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Updated: Nov 16, 2025

Temporomandibular Joint Pain Measurement by Bite Force and Von Frey Filament Assays in Mice
Published on: September 13, 2024
Temporomandibular inflammation regulates the matrix metalloproteinases MMP-2 and MMP-9 in limbic structures
Glauce C Nascimento1,2, Bruna B De Paula1, Raquel F Gerlach2
1Department of Psychology, Faculty of Philosophy, Science and Letters of Ribeirão Preto, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.
Abstract:
Temporomandibular disorder (TMD) is characterized by acute or chronic orofacial pain, which can be associated with inflammatory processes in the temporomandibular joint (TMJ) and emotional disorders. Peripheral and central sensitization in painful orofacial processes is common, and it can be triggered by peripheral inflammatory challenge with consequent neuroinflammation phenomena. Such neuroinflammation comes from inflammatory products from supportive cells, blood-brain barrier, and extracellular matrix. Here, we evaluated the possible recruitment of limbic structures for modified matrix metalloproteinases (MMPs) expression and activity during temporomandibular inflammation-induced orofacial persistent pain. The inflammatory process in TMJs of rats was induced by Freund's Complete Adjuvant (CFA) administration. The activity and expression of MMPs-2 and 9 were assessed by in situ zymography and conventional zymography, respectively. A glial colocalization with the MMPs was performed using immunofluorescence. The results evidenced both short- and long-term alterations on MMP-2 and -9 expression in the limbic structures following CFA-induced temporomandibular inflammation. The gelatinolytic activity was increased in the central amygdala, hippocampus, hypothalamus, ventrolateral periaqueductal gray (vlPAG), superior colliculus, and inferior colliculus. Finally, an increase of colocalization of MMP-2/GFAP and MMP-9/GFAP in CFA-induced inflammation groups was observed when compared with saline groups in the central amygdala and vlPAG. It is possible to suggest that glial activation is partly responsible for the production of gelatinases in the persistent orofacial pain, and it is involved in the initiation and maintenance of this process, indicating that inhibition of MMPs might be pursued as a potential new therapeutic target for TMD.
Insights
This study shows that matrix metalloproteinases (MMPs) in the brain
Area of Science:
- Neuroscience
- Pain Research
- Biochemistry
Background:
- Temporomandibular disorder (TMD) involves orofacial pain, potentially linked to inflammation and emotional issues.
- Neuroinflammation, involving inflammatory products and glial cells, plays a role in persistent pain.
- Matrix metalloproteinases (MMPs) are implicated in extracellular matrix remodeling and neuronal function.
Purpose of the Study:
- To investigate the role of limbic structures in matrix metalloproteinases (MMPs) expression and activity during temporomandibular inflammation-induced orofacial pain.
- To assess the impact of inflammation on MMP-2 and MMP-9 in specific brain regions.
- To explore the relationship between glial activation and MMPs in persistent orofacial pain.
Main Methods:
- Induction of temporomandibular joint (TMJ) inflammation in rats using Complete Freund's Adjuvant (CFA).
- Assessment of MMP-2 and MMP-9 activity and expression using zymography techniques.
- Immunofluorescence staining to evaluate glial colocalization with MMPs in limbic structures.
Main Results:
- CFA-induced TMJ inflammation caused short- and long-term alterations in MMP-2 and MMP-9 expression in limbic areas.
- Increased gelatinolytic activity of MMPs was observed in the central amygdala, hippocampus, hypothalamus, and midbrain PAG.
- Enhanced colocalization of MMP-2/GFAP and MMP-9/GFAP indicated glial activation in pain-related brain regions.
Conclusions:
- Glial activation contributes to gelatinase production in persistent orofacial pain.
- MMPs and associated glial responses are involved in the initiation and maintenance of TMD-related pain.
- Inhibition of MMPs presents a potential therapeutic target for managing TMD.
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