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Ryu, Ryu, Kim, Park, Kim, Chin, Kim, Cho, and Kuh: Bone Mineral Density Changes after Orchiectomy using a Scrotal Approach in Rats

Abstract

Objective

To investigate a suitable animal model for studies of male osteoporosis. Osteoporosis has a particularly high incidence in postmenopausal women, resulting in a substantial amount of research with respect to this disease in women. However, research on osteoporosis in men is still lacking.

Methods

Twenty 10-week-old male Sprague Dawley rats were used in this study, including 4 rats used to establish a baseline bone mineral density (BMD). The other 16 rats were divided into two groups: a sham surgery group (n=8), which underwent a sham operation, and an orchiectomized rat group (OCX) (n=8), which underwent bilateral OCX at 10 weeks of age. Bone mineral density was measured in 4 rats from both the sham surgery group and the OCX group 8 weeks after the surgery, while BMD in the remainder of the rats was measured 10 weeks post-surgery.

Results

Femoral BMD at 8 weeks post-surgery was found to be significantly lower in the OCX group compared to the sham group; a finding that was also similar 10 weeks post-surgery.

Conclusion

8 weeks after undergoing orchiectomy performed via a scrotal, white rats are a suitable model for studies of male osteoporosis.

INTRODUCTION

Korean society is rapidly aging in comparison to other developd countries. In 2000, Korea became an aging population with 7.2% of the total population aged 65 or older. It has been estimated that Korea will become an aged society in 2019, and a super-aged society in 202617). Hence, it is safe to assume that osteoporosis will become the next most important geriatric disease, following coronary artery disease (CAD) and diabetes mellitus (DM), resulting in rising costs to society for prevention and treatment.
Research on osteoporosis has so far been primarily performed on postmenopausal women, due to the high incidence of disease in this population. However, it is important to acknowledge that 14.5% of men who underwent spinal surgery had osteoporosis, which can result in higher reported morbidity and mortality if fracture was to occur10). This percentage is one-third of that found among women3). For this reason, research on male osteoporosis is essential.
Regarding osteoporosis in men, it has been reported that the androgen deprivation therapy used in patients with prostate cancer is complicated by osteoporosis4) and the high alkaline phosphatase levels in these patients14) allows us to deduce that bone loss is occurring in these patients. It is also known that continued use of androgen deprivation therapy in patients with prostate cancer results in a worsening of osteoporosis5). In these cases, anti-resorptive drugs, such as bisphosphonate, are used in prevention. Consequently, it is very important to understand their effect. Many articles have been published regarding the effects of anti-resorptive drugs in orchiectomized animal models of male osteoporosis1,6,11). However, before the effects of these drugs are evaluated in animal models, it is also important to validate whether the animal model is already compromised by osteoporosis.
The use of ovariectomized white rats as a female osteoporosis model, included specific procedural guidelines and disease development findings, has been reported15). However, similar reports on male osteoporosis animal models are scarce, except for articles dealing with male osteoporosis risk factors16,19) and histological analyses7) in orchiectomized white rats. We sought to evaluate these issues in detail, and to statistically verify changes in bone mineral density (BMD) in our research.
In this study, we focused on the verification of BMD changes over time in rats bilaterally orchiectomized via a scrotal approach (OCX), and to describe the specific procedures used to create our male osteopenia animal model.

MATERIALS AND METHODS

1. Animals

Twenty 10-week-old male rats purchased from Orient Bio (Gyonggi, Korea) (Sprague-Dawley, weight 210-220 g) were acclimated in a comfortable environment (temperature 22±4℃, humidity 65±5%, day-night cycle 6:00 AM-6:00 PM). The environment was specific pathogen free. Two rats were housed in each stainless steel wire cage. The experimental group was randomly selected. This study was approved by the Yonsei University Health System Institutional Animal Care and Use Committee.

2. Experimental Design

Four 10-week-old rats (control group) were sacrificed, their femora were removed, and BMD was measured in these femora. The living 16 rats were divided into two groups. The sham operation (SO) group (n=8), underwent a sham operation at 10 weeks of age, and the OCX group (n=8) underwent bilateral OCX, intended to change bone mineral density, at 10 weeks of age. Eight weeks after the OCX or SO, four rats from each of the two groups were sacrificed, and their femora were obtained and BMD was measured. Ten weeks after OCX or SO, the living rats in each group were sacrificed and the BMDs of their femora were measured. All rats were sacrificed using CO2 inhalation.

