This research is an independent study and did not receive any funding.

The protocol adheres to the ethical guidelines set by the Institutional Animal Care and Use Committee (IACUC) at Beijing University of Chinese Medicine, Protocol number BUCM-4-2022062001-2109. The protocol uses Sprague Dawley (SD) rats (SCXK(Jing)2019-0008), aged 8-10 weeks and weighing 200 g-250 g.
1. Adaptation training
<ol>
	<li>Albino rats generally have a visual range of less than 60 cm15. During the modeling process, place the rats in opaque cages and keep them as far away as possible from non-modeled rats (at least, other rats should be outside the maximum visual range of the modeled rats) to prevent them from experiencing traumatic stress.</li>
	<li>Turn on the power and set the treadmill to 10 m/min with a 0&#176; incline. Place the rats on the treadmill and ensure the movements are as gentle as possible to avoid stress. Do not use additional stimulation; the rats will naturally crawl forward because they are unfamiliar with the environment.</li>
	<li>The training lasts for 15 min. After the training, clean up the feces and urine left by the rats and spray alcohol to eliminate the animal odor. Then, prepare the next rat for training. 
	NOTE: If a rat refuses to walk on the treadmill for 5 minutes, exclude it&#160;from the study.</li>
	<li>Continue adaptive training until the end of the 1st week.</li>
</ol>
2. Measuring the maximum weight-bearing capacity in rats
<ol>
	<li>Prepare two test tubes, a hook, and a loop fastener approximately 80 cm long. Place steel balls into the test tubes, ensuring that the initial combined weight of the test tubes, the hook, and the loop fastener is 150 g. Prepare test tubes with different total weights in 10 g increments, with the maximum weight being 350 g.</li>
	<li>A researcher uses both hands to fasten rats using gloves (Figure 1). Another researcher places the test tube on the back of the rat about 1 cm from the midline of the back. Since this step does not require movement of the rat, perform fixation by simply wrapping the hook and loop fastener around the rat without using additional measures to secure the tube.</li>
	<li>Change the tube until the rat&#39;s maximum weight is reached. When the rat reaches maximum weight-bearing, it cannot stand when prodded or the experimenter leaves. Reduce the weight by 10 g to allow the rat to stand. This weight represents the rat&#39;s maximum weight-bearing capacity.</li>
</ol>
3. Preparation of weight load
<ol>
	<li>Since secure fixation is required during training, secure the objects using 1-1.5 m elastic therapeutic tape based on rat size, which has strong adhesion. Use clay to adjust the weight of the test tubes to reduce the swinging of the load.</li>
	<li>After weighing the weight of the test tubes and the fixation objects, add an appropriate amount of clay into the test tubes to adjust them to the target weight. Use a glass stirring rod to evenly spread the clay inside the test tubes. Clay concentrated at one end of the test tube may cause it to detach easily during training.</li>
	<li>Adjust the total weight of the adjusted test tubes and clay at 50% of the rat&#39;s maximum weight-bearing capacity (Figure 1A). Exceeding this weight will make it difficult for the rat to complete the training. Do not adjust the weight of the load again until the end of the experiment.</li>
</ol>
4. Establishing steroid-induced osteonecrosis of the femoral head model
<ol>
	<li>Use the methylprednisolone combined with lipopolysaccharide (LPS+MPS) method for SONFH model establishment16,17. Perform intraperitoneal injection of LPS (20 &#181;g/kg) using a standard needle at the midline of the rat&#39;s abdomen once every 24 h, for a total of 2 injections.</li>
	<li>After the last LPS injection, inject MPS (40 mg/kg) into the unilateral gluteal muscle 24 h after regular feeding and continue injections every 24 h, alternating between the two gluteal areas, for a total of three injections.</li>
</ol>
5. Tension-free weight-bearing immobilization using elastic therapeutic tape and treadmill training
<ol>
	<li>Mark the rat&#39;s back midline at 1-2 cm on both sides; this is the reference point for the weight load. Ensure the marks are appropriately positioned to prevent the rat from tipping or hindering movement during treadmill training.</li>
	<li>With one investigator fixing the rat using gloves, place one hand under the rat&#39;s armpit to secure the forelimb and jaw while the other hand secures the hind limbs and tail. Avoid excessive force to prevent stress or suffocation (Figure 1B).</li>
	<li>Adhere the elastic therapeutic tape to the test tube without applying tension to secure the load on the rat&#39;s back. In the process of winding, do not stretch the elastic therapeutic tape to achieve tension-free fixation. 
