Department of Oral Immunology and Infectious Diseases, University of Louisville School of Dentistry, Louisville, KY, 40202, USA.
Department of Oral Immunology and Infectious Diseases, University of Louisville School of Dentistry, Louisville, KY, 40202, USA.
Microb Pathog. 2018 Nov;124:145-151. doi: 10.1016/j.micpath.2018.08.019. Epub 2018 Aug 15.
Although pregnant women are prone to gingival inflammation, its mechanism remains unclear. Animal models are ideal for investigating immunological mechanisms in the periodontal disease. A murine model for ligature-induced periodontal disease has been modified and utilized to determine the susceptibility to periodontal inflammation and tissue damage in pregnant mice. Expression of different inflammatory mediators in the gingivae was determined by quantitative real-time PCR (qPCR). Inflammatory bone loss was determined by measuring the distance from the cementoenamel junction to the alveolar bone crest (CEJ-ABC). Oral bacterial number was determined by the CFU (Colony Forming Units) count from anaerobic culture of oral swabs. In our experiments, ligation itself did not cause higher gingival inflammation and bone loss in pregnant mice than non-pregnant mice, while ligation combined with P. gingivalis infection led to increased gingival inflammation and periodontal bone loss, accompanied by lower gingival expression of anti-inflammatory cytokines in pregnant mice. Our results indicated that P. gingivalis infection was important in inducing more severe periodontal diseases during pregnancy, which might be attributed to the down-regulated anti-inflammatory mechanisms, but not be associated with higher oral bacterial burden.
虽然孕妇容易发生牙龈炎症,但其机制尚不清楚。动物模型是研究牙周病免疫机制的理想模型。已经对结扎诱导牙周病的小鼠模型进行了改良,并用于确定妊娠小鼠对牙周炎症和组织损伤的易感性。通过实时定量 PCR(qPCR)测定牙龈中不同炎症介质的表达。通过测量从牙釉质牙骨质界到牙槽骨嵴的距离(CEJ-ABC)来确定炎症性骨丢失。通过口腔拭子厌氧培养的 CFU(集落形成单位)计数来确定口腔细菌数量。在我们的实验中,结扎本身不会导致妊娠小鼠的牙龈炎症和骨丢失高于非妊娠小鼠,而结扎结合 P. gingivalis 感染会导致牙龈炎症和牙周骨丢失增加,同时妊娠小鼠的牙龈抗炎细胞因子表达降低。我们的结果表明,P. gingivalis 感染在怀孕期间诱导更严重的牙周病中很重要,这可能归因于抗炎机制下调,但与更高的口腔细菌负荷无关。