Shidara Kie, Mohan Geetha, Evan Lay Yan-An, Jepsen Karl J, Yao Wei, Lane Nancy E
Center for Musculoskeletal Health, Department of Internal Medicine, University of California Davis Medical Center, Sacramento, CA, United States.
Department of Orthopaedic Surgery, University of Michigan, Ann Arbor, MI, United States.
J Orthop Translat. 2018 Jul 27;16:91-101. doi: 10.1016/j.jot.2018.07.001. eCollection 2019 Jan.
Glucocorticoids (GCs) are commonly prescribed as treatment for chronic inflammatory diseases. Prolonged use of GCs is a common cause of atraumatic osteonecrosis (ON) and secondary osteoporosis. Currently, there is no effective treatment for this disease; therefore, a reliable animal model would be useful to study both the pathology and novel treatment strategies for patients with the disease. The aim of this study was to establish a validated, reproducible model of GC-induced ON and bone loss in two different mouse strains (BALB/c and C57BL/6).
Seven-week-old male BALB/c ( = 32) and male C57BL/6 mice ( = 32) were randomised into placebo or GC groups and treated with daily 4 mg/L oral dexamethasone in drinking water for 90 days. Study outcome measures included histologic assessment of ON of the distal femur, bone mass and mechanical strength of tibia and lumbar vertebral body, osteoclast number, biochemical measure of bone formation and bone marrow fat quantitation.
GC-induced ON lesions were observed in the distal femur in 47% of the male BALB/c mice and 25% of the male C57BL/6 mice. GC treatment decreased the trabecular bone volume and serum pro-collagen type 1N-protease (P1NP) in BALB/c mice compared with the placebo ( < 0.05) and reduced tibial bone strength in both BALB/c and C57BL/6 mice. GC-treated BALB/c mice had significantly greater marrow fat levels compared to the placebo group.
GC-induced ON was more prevalent in the male BALB/c mice compared to the male C57BL/6 mice. GC treatment significantly reduced bone mass, bone formation measured by P1NP, bone strength and increased marrow fat levels in male BALB/c mice. Therefore, the use of male BALB/c mice strain is recommended for both diagnostic and therapeutic studies for the prevention and treatment of ON and bone loss following prolonged treatment with GCs.
GCs are commonly used to treat patients with various chronic inflammatory diseases, and this is associated with both the development of ON and bone loss. Our study confirmed that the BALB/c mouse strain treated for 90 days with GC may be useful for developing novel treatments for ON.
糖皮质激素(GCs)常用于慢性炎症性疾病的治疗。长期使用GCs是无创伤性骨坏死(ON)和继发性骨质疏松的常见原因。目前,针对这种疾病尚无有效的治疗方法;因此,一种可靠的动物模型对于研究该疾病患者的病理和新的治疗策略将很有用。本研究的目的是在两种不同的小鼠品系(BALB/c和C57BL/6)中建立一种经过验证的、可重复的GC诱导的ON和骨质流失模型。
将7周龄雄性BALB/c小鼠(n = 32)和雄性C57BL/6小鼠(n = 32)随机分为安慰剂组或GC组,通过在饮用水中每日口服4 mg/L地塞米松进行治疗,持续90天。研究结果指标包括对股骨远端ON的组织学评估、胫骨和腰椎椎体的骨量和力学强度、破骨细胞数量、骨形成的生化指标以及骨髓脂肪定量。
在47%的雄性BALB/c小鼠和25%的雄性C57BL/6小鼠的股骨远端观察到GC诱导的ON病变。与安慰剂组相比,GC治疗降低了BALB/c小鼠的小梁骨体积和血清I型前胶原N端蛋白酶(P1NP)(P < 0.05),并降低了BALB/c和C57BL/6小鼠的胫骨骨强度。与安慰剂组相比,经GC治疗的BALB/c小鼠的骨髓脂肪水平显著更高。
与雄性C57BL/6小鼠相比,GC诱导的ON在雄性BALB/c小鼠中更为普遍。GC治疗显著降低了雄性BALB/c小鼠的骨量、通过P1NP测量的骨形成、骨强度,并增加了骨髓脂肪水平。因此,建议使用雄性BALB/c小鼠品系进行预防和治疗GC长期治疗后ON和骨质流失的诊断和治疗研究。
GCs常用于治疗各种慢性炎症性疾病患者,这与ON的发生和骨质流失都有关。我们的研究证实,用GC治疗90天的BALB/c小鼠品系可能有助于开发ON的新治疗方法。