Antipruritic Effect of Cold-induced and Transient Receptor Potential-agonist-induced Counter-irritation on Histaminergic Itch in Humans

被引:27
作者
Andersen, Hjalte H. [1 ]
Melholt, Camilla [1 ]
Hilborg, Sigurd D. [1 ]
Jerwiarz, Anne [1 ]
Randers, Amalie [1 ]
Simoni, Amalie [1 ]
Elberling, Jesper [2 ]
Arendt-Nielsen, Lars [1 ]
机构
[1] Aalborg Univ, Fac Med, Dept Hlth Sci & Technol, SMI,Lab Expt Cutaneous Pain Res, Aalborg, Denmark
[2] Copenhagen Univ Hosp, Allergy Clin, Copenhagen, Denmark
关键词
itch; histamine; cold stimulation; TRPs; counter-irritation; TRPM8; TRPA1; TRP ION CHANNELS; NOCICEPTIVE SENSATIONS; INTERNATIONAL FORUM; ATOPIC-DERMATITIS; NEUROPATHIC PAIN; NOXIOUS HEAT; BLOOD-FLOW; HUMAN SKIN; MENTHOL; PRURITUS;
D O I
10.2340/00015555-2447
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
A frequent empirical observation is that cold-induced counter-irritation may attenuate itch. The aim of this randomized, single-blinded, exploratory study was to evaluate the counter-irritation effects of cold-stimulation and topical application of transient receptor potential TRPA1/M8-agonists (trans-cinnamaldehyde/Lmenthol, respectively), on histamine-induced itch, wheals and neurogenic inflammation in 13 healthy volunteers. Histamine 1% was applied to the volar forearms using skin prick-test lancets. Recorded outcome-parameters were itch intensity, wheal reactions, and neurogenic inflammation (measured by laser-speckle perfusion-imaging). Homotopic thermal counter-irritation was performed with 6 temperatures, ranging from 4 degrees C to 37 degrees C, using a 3 x 3-cm thermal stimulator. Chemical "cold-like" counter-irritation was conducted with 40% L-men-thol and 10% trans-cinnamaldehyde, while 5% doxepin was used as a positive antipruritic control/comparator. Cold counter-irritation stimuli from 4 degrees C to 22 degrees C inhibited itch in a stimulus-intensitydependent manner (p < 0.05) and, to a lesser extent, also wheal reactions and neurogenic inflammation. Chemical "cold-like" counter-irritation with both Lmenthol and trans-cinnamaldehyde had antipruritic efficacy similar to doxepin (p < 0.05). Cold-induced counter-irritation had an inhibitory effect on histaminergic itch, suggesting that agonists of cold transduction receptors could be of potential antipruritic value.
引用
收藏
页码:63 / 70
页数:8
相关论文
共 70 条
[11]   New aspects of itch pathophysiology: Component analysis of atopic itch using the 'Eppendorf Itch Questionnaire' [J].
Darsow, U ;
Scharein, E ;
Simon, D ;
Walter, G ;
Bromm, B ;
Ring, J .
INTERNATIONAL ARCHIVES OF ALLERGY AND IMMUNOLOGY, 2001, 124 (1-3) :326-331
[12]   Oral irritant properties of menthol - Sensitizing and desensitizing effects of repeated application and cross-desensitization to nicotine [J].
Dessirier, JM ;
O'Mahony, M ;
Carstens, E .
PHYSIOLOGY & BEHAVIOR, 2001, 73 (1-2) :25-36
[13]   TRP ion channels and temperature sensation [J].
Dhaka, Ajay ;
Viswanath, Veena ;
Patapoutian, Ardem .
ANNUAL REVIEW OF NEUROSCIENCE, 2006, 29 :135-161
[14]   The neurology of itch [J].
Dhand, Amar ;
Aminoff, Michael J. .
BRAIN, 2014, 137 :313-322
[15]   HC-030031, a TRPA1 selective antagonist, attenuates inflammatory- and neuropathy-induced mechanical hypersensitivity [J].
Eid, Samer R. ;
Crown, Eric D. ;
Moore, Eric L. ;
Liang, Hongyu A. ;
Choong, Kar-Chan ;
Dima, Shelley ;
Henze, Darrell A. ;
Kane, Stefanie A. ;
Urban, Mark O. .
MOLECULAR PAIN, 2008, 4
[16]   ICE FREEZES PAIN - A REVIEW OF THE CLINICAL EFFECTIVENESS OF ANALGESIC COLD THERAPY [J].
ERNST, E ;
FIALKA, V .
JOURNAL OF PAIN AND SYMPTOM MANAGEMENT, 1994, 9 (01) :56-59
[17]   THE EFFECTS OF THERMAL-STIMULATION ON CLINICAL AND EXPERIMENTAL ITCH [J].
FRUHSTORFER, H ;
HERMANNS, M ;
LATZKE, L .
PAIN, 1986, 24 (02) :259-269
[18]   Botulinum toxin type A reduces histamine-induced itch and vasomotor responses in human skin [J].
Gazerani, P. ;
Pedersen, N. S. ;
Drewes, A. M. ;
Arendt-Nielsen, L. .
BRITISH JOURNAL OF DERMATOLOGY, 2009, 161 (04) :737-745
[19]   Menthol desensitization of capsaicin irritation: Evidence of a short-term anti-nociceptive effect [J].
Green, BG ;
McAuliffe, BL .
PHYSIOLOGY & BEHAVIOR, 2000, 68 (05) :631-639
[20]  
HAGERMARK O, 1973, ACTA DERM-VENEREOL, V53, P363