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The effect of bone marrow mononuclear cells on vascularization and bone regeneration in steroid-induced osteonecrosis of the femoral head.

机译:激素引起的股骨头坏死中,骨髓单个核细胞对血管生成和骨再生的影响。

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OBJECTIVE: We examined whether implantation of autologous bone marrow mononuclear cells (BM-MNC) can augment neovascularization and bone regeneration in steroid-induced osteonecrosis of the femoral head. METHODS: Sixty-five 28-week-old male New Zealand white rabbits were divided into group I (left untreated, N=20), group II (core decompression, N=20) and group III (core decompression+autologous bone marrow cells implantation, N=25) after receiving an established inductive protocol for inducing steroid-associated ON. Four weeks later, these rabbits were euthanized, bilateral femora were dissected for micro-CT-based microangiography to assess vascularization, and then the osteonecrotic changes and repair processes were examined histopathologically. RESULTS: Quantitative analysis showed that new vessel formation in group III was significantly greater compared with other groups at 4 weeks after treatment. Penetrating capillary vessels number vessels number in group III (44.5+/-5.11) was significantly larger than that of group II (11.4+/-2.46) and group I (3.10+/-0.33) (p<0.01). The histologic and histomorphometric analysis revealed that the new bone volume was significantly higher in the group III than in the group I and II, 4 weeks after treatment. CONCLUSION: In this animal model, a combination of bone marrow mononuclear cells and core decompression enhance the neovascularization and the osteoinductive ability, resulting in bone regeneration. These findings confirm the preliminary clinical results obtained in humans that the implantation of bone marrow mononuclear cells is an effective and feasible method for treating early osteonecrosis.
机译:目的:我们研究了自体骨髓单个核细胞(BM-MNC)的植入是否可以促进类固醇激素引起的股骨头坏死的新生血管形成和骨再生。方法:将65只28周龄的雄性新西兰白兔分为I组(未经治疗,N = 20),II组(核心减压,N = 20)和III组(核心减压+自体骨髓细胞)植入,N = 25),然后接受已建立的诱导类固醇相关ON的诱导方案。四周后,对这些兔实施安乐死,解剖双侧股骨,进行基于微CT的微血管造影术以评估血管形成,然后组织病理学检查坏死的变化和修复过程。结果:定量分析表明,治疗后第4周,第三组的新血管形成明显高于其他组。第三组(44.5 +/- 5.11)的穿透性毛细血管数目明显高于第二组(11.4 +/- 2.46)和第一组(3.10 +/- 0.33)(p <0.01)。组织学和组织形态计量学分析显示,治疗后4周,III组的新骨体积明显高于I和II组。结论:在该动物模型中,骨髓单个核细胞与核心减压相结合可增强新血管形成和骨诱导能力,从而促进骨骼再生。这些发现证实了在人体中获得的初步临床结果,即骨髓单个核细胞的植入是治疗早期骨坏死的有效且可行的方法。

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