Center of System Biomedical Sciences, School of Medical Instrument and Food Engineering, University of Shanghai for Science and Technology, Shanghai 200093, People's Republic of China.
Osteoporos Int. 2011 Jun;22(6):1781-8. doi: 10.1007/s00198-010-1404-1. Epub 2010 Sep 29.
This study aimed to delineate the mechanism involved in type 1 diabetes-induced bone loss. The results revealed the alteration of vitamin D metabolic enzyme expression and the downregulation of renal calcium transporter abundance in type 1 diabetic mice.
The purpose of this study was to investigate the changes of the expression of vitamin D metabolic enzymes and transcellular calcium-transporting proteins in kidneys from mice with experimentally induced diabetes.
Male DBA/2J mice were injected with either vehicle (control) or streptozotocin (STZ) daily for five consecutive days. Bone mineral density was measured by peripheral quantitative computerized tomography, and bone histomorphology was analyzed by Safranin O staining. Real-time PCR and Western blotting were applied to determine the expression of target genes and proteins.
Type 1 diabetes produced high urinary calcium excretion and loss of trabecular bone measured at the proximal metaphysis of the tibia and the distal femur. Bone loss was associated with deterioration of trabecular bone microstructure. Quantified PCR results showed that mRNA expression level in the kidney of diabetic mice for 25-hydroxyvitamin D-24-hydroxylase was downregulated at week 10, while those for 25-hydroxyvitamin D-1α-hydroxylase were upregulated at week 20. In addition, mRNA expression levels for renal transient receptor potential V6, plasma membrane Ca-ATPase (PMCA)1b, and vitamin D receptor (VDR) genes were decreased in STZ-treated mice. Western blot analysis showed that protein expression of PMCA1b and VDR was significantly decreased in kidneys from STZ-treated mice compared to that of controls.
The limitation in this study is the lack of vitamin D, parathyroid hormone, and phosphorus levels in serum. However, the present study supports the conclusion that the underlying mechanism contributing to type 1 diabetes-associated bone loss may be alterations of vitamin D metabolic enzyme expression and associated decreases in expression of renal calcium transporters.
阐明 1 型糖尿病导致骨丢失的机制。结果揭示了 1 型糖尿病小鼠维生素 D 代谢酶表达改变和肾脏钙转运体丰度下调。
本研究旨在研究实验性诱导糖尿病小鼠肾脏中维生素 D 代谢酶表达的变化。
雄性 DBA/2J 小鼠连续 5 天每天注射载体(对照)或链脲佐菌素(STZ)。通过外周定量计算机断层扫描测量骨矿物质密度,并通过番红 O 染色分析骨组织形态计量学。实时 PCR 和 Western blot 用于确定靶基因和蛋白的表达。
1 型糖尿病导致尿钙排泄增加和胫骨近端干骺端和股骨远端小梁骨丢失。骨丢失与小梁骨微观结构恶化有关。定量 PCR 结果显示,糖尿病小鼠肾脏中 25-羟维生素 D-24-羟化酶的 mRNA 表达水平在第 10 周下调,而 25-羟维生素 D-1α-羟化酶的 mRNA 表达水平在第 20 周上调。此外,STZ 处理小鼠肾脏中瞬时受体电位 V6、质膜 Ca-ATP 酶(PMCA)1b 和维生素 D 受体(VDR)基因的 mRNA 表达水平降低。Western blot 分析显示,与对照组相比,STZ 处理小鼠肾脏中 PMCA1b 和 VDR 的蛋白表达显著降低。
本研究的局限性在于缺乏血清中维生素 D、甲状旁腺激素和磷的水平。然而,本研究支持这样的结论,即导致 1 型糖尿病相关骨丢失的潜在机制可能是维生素 D 代谢酶表达的改变和肾脏钙转运体表达的相关降低。