- Research article
- Open Access
A multi-factorial analysis of bone morphology and fracture strength of rat femur in response to ovariectomy
Journal of Orthopaedic Surgery and Research volume 13, Article number: 318 (2018)
Postmenopausal osteoporosis develops due to a deficiency of estrogen that causes a decrease in bone mass and changes in the macro- and micro-architectural structure of the bone, leading to the loss of mechanical strength and an increased risk of fracture. Although the assessment of bone mineral density (BMD) has been widely used as a gold standard for diagnostic screening of bone fracture risks, it accounts for only a part of the variation in bone fragility; thus, it is necessary to consider other determinants of bone strength. Therefore, we aimed to comprehensively evaluate the architectural changes of the bone that influence bone fracture strength, together with the different sensitivities of cortical and trabecular bone in response to ovariectomy (OVX).
Bone morphology parameters were separately analyzed both in cortical and in trabecular bones, at distal-metaphysis, and mid-diaphysis of OVX rat femurs. Three-point bending test was performed at mid-diaphysis of the femurs. Correlation of OVX-induced changes of morphological parameters with breaking force was analyzed using Pearson’s correlation coefficient.
OVX resulted in a decline in the bone volume of distal-metaphysis trabecular bone, but an increase in distal-metaphysis and mid-diaphysis cortical bone volume. Tissue mineral density (TMD) remained unchanged in both the trabecular and cortical bone of the distal metaphysis but decreased in cortical bone of the mid-diaphysis. The OVX significantly increased the breaking force at mid-diaphysis of the femurs.
OVX decreased the trabecular bone volume of the distal-metaphysis and increased the cortical bone volume of the distal-metaphysis and mid-diaphysis. Despite the reduction in TMD and increased cortical porosity, bone fracture strength increased in the mid-diaphysis after OVX. These results indicate that analyzing a single factor, i.e., BMD, is not sufficient to predict the absolute fracture risk of the bone, as OVX-induced bone response vary, depending on the bone type and location. Our results strongly support the necessity of analyzing bone micro-architecture and site specificity to clarify the true etiology of osteoporosis in a clinical setting.
The bone is a complex, dynamic, and hierarchical tissue that has various functions, including the architectural framework component of the body, protection of internal organs, and contribution to the maintenance of mineral homeostasis of body fluids. The macro- and micro-architecture of the bone changes with age, pathological conditions, and anatomical location; therefore, bone mechanical properties will change accordingly . Morphologically, there are two distinct types of bone: cortical bone and trabecular bone. The trabecular bone is mainly responsible for rapid bone turnover and regulating systemic mineral homeostasis, while cortical bone is responsible for constructing the body framework .
Osteoporosis is a skeletal disease with various pathogenesis and is caused by an imbalance in bone remodeling. Postmenopausal osteoporosis is developed by a deficiency of estrogen, resulting in a decrease in bone mass and changes in the macro- and micro-architectural structure of bone. As a result, postmenopausal osteoporosis leads to the loss of mechanical strength of the bone and increases the bone fracture risk . Clinically, bone mineral density (BMD) measured by dual-energy X-ray absorptiometry (DXA) remains the standard assessment of osteoporosis and bone fracture risk; a T score of less than or equal to − 2.5 decrease in BMD determines the onset of the disease . However, BMD is a surrogate marker of bone strength , accounting for only 60% of variation in bone fragility . From a mechanical perspective, bones are composed of different hierarchy levels, namely, whole bone geometry, microstructural properties, and intrinsic material properties . BMD is only one factor affecting the material properties of the bone; therefore, other determinants, such as bone mass and bone quality, also need to be considered as potential factors that contribute to bone fracture risks . Bone quality includes several aspects of bone structure and composition, including bone turnover, micro-architecture, the degree and distribution of mineralization, the extent of micro-damage, and the composition of bone matrix and mineral [8,9,10].
One of the parameters of bone quality, cortical porosity, occurs as a result of accelerated remodeling at the inner surface of long bones and causes trabeculation of the cortical bone. Recent studies revealed that cortical porosity also affects the mechanical properties of the bone [11, 12]. Accelerated bone resorption at the inner side of the cortical bone is frequently observed in patients with osteoporosis, and persistence of this condition leads to intra-cortical porosity, which can compromise bone strength . Studies in humans have shown a consistent relationship between cortical bone porosity and bone fracture risk which, notably, was largely undetected by conventional DXA-based BMD measurements [9, 13]. Currently, the evaluation of the parameters of bone quality has not been adopted for general diagnostic purposes. The contribution of each parameter of bone quality towards the risks of fracture is still unclear. Moreover, the limited resolution of radiographic imaging does not permit the detection of detailed architectural changes in the bone.
