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Masseter Muscular Weakness Affects Temporomandibular Synovitis Induced by Jaw Opening in Growing Rats
Author(s) -
Miho Ozaki,
Sawa Kaneko,
Kunimichi Soma
Publication year - 2008
Publication title -
the angle orthodontist
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.116
H-Index - 86
eISSN - 1945-7103
pISSN - 0003-3219
DOI - 10.2319/072407-342.1
Subject(s) - medicine , temporomandibular joint , masseter muscle , synovitis , hyperplasia , immunohistochemistry , nitric oxide synthase , anatomy , pathology , nitric oxide , arthritis
Objective: To evaluate the influence of impaired masseter function during growth on the development of temporomandibular synovitis. Materials and Methods: Sixteen 3-week-old male Wistar rats were classified into four groups. The first group served as control; and in the second group, jaw opening was forced for 3 hours when the rats were 9 weeks old. In the third and fourth groups, the masseter muscles were bilaterally resected at 3 weeks of age, and the rats in the fourth group were additionally forced to open their jaw at 9 weeks of age. All rats were sacrificed at 9 weeks. Temporomandibular joint (TMJ) tissue samples were processed for histology, and evaluated for cyclooxygenase-2 (COX-2) and inducible nitric oxide synthase (iNOS) expressions by immunohistochemistry to examine the inflammatory changes in the synovial membrane. Results: The control group showed noninflammatory changes. In the jaw-opening group, vascular dilation and weak COX-2 immunoreactivity were induced by jaw opening in the synovium. In the masseter-resection group, the masseter-resected rats exhibited moderate synovial changes while in the resection with opening group, the masseter-resected rats revealed more significant inflammatory changes including synovial hyperplasia, dilated vasculature, fibrin deposits, and intense immunoreactivity for COX-2 and iNOS, all caused by jaw opening. Conclusions: These results suggest that masseter activity in the growth period is an important factor in the induction of temporomandibular synovitis.

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