Kuraji Ryutaro, Fujita Miyako, Ito Hiroshi, Hashimoto Shuichi, Numabe Yukihiro
Department of Life Science Dentistry, The Nippon Dental University, 1-9-20 Fujimi, Chiyoda-ku, Tokyo, Tokyo, 102-8159, Japan.
Department of Periodontology, The Nippon Dental University School of Life Dentistry at Tokyo, 1-9-20 Fujimi, Chiyoda-ku, Tokyo, Tokyo, 102-8159, Japan.
Odontology. 2018 Apr;106(2):162-170. doi: 10.1007/s10266-017-0322-5. Epub 2017 Dec 14.
Recent studies have shown that periodontitis accelerates the progression of obesity-associated metabolic diseases. Thus, we examined the influence of periodontitis on serum biochemical parameters of metabolic disease in a diet-induced obesity (DIO) rat. First, we established the DIO model using ten male rats fed with either basal diet (lean group) or high-fat diet (DIO group) for 12 weeks. Second, to examine the interaction between periodontitis and obesity, we divided 24 DIO rats into the following four groups. (1) Porphyromonas gingivalis (Pg) group was applied with Pg around the maxillary first molar (M1). (2) Ligature group was applied with ligature placement around M1. (3) Ligature/Pg group was treated with both ligature placement and Pg. (4) Control was non-treatment group. Serum biochemical parameters and maxillary histopathology were evaluated at 12 weeks. The DIO model demonstrated significant increases in body weight, serum insulin, alanine aminotransaminase (ALT) levels, and insulin resistance (HOMA-IR) compared to the lean group. In the DIO ligature and ligature/Pg groups, alveolar bone resorption and inflammatory cell infiltration were significantly increased compared to the control. Serum levels of fasting glucose, lactate dehydrogenase, and uric acid were also significantly higher, while the liver damage markers ALT and aspartate aminotransferase were only higher in ligature/Pg group. However, we observed no significant differences between the Pg group and Control. The present study suggested a possibility that periodontitis induced by ligature placement changed serum metabolic parameter regarding organs such as the liver in DIO rat.
最近的研究表明,牙周炎会加速肥胖相关代谢疾病的进展。因此,我们在饮食诱导肥胖(DIO)大鼠中研究了牙周炎对代谢疾病血清生化参数的影响。首先,我们使用10只雄性大鼠建立DIO模型,分别用基础饮食(瘦素组)或高脂饮食(DIO组)喂养12周。其次,为了研究牙周炎与肥胖之间的相互作用,我们将24只DIO大鼠分为以下四组。(1)牙龈卟啉单胞菌(Pg)组在上颌第一磨牙(M1)周围应用Pg。(2)结扎组在M1周围放置结扎线。(3)结扎/Pg组同时进行结扎线放置和Pg处理。(4)对照组为未处理组。在12周时评估血清生化参数和上颌组织病理学。与瘦素组相比,DIO模型的体重、血清胰岛素、丙氨酸转氨酶(ALT)水平和胰岛素抵抗(HOMA-IR)显著增加。在DIO结扎组和结扎/Pg组中,与对照组相比,牙槽骨吸收和炎性细胞浸润显著增加。空腹血糖、乳酸脱氢酶和尿酸的血清水平也显著更高,而肝损伤标志物ALT和天冬氨酸转氨酶仅在结扎/Pg组中更高。然而,我们观察到Pg组和对照组之间没有显著差异。本研究表明,结扎诱导的牙周炎可能会改变DIO大鼠肝脏等器官的血清代谢参数。