Zhou Sheng, Wang Guanghu, Qiao Liang, Ge Qiting, Chen Dongyang, Xu Zhihong, Shi Dongquan, Dai Jin, Qin Jinzhong, Teng Huajian, Jiang Qing
The Center of Diagnosis and Treatment for Joint Disease, Drum Tower Hospital, Medical School, Nanjing University, Nanjing, Jiangsu 210008, P.R. China.
Joint Research Center for Bone and Joint Disease, Model Animal Research Center (MARC), Nanjing University, Nanjing, Jiangsu 210061, P.R. China.
Exp Ther Med. 2018 Apr;15(4):3623-3632. doi: 10.3892/etm.2018.5839. Epub 2018 Feb 6.
The ovariectomized (OVX) mouse model has been widely accepted to be suitable for the study of postmenopausal osteoporosis. However, whether C57BL/6J mice, a commonly used genetic background mouse strain, is an appropriate model for postmenopausal osteoporosis remains controversial. The present study investigated the effect of the OVX model on alterations in bone density and microarchitecture in C57BL/6J female mice of different ages. C57BL/6J mice were divided into 8-, 12- and 16-week-old groups (OVX, OVX and OVX) from the beginning of OVX. At 8 weeks post-surgery, the mice were anesthetized and micro-computed tomography was used to analyze the bone density and microarchitecture. The results revealed that OVX-induced loss of cancellous bone was greatest in OVX, moderate in OVX, and only a weak bone loss was observed in the OVX group when compared with the SHAM control group. In addition, the effect of genetic backgrounds in response to the OVX model were examined. Several other strains of mice, including inbred (BALB/c) and outbred (ICR and Kunming), were used in the present study, all of which were subjected to OVX at 8 weeks of age. The present findings revealed that the highest rate of bone loss was detected in C57BL/6J female mice. In addition, treatment with estrogen (17β-estradiol, 30 µg/kg five times per week) led to a significant increase in bone density in C57BL/6J mice compared with the other strains of mice. Therefore, these results may provide novel insights into the age- and strain-associated effect of OVX on regulating turnover of bone in female mice. The present findings also suggest 8-week-old C57BL/6J mice as an animal model for postmenopausal osteoporosis and preclinical testing of potential therapies for this disease.
卵巢切除(OVX)小鼠模型已被广泛认为适用于绝经后骨质疏松症的研究。然而,常用的遗传背景小鼠品系C57BL/6J小鼠是否是绝经后骨质疏松症的合适模型仍存在争议。本研究调查了OVX模型对不同年龄C57BL/6J雌性小鼠骨密度和微观结构改变的影响。从OVX开始,将C57BL/6J小鼠分为8周龄、12周龄和16周龄组(OVX组、OVX组和OVX组)。术后8周,将小鼠麻醉,使用微型计算机断层扫描分析骨密度和微观结构。结果显示,与假手术对照组相比,OVX诱导的松质骨丢失在8周龄OVX组中最大,12周龄OVX组中等,16周龄OVX组仅观察到轻微的骨质流失。此外,还研究了遗传背景对OVX模型反应的影响。本研究使用了其他几种小鼠品系,包括近交系(BALB/c)和远交系(ICR和昆明小鼠),所有这些小鼠在8周龄时均接受了OVX手术。目前的研究结果显示,C57BL/6J雌性小鼠的骨质流失率最高。此外,与其他品系的小鼠相比,用雌激素(17β-雌二醇,每周5次,每次30μg/kg)治疗可使C57BL/6J小鼠的骨密度显著增加。因此,这些结果可能为OVX对雌性小鼠骨转换调节的年龄和品系相关效应提供新的见解。目前的研究结果还表明,8周龄的C57BL/6J小鼠可作为绝经后骨质疏松症的动物模型以及该疾病潜在治疗方法的临床前测试模型。