Biomaterials Laboratory, Department of Restorative Dentistry, Rutgers School of Dental Medicine, NJ, USA; Department of Endodontics, University of the Pacific, Arthur A. Dugoni School of Dentistry, CA, USA.
Department of Ophthalmology and Visual Sciences, University of Wisconsin School of Medicine and Public Health, Madison, WI, USA.
Arch Oral Biol. 2022 Jul;139:105434. doi: 10.1016/j.archoralbio.2022.105434. Epub 2022 Apr 18.
This study was performed to evaluate the effect of type 1 diabetes mellitus (T1DM) on the microhardness of tooth enamel and dentine in mice.
Seventy male C57BL/6 J mice were used in this study. Thirty-five mice were rendered diabetic by administration of streptozotocin (STZ), and the remaining animals received citrate buffer (normal/non-diabetic). In each group, specimens were divided into 7 subgroups of 5 mice based on the time points 0, 1, 4, 8, 12, 20, and 28 weeks. The microhardness value (MHV) of the second molars' enamel and root dentine were tested with a Vickers microhardness tester. Five specimens from each subgroup were evaluated for dentinal tubular density by scanning electron microscope (SEM) and color dot map analysis to determine the color intensity of strontium (Sr) and magnesium (Mg) by using ImageJ software.
The MHV of enamel was significantly reduced in STZ specimens in time points of 12 weeks (STZ: 274.39 ± 15.42, normal: 291.22 ± 15.28), 20 weeks (STZ: 247.28 ± 19.65, normal: 290.68 ± 11.52), and 28 weeks (STZ: 232.87 ± 15.07, normal: 282.76 ± 10.36) (P < 0.05). When comparing the MHV of dentine in subgroups of the normal group, after 20 weeks (169.1 ± 7.5) and 28 weeks (168.6 ± 7.81), the MHV increased significantly (P < 0.05). However, in the STZ group, a significant reduction of MHV was noticed between 28 weeks (131.69 ± 6.2) specimens with other subgroups (P < 0.05).
T1DM negatively affected enamel and dentine microhardness, and enamel was influenced much more negatively and rapidly compared with dentine in diabetic groups.
本研究旨在评估 1 型糖尿病(T1DM)对小鼠牙釉质和牙本质微观硬度的影响。
本研究使用了 70 只雄性 C57BL/6J 小鼠。35 只小鼠通过链脲佐菌素(STZ)给药诱导糖尿病,其余动物给予柠檬酸盐缓冲液(正常/非糖尿病)。在每组中,根据 0、1、4、8、12、20 和 28 周的时间点,将标本分为 7 个 5 只小鼠亚组。使用维氏硬度测试仪测试第二磨牙釉质和根牙本质的微观硬度值(MHV)。每组 5 个标本通过扫描电子显微镜(SEM)和色点图分析评估牙本质小管密度,使用 ImageJ 软件确定锶(Sr)和镁(Mg)的颜色强度。
在 12 周(STZ:274.39±15.42,正常:291.22±15.28)、20 周(STZ:247.28±19.65,正常:290.68±11.52)和 28 周(STZ:232.87±15.07,正常:282.76±10.36)时,STZ 标本的牙釉质 MHV 显著降低(P<0.05)。在正常组的亚组中比较牙本质 MHV 时,在 20 周(169.1±7.5)和 28 周(168.6±7.81)后,MHV 显著增加(P<0.05)。然而,在 STZ 组中,28 周(131.69±6.2)标本与其他亚组相比,MHV 显著降低(P<0.05)。
T1DM 对牙釉质和牙本质微观硬度有负面影响,与糖尿病组的牙本质相比,牙釉质受到的影响更大且更快。