Estrogenic effects on temporomandibular disorder and pain

被引:3
作者
Stinson, Crystal [1 ]
Bellinger, Larry L. [1 ]
Puri, Jyoti [2 ]
Ahuja, Neelam [1 ]
Bender, Steven D. [3 ]
Kramer, Phillip R. [1 ]
机构
[1] Texas A&M Coll Dent, Dept Biomed Sci, Dallas, TX USA
[2] Adv Family Dent & Orthodont PC, Crest Hill, IL USA
[3] Texas A&M Coll Dent, Ctr Facial Pain & Sleep Med, Dallas, TX USA
关键词
orofacial; pain; sex; steroids; temporomandibular joint; TMD; SPINAL TRIGEMINAL NUCLEUS; RECEPTOR ALPHA-6 EXPRESSION; KAPPA-OPIOID RECEPTOR; MEDULLARY DORSAL-HORN; SEX-DIFFERENCES; JOINT INFLAMMATION; SPINOMEDULLARY JUNCTION; MENSTRUAL-CYCLE; NOCICEPTIVE RESPONSE; POSTMENOPAUSAL WOMEN;
D O I
10.1111/jabr.12164
中图分类号
B849 [应用心理学];
学科分类号
040203 ;
摘要
Purpose It has become more apparent that studies focusing on the effect of sex steroids on orofacial pain in humans and animals require careful attention to the methods of hormone replacement. As a result, the purpose of this review is to highlight differences in estrogen concentration and its effects on temporomandibular joint (TMJ) pain and behavior. Methods This literature review searched keywords TMJ, orofacial, pain, nociception sex steroids, estrous cycle, menstrual cycle estradiol, and progesterone. Results In the case of estrogen, the change in concentration was a consideration, as a rise in estrogen can lead to protective effects and a decrease in estrogen appears to exacerbate the pain response. The dosage and timing was important when administering sex steroids as many orofacial pain studies conducted on animals have used large pharmacologic dosages and/or have given the hormone in a nonphysiologic way that does not mimic natural secretion patterns. Conclusions The results demonstrate that when performing studies or experiments these factors can result in alteration of the pain or behavioral response, as well as, joint structure and inflammatory response. Therefore, these factors must be considered when designing experiments focused on determining the mechanisms of action for sex steroids.
引用
收藏
页数:30
相关论文
共 144 条
[41]   ENDORPHIN-MEDIATED INCREASES IN PAIN THRESHOLD DURING PREGNANCY [J].
GINTZLER, AR .
SCIENCE, 1980, 210 (4466) :193-195
[42]   Estrogenic effect on swelling and monocytic receptor expression in an arthritic temporomandibular joint model [J].
Guan, GQ ;
Kerins, CC ;
Bellinger, LL ;
Kramer, PR .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 2005, 97 (03) :241-250
[43]   BRADYKININ IS INCREASED DURING ACUTE AND CHRONIC INFLAMMATION - THERAPEUTIC IMPLICATIONS [J].
HARGREAVES, KM ;
TROULLOS, ES ;
DIONNE, RA ;
SCHMIDT, EA ;
SCHAFER, SC ;
JORIS, JL .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 1988, 44 (06) :613-621
[44]   Meal pattern analysis in response to temporomandibular joint inflammation in the rat [J].
Harper, RP ;
Kerins, CA ;
Talwar, R ;
Spears, R ;
Hutchins, B ;
Carlson, DS ;
McIntosh, JE ;
Bellinger, LL .
JOURNAL OF DENTAL RESEARCH, 2000, 79 (09) :1704-1711
[45]   Is use of exogenous estrogen associated with temporomandibular signs and symptoms? [J].
Hatch, JP ;
Rugh, JD ;
Sakai, S ;
Saunders, MJ .
JOURNAL OF THE AMERICAN DENTAL ASSOCIATION, 2001, 132 (03) :319-326
[46]  
Hotchkiss J., 1994, PHYSL REPROD, V2nd, P711
[47]   INDUCTION OF C-FOS-LIKE PROTEIN IN SPINAL-CORD NEURONS FOLLOWING SENSORY STIMULATION [J].
HUNT, SP ;
PINI, A ;
EVAN, G .
NATURE, 1987, 328 (6131) :632-634
[48]   VRl-, VRL-1- and P2X3 receptor-immunoreactive innervation of the rat temporomandibular joint [J].
Ichikawa, H ;
Fukunaga, T ;
Jin, HW ;
Fujita, M ;
Takano-Yamamoto, T ;
Sugimoto, T .
BRAIN RESEARCH, 2004, 1008 (01) :131-136
[49]   PHYSIOLOGICAL MECHANISMS OF NEUROPATHIC PAIN: THE OROFACIAL REGION [J].
Iwata, Koichi ;
Imamura, Yoshiki ;
Honda, Kuniya ;
Shinoda, Masamichi .
TRANSLATING MECHANISMS OF OROFACIAL NEUROLOGICAL DISORDER, 2011, 97 :227-250
[50]   ORGANIZATION OF HRP-LABELED TRIGEMINAL MANDIBULAR PRIMARY AFFERENT NEURONS IN THE RAT [J].
JACQUIN, MF ;
SEMBA, K ;
EGGER, MD ;
RHOADES, RW .
JOURNAL OF COMPARATIVE NEUROLOGY, 1983, 215 (04) :397-420