Assessing the modulation of cutaneous sensory fiber excitability using a fast perception threshold tracking technique.


Journal

Muscle & nerve
ISSN: 1097-4598
Titre abrégé: Muscle Nerve
Pays: United States
ID NLM: 7803146

Informations de publication

Date de publication:
10 2019
Historique:
received: 17 10 2018
revised: 14 05 2019
accepted: 14 05 2019
pubmed: 21 5 2019
medline: 15 1 2020
entrez: 21 5 2019
Statut: ppublish

Résumé

Topical application of lidocaine-and-prilocaine (LP) cream attenuates the functionality of small cutaneous nerve fibers. The aim of this human study was to measure the underlying excitability modulation of small cutaneous nerve fibers using a novel and fast perception threshold tracking (PTT) technique. Small sensory fibers were selectively blocked by 120-minute topical application of LP and confirmed by quantitative sensory testing. Excitability changes of small (activated by a specially designed pin electrode) and large (patch electrode) nerve fibers were assessed as the strength-duration relation and threshold electrotonus. The excitability assessed by the strength-duration relation and threshold electrotonus was significantly modulated for the small afferents (P < 0.05, Wilcoxon's test) but not the large afferents. This novel PTT technique was able to assess inhibition of membrane properties of small cutaneous fibers, suggesting the usefulness of the technique as a diagnostic method for assessing impairment of small fibers, as seen in many types of polyneuropathies.

Identifiants

pubmed: 31107560
doi: 10.1002/mus.26520
doi:

Substances chimiques

Anesthetics, Local 0
Lidocaine, Prilocaine Drug Combination 0

Types de publication

Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

367-375

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2019 Wiley Periodicals, Inc.