Development of site-specific osteoporosis in the trabecular bone is one of the most reproducible biological responses in ovariectomy (OVX) animal models; therefore, OVX has been widely used to understand the pathophysiology of osteoporosis and to evaluate the efficacy of anti-bone resorption treatment [14, 15]. On the contrary, the non-uniform bone reaction in response to OVX complicates the evaluation and understanding of osteoporosis pathogenesis [16,17,18]. It has been reported that OVX-induced osteoporosis caused reduction of the trabecular bone volume at the proximal tibial metaphysis, but exhibited no marked change in the cortical bone volume at the mid-diaphysis of the tibia and femur in rats . Although cortical bone, the major constituent of skeletal bone, is more responsible for bone strength, its response to OVX is still controversial .
While many studies have been conducted for decades, non-uniform skeletal response to OVX, especially between cortical bone and trabecular bone, tend to be overlooked. Moreover, given the importance of bone micro-architecture as a volumetric structure in the evaluation of fracture risk, it is necessary to consider other determinants of bone strength [8, 9]. Therefore, in the present study, through the use of high-resolution computed tomography and data-analyzing software to obtain 3D reconstructions, we aimed to comprehensively evaluate the architectural changes of the bone that influence bone fracture strength, together with different sensitivities of the cortical and trabecular bones in response to OVX.
Experimental animals and surgical procedures
A total of 13 female Wistar rats were purchased from Charles River Japan (Yokohama, Japan). Rats were randomly divided into two groups: six rats in the control group and seven rats in the ovariectomy-induced osteoporosis group (OVX group). Bilateral ovariectomy [21, 22] was performed in the OVX group at 10 weeks of age according to the protocol and the ethical guidelines of Niigata University (36-9). The animals were provided with commercially available pellet food and water ad libitum and kept under controlled light conditions of 12/12-h light/dark cycles throughout the experiment. Eight weeks after OVX was performed, all animals were euthanized, and both femurs were excised and immediately fixated in 4% formaldehyde for 3 days at 4 °C. Bone morphometry, cortical porosity, and mechanical testing were performed on the same sample. The experimental workflow of this study is shown in Fig. 1.
X-ray micro-computed tomography imaging
Micro-computed tomography (micro-CT) images of a section (3.5 mm × 4.5 mm × 2.0 mm) of the femur’s mid-diaphysis were taken. Scanning conditions of 75 Kv, 10 μA, and 9 μm of thickness were applied to obtain a detailed image of the sample, using ELE-scan micro-tomography (Nittetsu Elex Co. Ltd., Tokyo, Japan). A section of the distal metaphysis of the femur was also scanned to analyze the rat femur trabecular bone. The settings for this portion were similar to the mid-diaphysis at 75 Kv and 10 μA; however, since the area to be scanned was wider than the mid-diaphysis, the thickness of each slide was set to 14 μm. Along with the samples, a commercially available BMD phantom (Ratoc Systems, Tokyo, Japan) with different known densities was scanned using the same scan setting.
Three-dimensional reconstruction and bone morphometry
Three-dimensional (3D) volume reconstructions were done with the ELE-scan software and converted into stacks of TIFF files. Based on the image stacks, a 3D model of the samples was reconstructed and further analysis was performed using Tri/3D-BON software (Ratoc Systems, Tokyo, Japan) . For the analysis of the femur cortical bone, a region of interest (ROI) of 3.5 mm × 4.5 mm × 2.0 mm in size was taken from a section of the mid-diaphysis area. Trabecular bone was analyzed using a 5.5 mm × 7.0 mm × 1.75 mm section of the distal metaphysis. Analysis parameters used complied with the guidelines for the assessment of bone microstructure in rodents using micro-CT .
Cortical porosity and tissue mineral density analysis
Mid-diaphysis cortical porosity analysis was performed using an intensity threshold of 170 for all samples. Measurements were performed according to the protocols and manual guidelines provided by the software company. TMD analysis was performed using the BMD phantom as a density reference for all samples.
