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脊柱关节病HLA - B27转基因大鼠模型中骨强度降低。

Decreased bone strength in HLA-B27 transgenic rat model of spondyloarthropathy.

作者信息

Akhter M P, Jung L K L

机构信息

Medicine, Creighton University, Suite 4820, 610N, 30th Street, Omaha, NE 68131, USA.

出版信息

Rheumatology (Oxford). 2007 Aug;46(8):1258-62. doi: 10.1093/rheumatology/kem104. Epub 2007 May 27.

DOI:10.1093/rheumatology/kem104
PMID:17526927
Abstract

OBJECTIVE

To investigate the nature of osteopenia/osteoporosis in spondyloarthropathy, an inflammatory disorder, using the HLA-B27 transgenic rat model.

METHODS

HLA-B27 transgenic rats were housed individually and sacrificed at the peak of their disease (8-month-old). The spine and femurs were removed and stored in saline at -20 degrees C until analysis. The bone structure and strength were determined using a micro-computed tomography (micro-CT) device (Scanco Medical) and mechanical testing (Instron 5543). Vertebral bodies and femurs were scanned to determine trabecular structural properties in terms of bone volume (BV/TV), trabecular thickness, and spacing. After scanning, the mid-shaft femurs were subjected to a 3-point bending test (along anterior-posterior direction), the femoral necks were tested in bending, and the vertebral bodies (L4) were tested in compression. Structural (ultimate/yield load, stiffness) and apparent material (ultimate/yield stress, modulus) strength parameters were then determined.

RESULTS

The majority of the bone structural and strength parameters were significantly lower (P < 0.05) in the HLA-B27 transgenic rats as compared with control littermates. Micro-CT data suggested that the transgenic animals had lower BV/TV and trabecular thickness in their vertebral bodies. The poor trabecular structure observed in HLA-B27 rats is also indicative of the poor biomechanical strength properties in the vertebral bodies as well.

CONCLUSION

The HLA-B27 transgenic rats develop bone fragility similar to that seen in spondyloarthropathy and may be an important model for the study of osteoporosis in spondyloarthropathy.

摘要

目的

利用HLA - B27转基因大鼠模型研究脊柱关节炎(一种炎症性疾病)中骨质减少/骨质疏松的本质。

方法

将HLA - B27转基因大鼠单独饲养,并在疾病高峰期(8月龄)处死。取出脊柱和股骨,保存在-20℃的盐水中直至分析。使用微型计算机断层扫描(micro-CT)设备(Scanco Medical)和力学测试(Instron 5543)测定骨结构和强度。扫描椎体和股骨,以确定骨体积(BV/TV)、小梁厚度和间距方面的小梁结构特性。扫描后,对股骨中段进行三点弯曲试验(沿前后方向),对股骨颈进行弯曲试验,对椎体(L4)进行压缩试验。然后确定结构(极限/屈服载荷、刚度)和表观材料(极限/屈服应力、模量)强度参数。

结果

与对照同窝仔鼠相比,HLA - B27转基因大鼠的大多数骨结构和强度参数显著降低(P < 0.05)。Micro-CT数据表明,转基因动物椎体的BV/TV和小梁厚度较低。在HLA - B27大鼠中观察到的不良小梁结构也表明椎体的生物力学强度特性较差。

结论

HLA - B27转基因大鼠发生的骨脆性与脊柱关节炎中所见相似,可能是研究脊柱关节炎中骨质疏松的重要模型。

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