期刊文献+

去卵巢大鼠不同时期皮质骨与松质骨变化的显微CT观察 被引量:4

Micro-CT analysis of cortical and cancellous bone on left tibial in ovariectomized rats
原文传递
导出
摘要 目的应用显微CT观察去卵巢大鼠胫骨近端皮质骨与松质骨骨密度和骨微结构差异。方法40只7月龄SD大鼠,随机分为去卵巢(OVX)组和假手术(SHAM)组,每组20只,于手术后第3周及第15周处死。处死后剥离左侧胫骨,行显微CT三维扫描,扫描完成后选取距生长板远端2.5 mm、层厚0.4 mm骨组织为皮质骨感兴趣区域,选取距生长板远端0.7 mm、层厚1.2 mm骨组织为松质骨感兴趣区域行三维重建。获取二维最大密度投射图像及三维结构图像,并对感兴趣区的皮质骨和松质骨进行定量分析。结果3周时,OVX和SHAM组大鼠皮质骨面积分别为(0.43±0.13)、(0.31±0.06)mm^2;骨髓腔面积(10.31±1.98)、(8.44±1.25)mm^2,截面总面积(10.74±2.05)、(8.75±1.26)mm^2,截面惯性矩(4.10±0.73)、(3.49±0.37)mm^4,两组比较差异有统计学意义(均为P〈0.05)。第15周时,除OVX组皮质骨平均厚度低于SHAM组外(P〈0.05),其余各参数两组比较差异无统计学意义。15周OVX组大鼠左侧胫骨骨丢失敏感区域内皮质骨平均厚度和皮质骨面积较3周OVX组大鼠下降(P〈0.05)。SHAM组15周大鼠骨内径周长、骨外径周长和截面惯性矩增大,与3周比较,差异有统计学意义(P〈0.05)。3周时,OVX和SHAM组体积骨密度分别为(288.2±48.2)mg/mm^3和(408.4±51.6)mg/mm^3、组织骨密度(604.5±45.3) mg/mm^3和(686.7±40.0)mg/mm^3、骨体积分数(25.1±5.1)%和(33.6±4.1)%、骨小梁数量(6.04±2.94)个/mm和(9.85±2.83)个/mm,两组比较差异有统计学意义(均为P〈0.05),结构模型指数(分别为3.11±0.36)和2.58±0.36),小梁间隔为(0.37±0.22)mm和(0.14±0.10)mm,明显高于SHAM组(P〈0.05)。第15周时,OVX组体积骨密度、骨体积分数、骨小梁数量、结构模型指数和骨小梁间隔改变与SHAM组比较,差异有统计学意义(均为P〈0.05),但组织骨密度差别消失。OVX组大鼠15周较3周组织骨密度增加、骨小梁厚度增厚、骨小梁数量减少和骨小梁间隔增宽(P〈0.05)。结论大鼠去卵巢后,胫骨近端皮质骨与松质骨具有不同的骨量丢失方式和不同的微结构改变。早期松质骨骨密度明显下降,骨微结构发生退变;皮质骨厚度减少,其微结构改变则先于骨密度的下降,骨量在去卵巢后15周变化不大。 Objective To observe the changes of bone mass and microarchitecture in ovariectomized rat left tibia by Micro CT(μCT).Methods Forty seven-month-old SD rats were randomly divided into ovariectomized(OVX)and sham-operated(SHAM)groups,twenty in each group.After killed at 3^rdweek and 15^thweek aftersurgery,μCT scanning were performed in the left tibia in vitro.After scanning,the regions involving 0.4 mm slice thickness and 2.5 mm distance at the far end from tibial growth plate were selected as the region of interest(ROI)for cortical bone analysis.The regions selected as ROI of cancellous analysis,were involved in 1.2 mm slice thickness and 0.7 mm distance at the far end from tibial growth plate.After three dimension(3D) reconstruction,2D images of the maximum intensity projection and pictures of 3D microarchitecture were obtained,and bone mineral density(BMD)and microarchitectural parameters were quantitively identified.Results There were significant increases in Ct.Ar〔(0.43±0.13)mm^2 vs.(0.31±0.06)mm^2〕,Ma.Ar〔(10.31±1.98)mm^2 vs.(8.44±1.25)mm^2〕,Tt.Ar〔(10.74±2.05)mm^2 vs. (8.75±1.26)mm^2〕,and Mm〔(4.10±0.73)mm^2 vs.(3.49±0.37)mm^4〕in OVX group,compared with SHAM group at the 3^rdweek(all P〈0.05).While at the 15^thweek,only Ct.Th showed a decrease in OVX group(P〈0.05).In OVX group,Ct.Th and Ct.Ar were lower at 15 weeks than at 3 weeks.In SHAM group,In.Pro,Ot.Pm and Mm at 15 weeks were higher than those at 3 weeks (P〈0.05).At the 3^(rd)week OVX rats had much lower vBMD〔(288.2±48.2)mg/mm^3 vs(408.4±51.6)mg/mm3〕,tBMD〔(604.5±45.3)mg/mm^3 vs.(686.7±40.0)mg/mm^3〕,BVF〔(25.1±5.1)%vs.(33.6±4.1)%〕,and Tb.N〔(6.04±2.94)mm^(-1)vs.(9.85±2.83)mm^(-1)〕,but higher SMI〔(3.11±0.36)vs.(2.58±0.36)〕and Tb.Sp〔(0.37±0.22)vs.(0.14±0.10)〕mm than SHAM had(P〈0.05).At the 15th week,vBMD,BVF and Tb.N were still lower in OVX than in SHAM.SMI and Tb.Sp in OVX were also higher than in SHAM rats,but no significant difference of tBMD was found.In OVX group,the scores of tBMD,Tb.Th,Tb.N,Tb.Sp in the 15^thweek were higher than those in the 3^rdweek(P〈0.05).Conclusions The cortical bone and cancellous bone have different ways of bone mass losing and microarchitecture changing in proximal tibia of post-OVX rat.At early period,BMD and microarchitecture of cancellous are decreased obviously.The thickness of cortical bone is reduced,the microarchitecture change is earlier than BMD decreasing while bone mass has no obvious changing during 15 weeks post-OVX.
出处 《中华老年医学杂志》 CAS CSCD 北大核心 2008年第1期57-61,共5页 Chinese Journal of Geriatrics
基金 国家自然科学基金(30400514) 卫生部临床学科重点建设资助项目(2004-468-50)
关键词 体层摄影术 X线计算机 骨密度 骨质疏松 绝经后 Tomography,x-ray Bone density Dsteoporosis,postmenopausal
  • 相关文献