Three-point bending test
Following micro-CT imaging, samples were analyzed by a three-point universal testing machine (EZ Graph, Shimadzu, Kyoto, Japan). Three-point bending strength was set with a length span of 20 mm between the support points. The press head as well as the two support points were round to avoid shear load and damage to the samples . Samples were positioned horizontally, with the anterior surface facing upwards while the compressive force was directed perpendicular to the center of the bone shaft. Each bone was loaded with a constant crosshead speed of 1 mm/min until mechanical failure was reached. Data were obtained from the universal testing machine using Trapezium X v1.1.5 software (EZ Graph, Shimadzu, Tokyo, Japan). Data were then converted into a load-displacement plot, where the load is the force applied in newtons (N) and the displacement is in millimeters (mm). In order to determine the intrinsic properties of a material, the load-displacement data were further converted into a stress-strain graph , and mechanical properties were calculated.
All data were processed and analyzed using the independent Student’s t test analysis of variance to find the statistical difference between groups. A P value less than 0.05 was considered statistically significant. The correlations of regression models were evaluated using Pearson’s determination coefficient R2 to explore the relationship between the morphological characteristics and biomechanical parameters [27, 28].
Weight changes in the experimental animals were recorded throughout the experimental period (Fig. 2). During the period before OVX, both groups showed a steady increase in body weight, without any significant difference between groups. Two weeks after the bilateral OVX operation, the OVX group showed a significant increase in body weight compared to that in the control group and maintained this increase throughout the rest of the experimental period (up to 18 weeks).
Morphological characteristics of the femur distal-metaphysis
Representative 3D-reconstructed images of femur distal-metaphysis are shown in Fig. 3a. The numerical results of the trabecular bone analysis at femur distal-metaphysis are shown in Table 1. Eight weeks after OVX, while total volume (TV) was unchanged, a significant decrease was observed in bone volume (BV), bone surface (BS), bone surface density (BS/TV), and bone volume fraction (BV/TV). Meanwhile, trabecular separation (Tb.Sp), trabecular space (Tb.Spac), and trabecular thickness (Tb.Th) increased while trabecular number (Tb.N) decreased in the OVX group.
For mineral content, we analyzed TMD instead of BMD. TMD differs from BMD; TMD is calculated from the average attenuation value of the bone tissue only, whereas BMD assessment will include attenuation values from non-bone soft tissue in addition to the bone tissue. In trabecular bone, TMD was not statistically different between the control and OVX groups. Bone mineral content (BMC) and volumetric bone mineral density (vBMD) significantly decreased in the OVX group, reflecting the reduction of bone volume (BV).
The numerical results of the cortical bone analysis at the femur distal-metaphysis are shown in Table 2. The OVX group had a significant increase in total volume (TV), cortical bone volume (Ct.V), total cross-sectional area (Tt.Ar), cortical bone area (Ct.Ar), periosteal perimeter (Ps.Pm), and cortical thickness (Ct.Th). Although cortical area fraction (Ct.Ar/Tt.Ar), center-line length (CLL), total pore volume (Po.V), and cortical porosity (Ct.Po) were not significantly different, they had a tendency to be increased in the OVX group. Bone mineral content (BMC) increased in the OVX group due to the increases in cortical bone volume (Ct.V). TMD between the control and OVX groups was not significantly different.
Morphological characteristics of the femur mid-diaphysis
Reconstructed images of the femur mid-diaphysis are shown in Fig. 3b. The mid-diaphysis portion of the femur had a negligible amount of trabecular bone; therefore, quantitative analysis could not be done. The results of the cortical bone analysis are shown in Table 3. Quantitative analysis at the femur mid-diaphysis of the samples showed a significant increase of TV, Ct.V, Tt.Ar, Ct.Ar, Ps.Pm, and CLL; however, Ct.Ar/Tt.Ar and Ct.Th showed no differences. Regarding the porosity, Po.V and Ct.Po showed a significant increase in the OVX group. Although BMC was not altered, TMD decreased due to increases of Ct.V in the OVX group.
Mechanical test of the femur mid-diaphysis
The results of the femur mid-diaphysis three-point bending test are shown in Table 4. After 8 weeks, the OVX group had a significant increase in breaking force, breaking displacement, and breaking time; however, stiffness did not show a significant difference. Moreover, in analyzing the stress-strain graph, the OVX group showed a significant increase in fracture strength; however, Young’s modulus, ductility, resilience modulus, and toughness did not show significant differences.
