Effect of testosterone, raloxifene and estrogen replacement on the microstructure and biomechanics of metaphyseal osteoporotic bones in orchiectomized male rats
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- Stuermer, E.K., Sehmisch, S., Tezval, M. et al. World J Urol (2009) 27: 547. doi:10.1007/s00345-009-0373-5
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Currently, osteoporosis research is rarely undertaken in males but an increase in male life expectancy in the company of hypogonadism suggests the necessity for potential therapeutic options.
Materials and methods
In this study, the changes in bone structure under standardized testosterone- (T), raloxifene- (R) and estrogen (E)-supplemented diets were analyzed in osteoporotic castrated male rats.
Unexpected biomechanical results could be only explained by the histomorphometry, but not by BMD measurements obtained from the qCT. All tested substances showed a significant improvement in the trabecular network (trabecular bone area for C: 2.55 mm2, T: 4.25 mm2, R: 4.22 mm2 and E: 4.28 mm2), and suggests that the bone structure was preserved. For the metaphyseal cortical bone, a significant loss was detected in T (CBP: 18.7%) compared to R (CBP: 30.0%), E (CBP: 26.8%) and even to the osteoporotic control (CBP: 28.6%). This explains the observed early mechanical final failure after T supplementation. However, due to the preserved trabecular bone in T, the occurrence of the first microfractures (yL: 49 ± 21.4 N) was significantly later than in the osteoporotic control (yL: 39.5 ± 15.5 N). Raloxifene performed well in hindering the bone loss associated with osteoporosis. However, its effect (yL: 83.3 ± 16.5 N) did not approach the protective effect of E (yL: 99.2 ± 21.1 N).
Testosterone only preserved the deterioration of the trabecular bone but not of the cortical bone. Raloxifene prevented the bone loss associated with osteoporosis at all bony structures. This effect did not approach the protective effect of estrogen on trabecular bone, but it is more suitable for male individuals because it has no feminizing effects on the subject.
Osteoporosis has become a pertinent topic in public health today, primarily due to the ever increasing elderly population. Many of the current therapies target postmenopausal osteoporosis [1, 2], where estrogens have been shown to have potent anti-osteoporotic properties. However, an increase in life expectancy in males also suggests the necessity to develop potential alternative therapies since estrogens cannot be used in males because of their feminizing side effects. Osteoporosis research is rarely undertaken in males and there are few therapeutic options. Testosterone (T) is an essential hormone for maintenance of bone mass and androgens have anti-osteoporotic properties [3, 4]. However, the clinical significance of testosterone substitution in osteoporotic men with hypogonadism is still undefined. It is believed that estrogens mediate the primary bone-sparing effects of androgens only after aromatization . Aromatase gene expression and activity has been demonstrated in bones of male humans and rodents [6–8] Aromatase knock-out mice, as well as estrogen receptor α knock-out mice develop osteoporosis [7, 8]. Additionally, osteoblasts and osteoclasts were equally active in both control and testosterone-treated groups, while a reduction in their activities was associated with estrogen- and raloxifene-supplemented diets .
In males, osteoporosis occurs primarily due to slowly deteriorating testicular testosterone production. Therefore, T supplementation presents itself as an alternative treatment that was tested in the present study. In recent years, the discovery of selective estrogen receptor modulators (SERMs) has led to the availability of substances, which do not affect the mammary glands and gonads, but exert estrogenic, positive effects in bone. One such substance is raloxifene (R), which proved to have potent anti-osteoporotic effects in postmenopausal women [9, 10]. R appears to have no feminizing effect or negative effects on male gonads . Therefore, R was also tested in this study.
The castrated rat is an established model of osteoporosis [12, 13] and these animals develop substantial osteoporosis with the highest degree occurring in the metaphyseal tibia ; after 3 months, bone mass will decrease to about 35% in male animals [14, 15]. Consequently, bone density measurements are performed at the femoral neck for humans and in the proximal tibia for rats. The qCT is an established method used to quantify the effect of anti-osteoporotic agents in vivo [2, 16, 17]. Post-mortem microradiographs from undecalcified histological sections provide higher local resolution. Information about the trabeculae (i.e., number, length, width, localization etc.), and changes in cortical bone can also be obtained in detail.
Materials and methods
Animals and chemicals
The study protocol was approved by the regional government and conformed to German animal protection laws (permission Az: 509.42502/01-02.98 District Government of Braunschweig).