	NOTE: The elastic therapeutic tape used in this model is designed for taping during intense physical activities, providing high adhesion and elasticity18. Due to its high elasticity, it greatly reduces the impact on the rat&#39;s movement while crawling.</li>
	<li>Ask the second investigator to fix the test tube to the rat&#39;s back parallel to the rat&#39;s spine, with the fixation position based on the markings made, i.e., 1-2 cm away from the midline on both sides of the rat&#39;s back.</li>
	<li>To minimize the suffering of the rat, reduce the impact on the rat&#39;s movement, and decrease mortality caused by fixation, perform fixation without applying tension. Stick the test tube with adjusted weight onto the elastic therapeutic tape, then wrap the test tube around the rat&#39;s body using a tension-free technique.</li>
	<li>Ensure tension-free immobilization and maintain the original length of the elastic therapeutic tape without stretching in order to prevent any adverse effects on rat breathing and movement (Figure 1C).</li>
	<li>After wrapping the test tube around the rat&#39;s body, place the rat in an open space or a single cage, monitoring its breathing and direction. If signs of rapid breathing or mouth opening appear, promptly release the rat to prevent suffocation.
	<ol>
		<li>Ideal immobilization allows the rat to move freely and perform activities like drinking, lifting forelimbs, and feeding (Figure 1D). If immobilization is unsatisfactory, release temporarily and re-immobilize after 20 min to minimize stress on the rat due to repeated immobilization stimuli.</li>
	</ol>
	</li>
	<li>Turn on the power and set the treadmill to 1 m/min with a 0&#176; incline. The treadmill training time is 30 min. Gently transfer the rat onto the treadmill and begin the timer.</li>
	<li>Do not provide additional stimulation to the rat. If the rat cannot complete the 30 min training, place it in a cage for a 10 min rest without removing the fixation. 
	NOTE: The elastic therapeutic tape used in this study has excellent stretchability and adhesiveness. When properly secured without tension, long-term fixation will not cause the test tube to detach or result in suffocation and death of the rat.</li>
	<li>After the training, clean up the feces and urine left by the rats and spray alcohol to eliminate the animal odor.</li>
	<li>Avoid the above steps being seen by other rats and handle the animals as gently as possible to prevent animals from vocalizing, thus causing traumatic stress to other rats.</li>
	<li>Immediately release the rat from fixation after completing training (Figure 1E). During release, use fingers to press down on the rat&#39;s fur to protect it, minimizing fur loss during release (Figure 1F).</li>
</ol>
6. Animal grouping
<ol>
	<li>To study the impact of weight-bearing training on SONFH, randomly divide 60 rats into four groups.</li>
	<li>In the Control group, do not establish the common steroid-induced osteonecrosis of the femoral head (SONFH) model or perform weight-bearing training. In the Control+Load group, carry out weight-bearing training only, without establishing the steroid-induced osteonecrosis of the femoral head model. In the Model group, establish the steroid-induced osteonecrosis of the femoral head model only. In the Model+Load group, perform weight-bearing training after establishing the steroid-induced osteonecrosis of the femoral head model.</li>
</ol>
7. Euthanasia and specimen collection
<ol>
	<li>Place the rats into a small animal euthanasia chamber and inject enough carbon dioxide to achieve a concentration higher than 5%. Once the rats lose consciousness, administer a dose of 0.3 mL/kg of body weight of a 20% potassium chloride solution, totaling 20 mL, via an intracardiac injection.</li>
	<li>Monitor the rats&#39; breathing and heartbeat to ensure they experience no pain or discomfort during euthanasia. Confirm death by checking for the absence of breathing and heartbeat. Spray alcohol to clean away any odor.</li>
	<li>Post-euthanasia, dissect the rat&#39;s hip region and extract the femoral head while keeping the femur intact. Perform a microCT scan following pretreatment, followed by Hematoxylin-Eosin (HE) staining.</li>
</ol>
8. Hematoxylin-Eosin staining
<ol>
	<li>After the modeling is completed, euthanize the rats. Remove the femurs for HE staining.</li>
	<li>Soak the rat femurs in 4% paraformaldehyde for 24 h to preserve biological tissues as specimens. Soak the rat femur specimens in 5% formic acid for decalcification for 5 days.</li>
	<li>Section the specimens into 5 &#181;m slices for HE staining. 
