Also, the different study durations are likely to play a role, as new bone formed in response to PTH is probably undermineralized; however, mineralization
may increase thereafter. It should be noted that CT-based measurements of the degree of mineralization may be less reliable than other methods such as back-scattered electron imaging and microradiographic techniques. The unaffected cortical mineral density is supported by the bending results. Our bending data agree with three-point bending tests in the femur where an increase in ultimate load and extrinsic stiffness after PTH treatment was found in ovariectomized rats [39, 40]. It can be seen that the trends between groups in ultimate load, extrinsic stiffness, and calculated polar moment of inertia are similar, which indicates that the polar moment of inertia was a
good predictor of ultimate load LY2603618 datasheet and extrinsic stiffness. Ultimate displacement did not differ between all groups, which suggests that the newly formed bone was of similar quality as the old bone and indicates that PTH treatment did not lead to more brittle or ductile mechanical behavior. This is further supported by unaltered tissue mineralization values in the diaphyseal tissue, i.e., cortical bone. Individual trabeculae were tracked over time during PTH treatment in all rats by using image registration software. With this method, we were able to monitor bone formation after PTH treatment on a microlevel and gather insight into how selleck kinase inhibitor and where PTH treatment leads to new bone. In many trabeculae, it appeared that in the first 2 weeks, mostly cavities DCLK1 were filled, while later on bone was added to the outer surface. It has been suggested that increases in bone mass after PTH occur by remodeling- and modeling-based bone formation [41] and
plasma markers in PTH-treated patients have shown that modeling increases directly after the onset of treatment [42]. Our data suggest that in rats, initially remodeling-based bone formation takes place, as cavities are filled with bone, while later, modeling-based bone formation is more pronounced as bone is added to the outer LY2874455 clinical trial surface, which does not appear to have been resorbed first. This will need to be further validated. For several other trabeculae, it was seen that ovariectomy led to severe disruption of the trabecula to the point of almost complete cleavage after segmentation of the images. PTH treatment led to bone deposition there where most beneficial, resulting in full restoral of the trabecula. This could be explained by Frost’s mechanostat, which states that bone is deposited where strains and stresses are the highest. Since in an almost cleaved trabecula merely a thin line of bone was present at certain locations, strains and stresses would be the highest at these locations leading to bone formation there. This suggests that PTH-induced bone formation is, at least in part, mechanically driven.
Related posts:
- Vertebroplasty does not play a role in further fracture preventio
- NOX does not play a role in experimental steatosis and the genera
- T-helper (TH1) CD4+ cells expressing INF-γ play a critical role i
- Fludarabine Fludara study period was significantly increased with cant
- They might thus play a role in modulating spinal activity in adva