Forty-four 3-month-old male Sprague-Dawley rats (Winkelmann, Borken, Germany) weighing 220–260 g were orchidectomized under Rompun/Ketanest anesthesia (3.5 V/V, 1 ml/kg BW). After the operating procedure, animals were divided into four groups: Group I received phytoestrogen-free pelleted food (where protein supplementation was substituted with potato proteins); Group II received phytoestrogen-free food supplemented with T (in the form of testosterone propionate) with the average intake of 50 mg T/day; Group III received phytoestrogen-free food supplemented with R where the average intake was 3.35 mg R/day; Group IV received phytoestrogen-free food supplemented with E (in the form of estradiol benzoate), where the average food and E intake per animal per day was 20 g and 0.5 mg, respectively.
Drugs were used in established concentrations [2, 6, 17–19]. Animals were fed with these specific diets for 12 weeks, after which time they were sacrificed under anesthesia. Both tibiae were prepared as follows: skin, muscles and tendons were removed and the fibula was separated at the synostosis. Tibiae were immediately stored at −80°C prior to histological embedding. The metaphysis of the left tibia was used for immunohistochemical investigations as previously described [6, 16].
Collected blood samples were allowed to clot and then centrifuged at 3,000 g, 10 min. Serum concentrations of T and estradiol-17β were quantified using Euless (Roche, Mannheim, Germany) and DSL (Webster, TX, USA) commercial immunoassays, respectively. To avoid the difference in T and estradiol level, all blood samples are taken at a certain time in the mornings.
Twelve weeks after orchidectomy or on supplemented diets with T, R and E, total BMD, total bone area (TBA), trabecular density and trabecular area of the proximal tibial metaphysis were recorded by qCT (STRATEC XCT 4.50, Stratec Inc., Pforzheim, Germany) in anesthetized animals. The scanner was positioned in the proximal plane of the left tibial metaphysis and a coronal computed radiograph (Scout view) in the distal direction was carried out. Image acquisition, processing and calculation were performed using the software package (XCT 5.40, STRATEC Inc. Pforzheim, Germany). Trabecular values were calculated by acquiring data within the default threshold of 280–710 mg/cm3. Cortical area and cortical density were calculated from a slice sampled 15 mm distal to the growth plate. A density above 710 mg/mm3 was regarded to be cortical bone.
A ZWICK-testing machine type 145660Z020/TND (Zwick/Roell, Ulm, Germany) with a measuring range from 2 to 200 N at a relative accuracy of 0.2% at 0.4%FN and a newly developed device as previously described  were used for mechanical testing of the metaphyseal tibia. Strength admission was recorded using “testXpert” software. The speed of the feed motion was 50 mm/s and the automatic switch off-pressure was set at 300 N. The left tibiae were thawed and continuously moistened with isotonic saline solution during the test. The procedure was performed blindly with regard to the test groups.
Preparation for microscopy and microradiography
After biomechanical testing, complete tibiae were defatted in an alcohol series, stained with basic fuchsine (Chroma-Gesellschaft, Koengen, Germany) and embedded in methyl methacrylate. After polymerization, 100 μm (± 10) thick sections were cut parallel to the surface of the knee joint using a specifically designed diamond-coated saw (Leica SP 1600 saw microtome, Bensheim, Germany) with a blade thickness of 300 μm. The level of the sections was calculated in order to obtain one specific section corresponding to 2 mm distal to the growth plate. Therefore, this section corresponds to the qCT slice, as described above. Microradiographies were performed on KODAK Professional Industrex SR45 film (100 NIF) on a Faxitron X-Ray System (Hewlett-Packard, San Diego, CA, USA) as previously described. The bone sections were exposed for 6 min at 40 kV and the resolution of the images was approximately 0.5 μm. The film was analyzed qualitatively and quantitatively under the microscope.
Qualitative and quantitative bone morphometry
Quantitative analysis of bone tissue was digitally determined in the microradiographs using the Quantimet system (Leica DM-RXE and Leica QWIN, Bensheim, Germany) after digital imaging with the Leica DC200 camera. The following data were evaluated: TBA, trabecular bone area (Tb.Ar.), percentage of trabecular bone (Tb.P.), trabecular length (Tb.Ln.), number of trabecular nodes (N.Nd.), cortical bone area (Cb.Ar.), percentage of cortical bone, cortical width lateral (Ct.Wi.l.), cortical width medial (Ct.Wi.m.) and the ratio of cancellous bone area and Tb.Ar. The last value represents the trabecular density. Finally, fracture lines from the previously performed biomechanical testing  were analyzed qualitatively.
For statistical analyses, the mean values and standard deviations for each parameter were calculated. The differences between the four tested substances were assessed using ANOVA followed by the Tukey–Kramer post hoc test. For determining the correlation between the microradiographic and biomechanical data, Pearson’s correlation coefficient (r) was calculated. This value can range from −1.0 to 1.0 (where −1.0 = perfect negative correlation, 0.0 = no correlation and 1.0 = perfect positive correlation).