To determine the correlation of OVX-induced changes of selected morphological characteristics (i.e., Ct.V, Ct.Po, and TMD) with breaking force, the Pearson correlation coefficient was calculated. The results of the correlation analysis are shown in Fig. 4. A strong positive correlation between Ct.V and breaking force was observed. In contrast, Ct.Po showed a weak positive correlation with breaking force. Conversely, TMD showed a strong negative correlation with breaking force.
The OVX animal model has been widely used to understand the pathophysiology of osteoporosis and to evaluate the efficacy of anti-bone resorption treatment. The OVX-induced early bone loss occurs mainly in the trabecular bone; however, micro-architectural changes in the cortical bone and their correlation with the changes in the trabecular bone are still unclear. Therefore, in the present study, bone morphological parameters were separately analyzed both at cortical and trabecular bones in response to OVX using rat femurs. Interestingly, OVX resulted in contradictory results between trabecular and cortical bone. Bone volume decreased in the trabecular bone of distal metaphysis but increased in the cortical bone of distal metaphysis and mid-diaphysis; TMD remained unchanged in both trabecular and cortical bone of the distal metaphysis but decreased in the cortical bone of the mid-diaphysis. More surprisingly, the fracture strength of mid-diaphysis was significantly increased in response to OVX. The data obtained in this study are summarized in Table 5.
In response to OVX, a significant increase in bone volume and size was observed in the cortical bone of femur metaphysis, which demonstrated a strong positive correlation with the changes in breaking force (Table 4). Increases in the external diameter of the long bones with a concomitant increase in bone strength following OVX in rats have been also previously reported [4, 5, 29,30,31,32]. It is important to note that OVX cannot be considered to induce a bone-specific estrogen deficiency. OVX is reported to induce hyperphagia, leading to weight gain and increased adiposity , because estrogen regulates food intake via anorexigenic pathways of the central nervous system . In addition, bone-specific deletion of estrogen signaling, using genetically-manipulable transgenic mice, did not show significant phenotypes in cortical bone [35, 36] and phenotypes vary among age, sex, and mouse lines . Further studies are necessary to elucidate the precise function of estrogen-signaling on cortical bone homeostasis.
BMD measurement by DXA has been the gold standard assessment of osteoporosis; however, it accounts only partially towards fracture risk . Although BMD is calculated as the mass of mineral per volume of bone, the images obtained by DXA cannot differentiate the trabecular bone from soft tissue. Due to the limitation of image resolution, the porous trabecular bone is considered as a solid material. Consequently, conventional BMD measurement represents the aspects of both volume and material mineral density of the trabecular bone. Since our data were 3D-based, we calculated the volumetric BMD (vBMD) instead of conventional 2D-based BMD. Our results clearly demonstrated that OVX significantly decreased the volume of trabecular bone at the distal metaphysis, and vBMD decreased accordingly. However, TMD, representing solid material mineral density, did not change. Our high-resolution image analysis revealed that the decline of vBMD by OVX is mainly because of the decreased trabecular bone volume, and not because of the changes in bone mineral density. In addition, OVX decreased the TMD at the cortical bone of the mid-diaphysis, but did not affect the trabecular or cortical bone of the distal metaphysis, indicating a site-specific bone reaction in response to OVX. These results strongly support the necessity of analyzing bone micro-architecture and site specificity to clarify the true etiology of osteoporosis in a clinical setting.
In this study, bone volume, external perimeter, and cortical porosity increased, while TMD decreased in the cortical bone of the femur mid-diaphysis. Increases in cortical thickness and perimeter are associated with higher bone strength. Cortical perimeter and cross-sectional area are crucial geometric parameters of bone strength, because increasing a hollow cylinder diameter provides exponential increases in resistance to bending and torsion without requiring increases in bone mass . In line with our observations, a previous study reported that OVX significantly decreased BMD, but increased cross-sectional area and inertia tolerance on the femoral neck; consequently, femoral necks in OVX rats had greater stiffness than in the controls . A human study also showed that fractures were more frequent in individuals with lower cortical thickness, while no association was seen between fracture and cortical BMD , indicating that individuals with identical BMD values can have different architectural characteristics of the cortical bone and, therefore, different fracture risks [9, 13]. It has also been reported that the trabecular connectivity contributes more to the bone mechanical strength than BMD in human calcaneal bone . Thus, the assessment of multiple factors such as bone morphology, bone composition, and bone properties besides BMD is necessary to determine the absolute fracture risk of bone .
