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Assessment of Alloxan-Induced Diabetic Rats as a Periodontal Disease Model Using a Selective Cyclooxygenase (COX)-2
Yutaka Nakahara1, Kiyokazu Ozaki1, Tomoya Sano1
1Department of Pathology, Faculty of Pharmaceutical Sciences, Setsunan University, 45-1 Nagaotoge-cho, Hirakata, Osaka 573-0101, Japan.
Diabetic rats treated with alloxan develop dental caries, not periodontal disease (PD). Hyperglycemia may worsen caries progression, potentially leading to apical periodontitis and secondary periodontal inflammation.
Area of Science:
- Oral pathology
- Endocrinology
- Periodontology
Background:
- Long-term hyperglycemia in alloxan-treated rats has been suggested to induce periodontal disease (PD).
- Previous studies in this model identified dental caries, suggesting concurrent occurrence of both pathologies.
Purpose of the Study:
- To evaluate alloxan-induced diabetic rats as a model for periodontal disease (PD).
- To assess the efficacy of a selective COX-2 inhibitor in managing PD in this model.
Main Methods:
- Six-week-old female F344 rats were divided into control, alloxan-induced diabetic (AL), and alloxan-induced diabetic with etodolac (AL+Et) groups.
- Animals were euthanized at 26 weeks for histopathological examination of oral tissues.
- A selective COX-2 inhibitor (etodolac) was administered to assess its effect on periodontal inflammation.
Main Results:
- The AL group exhibited enhanced gingivitis, marginal periodontitis, and alveolar bone resorption alongside dental caries compared to controls.
- The COX-2 inhibitor (etodolac) did not reduce periodontal inflammation in the AL+Et group.
- Periodontitis was minimal around healthy molars, and gingivitis was only slightly worse than controls in the AL group; inflammation correlated with caries severity.
Conclusions:
- Alloxan-induced diabetic rats serve as a model for dental caries, not periodontal disease (PD).
- Hyperglycemia in this model may facilitate caries progression to apical periodontitis.
- Associated inflammation might extend to surrounding periodontal tissues, mimicking PD features.
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