Alhashim Abdulmohsin, Capehart Kim, Tang Jocelyn, Saad Karim M, Abdelsayed Rafik, Cooley Marion A, Williams Jan M, Elmarakby Ahmed A
Departments of General Dentistry and Oral Biology & Diagnostic Sciences, Dental College of Georgia, Augusta University, Augusta, GA 30912, USA.
Oral Biology & Diagnostic Sciences, Dental College of Georgia, Augusta University, Augusta, GA 30912, USA.
Dent J (Basel). 2024 Dec 27;13(1):14. doi: 10.3390/dj13010014.
The incidence of obesity has dramatically increased worldwide. Obesity has been shown to exacerbate the progression of periodontal disease. Studies suggest a sex difference in periodontitis, whereby males are more sensitive to periodontal inflammation compared to females. In the current study, it was hypothesized that obesity drives periodontal inflammation and bone loss in both sexes. Utilizing leptin receptor mutant (SS mutant) rats as a genetic model of obesity, 11-12-week-old male and female lean Dahl salt-sensitive (SS) rats and obese SS mutant rats were used to investigate sex differences in obesity-induced periodontal inflammation. Body weight, insulin, hemoglobin A1c and cholesterol levels were significantly elevated in the obese SS mutant strain vs. the lean SS strain within the same sex. Sex differences in body weight and plasma hemoglobin A1c were only observed in obese SS mutant rats, with males having significantly greater body weight and hemoglobin A1c vs. females. Plasma thiobarbituric acid reactive substances (TBARs) and monocyte chemoattractant protein-1 (MCP-1), markers of systemic oxidative stress and inflammation, respectively, were significantly elevated in obese SS mutant rats vs. lean SS rats, with no sex differences in these parameters in either rat strains. Although micro-CT analyses of the maxillary first molar alveolar bone from obese SS mutant rats revealed no evidence of bone loss and/or sex differences, immuno-histochemical analysis revealed significant elevations in periodontal IL-6 and decreases in IL-10 in obese SS mutant rats vs. lean SS rats, with no apparent sex differences in these parameters. Obesity increases systemic and periodontal inflammation, without evidence of bone loss or apparent sex differences in SS mutant rats.
肥胖症的发病率在全球范围内急剧上升。肥胖已被证明会加剧牙周病的进展。研究表明牙周炎存在性别差异,即与女性相比,男性对牙周炎症更为敏感。在本研究中,我们假设肥胖会导致两性的牙周炎症和骨质流失。利用瘦素受体突变(SS突变)大鼠作为肥胖的遗传模型,选用11 - 12周龄的雄性和雌性瘦型达尔盐敏感(SS)大鼠以及肥胖的SS突变大鼠,来研究肥胖诱导的牙周炎症中的性别差异。与同性别瘦型SS品系相比,肥胖SS突变品系的体重、胰岛素、糖化血红蛋白和胆固醇水平显著升高。仅在肥胖SS突变大鼠中观察到体重和血浆糖化血红蛋白的性别差异,雄性大鼠的体重和糖化血红蛋白显著高于雌性。肥胖SS突变大鼠的血浆硫代巴比妥酸反应物质(TBARs)和单核细胞趋化蛋白-1(MCP-1),分别作为全身氧化应激和炎症的标志物,与瘦型SS大鼠相比显著升高,两种品系大鼠在这些参数上均无性别差异。尽管对肥胖SS突变大鼠上颌第一磨牙牙槽骨的显微CT分析未发现骨质流失和/或性别差异的证据,但免疫组织化学分析显示,与瘦型SS大鼠相比,肥胖SS突变大鼠的牙周IL-6显著升高,IL-10降低,这些参数无明显性别差异。肥胖会增加全身和牙周炎症,在SS突变大鼠中没有骨质流失或明显性别差异的证据。