Evidence map›Paper›PMID 41436118›Full record

ArticleJournal of oral & facial pain and headache2025

Up-regulation of peripheral and central CGRP expression combined with subchondral bone remodeling in rat MIA-induced TMJOA model.

Liqin Xu, Henghua Jiang, Qijun Xu, Wei Fang

Abstract read
In one paragraph

Article in Journal of oral & facial pain and headache, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

4 authors.

Liqin Xu *State Key Laboratory Breeding Base of Basic Science of Stomatology (Hubei-MOST) & Key Laboratory of Oral Biomedicine Ministry of Education (KLOBM), School and Hospital of Stomatology, Wuhan University, 430079 Wuhan, Hubei, China.
Henghua Jiang *State Key Laboratory Breeding Base of Basic Science of Stomatology (Hubei-MOST) & Key Laboratory of Oral Biomedicine Ministry of Education (KLOBM), School and Hospital of Stomatology, Wuhan University, 430079 Wuhan, Hubei, China.
Qijun XuDepartment of Plastic Surgery, The Third Hospital of Wuhan, 430060 Wuhan, Hubei, China.
Wei FangDepartment of Oral and Maxillofacial Surgery, School and Hospital of Stomatology, Wuhan University, 430079 Wuhan, Hubei, China.

Funding

National Science Foundation of China No. 81771100 and No. 81671013
6 · The paper itself

Abstract

backgroundTemporomandibular joint osteoarthritis (TMJOA) is a pathological condition marked by subchondral bone remodeling. Osteoarthritis can lead to TMJ pain, nevertheless, the relationship between nociceptive mechanisms and subchondral bone in TMJOA still unclear.

methodsIn the present investigation, a rat TMJOA model was established via intra-articular administration of monosodium iodoacetate (MIA). Following the induction of MIA-triggered TMJOA, tissue samples were collected from the TMJ condyle, trigeminal system components including ganglion (TG) and nucleus caudalis (TNC), and hippocampal formation. Micro-computed tomography (Micro-CT) was employed to evaluate subchondral bone degeneration in the TMJ, while tartrate-resistant acid phosphatase (TRAP) staining was conducted to measure the activity of osteoclasts in the subchondral bone. Furthermore, immunofluorescence (IF) staining was performed to detect the expression of calcitonin gene related peptide (CGRP) in the TMJ subchondral bone. Afterwards, immunohistochemistry (IHC) was used to detect the expression of CGRP in the TG, TNC and hippocampus tissues. The experimental results were expressed as mean ± Standard Error of the Mean (SEM) values and two-way Analysis of Variance (ANOVA) with Student-Newman-Keuls

resultsCompared with the control group, Micro-CT results revealed progressive condylar degeneration over time. Consistently, MIA-induced TMJOA rats demonstrated a pronounced accumulation of TRAP-positive osteoclasts in the subchondral bone. The expression of CGRP in the TMJ subchondral bone, TG, TNC and hippocampus tissues was also obviously increased in MIA-induced TMJOA rats.

conclusionsMIA-induced rat TMJOA pain could be attributed to the augmented exprssion of CGRP in the TMJ subchondral bone, TG, TNC and hippocampus tissues. An elevated level of CGRP stimulated nociception which was implicated in the development of peripheral and central sensitization in TMJOA pain.

Indexed as

Bone RemodelingCalcitonin Gene-Related PeptideOsteoarthritisTemporomandibular Joint DisordersAnimalsDisease Models, AnimalHippocampusIodoacetic AcidMaleMandibular CondyleOsteoclastsRatsRats, Sprague-DawleyTrigeminal GanglionUp-RegulationX-Ray MicrotomographyCalcitonin Gene-Related PeptideIodoacetic AcidCalcitonin gene related peptideMonosodium iodoacetateOsteoarthritisPainSubchondral boneTemporomandibular joint

Identifiers

PMID41436118
PMCPMC12727174

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.