Références

Lelic D, Mørch CD, Hennings K, Andersen OK, Drewes AM. Differences in perception and brain activation following stimulation by large versus small area cutaneous surface electrodes. Eur J Pain 2012;16:827-837.
Nilsson HJ, Levinsson A, Schouenborg J. Cutaneous field stimulation (CFS): a new powerful method to combat itch. Pain 1997;71:49-55.
Klein T, Magerl W, Hopf HC, Sandkühler J, Treede RD. Perceptual correlates of nociceptive long-term potentiation and long-tern depression in humans. J Neurosci 2004;24:964-971.
Inui K, Tran TD, Hoshiyama M, Kakigi R. Preferential stimulation of A-delta fibers by intra-epidermal needle electrode in humans. Pain 2002;96:247-252.
Kaube H, Katsarava Z, Käufer T, Diener H, Ellrich J. A new method to increase nociception specificity of the human blink reflex. Clin Neurophysiol 2000;111:413-416.
Mørch CD, Hennings K, Andersen OK. Estimating nerve excitation thresholds to cutaneous electrical stimulation by finite element modelling combined with a stochastic branching nerve fiber model. Med Biol Eng Comput 2011;49:385-395.
Motogi J, Sugiyama Y, Laakso I, Hirata A, Inui K, Tamura M, et al. Why intra-epidermal electrical stimulation achieves stimulation of small fibres selectively: a simulation study. Phys Med Biol 2016;61:4479-4490.
Provitera V, Nolano M, Pagano A, Caporaso G, Stancanelli A, Santoro L. Myelinated nerve endings in human skin. Muscle Nerve 2007;35:767-775.
Bostock H, Cikurel K, Burke D. Threshold tracking techniques in the study of human peripheral nerve. Muscle Nerve 1998;21:137-158.
Krishnan AV, Lin CS, Park SB, Kiernan MC. Axonal ion channels from bench to bedside: a translational neuroscience perspective. Prog Neurobiol 2009;89:288-313.
Kiernan MC, Lin CS, Andersen KV, Murray NM, Bostock H. Clinical evaluation of excitability measures in sensory nerve. Muscle Nerve 2001;24:883-892.
Hennings K, Frahm KS, Petrini L, Andersen OK, Arendt-Nielsen L, Mørch CD. Membrane properties in small cutaneous nerve fibers in humans. Muscle Nerve 2017;55:195-201.
Kodaira M, Inui K, Kakigi R. Evaluation of nociceptive Aδ- and C-fiber dysfunction with lidocaine using intraepidermal electrical stimulation. Clin Neurophysiol 2014;125:1870-1877.
Otsuru N, Inui K, Yamashiro K, Miyazaki T, Takeshima Y, Kakigi R. Assessing Aδ fiber function with lidocaine using intraepidermal electrical stimulation. J Pain 2010;11:621-627.
Gammaitoni AR, Alvarez NA, Galer BS. Safety and tolerability of the lidocaine patch 5%, a targeted peripheral analgesic: a review of the literature. J Clin Pharmacol 2003;43:111-117.
Krumova EK, Zeller M, Westermann A, Maier C. Lidocaine patch (5%) produces a selective, but incomplete block of Aδ and C fibers. Pain 2012;153:273-280.
Bjerring P, Arendt-Nielsen L. Depth and duration of skin analgesia to needle insertion after topical application of EMLA cream. Br J Anaesth 1990;64:173-177.
Arendt-Nielsen L, Bjerring P. The effect of topically applied anaesthetics (EMLA cream) on threshold to thermode and argon laser stimulation. Acta Anaesthesiol Scand 1989;33:469-473.
Wehrfritz A, Namer B, Ihmsen H, Mueller C, Filitz J, Koppert W, et al. Differential effects on sensory functions and measures of epidermal nerve fiber density after application of a lidocaine patch (5%) on healthy human skin. Eur J Pain 2011;15:907-912.
Weiss G. Sur la possibilité de rendre comparables entre eux les appareils servant l'excitation electrique. Arch Ital Biol 1901;35:413-446.
Mogyoros I, Kiernan MC, Burke D. Strength-duration properties of human peripheral nerve. Brain 1996;199:439-447.
Mouraux A, Iannetti GD, Plaghki L. Low intensity intra-epidermal electrical stimulation can activate Aδ-nociceptors selectively. Pain 2010;150:199-207.
Burke D, Kiernan MC, Bostock H. Excitability of human axons. Clin Neurophysiol 2001;112:1575-1585.
Gold MS, Shuster MJ, Levine JD. Characterization of six voltage-gated K+ currents in adult rat sensory neurons. J Neurophysiol 1996;75:2629-2646.
Akopian AN, Sivilotti L, Wood JN. A tetrodotoxin-resistant voltage-gated sodium channel expressed by sensory neurons. Nature 1996;379:257-262.
Djouhri L, Fang X, Okuse K, Wood JN, Berry CM, Lawson SN. The TTX-resistant sodium channel Nav1.8 (SNS/PN3): expression and correlation with membrane properties in rat nociceptive primary afferent neurons. J Physiol 2003;550:739-752.
Phuket TR, Covarrubias M. Kv4 channels underlie the subthreshold-operating A-type K-current in nociceptive dorsal root ganglion neurons. Front Mol Neurosci 2009;2:3.
Catterall WA, Goldin AL, Waxman SG. International Union of Pharmacology. XLVII. Nomenclature and structure-function relationships of voltage-gated sodium channels. Pharmacol Rev 2005;57:397-409.
Dib-Hajj SD, Cummins TR, Black JA, Waxman SG. Sodium channels in normal and pathological pain. Annu Rev Neurosci 2010;33:325-347.
Panizza M, Nilsson J, Roth BJ, Rothwell J, Hallett M. The time constants of motor and sensory peripheral nerve fibers measured with the method of latent addition. Electroencaphalogr Clin Neurophysiol 1994;93:147-154.
Doll RJ, Maten AC, Spaan SP, Veltink PH, Buitenweg JR. Effect of temporal stimulus properties on the nociceptive detection probability using intra-epidermal electrical stimulation. Exp Brain Res 2016;234:219-227.
Elmariah SB, Lerner EA. Topical therapies for pruritus. Semin Cutan Med Surg 2011;30:118-126.
Rolke R, Magerl W, Campbell KA, Schalber C, Caspari S, Birklein F, et al. Quantitative sensory testing: a comprehensive protocol for clinical trials. Eur J Pain 2006;10:77-88.
Lauria G, Dacci P, Lombardi R, Cazzato D, Porretta-Serapiglia C, Taiana M, et al. Side and time variability of intraepidermal nerve fiber density. Neurology 2015;84:2368-2371.
Ziegler D, Papanas N, Zhivov A, Allgeier S, Winter K, Ziegler I, et al. Early detection of nerve fiber loss by corneal confocal microscopy and skin biopsy in recently diagnosed type 2 diabetes. Diabetes 2014;63:2454-2463.
Devigili G, Tugnoli V, Penza P, Camozzi F, Lombardi R, Melli G, et al. The diagnostic criteria for small fibre neuropathy: from symptoms to neuropathology. Brain 2008;131:1912-1925.
Raputova J, Srotova I, Vlckova E, Sommer C, Üceyler N, Birklein F, et al. Sensory phenotype and risk factors for painful diabetic neuropathy: a cross-sectional observational study. Pain 2017;158:2340-2353.
Themistocleous AC, Ramirez JD, Shillo PT, Lees JG, Selvarajah D, Orengo C, et al. The Pain in Neuropathy Study (PiNS): a cross-sectional observational study determining the somatosensory phenotype of painful and painless diabetic neuropathy. Pain 2016;157:1132-1145.

Auteurs

Tatiana Nielson Hoberg (T)

Department of Health Science and Technology, Center for Sensory-Motor Interaction (SMI), Aalborg University, Fredrik Bajers Vej 7 D3, 9220 Aalborg Ø, Denmark.

Steffen Frahm (S)

Center for Neuroplasticity and Pain, SMI, Department of Health Science and Technology, Aalborg University, Aalborg, Denmark.

Kristian Hennings (K)

Department of Health Science and Technology, Center for Sensory-Motor Interaction (SMI), Aalborg University, Fredrik Bajers Vej 7 D3, 9220 Aalborg Ø, Denmark.

Lars Arendt-Nielsen (L)

Department of Health Science and Technology, Center for Sensory-Motor Interaction (SMI), Aalborg University, Fredrik Bajers Vej 7 D3, 9220 Aalborg Ø, Denmark.
Center for Neuroplasticity and Pain, SMI, Department of Health Science and Technology, Aalborg University, Aalborg, Denmark.

Carsten Dahl Mørch (C)

Department of Health Science and Technology, Center for Sensory-Motor Interaction (SMI), Aalborg University, Fredrik Bajers Vej 7 D3, 9220 Aalborg Ø, Denmark.
Center for Neuroplasticity and Pain, SMI, Department of Health Science and Technology, Aalborg University, Aalborg, Denmark.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH