State Key Laboratory of Oral Diseases, National Clinical Research Center for Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
Guanghua School of Stomatology, Hospital of Stomatology, Sun Yat-sen University, Guangzhou, China; Guangdong Provincial Key Laboratory of Stomatology, Guangzhou, China.
Arch Oral Biol. 2017 Nov;83:76-84. doi: 10.1016/j.archoralbio.2017.06.033. Epub 2017 Jul 5.
Intermittent administration of parathyroid hormone (PTH) has been demonstrated to have anabolic effects on bone metabolism and is approved for use in the treatment of osteoporosis. This study evaluates the role of intermittent PTH administration on alveolar bone loss in streptozotocin (STZ)-induced diabetic rats.
Fifty male Sprague Dawley rats were randomly divided into the following five groups: (1) a control group (saline placebo without ligature and STZ injection), (2) a PTH group (PTH administration without ligature and STZ injection), (3) an L group (saline placebo with ligature), (4) an L+STZ group (saline placebo with ligature and STZ injection), and (5) an L+STZ+PTH group (PTH administration with ligature and STZ injection). PTH was administered at 75μg/kg per dose four times a week for 28days. Subsequently, all rats were sacrificed, and their mandibles were extracted for micro-computed tomography (micro-CT) scanning, as well as histological and immunochemical evaluation.
Micro-CT scanning demonstrated the anabolic effect of PTH on alveolar bone metabolism in STZ-induced diabetic rats (P<0.05), and histomorphometry indicated that PTH inhibited inflammation of the periodontium and increased the level of osteoblastic activity (P<0.05). Immunochemical evaluation showed that rats subjected to both ligature placement and STZ injection had the highest receptor activator of nuclear factor kappa B ligand (RANKL)/osteoprotegerin (OPG) ratio and that PTH administration decreased this ratio.
Intermittent systemic PTH administration effectively reduced alveolar bone loss and ameliorated the manifestation of experimental periodontitis in STZ-induced diabetic rats.
甲状旁腺激素(PTH)的间歇性给药已被证明对骨代谢具有合成代谢作用,并且已被批准用于治疗骨质疏松症。本研究评估了间歇性 PTH 给药对链脲佐菌素(STZ)诱导的糖尿病大鼠牙槽骨丢失的作用。
50 只雄性 Sprague Dawley 大鼠随机分为以下五组:(1)对照组(无结扎和 STZ 注射的生理盐水安慰剂),(2)PTH 组(无结扎和 STZ 注射的 PTH 给药),(3)L 组(结扎的生理盐水安慰剂),(4)L+STZ 组(结扎和 STZ 注射的生理盐水安慰剂),和(5)L+STZ+PTH 组(结扎和 STZ 注射的 PTH 给药)。每周 4 次给予 PTH 75μg/kg 剂量,共 28 天。随后,所有大鼠被处死,取出下颌骨进行微计算机断层扫描(micro-CT)扫描,以及组织学和免疫化学评估。
micro-CT 扫描显示 PTH 对 STZ 诱导的糖尿病大鼠牙槽骨代谢具有合成代谢作用(P<0.05),组织形态计量学表明 PTH 抑制牙周炎的炎症并增加成骨细胞活性水平(P<0.05)。免疫化学评估显示,同时结扎和注射 STZ 的大鼠具有最高的核因子κB 配体(RANKL)/骨保护素(OPG)比值,而 PTH 给药降低了该比值。
间歇性全身 PTH 给药可有效减少牙槽骨丢失,并改善 STZ 诱导的糖尿病大鼠实验性牙周炎的表现。