The mean serum concentration of testosterone in the T-treated animals was 4.2 ± 0.8 ng/ml and in the estradiol-17β-treated animals, the mean E level was 51.6 ± 4.6 pg/ml. Both hormone levels fall within the normal circadian physiological range of male and female rats; hence these animals can be referred as normal (positive) controls. There is currently no established method to determine the serum levels of raloxifene.
At the time of castration, the average body weight for control animals was 242.8 ± 7.0 g and for the T-, R- and E-treated groups, 259.3 ± 45.2, 280.3 ± 26.1 and 245.2 ± 13.3 g, respectively. The average body weight of R-treated rats was significantly higher than for control and E-treated animals. Three months after castration, diverse increases in weight were observed amongst the animal groups, the control and T-treated animals weighed 392.8 ± 19.7 g (+38.2%) and 393.4 ± 23.4 g (+34.1%), respectively, whereas treatments with R and E were associated with a significantly lower animal body weights of 319.3 ± 22.0 g (+12.2%) and 270.1 ± 18.9 g (+9.3%), respectively. For E this is a well-known effect [20, 21].
BMD and bone areas (qCT)
Microradiography and morphometry
Morphological analysis of the cortical and trabecular bone in the microradiographic sections 2 mm distally to the growth plate in the metaphyseal tibia in male rats
Total bone area (mm2; mean)
23.66 ± 2.26
24.67 ± 3.11
23.37 ± 3.39
20.99 ± 2.54a
Trabecular bone area (mm2; mean)
2.553 ± 0.90
4.253 ± 1.18a
4.223 ± 1.10a
4.276 ± 0.99a
Percentage of trabecular bone (%; mean)
10.62 ± 2.994
17.01 ± 3.223a
17.95 ± 3.371a
20.18 ± 2.909a
Trabecular bone area/cancellous bone area ratio (Tb.Ar./Cn.Ar.) (mean)
7.40 ± 3.01
4.87 ± 0.68a
4.19 ± 0.71a
3.70 ± 0.53a
Trabecular length (μm; mean)
102.7 ± 7.28
99.45 ± 5.11
108.2 ± 9.74
103.2 ± 5.88
Number of nodes (mean)
150.3 ± 59.87
311.1 ± 140.10a
306.1 ± 129.40a
365.6 ± 122.20a
Cortical bone area (mm2; mean)
6.701 ± 0.62
4.443 ± 1.61a
6.165 ± 0.77a
5.575 ± 0.64a
Percentage of cortical bone (%; mean)
28.59 ± 3.98
18.68 ± 8.41a
30.02 ± 4.41
26.77 ± 3.10
Cortical width lateral (μm; mean)
457.7 ± 48.29
388.0 ± 48.29a
498.6 ± 36.87a
396.2 ± 23.74a
Cortical width medial (μm; mean)
324.1 ± 21.33
254.4 ± 41.95a
349.0 ± 42.60
273.8 ± 34.68a
Pearson correlation test
Positive and negative correlations of the morphological data of the microradiographies and biomechanical testing evaluated in the Pearson test
Total bone area
Trabecular bone area
Number of nodes
Cortical bone area
Percentage of cortical bone
Average cortical width
Analysis of the post-mortem fracture lines
Examination of the microradiographs allowed the differences in the fracture lines from the biomechanical testing to be determined in all groups. In an example picture from an osteoporotic control (Fig. 4a, e), the main fracture line is clearly visible. In this group fracture lines failed in a burst-like fashion with no regard for the bone architecture and matrix. In contrast, in the E-supplemented group, the main fracture line spread with many comminutions of various lengths (Fig. 4d, h) and the force appeared to propagate directly through those bone structures with least resistance (i.e., the fracture “cuts” through the thinnest trabecular junctions). In the R group (Fig. 4c, g), this phenomenon was less developed compared to the E group, although more visible. After T supplementation, less comminution were found, although the trabecular network was nearly as dense as those present in R- and E-treated bones (Fig. 4b, f). However, the administered force affected the trabecular structures more than in the other groups because of the weaker cortical bone.
Management of hypogonadism and its related morbidities in male is still a dilemma in medicine. Hypogonadism has been accepted as a significant risk factor for the development of male osteoporosis. However, studies regarding therapy of osteoporosis in males are rare in comparison to those of postmenopausal females. The orchidectomized rat is currently an accepted animal model of male hypogonadism and osteoporosis [22, 23].
