Females have greater susceptibility to develop ongoing pain and central sensitization in a rat model of temporomandibular joint pain.


Journal

Pain
ISSN: 1872-6623
Titre abrégé: Pain
Pays: United States
ID NLM: 7508686

Informations de publication

Date de publication:
09 2019
Historique:
entrez: 21 8 2019
pubmed: 21 8 2019
medline: 28 7 2020
Statut: ppublish

Résumé

Temporomandibular joint osteoarthritis (TMJOA) is a prevalent source of temporomandibular joint disorder (TMD). Women are more commonly diagnosed with TMD and are more likely to seek care at tertiary orofacial pain clinics. Limited knowledge regarding mechanisms underlying temporomandibular joint (TMJ) pain impairs development of improved pain management strategies. In a rat model of unilateral TMJOA, monosodium iodoacetate (MIA) produces joint pathology in a concentration-dependent manner. Unilateral MIA produces alterations in meal patterns in males and females without altering overnight time spent eating or weight across 2 weeks. Monosodium iodoacetate (80 mg/mL)-treated males develop ongoing pain within 2 weeks after MIA injection. Females develop ongoing pain at a 5-fold lower MIA concentration (16.6 mg/m). Monosodium iodoacetate (80 mg/mL)-treated males show spread of tactile hypersensitivity across the face during the first week after injection and then to the fore paws and hind paws during the second week after injection, indicating development of central sensitization. At the lower dose, female rats demonstrate a similar spread of tactile hypersensitivity, whereas male rats do not develop ongoing pain or spread of tactile hypersensitivity outside the area of the ipsilateral temporomandibular joint. These observations indicate that females have a higher susceptibility to development of ongoing pain and central sensitization compared with male rats that is not due to differences in MIA-induced joint pathology. This model of TMJOA pain can be used to explore sex differences in pain processes implicated in development of neuropathic pain, ongoing pain, and central sensitization, allowing for development of individualized strategies for prevention and treatment of TMD joint pain.

Identifiants

pubmed: 31430262
doi: 10.1097/j.pain.0000000000001598
pii: 00006396-201909000-00014
pmc: PMC7092504
mid: NIHMS1527478
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

2036-2049

Subventions

Organisme : NIGMS NIH HHS
ID : P20 GM103643
Pays : United States
Organisme : NIGMS NIH HHS
ID : U54 GM115516
Pays : United States

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Auteurs

Sébastien Sannajust (S)

Department of Biomedical Sciences, College of Osteopathic Medicine, Biddeford, ME, United States.
Center for Excellence in the Neurosciences, University of New England, Biddeford, ME, United States.

Ian Imbert (I)

Department of Biomedical Sciences, College of Osteopathic Medicine, Biddeford, ME, United States.

Victoria Eaton (V)

Department of Biomedical Sciences, College of Osteopathic Medicine, Biddeford, ME, United States.
Center for Excellence in the Neurosciences, University of New England, Biddeford, ME, United States.

Terry Henderson (T)

Center for Molecular Medicine, Maine Medical Center Research Institute, Scarborough, ME, United States.

Lucy Liaw (L)

Center for Molecular Medicine, Maine Medical Center Research Institute, Scarborough, ME, United States.

Meghan May (M)

Department of Biomedical Sciences, College of Osteopathic Medicine, Biddeford, ME, United States.

Mary F Barbe (MF)

Department of Anatomy and Cell Biology, Temple University, Lewis Katz School of Medicine, Philadelphia, PA, United States.

Tamara King (T)

Department of Biomedical Sciences, College of Osteopathic Medicine, Biddeford, ME, United States.
Center for Excellence in the Neurosciences, University of New England, Biddeford, ME, United States.

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Classifications MeSH