Zawawi Muhamad S F, Marino Victor, Perilli Egon, Cantley Melissa D, Xu Jiake, Purdue P Edward, Dharmapatni Anak A S S K, Haynes David R, Crotti Tania N
Discipline of Anatomy and Pathology, School of Medical Sciences, The University of Adelaide, Adelaide, SA, Australia.
School of Medical Sciences, Universiti Sains Malaysia, Malaysia.
J Biomed Mater Res A. 2015 Nov;103(11):3572-9. doi: 10.1002/jbm.a.35484. Epub 2015 May 29.
The study aimed to determine the effects of parthenolide (PAR) on bone volume (BV) and bone surface resorption as assessed by live-animal microcomputed tomography (μCT) and possible osteocyte death as indicated by empty lacunae histologically in polyethylene (PE) particle-induced calvarial osteolysis in mice. Baseline μCT scans were conducted 7 days preimplantation of 2 × 10(8) PE particles/mL over the calvariae (day 0). PAR at 1 mg/kg/day was subcutaneously injected on days 0, 4, 7, and 10. At day 14, BV and surface resorption was analyzed with μCT. Calvarial tissue was processed for histomorphometric osteocyte evaluation. Serum was analyzed for type-1 carboxy-terminal collagen crosslinks (CTX-1) and osteoclast associated receptor (OSCAR) levels by ELISA. PE significantly decreased BV (p = 0.0368), increased surface bone resorption area (p = 0.0022), and increased the percentage of empty lacunae (p = 0.0043). Interestingly, PAR significantly reduced the resorption surface area (p = 0.0022) and the percentage of empty osteocyte lacunae (p = 0.0087) in the PE-calvariae, but it did not affect BV, serum CTX-1 or OSCAR levels. The ability of PAR to inhibit PE-induced surface bone erosion may better reflect the in vivo situation, where bone resorption occurs on the surface at the bone-implant interface and may also be related to the role of osteocytes in this pathology.
本研究旨在通过活体动物微型计算机断层扫描(μCT)评估小白菊内酯(PAR)对骨体积(BV)和骨表面吸收的影响,以及通过组织学检查空陷窝来评估聚乙烯(PE)颗粒诱导的小鼠颅骨骨溶解中可能出现的骨细胞死亡情况。在颅骨植入2×10(8)个PE颗粒/mL前7天(第0天)进行基线μCT扫描。在第0、4、7和10天皮下注射1 mg/kg/天的PAR。在第14天,用μCT分析BV和表面吸收情况。对颅骨组织进行处理以进行组织形态计量学骨细胞评估。通过酶联免疫吸附测定(ELISA)分析血清中1型羧基末端胶原交联物(CTX-1)和破骨细胞相关受体(OSCAR)水平。PE显著降低了BV(p = 0.0368),增加了表面骨吸收面积(p = 0.0022),并增加了空陷窝百分比(p = 0.0043)。有趣的是,PAR显著降低了PE-颅骨中的吸收表面积(p = 0.0022)和空骨细胞陷窝百分比(p = 0.0087),但它不影响BV、血清CTX-1或OSCAR水平。PAR抑制PE诱导的表面骨侵蚀的能力可能更好地反映体内情况,即骨吸收发生在骨-植入物界面的表面,这也可能与骨细胞在这种病理过程中的作用有关。