A new hypothesis of sex-differences in temporomandibular disorders: Estrogen enhances hyperalgesia of inflamed TMJ through modulating voltage-gated sodium channel 1.7 in trigeminal ganglion?

被引:21
作者
Bi, Rui-Yun [1 ]
Ding, Yun [1 ]
Gan, Ye-Hua [2 ,3 ]
机构
[1] Peking Univ, Sch & Hosp Stomatol, Dent Ctr 3, Beijing 100088, Peoples R China
[2] Peking Univ, Sch & Hosp Stomatol, Cent Lab, Beijing 100088, Peoples R China
[3] Peking Univ, Sch & Hosp Stomatol, Ctr Temporomandibular Disorders & Orofacial Pain, Beijing 100088, Peoples R China
关键词
INFLAMMATORY PAIN; RECEPTOR; NA(V)1.7; JOINT; SCN9A; RAT; NEURONS; ACTIVATION; EXPRESSION; ALLODYNIA;
D O I
10.1016/j.mehy.2014.12.010
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Objective: Temporomandibular disorders (TMD) are an assorted set of clinical conditions characterized mainly by pain in the temporomandibular joint (TMJ). TMJ inflammation or synovitis is frequently observed in TMD patients and is the major reason for TMD pain. TMD is prevalent in women of childbearing age, at least twice than in men, implying that estrogen may be involved in TMD pain processing. Estrogen affects a cell mainly through the estrogen receptors (ER). The estrogen-ER complex binds to estrogen response element sequences (ERE) in the promoter region of specific genes and then exerts its regulatory potential. The voltage-gated sodium channel 1.7 (Nav1.7), whose single disruption leads to a complete loss of pain, amplifies weak stimuli in the neurons and acts as the threshold channel for firing action potentials and plays a prominent role in pain perception, including inflammatory pain. Furthermore, our previous study showed that trigeminal ganglionic Nav1.7 was involved in the hyperalgesia of the inflamed TMJ. We propose that estrogen may enhance hyperalgesia of inflamed TMJ through decrease nociceptive threshold of TMJ or inflamed TMJ by modulating both expression and channel threshold of Nav1.7 in trigeminal ganglion. (c) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:100 / 103
页数:4
相关论文
共 33 条
[1]   Sex differences in brainstem neural activation after injury to the TMJ region [J].
Bereiter, DA .
CELLS TISSUES ORGANS, 2001, 169 (03) :226-237
[2]   Involvement of trigeminal ganglionic Nav1.7 in hyperalgesia of inflamed temporomandibular joint is dependent on ERK1/2 phosphorylation of glial cells in rats [J].
Bi, R-Y. ;
Kou, X-X. ;
Meng, Z. ;
Wang, X-D. ;
Ding, Y. ;
Gan, Y-H. .
EUROPEAN JOURNAL OF PAIN, 2013, 17 (07) :983-994
[3]   Nav1.7 sodium channel expression in human lingual nerve neuromas [J].
Bird, E. V. ;
Robinson, P. P. ;
Boissonade, F. M. .
ARCHIVES OF ORAL BIOLOGY, 2007, 52 (05) :494-502
[4]   Changes in the expression of tetrodotoxin-sensitive sodium channels within dorsal root ganglia neurons in inflammatory pain [J].
Black, JA ;
Liu, SJ ;
Tanaka, M ;
Cummins, TR ;
Waxman, SG .
PAIN, 2004, 108 (03) :237-247
[5]  
Cairns BE, 2003, J OROFAC PAIN, V17, P317
[6]  
Carlsson GE, 1999, J OROFAC PAIN, V13, P232
[7]   Origin of sensory and autonomic innervation of the rat temporomandibular joint: A retrograde axonal tracing study with the fluorescent dye fast blue [J].
Casatti, CA ;
Frigo, L ;
Bauer, JA .
JOURNAL OF DENTAL RESEARCH, 1999, 78 (03) :776-783
[8]   An SCN9A channelopathy causes congenital inability to experience pain [J].
Cox, James J. ;
Reimann, Frank ;
Nicholas, Adeline K. ;
Thornton, Gemma ;
Roberts, Emma ;
Springell, Kelly ;
Karbani, Gulshan ;
Jafri, Hussain ;
Mannan, Jovaria ;
Raashid, Yasmin ;
Al-Gazali, Lihadh ;
Hamamy, Henan ;
Valente, Enza Maria ;
Gorman, Shaun ;
Williams, Richard ;
McHale, Duncan P. ;
Wood, John N. ;
Gribble, Fiona M. ;
Woods, C. Geoffrey .
NATURE, 2006, 444 (7121) :894-898
[9]   Voltage-Gated Sodium Channels: Therapeutic Targets for Pain [J].
Dib-Hajj, Sulayman D. ;
Black, Joel A. ;
Waxman, Stephen G. .
PAIN MEDICINE, 2009, 10 (07) :1260-1269
[10]   Sex-related differences in NMDA-evoked rat masseter muscle afferent discharge result from estrogen-mediated modulation of peripheral NMDA receptor activity [J].
Dong, X-D. ;
Mann, M. K. ;
Kumar, U. ;
Svensson, P. ;
Arendt-Nielsen, L. ;
Hu, J. W. ;
Sessle, B. J. ;
Cairns, B. E. .
NEUROSCIENCE, 2007, 146 (02) :822-832