We observed a contradictory result between the trabecular and cortical bones at the distal metaphysis, which demonstrated increased cortical bone volume but decreased trabecular bone volume. Different sensitivity to OVX between cortical and trabecular bone is most likely due to the available bone surface . In addition, recent studies have made progress elucidating a molecular cue controlling the bone type-specific response to OVX, which involves a differential expression pattern of two distinct estrogen receptors (ER), ERα and ERβ. The predominant form of ER, ERα, is expressed in both cortical and trabecular bone, while ERβ, which acts as a natural antagonist to ERα , is highly expressed in trabecular bone compared with that in cortical bone . The different expression patterns of these ERs would lead to different sensitivities to the OVX-induced estrogen deficiency. Nevertheless, more precise analysis and longer periods of observation are needed in order to clearly verify this notion.
In our results, cortical porosity of the mid-diaphysis was significantly higher in OVX rats, but did not have a substantial impact on bone strength. However, it has reported that the increase in cortical porosity associated with the initial stages of the bone remodeling process may actually weaken the bone tissue . In our experimental setting, OVX affected not only cortical porosity, but also other bone morphological parameters, e.g., bone volume and external perimeter, thus, evaluating the absolute contribution of cortical porosity to the fracture strength is particularly challenging. Further studies, such as finite element analysis, will reveal the absolute significance of cortical porosity on the mechanical properties of bone.
In the present study, OVX resulted in a decline in the bone volume of distal metaphysis trabecular bone, but an increase in the bone volume of the distal metaphysis and mid-diaphysis cortical bone. Despite the reduction in TMD and increases in cortical porosity, bone fracture strength increased in the mid-diaphysis after OVX. This suggests that OVX-induced changes in volume/size seemed to be a major determinant of breaking force at the mid-diaphysis of a rat femur. These results clearly indicate that analyzing a single factor, i.e., BMD, is not sufficient to predict the absolute fracture risk of the bone, as OVX-induced bone response vary, depending on the bone type and location. Taken together, understanding the different sensitivities to estrogen deficiency with regard to their impact on bone location and bone type is essential. Further studies are necessary to elucidate the relationship between site-specific OVX-induced changes in both macro-and micro-morphological characteristics and the fracture risk of bone.
Bone mineral content
Bone mineral density
Center line length
Cortical bone area
Cortical bone volume
Total pore volume
Region of interest
- Tb.N :
- Tb.Sp :
- Tb.Spac :
- Tb.Th :
Tissue mineral density
Total cross-sectional area
Burstein AH, Reilly DT, Martens M. Aging of bone tissue: mechanical properties. J Bone Joint Surg Am. 1976;58(1):82–6.
Rho JY, Kuhn-Spearing L, Zioupos P. Mechanical properties and the hierarchical structure of bone. Med Eng Phys. 1998;20(2):92–102.
Bala Y, Zebaze R, Ghasem-Zadeh A, Atkinson EJ, Iuliano S, Peterson JM, Amin S, Bjornerem A, Melton LJ 3rd, Johansson H, et al. Cortical porosity identifies women with osteopenia at increased risk for forearm fractures. J Bone Miner Res. 2014;29(6):1356–62.
Ammann P, Rizzoli R. Bone strength and its determinants. Osteoporos Int. 2003;14(Suppl 3):S13–8.
Miller PD. Bone strength and surrogate markers: the first, second, and third fiddle. J Bone Miner Res. 2012;27(8):1623–6.
Muller R. Hierarchical microimaging of bone structure and function. Nat Rev Rheumatol. 2009;5(7):373–81.
NIH Consensus Development Panel on Osteoporosis Prevention, Diagnosis, and Therapy. Osteoporosis prevention, diagnosis, and therapy. JAMA. 2000;17(1):1–45.
Cole JH, van der Meulen MC. Whole bone mechanics and bone quality. Clin Orthop Relat Res. 2011;469(8):2139–49.
