Bauer Natali B, Khassawna Thaqif El, Goldmann Fee, Stirn Martina, Ledieu David, Schlewitz Gudrun, Govindarajan Parameswari, Zahner Daniel, Weisweiler David, Schliefke Nathalie, Böcker Wolfgang, Schnettler Reinhard, Heiss Christian, Moritz Andreas
Department of Veterinary Clinical Sciences, Clinical Pathology and Clinical Pathophysiology, Justus-Liebig University Giessen, Frankfurterstraße 126, 35392 Giessen, Germany.
Laboratory of Experimental Trauma Surgery, Justus-Liebig-University of Giessen, KerkraderStrasse 9, 35392 Giessen, Germany.
Exp Toxicol Pathol. 2015 Apr;67(4):287-96. doi: 10.1016/j.etp.2015.01.004. Epub 2015 Mar 12.
An experimental rat model served for evaluation of bone- and energy metabolism in early and late stages of osteoporosis. For the early stage, we hypothesized that bilateral ovariectomy (OVX)+multi-deficiency diet (OVXD; depletion of vitamin D, calcium, vitamin K, phosphorus) would induce increased bone turnover while the late stage would be characterized by enhanced bone catabolism. Obesity, insulin resistance and hyperleptinemia would be seen during the whole course of disease. Healthy female Sprague Dawley rats (n=41) aged 10 weeks were randomly assigned to sham and treatment groups and sacrificed at 3, 12, and 14 months after the study began.
In the early phase, OVXD was associated with an increase in body weight, but not, however, in later stages. There was a decrease in bone mineral density and relative bone volume (BV/TV) as assessed by Dual Energy X-ray Absorptiometry and micro computed tomography that was most severe in the later stages of disease, indicating bone catabolism. Osteocalcin limiting bone formation was increased initially, whereas later stages (14 months) were characterized by elevated osteopontin, suggesting bone remodeling. Severe hyperparathyroidism was present during all stages of disease. Only the early phases of disease were characterized by hyperinsulinemia and increased adrenocorticotrophic stimulating hormone, whereas in the late stage hypoleptinemia rather than hyperleptinemia was seen.
Markers of bone and energy metabolism reflected both an increased bone turn over and ongoing bone remodeling associated with initial hyperinsulinemia. Osteopontin and osteocalcin can be used to differentiate early and late stages of osteoporosis.
采用实验性大鼠模型评估骨质疏松症早期和晚期的骨骼与能量代谢。对于早期阶段,我们假设双侧卵巢切除术(OVX)+多种营养素缺乏饮食(OVXD;维生素D、钙、维生素K、磷缺乏)会导致骨转换增加,而晚期则以骨分解代谢增强为特征。在疾病的整个过程中会出现肥胖、胰岛素抵抗和高瘦素血症。将41只10周龄的健康雌性斯普拉格-道利大鼠随机分为假手术组和治疗组,并在研究开始后的3、12和14个月处死。
在早期阶段,OVXD与体重增加有关,但在后期阶段则不然。通过双能X线吸收法和微型计算机断层扫描评估,骨矿物质密度和相对骨体积(BV/TV)降低,在疾病后期最为严重,表明存在骨分解代谢。最初,限制骨形成的骨钙素增加,而后期阶段(14个月)的特征是骨桥蛋白升高,提示骨重塑。在疾病的所有阶段均存在严重的甲状旁腺功能亢进。只有疾病的早期阶段表现为高胰岛素血症和促肾上腺皮质激素增加,而在后期则出现低瘦素血症而非高瘦素血症。
骨骼和能量代谢标志物既反映了骨转换增加,也反映了与初始高胰岛素血症相关的持续骨重塑。骨桥蛋白和骨钙素可用于区分骨质疏松症的早期和晚期阶段。