Department of Stomatology, 2nd Hospital, Shanxi Medical University, Taiyuan, Shanxi, China.
School of Basic Medicine, Shanxi Medical University, Taiyuan, Shanxi, China.
Front Endocrinol (Lausanne). 2023 Jan 23;14:1098702. doi: 10.3389/fendo.2023.1098702. eCollection 2023.
To observe the elongation of the axial tooth movement in the unopposed rodent molar model with type 1 diabetes mellitus and explore the pathological changes of periodontal ligament and alveolar bone, and their correlation with tooth axial movement.
The 80 C57BL/6J mice were randomly divided into the streptozotocin(STZ)-injected group (n = 50) and the control group (n = 30). Mice in the streptozotocin(STZ)-injected group were injected intraperitoneal with streptozotocin (STZ), and mice in the control group were given intraperitoneal injection of equal doses of sodium citrate buffer. Thirty mice were randomly selected from the successful models as the T1DM group. The right maxillary molar teeth of mice were extracted under anesthesia, and allowed mandibular molars to super-erupt. Mice were sacrificed at 0, 3, 6,9, and 12 days. Tooth elongation and bone mineral density (BMD) were evaluated by micro-CT analysis(0,and 12 days mice). Conventional HE staining, Masson staining and TRAP staining were used to observe the changes in periodontal tissue(0, 3, 6, 9, and 12 days mice). The expression differences of SPARC, FGF9, BMP4, NOGGIN, and type I collagen were analyzed by RT-qPCR.
After 12 days of tooth extraction, our data showed significant super-eruption of mandibular mouse molars of the two groups. The amount of molar super-eruption in the T1DM group was 0.055mm( ± 0.014mm), and in the control group was 0.157( ± 0.017mm). The elongation of the T1DM mice was less than that of the control mice(<0.001). It was observed that the osteoclasts and BMD increased gradually in both groups over time. Compared with the control group, the collagen arrangement was more disordered, the number of osteoclasts was higher (<0.05), and the increase of bone mineral density was lower(2.180 ± 0.007g/cm vs. 2.204 ± 0.006g/cm, <0.001) in the T1DM group. The relative expression of SPARC, FGF9, BMP4, and type I collagen in the two groups increased with the extension of tooth extraction time while NOGGIN decreased. The relative expression of all of SPARC, FGF9, BMP4, and type I collagen in the T1DM group were significantly lower, and the expression of NOGGIN was higher than that in the control group (<0.05).
The axial tooth movement was inhibited in type 1 diabetic mice. The result may be associated with the changes of periodontal ligament osteoclastogenic effects and alveolar bone remodeling regulated by the extracellular matrix and osteogenesis-related factors.
观察 1 型糖尿病非配对啮齿动物模型中轴牙移动的伸长情况,并探讨牙周韧带和牙槽骨的病理变化及其与牙齿轴向运动的关系。
将 80 只 C57BL/6J 小鼠随机分为链脲佐菌素(STZ)注射组(n = 50)和对照组(n = 30)。STZ 注射组小鼠腹腔内注射链脲佐菌素(STZ),对照组小鼠腹腔内注射等量柠檬酸缓冲液。30 只成功模型的小鼠被随机选为 T1DM 组。在麻醉下取出小鼠右侧上颌磨牙,并允许下颌磨牙超萌出。0、3、6、9 和 12 天时,通过 micro-CT 分析评估牙齿伸长和骨矿物质密度(BMD)。0、3、6、9 和 12 天时的小鼠进行常规 HE 染色、Masson 染色和 TRAP 染色,观察牙周组织的变化。通过 RT-qPCR 分析分析 SPARC、FGF9、BMP4、NOGGIN 和 I 型胶原的表达差异。
在牙齿拔出后 12 天,两组下颌小鼠磨牙的超萌出明显。T1DM 组磨牙超萌出量为 0.055mm(±0.014mm),对照组为 0.157(±0.017mm)。T1DM 组小鼠的牙伸长量小于对照组(<0.001)。结果表明,两组的破骨细胞和 BMD 随时间逐渐增加。与对照组相比,T1DM 组胶原排列更为紊乱,破骨细胞数量更高(<0.05),骨矿物质密度增加较低(2.180 ± 0.007g/cm 与 2.204 ± 0.006g/cm,<0.001)。两组 SPARC、FGF9、BMP4 和 I 型胶原的相对表达随牙齿拔出时间的延长而增加,而 NOGGIN 则减少。T1DM 组的 SPARC、FGF9、BMP4 和 I 型胶原的相对表达均明显低于对照组,而 NOGGIN 的表达高于对照组(<0.05)。
1 型糖尿病小鼠的轴向牙齿移动受到抑制。结果可能与细胞外基质和骨生成相关因子调节的牙周韧带成骨细胞生成作用以及牙槽骨重塑的变化有关。