Department of Nutrition and Exercise Physiology, University of Missouri, Columbia, MO, United States.
Department of Nutrition and Exercise Physiology, University of Missouri, Columbia, MO, United States; Research Service-Harry S Truman Memorial Veterans Medical Center, Columbia, MO, United States.
Bone. 2017 Dec;105:200-211. doi: 10.1016/j.bone.2017.09.003. Epub 2017 Sep 9.
Obesity and type 2 diabetes (T2D) increase fracture risk; however, the association between obesity/T2D may be confounded by consumption of a diet high in fat, sucrose, and cholesterol (HFSC).
The study objective was to determine the main and interactive effects of obesity/T2D and a HFSC diet on bone outcomes using hyperphagic Otuska Long Evans Tokushima Fatty (OLETF) rats and normophagic Long Evans Tokushima Otsuka (LETO) controls.
At 8weeks of age, male OLETF and LETO rats were randomized to either a control (CON, 10 en% from fat as soybean oil) or HFSC (45 en% from fat as soybean oil/lard, 17 en% sucrose, and 1wt%) diet, resulting in four treatment groups. At 32weeks, total body bone mineral content (BMC) and density (BMD) and body composition were measured by dual-energy X-ray absorptiometry, followed by euthanasia and collection of blood and tibiae. Bone turnover markers and sclerostin were measured using ELISA. Trabecular microarchitecture of the proximal tibia and geometry of the tibia mid-diaphysis were measured using microcomputed tomography; whole-bone and tissue-level biomechanical properties were evaluated using torsional loading of the tibia. Two-factor ANOVA was used to determine main and interactive effects of diet (CON vs. HFSC) and obesity/T2D (OLETF vs. LETO) on bone outcomes.
Hyperphagic OLEFT rats had greater final body mass, body fat, and fasting glucose than normophagic LETO, with no effect of diet. Total body BMC and serum markers of bone formation were decreased, and bone resorption and sclerostin were increased in obese/T2D OLETF rats. Trabecular bone volume and microarchitecture were adversely affected by obesity/T2D, but not diet. Whole-bone and tissue-level biomechanical properties of the tibia were not affected by obesity/T2D; the HFSC diet improved biomechanical properties only in LETO rats.
Obesity/T2D, regardless of diet, negatively impacted the balance between bone formation and resorption and trabecular bone volume and microarchitecture in OLETF rats.
肥胖和 2 型糖尿病(T2D)会增加骨折风险;然而,肥胖/T2D 之间的这种关联可能会受到高脂肪、蔗糖和胆固醇(HFSC)饮食的影响。
本研究旨在通过肥胖/高血糖 Otuska 长耳东津肥胖(OLETF)大鼠和正常血糖长耳东津 Otuka(LETO)对照,确定肥胖/T2D 与 HFSC 饮食对骨骼的主要和交互作用。
8 周龄时,雄性 OLETF 和 LETO 大鼠随机分为对照组(CON,10%来自大豆油的脂肪)或 HFSC 组(45%来自大豆油/猪油的脂肪、17%蔗糖和 1%wt%胆固醇),共 4 个处理组。32 周时,采用双能 X 射线吸收法测量全身骨矿物质含量(BMC)和密度(BMD)和身体成分,随后处死并采集血液和胫骨。采用 ELISA 法测定骨转换标志物和硬化蛋白。采用 microCT 法测定胫骨近端小梁微结构和胫骨中轴几何形状;采用胫骨扭转加载法评价全骨和组织水平的生物力学性能。采用双因素方差分析确定饮食(CON 与 HFSC)和肥胖/T2D(OLETF 与 LETO)对骨骼的主要和交互作用。
多食的 OLEFT 大鼠的终体重、体脂和空腹血糖均高于正常摄食的 LETO 大鼠,饮食无影响。肥胖/T2D 的 OLETF 大鼠全身 BMC 和骨形成标志物血清减少,骨吸收和硬化蛋白增加。肥胖/T2D 对小梁骨体积和微结构有不良影响,但饮食无影响。肥胖/T2D 对胫骨的整体和组织水平的生物力学性能没有影响;HFSC 饮食仅改善 LETO 大鼠的生物力学性能。
肥胖/T2D 无论饮食如何,都会对 OLETF 大鼠的骨形成与吸收平衡以及小梁骨体积和微结构产生负面影响。