Dynamic and static components of mechanical hyperalgesia in human hairy skin - PubMed (original) (raw)
Dynamic and static components of mechanical hyperalgesia in human hairy skin
Martin Koltzenburg et al. Pain. 1992 Nov.
Erratum in
- Pain 1993 Jun;53(3):363
Abstract
The principle finding of the present study is that there are two types of mechanical hyperalgesia developing in human hairy skin following injurious stimuli. Mechanical hyperalgesia comprises a dynamic component (brush-evoked pain, allodynia) signalled by large myelinated afferents and a static component (hyperalgesia to pressure stimuli) signalled by unmyelinated afferents. While the static component is only found in the injured area, the dynamic component also extends into a halo of undamaged tissue surrounding the injury. The irritant chemicals, mustard oil or capsaicin, were applied transdermally in 20 subjects to a patch (2 x 2 cm) of hairy skin. Both substances evoked burning pain and hyperalgesia to mechanical stimuli. While stroking normal skin with a cotton bud was perceived only as touch prior to chemical stimulation, there was a distinctly unpleasant sensation afterwards. This component of mechanical hyperalgesia persisted for at least 30 min and was present in the skin exposed to the irritants (primary hyperalgesia) as well as in a zone of untreated skin surrounding the injury (secondary hyperalgesia) measuring 38 +/- 4 cm2 after capsaicin. Pressure pain thresholds dropped to 55 +/- 8% of baseline level after mustard oil and to 46 +/- 9% after capsaicin. However, this drop of thresholds was short-lived, lasting 5 min following mustard oil but persisting more than 30 min following capsaicin treatment. The reduction of pressure pain thresholds was only observed for treated skin areas, but not in the surrounding undamaged tissue from where brush-evoked pain could be evoked. When pressure pain thresholds were lowered, the pain had a burning quality which differed distinctly from the quality of brush-evoked pain. On-going burning pain and both types of mechanical hyperalgesia were critically temperature dependent. Mildly cooling the skin provided instant relief from on-going pain, abolished brush-evoked pain and normalized pressure pain thresholds. Rewarming resulted in a reappearance of on-going pain and hyperalgesia. The effect of a nerve compression block of the superficial radial nerve on these sensations was tested in 14 experiments. When the ability to perceive light touch had been abolished, there was also no touch-evoked pain, indicating that this component of mechanical hyperalgesia is mediated by large-diameter primary afferents. At a later stage of the block when the subjects' ability to perceive cold stimuli had also been lost, application of cool stimuli still eliminated on-going burning pain, suggesting that pain relief afforded by cooling the skin acts at the peripheral receptor level and not by central masking.(ABSTRACT TRUNCATED AT 400 WORDS)
Similar articles
- Nociceptor modulated central sensitization causes mechanical hyperalgesia in acute chemogenic and chronic neuropathic pain.
Koltzenburg M, Torebjörk HE, Wahren LK. Koltzenburg M, et al. Brain. 1994 Jun;117 ( Pt 3):579-91. doi: 10.1093/brain/117.3.579. Brain. 1994. PMID: 8032867 - Roles of capsaicin-insensitive nociceptors in cutaneous pain and secondary hyperalgesia.
Magerl W, Fuchs PN, Meyer RA, Treede RD. Magerl W, et al. Brain. 2001 Sep;124(Pt 9):1754-64. doi: 10.1093/brain/124.9.1754. Brain. 2001. PMID: 11522578 - Neurogenic hyperalgesia: the search for the primary cutaneous afferent fibers that contribute to capsaicin-induced pain and hyperalgesia.
Baumann TK, Simone DA, Shain CN, LaMotte RH. Baumann TK, et al. J Neurophysiol. 1991 Jul;66(1):212-27. doi: 10.1152/jn.1991.66.1.212. J Neurophysiol. 1991. PMID: 1919668 - Peripheral and central mechanisms of cutaneous hyperalgesia.
Treede RD, Meyer RA, Raja SN, Campbell JN. Treede RD, et al. Prog Neurobiol. 1992;38(4):397-421. doi: 10.1016/0301-0082(92)90027-c. Prog Neurobiol. 1992. PMID: 1574584 Review. - Human surrogate models of central sensitization: A critical review and practical guide.
Quesada C, Kostenko A, Ho I, Leone C, Nochi Z, Stouffs A, Wittayer M, Caspani O, Brix Finnerup N, Mouraux A, Pickering G, Tracey I, Truini A, Treede RD, Garcia-Larrea L. Quesada C, et al. Eur J Pain. 2021 Aug;25(7):1389-1428. doi: 10.1002/ejp.1768. Epub 2021 May 8. Eur J Pain. 2021. PMID: 33759294 Free PMC article. Review.
Cited by
- Visceral nociceptive afferent facilitates reaction of subnucleus reticularis dorsalis to acupoint stimulation in rats.
Li L, Yu L, Rong P, Ben H, Li X, Zhu B, Chen R. Li L, et al. Evid Based Complement Alternat Med. 2013;2013:931283. doi: 10.1155/2013/931283. Epub 2013 May 15. Evid Based Complement Alternat Med. 2013. PMID: 23762171 Free PMC article. - Selective mediation of nerve injury-induced tactile hypersensitivity by neuropeptide Y.
Ossipov MH, Zhang ET, Carvajal C, Gardell L, Quirion R, Dumont Y, Lai J, Porreca F. Ossipov MH, et al. J Neurosci. 2002 Nov 15;22(22):9858-67. doi: 10.1523/JNEUROSCI.22-22-09858.2002. J Neurosci. 2002. PMID: 12427842 Free PMC article. - Intradermal capsaicin as a neuropathic pain model in patients with unilateral sciatica.
Aykanat V, Gentgall M, Briggs N, Williams D, Yap S, Rolan P. Aykanat V, et al. Br J Clin Pharmacol. 2012 Jan;73(1):37-45. doi: 10.1111/j.1365-2125.2011.04059.x. Br J Clin Pharmacol. 2012. PMID: 21740458 Free PMC article. - No association of polymorphisms in the serotonin transporter gene with thermal pain sensation in healthy individuals.
Schaldemose EL, Horjales-Araujo E, Demontis D, Børglum AD, Svensson P, Finnerup NB. Schaldemose EL, et al. Mol Pain. 2014 Dec 4;10:76. doi: 10.1186/1744-8069-10-76. Mol Pain. 2014. PMID: 25472558 Free PMC article. - Similar excitability through different sodium channels and implications for the analgesic efficacy of selective drugs.
Xie YF, Yang J, Ratté S, Prescott SA. Xie YF, et al. Elife. 2024 Apr 30;12:RP90960. doi: 10.7554/eLife.90960. Elife. 2024. PMID: 38687187 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical