Tomaszewska Ewa, Dobrowolski Piotr, Muszyński Siemowit, Donaldson Janine, Gołyński Marcin, Zwolska Jowita, Szadkowski Mateusz, Osęka Maciej, Mielnik-Błaszczak Maria, Balicki Ireneusz
Department of Animal Physiology, Faculty of Veterinary Medicine, University of Life Sciences in Lublin, 20-950 Lublin, Poland.
Department of Functional Anatomy and Cytobiology, Institute of Biology, Maria Curie Sklodowska University, 20-033 Lublin, Poland.
J Clin Med. 2024 Sep 20;13(18):5595. doi: 10.3390/jcm13185595.
This longitudinal study examined the early effects of type 1 diabetes on bone mechanical properties and metabolic markers in mature rats, focusing on the natural progression of diabetes-induced changes without external treatments. : Forty-eight 8-month-old male Wistar rats were divided into two groups, with one group receiving a single dose of streptozotocin (STZ, 60 mg/kg). Assessments were performed 2, 4, and 8 weeks post-administration, including serum biochemical analyses, bone marker assessments, and mechanical bone tests. The data were analyzed using two-way ANOVA to evaluate the impact of time and treatment. : At 2 weeks, diabetic rats showed increased fasting blood glucose ( < 0.001), decreased insulin levels ( = 0.03), and changes in HOMA markers ( < 0.001), liver enzymes ( < 0.001), inflammatory markers ( < 0.001), and bone metabolism markers (osteocalcin ( < 0.001), OPG ( = 0.006), RANKL ( < 0.001), and OPG/RANKL ratio ( < 0.001)), with initial alterations in bone geometry. By week 4, decreased body weight in the diabetic group ( < 0.001) led to further changes in bone geometry and initial differences in mechanical properties. At 8 weeks, significant declines in body ( < 0.001) and bone ( < 0.001) weights were observed, along with further deterioration in bone geometry and mechanical properties. : The study highlights the significant impact of STZ-induced diabetes on bone health as early as two weeks post-STZ administration, with marked temporal changes in biochemical markers and mechanical properties.
这项纵向研究考察了1型糖尿病对成熟大鼠骨骼力学性能和代谢标志物的早期影响,重点关注糖尿病诱导变化的自然进展,未进行外部治疗。48只8个月大的雄性Wistar大鼠被分为两组,其中一组接受单剂量链脲佐菌素(STZ,60mg/kg)。在给药后2周、4周和8周进行评估,包括血清生化分析、骨标志物评估和骨力学测试。使用双向方差分析对数据进行分析,以评估时间和治疗的影响。在2周时,糖尿病大鼠空腹血糖升高(<0.001),胰岛素水平降低(=0.03),HOMA标志物、肝酶(<0.001)、炎症标志物(<0.001)和骨代谢标志物(骨钙素(<0.001)、骨保护素(OPG,=0.006)、核因子κB受体活化因子配体(RANKL,<0.001)和OPG/RANKL比值(<0.001))发生变化,同时骨几何形状出现初始改变。到第4周时,糖尿病组体重下降(<0.001)导致骨几何形状进一步改变和力学性能出现初始差异。在8周时,观察到体重(<0.001)和骨重量(<0.001)显著下降,同时骨几何形状和力学性能进一步恶化。该研究强调,STZ诱导的糖尿病在STZ给药后两周就对骨骼健康产生了重大影响,生化标志物和力学性能随时间发生显著变化。