Guo Yubo, Wang Lili, Ma Rufeng, Mu Qianqian, Yu Na, Zhang Yi, Tang Yuqing, Li Yu, Jiang Guangjian, Zhao Dandan, Mo Fangfang, Gao Sihua, Yang Meijuan, Kan Feifei, Ma Qun, Fu Min, Zhang Dongwei
Preclinical Medicine School, Beijing University of Chinese Medicine, Beijing 100029, China.
Diabetes Research Center, Beijing University of Chinese Medicine, Beijing 100029, China.
Life Sci. 2016 Mar 1;148:24-30. doi: 10.1016/j.lfs.2016.02.056. Epub 2016 Feb 15.
To assess the beneficial effects of JiangTang XiaoKe (JTXK) granule on the bone metabolism in high fat diet (HFD) fed KK-Ay diabetic mice.
The KK-Ay mice were used as a diabetic model, while C57BL/6 mice were utilized as the non-diabetic control. The left tibia was used for determining bone mineral density (BMD) and bone ash coefficient. The HE and alizarin red S staining of femur were employed to evaluate bone pathology and calcium deposition. The expressions of alkaline phosphatase (ALP), insulin growth factor 1 (IGF-1) and cathepsin K were assessed by western blotting and immunohistochemical staining.
JTXK granule significantly improved the bone ash coefficient, the distribution of trabecular bone and the calcification nodules deposition in KK-Ay mice with diabetes. IGF-1 and ALP expressions were significantly decreased, and cathepsin K expression was dramatically increased in the HFD fed KK-Ay diabetic model mice, which can be reversed by JTXK granule treatment. JTXK granule at medium or high dosage was more efficient in improving diabetic bone quality when compared with that in mice with a low dosage. However, the BMD values in each group of KK-Ay diabetic mice were not significantly different.
We demonstrate that cathepsin K expression is increased in KK-Ay diabetic mouse model. JTXK granule treatment inhibits osteoclastic bone resorption and promotes the new bone formation by decreasing cathepsin K activity and increasing IGF-1 and ALP levels. These changes may contribute to the increase of bone strength and thus reducing the risk of bone fractures.
评估降糖消颗粒对高脂饮食喂养的KK-Ay糖尿病小鼠骨代谢的有益作用。
将KK-Ay小鼠作为糖尿病模型,C57BL/6小鼠作为非糖尿病对照。取左侧胫骨测定骨密度(BMD)和骨灰系数。采用苏木精-伊红(HE)染色和茜素红S染色评估股骨的骨病理学和钙沉积情况。通过蛋白质免疫印迹法和免疫组织化学染色评估碱性磷酸酶(ALP)、胰岛素生长因子1(IGF-1)和组织蛋白酶K的表达。
降糖消颗粒显著改善了糖尿病KK-Ay小鼠的骨灰系数、小梁骨分布和钙化结节沉积。在高脂饮食喂养的KK-Ay糖尿病模型小鼠中,IGF-1和ALP表达显著降低,组织蛋白酶K表达显著增加,而降糖消颗粒治疗可使其逆转。与低剂量组相比,中、高剂量的降糖消颗粒在改善糖尿病小鼠骨质量方面更有效。然而,各KK-Ay糖尿病小鼠组的BMD值无显著差异。
我们证明在KK-Ay糖尿病小鼠模型中组织蛋白酶K表达增加。降糖消颗粒治疗通过降低组织蛋白酶K活性、增加IGF-1和ALP水平来抑制破骨细胞骨吸收并促进新骨形成。这些变化可能有助于增加骨强度,从而降低骨折风险。