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Modulation of Temporomandibular Joint Nociception and Inflammation in Male Rats After Administering a Physiological Concentration of 17β-oestradiol

Overview
Journal Eur J Pain
Publisher Wiley
Date 2012 Jun 21
PMID 22715057
Citations 6
Authors
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Abstract

Background: Previous studies have shown 17β-estradiol will reduce temporomandibular joint (TMJ) inflammation and hypersensitivity in female rats. Although male rats contain significant amounts of oestradiol, it was unknown whether a physiological concentration of 17β-estradiol would attenuate male TMJ inflammation and nociception.

Methods: Intact and castrated rats were given a physiological concentration of oestradiol to examine first, if oestradiol will affect male TMJ nociception/inflammation and, second, if administration of oestradiol would act synergistically with endogenous male hormones to attenuate TMJ nociception. The hormonally treated rats were given TMJ injections of complete Freund's adjuvant (CFA) and then nociception was measured using a validated method in which a lengthening in meal duration is directly correlated to the intensity of deep TMJ nociception. Inflammation was assayed by quantitating pro-inflammatory gene expression.

Results: Meal duration was significantly lengthened after TMJ CFA injection and this lengthening was significantly attenuated in the castrated but not intact males after administering a physiological concentration of oestradiol. A physiological concentration of 17β-estradiol also significantly increased IL-6 expression in the inflamed TMJ of castrated males while 17β-estradiol did not alter IL-1β, CXCL2 and CCL20 expression. Castration increased pro-inflammatory mediators IL-6, IL-1β and CXCL2 suggesting male sex hormones were anti-inflammatory. Calcitonin gene-related peptide in the trigeminal ganglia was unchanged.

Conclusions: Similar to females, male rats with TMJ inflammation showed a reduced nociceptive response after treatment with a physiological concentration of oestradiol suggesting the effects of oestradiol treatment were not constrained by organizational processes in the males.

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References
1.
Tominaga K, Habu M, Sukedai M, Hirota Y, Takahashi T, Fukuda J . IL-1 beta, IL-1 receptor antagonist and soluble type II IL-1 receptor in synovial fluid of patients with temporomandibular disorders. Arch Oral Biol. 2004; 49(6):493-9. DOI: 10.1016/j.archoralbio.2003.12.008. View

2.
LeResche L . Epidemiology of temporomandibular disorders: implications for the investigation of etiologic factors. Crit Rev Oral Biol Med. 1997; 8(3):291-305. DOI: 10.1177/10454411970080030401. View

3.
Tashiro A, Okamoto K, Bereiter D . Rapid estrogenic effects on TMJ-responsive brainstem neurons. J Dent Res. 2011; 91(2):210-4. PMC: 3261121. DOI: 10.1177/0022034511428156. View

4.
Hirota K, Yoshitomi H, Hashimoto M, Maeda S, Teradaira S, Sugimoto N . Preferential recruitment of CCR6-expressing Th17 cells to inflamed joints via CCL20 in rheumatoid arthritis and its animal model. J Exp Med. 2007; 204(12):2803-12. PMC: 2118525. DOI: 10.1084/jem.20071397. View

5.
Kopp S . The influence of neuropeptides, serotonin, and interleukin 1beta on temporomandibular joint pain and inflammation. J Oral Maxillofac Surg. 1998; 56(2):189-91. DOI: 10.1016/s0278-2391(98)90867-9. View