The effects of testosterone may be mediated directly by the androgen receptor or indirectly, via aromatization into estrogens and subsequent stimulation of estrogen receptors (ER-α and ER-β) [24, 25]. It preserved the trabecular structure (Tr.Ar., N.Nd.) significantly compared to the osteoporotic control. The protective effect was nearly as good as for estrogen and raloxifene (Fig. 1a, b). The investigation of the metaphyseal cortical bone in the microradiography showed interesting results regarding testosterone. In contrast to results described by other authors [23–25], a significant deterioration in cortical bone was found after T supplementation. Cortical bone was more reduced than in the R- and E-treated groups, even more than in the osteoporotic control. The reason for this lack of conformity may be that metaphyseal (tibial) bone was investigated instead of diaphyseal bone, as was investigated in these other previous studies. A possible explanation for this phenomenon may be that the cortical bone has less androgen and/or estrogen receptors, but that has not been proved yet.
The structural changes after testosterone-supplementation could explain the comparatively poor results in the biomechanical tests (Fig. 3). The reduced cortical bone failed early and led to a low Fmax. However, the dense trabecular structure (Tr.Ar., N.Nd.) did protect the bone since it had high elasticity. Therefore, the yL is significantly higher than in the osteoporotic C. Microfracturing, which is the basis of the osteoporotic fracture, occurred later in T than in C. These data suggest that if T is to be used in treatment of osteoporosis, it needs to be supplemented by another bone-sparing substance, i.e., bisphosphonates as an osteoclast inhibitor.
Estrogen plays a key role in male skeletal growth [26, 27]. In this study preserved the trabecular bone more than T and R. It is well-acknowledged that estrogen application in rats’ results in smaller animals with a lower body weight . Therefore, the significantly smaller TBA must be taken into consideration; the number of nodes and relation of trabecular volume to tissue volume to cancellous volume were remarkably high. However, supplementation of E does not seem to improve the cortical bone in comparison to C. When considering biomechanical features, this had no negative effect since the comparable thin cortical bones seemed to have good elasticity and resistance to forces. The measured yL for E was the highest and significantly better than for C, T and R. Plastic deformation and microfracturing occurred very late. In terms of Fmax, the bone quality was significantly better than in C and T; only R showed equal results to E. E protected the physiological bony structure with a defined mixture of elastic and calcified tissues.
The SERM raloxifene that had been proved to prevent postmenopausal osteoporosis [9, 10] was also investigated. It did not bind to androgen receptors, had no effects on male reproduction (sperm production/quality, testicular weight and histopathology)  and had positive effects on the serum cholesterol  and the elasticity of vessels . Therefore, it may also be a good option in the treatment of osteoporosis in males. In osteoporotic rats, it mimicked most preserving effects of E, but did not yet reach the levels that E did in all parameters. Supplementation of R preserved the structure of the osteoporotic bones significantly. This was true for the metaphyseal cortical bone as well as the trabecular bone. In comparison to E, R preserved cortical bone more, but the trabecular bone was preserved less well than E. Overall, the bone volume (per tissue volume) was highest in R. That supports the well-acknowledged fact that the structure of bone is more important than the bone mass regarding the question of capacitance. The final failure (Fmax) for R was equal to E. But the yield load, which is more interesting in osteoporosis, was significantly lower than in E. Fatigue fractures in osteoporosis as the result of the sum of microfractures would occur significantly earlier. Regarding the prophylaxis of osteoporosis E outperforms R.
The morphological analysis with the qCT and microradiography showed that the tested substances T, R and E improved the trabecular structure. The qCT seemed to be less qualified for analysis of the minor metaphyseal cortical bone. Microradiography was able to illustrate the different influences of the tested substances more precisely.
In clinical practice, microscopic evaluation or non-invasive biomechanical measurement of bone quality for diagnostics or therapy of osteoporosis is not possible. It is well-known that the true individual risk of fracture cannot be measured by BMD alone. However, there is yet to be an alternative device for estimating individual bone quality in vivo. Micro-CTs for clinical examinations of human bone are rare worldwide. They provide more detailed, but also indirect parameters to estimate fracture risk. In the future, it may be helpful to also investigate the non-calciferous bone matrix and its changes during developing osteoporosis (e.g., by an exploratory excision) because of its important influence on the elasticity and brittleness of bone.
Testosterone only improved the trabecular bone structure, however due to the loss of cortical bone, fragility was nearly the same as that for osteoporotic bone. R had a good effect and hindered the bone loss associated with osteoporosis at trabecular structures. However, its effect did not approach the protective effect of E on the incidence of microfractures, which form the basis of osteoporotic fractures. E inhibited growth and induced smaller tibiae in rat, which was also advantageous. Nevertheless, Raloxifene may be a potential male osteoporosis treatment, as estrogen cannot be used in males because of its feminizing effects.
Conflict of interest statement
There is no conflict of interest.
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