Mattila P T, Knuuttila M L, Svanberg M J
Institute of Dentistry, University of Oulu, Finland.
Metabolism. 1998 May;47(5):578-83. doi: 10.1016/s0026-0495(98)90243-8.
The effects of 10% and 20% dietary xylitol supplementation on the biomechanical properties, trabeculation, and mineral content of long bones were studied in streptozotocin-diabetic rats. Forty 3-month-old male Wistar rats were divided randomly into four groups of 10. Rats in three groups were administered a single injection of streptozotocin (50 mg/kg body weight) to induce type I diabetes, while animals in the fourth group were given a sham injection of physiological saline. The sham-injected group and one of the streptozotocin-diabetic groups were fed the basal diet, while the two diabetic groups were fed the same diet supplemented with 10% and 20% xylitol (wt/wt). After 3 months, the rats were killed and the long bones were prepared for analysis. The 10% and 20% dietary xylitol supplementation significantly prevented the type I diabetes-induced decrease in the mechanical stress resistance of the tibia in the three-point bending test, the shear stress of the femur in the torsion test, and the stress resistance of the femoral neck in the loading test. No statistically significant differences were found between any groups in the values for strain or Young's modulus in the three-point bending test, or in the values for the shear modulus of elasticity in the torsion test. These findings indicate that dietary xylitol protects against the weakening of the bone strength properties of both cortical and trabecular bone without affecting the elastic-plastic properties. Supplementation with 10% and 20% dietary xylitol significantly prevented the type I diabetes-induced decrease of humeral ash weight and tibial density. Histomorphometric data for the secondary spongiosa of the proximal tibia showed that 10% and 20% dietary xylitol supplementation also significantly prevented the type I diabetes-induced loss of trabecular bone volume. In conclusion, dietary xylitol supplementation protects against the weakening of bone biomechanical properties in streptozotocin-diabetic rats. This is related to the preserved bone mineral content and preserved trabecular bone volume.
研究了在链脲佐菌素诱导的糖尿病大鼠中,饮食中添加10%和20%木糖醇对长骨生物力学性能、小梁结构和矿物质含量的影响。将40只3个月大的雄性Wistar大鼠随机分为四组,每组10只。三组大鼠单次注射链脲佐菌素(50 mg/kg体重)以诱导I型糖尿病,而第四组动物则注射生理盐水作为假注射。假注射组和其中一组链脲佐菌素诱导的糖尿病组喂食基础饮食,而另外两组糖尿病组喂食添加了10%和20%木糖醇(重量/重量)的相同饮食。3个月后,处死大鼠并准备对长骨进行分析。在三点弯曲试验中,饮食中添加10%和20%木糖醇显著预防了I型糖尿病诱导的胫骨抗机械应力能力下降;在扭转试验中,显著预防了股骨剪切应力下降;在加载试验中,显著预防了股骨颈抗应力能力下降。在三点弯曲试验中,各组之间在应变值或杨氏模量方面,以及在扭转试验中弹性剪切模量值方面,均未发现统计学上的显著差异。这些结果表明,饮食中的木糖醇可防止皮质骨和小梁骨的骨强度特性减弱,而不影响弹塑性特性。饮食中添加10%和20%木糖醇显著预防了I型糖尿病诱导的肱骨灰重和胫骨密度下降。胫骨近端二级海绵体的组织形态计量学数据显示,饮食中添加10%和20%木糖醇也显著预防了I型糖尿病诱导的小梁骨体积丢失。总之,饮食中添加木糖醇可防止链脲佐菌素诱导的糖尿病大鼠骨生物力学性能减弱。这与保留的骨矿物质含量和保留的小梁骨体积有关。