School of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing 100029, China.
Department of Bone Metabolism, School and Hospital of Stomatology, Cheeloo College of Medicine, Shandong University & Shandong Key Laboratory of Oral Tissue Regeneration & Shandong Engineering Laboratory for Dental Materials and Oral Tissue Regeneration & Shandong Provincial Clinical Research Center for Oral Diseases, Jinan 250012, China.
Medicina (Kaunas). 2023 Aug 3;59(8):1414. doi: 10.3390/medicina59081414.
The incidence of diabetic osteoporosis, an important complication of diabetes mellitus, is increasing gradually. This study investigated the combined effect of the Zuogui pill (ZGP) and eldecalcitol (ED-71), a novel vitamin D analog, on type 2 diabetic osteoporosis (T2DOP) and explored their action mechanism. Blood glucose levels were routinely monitored in db/db mice while inducing T2DOP. We used hematoxylin and eosin staining, Masson staining, micro-computed tomography, and serum biochemical analysis to evaluate changes in the bone mass and blood calcium and phosphate levels of mice. Immunohistochemical staining was performed to assess the osteoblast and osteoclast statuses. The MC3T3-E1 cell line was cultured in vitro under a high glucose concentration and induced to undergo osteogenic differentiation. Quantitative real-time polymerase chain reaction, Western blot, immunofluorescence, ALP, and alizarin red staining were carried out to detect osteogenic differentiation and PI3K-AKT signaling pathway activity. ZGP and ED-71 led to a dramatic decrease in blood glucose levels and an increase in bone mass in the db/db mice. The effect was strongest when both were used together. ZGP combined with ED-71 promoted osteoblast activity and inhibited osteoclast activity in the trabecular bone region. The in vitro results revealed that ZGP and ED-71 synergistically promoted osteogenic differentiation and activated the PI3K-AKT signaling pathway. The PI3K inhibitor LY294002 or AKT inhibitor ARQ092 altered the synergistic action of both on osteogenic differentiation. The combined use of ZGP and ED-71 reduced blood glucose levels in diabetic mice and promoted osteogenic differentiation through the PI3K-AKT signaling pathway, resulting in improved bone mass. Our study suggests that the abovementioned combination constitutes an effective treatment for T2DOP.
糖尿病性骨质疏松症是糖尿病的一种重要并发症,其发病率逐渐升高。本研究探讨了左归丸(ZGP)与新型维生素 D 类似物艾地骨化醇(ED-71)联合应用对 2 型糖尿病性骨质疏松症(T2DOP)的影响,并探讨了其作用机制。在诱导 db/db 小鼠发生 T2DOP 时,常规监测其血糖水平。我们采用苏木精-伊红染色、Masson 染色、微计算机断层扫描和血清生化分析来评估小鼠的骨量和血钙、血磷水平变化。采用免疫组织化学染色来评估成骨细胞和破骨细胞状态。体外培养 MC3T3-E1 细胞系于高糖浓度下,并诱导其向成骨细胞分化。采用实时定量聚合酶链反应、Western blot、免疫荧光、碱性磷酸酶(ALP)和茜素红染色检测成骨细胞分化和 PI3K-AKT 信号通路活性。ZGP 和 ED-71 可显著降低 db/db 小鼠的血糖水平并增加其骨量,两者联合使用效果最强。ZGP 联合 ED-71 可促进骨小梁区域的成骨细胞活性并抑制破骨细胞活性。体外实验结果表明,ZGP 和 ED-71 协同促进成骨细胞分化并激活 PI3K-AKT 信号通路。PI3K 抑制剂 LY294002 或 AKT 抑制剂 ARQ092 改变了两者对成骨细胞分化的协同作用。ZGP 和 ED-71 的联合使用可降低糖尿病小鼠的血糖水平,并通过 PI3K-AKT 信号通路促进成骨细胞分化,从而改善骨量。本研究表明,上述联合治疗可有效治疗 T2DOP。