Fonseca H, Moreira-Goncalves D, Coriolano HJ, Duarte JA. Bone quality: the determinants of bone strength and fragility. Sports Med. 2014;44(1):37–53.
Kuroshima S, Kaku M, Ishimoto T, Sasaki M, Nakano T, Sawase T. A paradigm shift for bone quality in dentistry: a literature review. J Prosthodont Res. 2017;61(4):353–62.
Cooper DM, Kawalilak CE, Harrison K, Johnston BD, Johnston JD. Cortical bone porosity: what is it, why is it important, and how can we detect it? Curr Osteoporos Rep. 2016;14(5):187–98.
Bjornerem A. The clinical contribution of cortical porosity to fragility fractures. Bonekey Rep. 2016;5:846.
Farr JN, Khosla S. Determinants of bone strength and quality in diabetes mellitus in humans. Bone. 2016;82:28–34.
Lelovas PP, Xanthos TT, Thoma SE, Lyritis GP, Dontas IA. The laboratory rat as an animal model for osteoporosis research. Comp Med. 2008;58(5):424–30.
Jee WS, Yao W. Overview: animal models of osteopenia and osteoporosis. J Musculoskelet Neuronal Interact. 2001;1(3):193–207.
Francisco JI, Yu Y, Oliver RA, Walsh WR. Relationship between age, skeletal site, and time post-ovariectomy on bone mineral and trabecular microarchitecture in rats. J Orthop Res. 2011;29(2):189–96.
Wronski TJ, Cintron M, Doherty AL, Dann LM. Estrogen treatment prevents osteopenia and depresses bone turnover in ovariectomized rats. Endocrinology. 1988;123(2):681–6.
Jiang Y, Zhao J, Genant HK, Dequeker J, Geusens P. Long-term changes in bone mineral and biomechanical properties of vertebrae and femur in aging, dietary calcium restricted, and/or estrogen-deprived/-replaced rats. J Bone Miner Res. 1997;12(5):820–31.
Zhang Y, Lai WP, Leung PC, Wu CF, Wong MS. Short- to mid-term effects of ovariectomy on bone turnover, bone mass and bone strength in rats. Biol Pharm Bull. 2007;30(5):898–903.
Osterhoff G, Morgan EF, Shefelbine SJ, Karim L, McNamara LM, Augat P. Bone mechanical properties and changes with osteoporosis. Injury. 2016;47(Suppl 2):S11–20.
Kaku M, Rocabado JMR, Kitami M, Ida T, Uoshima K. Royal jelly affects collagen crosslinking in bone of ovariectomized rats. J Funct Foods. 2014;7:398–406.
Sarkar A, Datta P, Gomes A, Gupta SCD, Gomes A. Anti-osteoporosis and anti-osteoarthritis activity of fresh water snail (Viviparous bengalensis) flesh extract in experimental animal model. Open J Rheumatol Autoimmune Dis. 2013;03(01):10–7.
Ida T, Kaku M, Kitami M, Terajima M, Rosales Rocabado JM, Akiba Y, Nagasawa M, Yamauchi M, Uoshima K. Extracellular matrix with defective collagen cross-linking affects the differentiation of bone cells. PLoS One. 2018;13(9):e0204306.
Bouxsein ML, Boyd SK, Christiansen BA, Guldberg RE, Jepsen KJ, Muller R. Guidelines for assessment of bone microstructure in rodents using micro-computed tomography. J Bone Miner Res. 2010;25(7):1468–86.
Jamsa T, Jalovaara P, Peng Z, Vaananen HK, Tuukkanen J. Comparison of three-point bending test and peripheral quantitative computed tomography analysis in the evaluation of the strength of mouse femur and tibia. Bone. 1998;23(2):155–61.
Ong KL, Lovald S, Black J: Orthopaedic biomaterials in research and practice, Second Edition: CRC Press; London, 2014.
Pandithevan P, Saravana Kumar G. Reconstruction of subject-specific human femoral bone model with cortical porosity data using macro-CT. Virtual and Physical Prototyping. 2009;4(3):115–29.
McCalden RW, McGeough JA, Court-Brown CM. Age-related changes in the compressive strength of cancellous bone. The relative importance of changes in density and trabecular architecture. J Bone Joint Surg Am. 1997;79(3):421–7.