3. Femur BMD Measurement

Rats were euthanized at weeks 10, 18, and 20, and both femora from each rat were obtained. BMD was measured in the femora using micro computed tomography (CT): SkyScan 1173 (Bruker-CT, Kartuizersweg 3B 2550 Kontich, Belgium) and NRecon (Ver. 1.6.9.4) software (Fig. 1).

4. Orchiectomy and Sham Operation Procedure

Anesthesia was induced with 5% isoflurane and Rompun (2.5mg/kg, Bayer Korea) and Zoletil (5mg/kg, Virbac Korea) were injected intra-peritoneally for generalized anesthesia. 2.5% isoflurane and oxygen were administered via a coaxial nose cone for anesthesia maintenance. Bilateral orchiectomy was performed via a scrotal approach. The anesthetized rat was placed supine on the operating table and its position was fixed using sticking tape. The scrotal hair was bilaterally shaved (Fig. 2A). A betadine prep was performed as an aseptic maneuver (Fig. 2B). If the cremaster muscle was stimulated during the betadine prep, resulting in ascension of the testes, a downward stroke was performed to lower the testes back into place. A small, 1.0-cm median incision was made through the skin at the tip of the scrotum(Fig. 2C). The cremaster muscles were opened with a small, 7-mm incision. At the entrance to the scrotal cavity, the testicular fat pad was located and pulled through the incision using blunt forceps. The cauda epididymis was pulled out along with the testis, followed by the caput epididymis, the vas deferens and the testicular blood vessels (Fig. 2D). After identifying the testis, epididymis, vas deferens and testicular blood vessels, a single ligature was placed on the spermatic cord around the vas deferens and the blood vessels (Fig. 2E). The testis and epididymis were removed. This procedure was repeated for on the other testis and epididymis. The cremaster muscle and scrotal skin were sutured layer by layer (Fig. 2F).
The same preparation was performed on animals in the sham operation group, allowing the authors to visually identify the testis, epididymis, vas deferens and testicular blood vessels. After visual identification, the cremaster muscle and skin were sutured without ligation or resection.

5. Statistical Analysis

Statistical analysis was performed using SPSS software (version 20.0, Chicago, IL, USA). The Mann-Whitney test was used to compare values between the SO group and the OCX group, and the Wilcoxon signed-rank test was used to compare the mean values of BMD within the same group. Probability values <0.05 were considered statistical significant.

RESULTS

No procedural deaths occurred during the course of the experiment. Micro CT scan revealed male osteoporosis in orchiectomy group at POD 8 weeks and POD 10 weeks. There are marked deficiencies in trabecular bone (Fig. 3). Baseline BMD was measured in 10-week-old rats (control group) and a value of 0.244±0.073 g/cm3 was obtained. The mean femur BMD was significantly different between the OCX rats and the sham operation rats eight weeks after OCX (0.363±0.048 g/cm3 vs. 0.205±0.019 g/cm3, p=0.029). The mean femur BMD was also significantly different between the OCX rats and the sham operation rats ten weeks after OCX (0.451±0.076 g/cm3 vs. 0.280±0.008 g/cm3, p=0.029) (Table 1 and Fig. 4). No significant differences in chronologic BMD were found in the same groups, in accordance with Wilcoxon signedranked test.

