychophysical and electrophysiological data were consistent with the ability of short high intensity infrared laser pulses to selectively produce Aδ mediated pain and of longer pulses to selectively produce C fiber mediated thermal pain. Thus, the use of these or similar protocols may be useful in developing and testing novel therapeutics based on the differential molecular mechanisms underlying activation of the two fiber types (e.g., TRPV1, TRPV2, etc). In addition, these protocol may be useful in determining the fiber mediation of different clinical pain types which may, in turn be useful in treatment choice.
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spelling pubmed-30706692011-04-05 Selective nociceptor activation in volunteers by infrared diode laser Tzabazis, Alexander Z Klukinov, Michael Crottaz-Herbette, Sonia Nemenov, Mikhail I Angst, Martin S Yeomans, David C Mol Pain Research BACKGROUND: Two main classes of peripheral sensory neurons contribute to thermal pain sensitivity: the unmyelinated C fibers and thinly myelinated Aδ fibers. These two fiber types may differentially underlie different clinical pain states and distinctions in the efficacy of analgesic treatments. Methods of differentially testing C and Aδ thermal pain are widely used in animal experimentation, but these methods are not optimal for human volunteer and patient use. Thus, this project aimed to provide psychophysical and electrophysiological evidence that whether different protocols of infrared diode laser stimulation, which allows for direct activation of nociceptive terminals deep in the skin, could differentially activate Aδ or C fiber thermonociceptors in volunteers. RESULTS: Short (60 ms), high intensity laser pulses (SP) evoked monomodal "pricking" pain which was not enhanced by topical capsaicin, whereas longer, lower power pulses (LP) evoked monomodal "burning" pain which was enhanced by topical capsaicin. SP also produced cortical evoked EEG potentials consistent with Aδ mediation, the amplitude of which was directly correlated with pain intensity but was not affected by topical capsaicin. LP also produced a distinct evoked potential pattern the amplitude of which was also correlated with pain intensity, which was enhanced by topical capsaicin, and the latency of which could be used to estimate the conduction velocity of the mediating nociceptive fibers. CONCLUSIONS: Psychophysical and electrophysiological data were consistent with the ability of short high intensity infrared laser pulses to selectively produce Aδ mediated pain and of longer pulses to selectively produce C fiber mediated thermal pain. Thus, the use of these or similar protocols may be useful in developing and testing novel therapeutics based on the differential molecular mechanisms underlying activation of the two fiber types (e.g., TRPV1, TRPV2, etc). In addition, these protocol may be useful in determining the fiber mediation of different clinical pain types which may, in turn be useful in treatment choice. BioMed Central 2011-03-22 /pmc/articles/PMC3070669/ /pubmed/21426575 http://dx.doi.org/10.1186/1744-8069-7-18 Text en Copyright ©2011 Tzabazis 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
Tzabazis, Alexander Z
Klukinov, Michael
Crottaz-Herbette, Sonia
Nemenov, Mikhail I
Angst, Martin S
Yeomans, David C
Selective nociceptor activation in volunteers by infrared diode laser
title Selective nociceptor activation in volunteers by infrared diode laser
title_full Selective nociceptor activation in volunteers by infrared diode laser
title_fullStr Selective nociceptor activation in volunteers by infrared diode laser
title_full_unstemmed Selective nociceptor activation in volunteers by infrared diode laser
title_short Selective nociceptor activation in volunteers by infrared diode laser
title_sort selective nociceptor activation in volunteers by infrared diode laser
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3070669/
https://www.ncbi.nlm.nih.gov/pubmed/21426575
http://dx.doi.org/10.1186/1744-8069-7-18
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