参考文献18

  • 1Thompson DD, Simmons HA, Pirie CM, et al. FDA guidelines and animal models for osteoporosis. Bone, 1995, 17(4 Suppl): 125S-133S.
  • 2Mitlak BH, Schoenfeld D, Neer RM. Accuracy, precision, and utility of spine and whole-skeleton mineral measurements by DXA in rats. J Bone Miner Res, 1994, 9:119-126.
  • 3McErlain DD, Chhem RK, Bohay RN, et al. Micro- computed tomography of a 500-year-old tooth: technical note. Can Assoc Radiol J, 2004, 55: 242-245.
  • 4Choplin RH, Buckwalter KA, Rydberg J, et al. CT with 3D rendering of the tendons of the foot and ankle: technique, normal anatomy, and disease. Radiographics, 2004, 24:343-356.
  • 5Wergedal JE, Veskovlc K, Hellan M, et al. Patients with van buchem disease, an osteosclerotlc genetic disease, have elevated bone formation markers, higher bone density, and greater derived polar moment of inertia than normal. J Clin Endocrinol Metab, 2003, 88:5778-5783.
  • 6Ito M, Nishida A, Aoyagi K, et al. Effects of risedronate on trabecular microstructure and biomechanical properties in ovariectomized rat tibia. Osteoporos Int, 2005, 16:1042-1048.
  • 7Jiang Y, Zhao J, Liao EY, et al. Application of micro- CT assessment of 3-D bone microstructure in preclinical and clinical studies. J Bone Miner Metab, 2005, 23: 122-131.
  • 8van Trommel MF, Kroon HM, Bloem JL, et al. MR imaging based strategies in limb salvage surgery for osteosareoma of the distal femur. Skeletal Radiol, 1997, 26:636-641.
  • 9Cohen IJ, Hadar H, Schreiber R, et al. Primary bone tumor resectability: the value of serial MRI studies in the determination of the feasibility, timing, and extent of tumor resection. J Pedlatr Orthop, 1994, 14: 781-787.
  • 10Yang J, Pham SM, Crabbe DL. High-resolution Micro-CT evaluation of mid- to long-term effects of estrogen deficiency on rat trabecular bone. Acad Radiol, 2003, 10:1153-1158.

同被引文献37

  • 1刘洁,李伟,董明纲.新一代骨转换标志物研究现状[J].中国临床医学,2006,13(1):102-104. 被引量:6
  • 2邹丽宜,吴铁,崔燎.丹参抑制泼尼松大鼠骨质丢失[J].中成药,2006,28(4):537-540. 被引量:12
  • 3魏雅楠,苗懿德,刘忠厚,刘杰.骨代谢生化标志物的临床进展——不同国家和地区绝经前后女性骨代谢标志物参考值回顾分析[J].中国骨质疏松杂志,2007,13(7):455-468. 被引量:23
  • 4Delmas PD,Seeman E.Changes in bone mineral density explain little of the reduction in vertebral or nonvertebral fracture risk with anti-resorptive therapy.Bone,2004,34:599-604.
  • 5Dai RC,Liao EY,Yang C,et al.Microcracks:an alternative index for evaluating bone biomechanical quality.J Bone Miner Metabol,2004,22:215-223.
  • 6Weinstein RS,Powers CC,Parfitt AM,et al.Preservation of osteocyte viability by bisphosphonates contributes to bone strength in glucocorticoid-treated mice independently of BMD:An unappreciated determinant of bone strength.J Bone Miner Res,2002,17:156.
  • 7Hazenberga JG,Freeleyc M,Foran E.Microdamage:a cell transducing mechanism based on ruptured osteocyte processes.J Biomech,2006,39:2096-2103.
  • 8Fanti P,Monier-Faugere MC,Geng Z,et al.The phytoestrogen genistein reduces bone loss in shortterm ovariectomized rats.Osteoporos Int,1998,8:274-281.
  • 9Allen MR,Iwata K,Sato M,et al.Raloxifene enhances vertebral mechanical properties independent of bone density.Bone,2006,39:1130-1135.
  • 10Sheng Z,Dai R,Wu X,et al.Regionally specific compensation for bone loss in the tibial trabeculae of estrogen-deficient rats.Acta Radiologica,2007,48:531-539.

引证文献4

二级引证文献20

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部