Neovascularization of osteoporotic metaphyseal bone defects: A morphometric micro-CT study
Neovascularization of osteoporotic metaphyseal bone defects: A morphometric micro-CT study
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DOI:
10.1016/j.mvr.2015.10.005
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发表时间:
2016-05-01
影响因子:
3.1
通讯作者:
Langheinrich, Alexander C.
中科院分区:
文献类型:
--
作者:
Kampschulte, Marian;Krombach, Gabriele A.;Langheinrich, Alexander C.
Purpose: Neovascularization is essential for bone regeneration in fractures. This study aimed to investigate the microvascular morphology and distribution in the non-injured femur and the neovascularization of the metaphyseal critical size defect in a small animal model of osteoporosis.Materials and methods: Female rats (n = 7) were ovariectomized (OVX) and received a multideficiency diet. Three months after OVX, a 5 mm wedge shaped critical size defect was cut at the distal femoral metaphysis and stabilized with a T-shaped mini-plate. After six weeks, the animals were euthanized, and femora were removed and decalcified for micro-CT measurement of fracture neovascularization.Results: No fracture healing was observed along the critical size defects. In the non-injured bone, micro-vessel distribution showed a specific pattern, thereby enabling a differentiation between epi-, meta- and diaphysis. Micro-CT based morphometry revealed a significant reduction of the vascular volume fraction as well as the vascular thickness (p < 0.001) in the critical size defect compared to the intact contralateral femur. Blood volume related vascular surface (vascular surface/volume) increased significantly (p < 0.001). Connectivity density and tissue volume related vascular surface (vascular surface density) did not change significantly.Conclusions: Micro-CT based vascular morphometry demonstrated differences between epi-, meta- and diaphysis in the non-injured bone as well as differences between the critical size defect and the non-injured metaphysis. As angiogenesis is a crucial prerequisite that precedes osteogenesis, our results may influence further evaluation of osteoconductive or osteogenic biomaterials in this small animal model of osteoporosis. (C) 2015 Elsevier Inc. All rights reserved.