DISCUSSION

The incidence of osteoporosis is rising in concordance with the rise in the geriatric population. Hence, understanding the etiology of osteoporosis will become helpful in improving the prognosis of spinal fusion surgery in osteoporotic patients. The morbidity and mortality of fracture in male osteoporosis patients are higher than those in the female population10), which necessitates additional research on osteoporosis in men. In the current study, we analyzed changes in BMD in a representative animal model (bilateral OCX rat). Having an osteoporosis animal model in which to analyze bone quality is essential for research evaluating the effects and safety of treatments. OCX is classified as a gonadectomy which, along with ovariectomy, is a method for establishing an osteoporotic animal model12). This method is thought to be highly relevant to and representative of prostate cancer patients with osteoporosis undergoing therapeutic androgen deprivation. There have been many articles that have used ovariectomized rats as models for osteoporosis in postmenopausal women13). However, studies that detail the creation of precise male osteoporosis animal models and provide accompanying data on chronologic BMD results in these models have been lacking. Therefore, we sought to outline the procedures we used and report the resulting changes in BMD we observed in the current study.
Orchiectomy can be performed by a few different methods. Surgical methods differ in the direction of approach and location of incisions. The usual approaches are on the scrotal and abdominal sides, and the skin incisions usually made are single midline scrotal, double median scrotal and midline abdominal incisions. We performed orchiectomy in rats using double median scrotal incisions. We chose this method because the double median scrotal incision requires the shortest incision relative to the other possible single midline incisions. We also chose to use a scrotal approach because it allows for faster location of the testis, compared to an abdominal approach; thereby shortening the duration of operation. This study reports the sequential delineation of orchiectomy using double median scrotal incisions.
Previous studies have not been clear regarding the appropriate age of rats for the model or on the timing of significant BMD decreases after OCX when using the OCX rat model. In cases of ovariectomy, growing female rats tend to show a more sensitive skeletal response compared to aged female rats18). If skeletally immature rats are used, a low peak bone mass is achieved. This is considered to be a high risk factor for human osteoporotic problems. This trait is why the skeletally immature rat is an appropriate animal model for research on endocrine, nutritional and environmental factors, all of which can influence peak bone mass12). We believed that growing orchiectomized rats would also show a greater response in their skeletal systems. Although rats reach sexual maturity at the age of 10 weeks, their skeleton is considered mature after 10 months8). Because there is a time difference between endocrinologic maturation and skeletal system maturation, low peak bone mass was obtained by using 10-week-old orchiectomized rats.
There are a few reports of decreasing bone mass starting 4 weeks after ovariectomy, which led to considerable bone mass loss at 8 and 10 weeks2,9). Although there are studies which found decreasing bone mass after orchiectomy and reports of osteoporosis following androgen deprivation in patients with prostate cancer, studies regarding the exact timing of this decline were lacking. This study revealed the exact timing of decreasing bone quality with serial measurement using micro computed tomography. Both the 8-week and 10-week postorchiectomy groups showed statistically significant reductions in bone mass in our study. However, BMD in the 8-week group was determined to be lower. Hence if one were to conduct a study using an animal model of male osteoporosis to evaluate many bone related variables and BMD measurements, our 8-week post-orchiectomy animal model would be most suited to this purpose.
Bone mass was shown to rise between weeks 8 and 10 after orchiectomy. In our study, as only 4 rats were used, the mean BMD we measured may not have been a precise representative of the entire rat species BMD. We believe that the increase in BMD observed after orchiectomy may have been due to other compensatory actions for the lack of sex hormones. Furthermore, because a histologic evaluation of osteoid numbers after OCX was not conducted in the current study, further research pursuing chemical markers and using a pathological evaluation may be required.

CONCLUSION

Osteoporotic animal models can be easily established using bilateral orchiectomy, the details of which we have described above. Statistically significant decreases in bone mass were observed starting at 8 weeks post-operation. Bone mass increased over time even after bilateral orchiectomy, but was still statistically significant compared to the sham operation group when measured at the same time.

References

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Fig. 1

BMD measurement using NRecon software. BMD was measured in the femora using micro computed tomography: SkyScan 1173 (Bruker-CT, Kartuizersweg 3B 2550 Kontich, Belgium) and NRecon (Ver. 1.6.9.4) software.

kjs-12-55-g001.jpg
Fig. 2

Procedures for orchiectomy in rat. Anesthetized rat was laid supine on the operating table. Scrotal shaving was done (A). Betadine prep was performed as an aseptic maneuver (B). A small, 1.0-cm median incision was made through the skin at the tip of the scrotum(C). The cremaster muscles were opened with a small 7-mm incision. Thick black arrow: cremaster muscle. The testicular fat pad was localized and pulled through the incision using blunt forceps. The cauda epididymis was pulled out along with the testis, followed by the caput epididymis, the vas deferens and the testicular blood vessels (D). A single ligature was placed around the vas deferens and blood vessels (E). The testis was then removed. This procedure was repeated for the other testis. Muscle and skin were sutured layer by layer (F). Thick white arrow: Testis and epididymis surrounded by fat pad were totally removed.

kjs-12-55-g002.jpg
Fig. 3

Micro CT Axial images of femora. (A, C) shows Sham group rats, each rats are POD 8 weeks and POD 10 weeks. (B, D) shows OCX group rats, each rats are 8 weeks and 10 weeks.

kjs-12-55-g003.jpg
Fig. 4

The changes in BMD(g/cm3) in the Sham and OCX groups. The measured BMD was lowest at 8 weeks, after which BMD increased.

kjs-12-55-g004.jpg
Table 1

The changes in BMD(Mean±SD g/cm3) of Sham and OCX groups

kjs-12-55-i001.jpg

POD, post operation date; Sham, sham surgery group; OCX, orchiectomy group.



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