	NOTE: Empty lacunae refer to the situation in bone tissue19 where the lacunae, which should normally contain osteocytes, are devoid of these cells. It is an important indicator for assessing the health of bone tissue. In the pathological process of bone necrosis, insufficient blood supply may cause osteocyte death, leading to empty lacunae. In the diagnosis and evaluation of bone necrosis, the number and distribution of empty lacunae are important parameters for measuring the severity of the disease20,21.
	<ol>
		<li>Place rat femoral specimens into melted paraffin (56-60 &#176;C), first soaking in low-melting-point paraffin, if necessary, then gradually transfer to higher melting point paraffin, each time for about 1 h, to ensure thorough infiltration of the tissue with paraffin.</li>
		<li>Prepare embedding molds and pour melted paraffin into the molds to the appropriate depth. Retrieve the tissue samples from the paraffin using forceps after soaking, remove excess paraffin, and place them in molds. Cool to room temperature to solidify the paraffin, forming paraffin blocks.</li>
		<li>Using a paraffin microtome, cut the embedded paraffin blocks into 5 &#181;m thick sections.</li>
	</ol>
	</li>
	<li>Bake the rat femoral specimens with attached slices in a slide warmer for 1 h to enhance the adhesion between the slices and coverslip and reduce floating during subsequent staining processes.</li>
	<li>Immerse the baked slices sequentially in pure xylene to remove paraffin, followed by a series of dehydration through absolute ethanol, gradient ethanol (100%, 95%, 80%, 70%), and water, for 2 min each, completing the deparaffinization and rehydration process.</li>
	<li>Immerse the deparaffinized slices in a hematoxylin staining solution and stain for 10 min. Rinse with running water to remove unbound hematoxylin.</li>
	<li>Immerse the hematoxylin-stained sections in eosin staining solution and stain for 2 min to color the cytoplasm and connective tissue. Rinsed with a 1% acetic acid solution to fix the staining effect.</li>
	<li>Immerse the rat femoral bone specimen slices sequentially in 70%, 80%, 90%, 95%, and 100% ethanol, with each gradient for 2 min, gradually removing moisture.</li>
	<li>Immerse the rat femoral bone specimen slices in pure xylene for transparency, followed by rinsing with running water to remove the xylene. Apply neutral mounting resin, covering the slides, gently tapping to remove air bubbles, and allowing the mounting medium to solidify to complete the mounting process.</li>
	<li>Using the randomizr package in R, select 30 HE-stainedslides for each group and allocate 15 slides each to two researchers. Without informing them of the groupings, ask the researchers to calculate the empty lacunae rate of the slidesand collect the results for statistical analysis.</li>
</ol>
9. MicroCT analysis
<ol>
	<li>After the modeling is completed, euthanize the rats. Remove the femurs for Hematoxylin-Eosin staining.</li>
	<li>Soak the rat femurs in 4% paraformaldehyde for 24 h to preserve biological tissues as specimens. Place the rat femurs in the small animal-specific microCT device.</li>
	<li>Set the microCT scanning conditions as follows: X-ray voltage: 80 kV, Current: 100 &#181;A, Single exposure time: 50 ms, scanning resolution: 25 &#181;m. Perform scans at intervals of 0.5&#176;, focusing on the trabecular bone from beneath the cartilage to the upper part of the epiphysis as the region of interest.</li>
	<li>Define the area above the rat femoral neck as the region of interest.</li>
	<li>Perform coronal plane reconstruction of the scanning results using microCT device and collect bone morphometric measurements generated by the built-in software of the microCT device. Record the following observed indices: Total Volume (TV), Percent Bone Volume (BV/TV), Bone Surface/Volume Ratio (BS/BV), Structure Thickness (Tb.Th), Structure Separation (Tb.Sp), Number of Bone (Tb.N), Bone Density (BD).</li>
</ol>
10. Statistical analysis
<ol>
	<li>Present the data as the mean &#177; standard deviation (SD). