AJP - Regu Fuel your research with LabChart
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
 QUICK SEARCH:   [advanced]


     


Am J Physiol Regul Integr Comp Physiol (February 9, 2006). doi:10.1152/ajpregu.00835.2005
This Article
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
291/2/R343    most recent
00835.2005v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Flake, N. M
Right arrow Articles by Gold, M. S
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Flake, N. M
Right arrow Articles by Gold, M. S
Submitted on November 30, 2005
Accepted on February 7, 2006

TESTOSTERONE AND ESTROGEN HAVE OPPOSING ACTIONS ON INFLAMMATION-INDUCED PLASMA EXTRAVASATION IN THE RAT TEMPOROMANDIBULAR JOINT

Natasha M Flake1, Tracey O Hermanstyne1, and Michael S Gold2*

1 Biomedical Sciences, University of Maryland, Baltimore Dental School, Baltimore, MD, USA
2 Biomedical Sciences, University of Maryland, Baltimore Dental School, Baltimore, MD, USA; Anatomy and Neurobiology, University of Maryland, Baltimore School of Medicine, Baltimore, MD, USA; Program in Neuroscience, University of Maryland, Baltimore, Baltimore, MD, USA

* To whom correspondence should be addressed. E-mail: mgold{at}umaryland.edu.

The present study was designed to test the hypothesis that estrogen exacerbates inflammation of the temporomandibular joint (TMJ). Evans Blue dye was used in order to quantify plasma extravasation (PE) around the rat TMJ. In an initial set of experiments, TMJ PE was compared in naive intact male and female rats as well as in both groups following complete Freund's adjuvant (CFA)-induced inflammation of the TMJ. In contrast to our hypothesis, TMJ PE was significantly greater in both naive and CFA-inflamed male rats than in females. In order to determine whether these differences were due to gonadal hormones, 4 additional groups of rats were studied which included gonadectomized (Gx) males and females, Gx males with chronic testosterone (T) replacement, and Gx females with chronic estrogen (E) replacement. The sex difference in baseline TMJ PE appeared to reflect the actions of T. However, in the presence TMJ inflammation, T augmented TMJ PE in males, while E attenuated TMJ PE in females. Changes in PE were also assessed in the contralateral TMJ. Results from this analysis indicated that there is a transient contralateral increase in TMJ PE in females but not males. Given that there is an inverse relationship between PE and joint damage, our results suggest that testosterone may mitigate but estrogen may exacerbate TMJ damage, particularly in the presence of overt inflammation. Importantly, our results may help explain both the higher prevalence and severity of temporomandibular disorder (TMD) pain in females versus males.




This article has been cited by other articles:


Home page
Am. J. Physiol. Regul. Integr. Comp. Physiol.Home page
K. J. Berkley, S. S. Zalcman, and V. R. Simon
Sex and gender differences in pain and inflammation: a rapidly maturing field
Am J Physiol Regulatory Integrative Comp Physiol, August 1, 2006; 291(2): R241 - R244.
[Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
Visit Other APS Journals Online
Copyright © 2006 by the American Physiological Society.