Experimental repetitive mild traumatic brain injury induces deficits in trabecular bone microarchitecture and strength in mice

被引:1
|
作者
Chandrasekhar Kesavan [1 ,2 ]
Nikita M Bajwa [1 ]
Heather Watt [1 ]
Subburaman Mohan [1 ,2 ,3 ]
机构
[1] Musculoskeletal Disease Center, VA Loma Linda Healthcare System  2. Department of Medicine
[2] Department of Orthopedic Surgery, Loma Linda University
关键词
IGF; TBI; Experimental repetitive mild traumatic brain injury induces deficits in trabecular bone microarchitecture and strength in mice;
D O I
暂无
中图分类号
R651.15 [];
学科分类号
1002 ; 100210 ;
摘要
To evaluate the long-term consequence of repetitive mild traumatic brain injury(m TBI) on bone, m TBI was induced in 10-week-old female C57 BL/6 J mice using a weight drop model, once per day for 4 consecutive days at different drop heights(0.5, 1 and 1.5 m) and the skeletal phenotype was evaluated at different time points after the impact. In vivo micro-CT(μ-CT) analysis of the tibial metaphysis at 2, 8 and 12 weeks after the impact revealed a 5%–32% reduction in trabecular bone mass. Histomorphometric analyses showed a reduced bone formation rate in the secondary spongiosa of 1.5 m impacted mice at 12 weeks post impact. Apparent modulus(bone strength), was reduced by 30%(P o 0.05) at the proximal tibial metaphysis in the 1.5 m drop height group at 2 and 8 weeks post impact. Ex vivo μ-CT analysis of the fifth lumbar vertebra revealed a significant reduction in trabecular bone mass at 12 weeks of age in all three drop height groups. Serum levels of osteocalcin were decreased by 22%, 15%, and 19% in the 0.5, 1.0 and 1.5 m drop height groups, respectively,at 2 weeks post impact. Serum IGF-I levels were reduced by 18%–32% in m TBI mice compared to contro1 mice at 2 weeks post impact. Serum osteocalcin and IGF-I levels correlated with trabecular BV/TV(r2= 0.14 and 0.16, P o 0.05). In conclusion, repetitive m TBI exerts significant negative effects on the trabecular bone microarchitecture and bone mechanical properties by influencing osteoblast function via reduced endocrine IGF-I actions.
引用
收藏
页码:357 / 366
页数:10
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