Home About us Contact
|
Home About us Contact | ||
|
|
||
Osteoporotic Bone (osteoporotic + bone)
Selected AbstractsTrabecular Bone Tissue Strains in the Healthy and Osteoporotic Human Femur,JOURNAL OF BONE AND MINERAL RESEARCH, Issue 10 2003B Van Rietbergen Quantitative information about bone tissue-level loading is essential for understanding bone mechanical behavior. We made microfinite element models of a healthy and osteoporotic human femur and found that tissue-level strains in the osteoporotic femoral head were 70% higher on average and less uniformly distributed than those in the healthy one. Introduction: Bone tissue stresses and strains in healthy load-adapted trabecular architectures should be distributed rather evenly, because no bone tissue is expected to be overloaded or unused. In this study, we evaluate this paradigm with the use of microfinite element (,FE) analyses to calculate tissue-level stresses and strains for the human femur. Our objectives were to quantify the strain distribution in the healthy femur, to investigate to what extent this distribution is affected by osteoporosis, to determine if osteoporotic bone is simply bone adapted to lower load levels, and to determine the "safety factor" for trabecular bone. Materials and Methods: ,FE models of a healthy and osteoporotic proximal femur were made from microcomputed tomography images. The models consisted of over 96 and 71 million elements for the healthy and osteoporotic femur, respectively, and represented their internal and external morphology in detail. Stresses and strains were calculated for each element and their distributions were calculated for a volume of interest (VOI) of trabecular bone in the femoral head. Results: The average tissue-level principal strain magnitude in the healthy VOI was 304 ± 185 microstrains and that in the osteoporotic VOI was 520 ± 355 microstrains. Calculated safety factors were 8.6 for the healthy and 4.9 for the osteoporotic femurs. After reducing the force applied to the osteoporotic model to 59%, the average strain compared with that of the healthy femur, but the SD was larger (208 microstrains). Conclusions: Strain magnitudes in the osteoporotic bone were much higher and less uniformly distributed than those in the healthy one. After simulated joint-load reduction, strain magnitudes in the osteoporotic femur were very similar to those in the healthy one, but their distribution is still wider and thus less favorable. [source] The Effect of In Vivo Mechanical Loading on Estrogen Receptor , Expression in Rat Ulnar Osteocytes,,JOURNAL OF BONE AND MINERAL RESEARCH, Issue 9 2002P. J. Ehrlich Abstract The presence of estrogen receptor , (ER,) in osteocytes was identified immunocytochemically in transverse sections from 560 to 860 ,m distal to the midshaft of normal neonatal and adult male and female rat ulnas (n = 3 of each) and from adult male rat ulnas that had been exposed to 10 days of in vivo daily 10-minute periods of cyclic loading producing peak strains of either ,3000 (n = 3) or ,4000 microstrain (n = 5). Each animal ambulated normally between loading periods, and its contralateral ulna was used as a control. In animals in which limbs were subject to normal locomotor loading alone, 14 ±1.2% SEM of all osteocytes in each bone section were ER, positive. There was no influence of either gender (p = 0.725) or age (p = 0.577) and no interaction between them (p = 0.658). In bones in which normal locomotion was supplemented by short periods of artificial loading, fewer osteocytes expressed ER, (7.5 ± 0.91% SEM) than in contralateral control limbs, which received locomotor loading alone (14 ± 1.68% SEM; p = 0.01; median difference, 6.43; 95% CI, 2.60, 10.25). The distribution of osteocytes expressing ER, was uniform across all sections and thus did not reflect local peak strain magnitude. This suggests that osteocytes respond to strain as a population, rather than as individual strain-responsive cells. These data are consistent with the hypothesis that ER, is involved in bone cells' responses to mechanical strain. High strains appear to decrease ER, expression. In osteoporotic bone, the high strains assumed to accompany postmenopausal bone loss may reduce ER, levels and therefore impair the capacity for appropriate adaptive remodeling. [source] Osseointegration of titanium alloy and HA-coated implants in healthy and ovariectomized animals: a histomorphometric studyCLINICAL ORAL IMPLANTS RESEARCH, Issue 11 2009Guaracilei Maciel Vidigal Jr Abstract Objectives: The objective of the present study is to evaluate the response to dental implants in healthy and osteoporotic bone. Materials and methods: Ten ovariectomized (OVX) New Zealand rabbits submitted to a hypocalcic diet and 10 sham-aged rabbits were used. All animals were submitted to bone mineral density (BMD) measurements before ovariectomy, and also 4 months afterwards, using dual energy X-ray absorptiometry. The BMD measurements showed a significant loss of bone mass, between the first and second examinations, only in the experimental group (P<0.05). After the bone mass loss induction period, three different implants were installed in the proximal tibia metaphisis of each animal: a titanium alloy implant (Ti), a plasma-spray hydroxyapatite-coated implant (HA-PS), and another implant coated with hydroxyapatite with the biomimetic process (HA-B). Results: After 3 months, histomorphometry showed a bone-to-implant contact (BIC) for Ti implants of 73.09±13.74% in healthy and 66.09±30.01% in OVX animals. The BIC for the HA-PS was 64.83±15.65% and 90.17±8.14% for healthy and OVX animals, respectively, and 88.66±5.30% and 87.96±10.71% for the HA-B implants placed in the same conditions. The differences between the implants in healthy and OVX conditions were not statistically significant (P>0.05). The only significant difference within groups was observed in the healthy animals between HA-B and Ti implants (P<0.06). Conclusion: Within the parameters used in this animal model it was not possible to observe BIC differences between osteoporotic and healthy animals. [source] In vivo anabolic effect of strontium on trabecular bone was associated with increased osteoblastogenesis of bone marrow stromal cells,JOURNAL OF ORTHOPAEDIC RESEARCH, Issue 9 2010Songlin Peng Abstract In vitro studies have demonstrated that strontium (Sr) could increase osteogenic differentiation of bone marrow stromal cells (BMSCs). We investigated the in vivo effect of Sr on BMSCs. Thirty-six female rats were randomly divided into the following groups: sham operated and treated with either vehicle (Sham,+,Veh) or Sr compound (Sham,+,Sr) and ovariectomized and treated with either vehicle (OVX,+,Veh) or Sr compound (OVX,+,Sr). Vehicle and Sr were orally administrated daily starting immediately after the surgery and continuing for 12 weeks. The anabolic effect of Sr on trabecular bone was determined at the structural and tissue level by microCT and histomorphometry, respectively. Colony formation assays demonstrated that BMSCs exhibited higher osteogenic colony but lower adipogenic colony in Sr-treated versus Veh-treated OVX rats. The mRNA level of osteogenic genes was higher, while the mRNA level of adipogenic genes was lower in BMSCs from Sr-treated versus Veh-treated Sham and OVX rats. The effect of Sr on rat BMSCs was reproducible in human BMSCs. Taken together, this study suggests that the anabolic effect of Sr on normal or osteoporotic bones is associated with increased osteoblastic differentiation of BMSCs. © 2010 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 28:1208,1214, 2010 [source] | ||||||||||