Bagi CM, DeLeon E, Ammann P, Rizzoli R, Miller SC. Histo-anatomy of the proximal femur in rats: impact of ovariectomy on bone mass, structure, and stiffness. Anat Rec. 1996;245(4):633–44.
Turner RT, Vandersteenhoven JJ, Bell NH. The effects of ovariectomy and 17 beta-estradiol on cortical bone histomorphometry in growing rats. J Bone Miner Res. 1987;2(2):115–22.
Aerssens J, van Audekercke R, Talalaj M, Geusens P, Bramm E, Dequeker J. Effect of 1alpha-vitamin D3 and estrogen therapy on cortical bone mechanical properties in the ovariectomized rat model. Endocrinology. 1996;137(4):1358–64.
Danielsen CC, Mosekilde L, Svenstrup B. Cortical bone mass, composition, and mechanical properties in female rats in relation to age, long-term ovariectomy, and estrogen substitution. Calcif Tissue Int. 1993;52(1):26–33.
McElroy JF, Wade GN. Short- and long-term effects of ovariectomy on food intake, body weight, carcass composition, and brown adipose tissue in rats. Physiol Behav. 1987;39(3):361–5.
Coll AP, Farooqi IS, O'Rahilly S. The hormonal control of food intake. Cell. 2007;129(2):251–62.
Nicks KM, Fujita K, Fraser D, McGregor U, Drake MT, McGee-Lawrence ME, Westendorf JJ, Monroe DG, Khosla S. Deletion of estrogen receptor beta in osteoprogenitor cells increases trabecular but not cortical bone mass in female mice. J Bone Miner Res. 2016;31(3):606–14.
Martin-Millan M, Almeida M, Ambrogini E, Han L, Zhao H, Weinstein RS, Jilka RL, O'Brien CA, Manolagas SC. The estrogen receptor-alpha in osteoclasts mediates the protective effects of estrogens on cancellous but not cortical bone. Mol Endocrinol. 2010;24(2):323–34.
Windahl SH, Andersson G, Gustafsson J-Å. Elucidation of estrogen receptor function in bone with the use of mouse models. Trends Endocrinol Metab. 2002;13(5):195–200.
Taes Y, Lapauw B, Griet V, De Bacquer D, Goemaere S, Zmierczak H, Kaufman JM. Prevalent fractures are related to cortical bone geometry in young healthy men at age of peak bone mass. J Bone Miner Res. 2010;25(6):1433–40.
Mittra E, Rubin C, Gruber B, Qin YX. Evaluation of trabecular mechanical and microstructural properties in human calcaneal bone of advanced age using mechanical testing, microCT, and DXA. J Biomech. 2008;41(2):368–75.
Guler Okyay A, Kavak S, Turktas U, Alkis I, Guner S, Aksakal B. Biomechanical effects of menopause in ovariectomized rats’ femurs. Gynecol Endocrinol. 2014;30(1):62–5.
McNamara LM, Ederveen AG, Lyons CG, Price C, Schaffler MB, Weinans H, Prendergast PJ. Strength of cancellous bone trabecular tissue from normal, ovariectomized and drug-treated rats over the course of ageing. Bone. 2006;39(2):392–400.
Bord S, Horner A, Beavan S, Compston J. Estrogen receptors alpha and beta are differentially expressed in developing human bone. J Clin Endocrinol Metab. 2001;86(5):2309–14.
Kutz M. Keaveny: Standard Handbook of Biomedical Engineering and Design. Chapter 8. New York: McGraw-Hill; 2003.
This study was supported by a Grant-in-Aid for Scientific Research from the Japan Society for the Promotion of Science (JSPS) (JP15KK0337 and 18H02989 to MKa).
Availability of data and materials
All data generated or analyzed during this study are included in this published article. Additional data may be available from the corresponding author on reasonable request.
Ethics approval and consent to participate
This study was approved by the animal review committee of Niigata University (approval number: 36-9). All animal experiments were performed according to the protocol and the ethical guidelines of Niigata University.
Consent for publication
The authors declare that they have no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Rosales Rocabado, J.M., Kaku, M., Nozaki, K. et al. A multi-factorial analysis of bone morphology and fracture strength of rat femur in response to ovariectomy. J Orthop Surg Res 13, 318 (2018) doi:10.1186/s13018-018-1018-4
- Bone quality
- Bone architecture
- Tissue mineral density
- Cortical porosity
- Bone fracture risk