Temporomandibular inflammation regulates the matrix metalloproteinases MMP-2 and MMP-9 in limbic structures.
Glauce C do NascimentoBruna B De PaulaRaquel F GerlachChristie Ramos Andrade Leite-PanissiPublished in: Journal of cellular physiology (2021)
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.
Keyphrases
- oxidative stress
- diabetic rats
- blood brain barrier
- poor prognosis
- neuropathic pain
- induced apoptosis
- chronic pain
- extracellular matrix
- drug induced
- high glucose
- pain management
- cell migration
- cerebral ischemia
- high resolution
- traumatic brain injury
- functional connectivity
- early stage
- spinal cord injury
- intensive care unit
- liver failure
- resting state
- cell death
- cell cycle arrest
- brain injury
- hepatitis b virus
- stress induced
- inflammatory response
- spinal cord
- postoperative pain
- aortic dissection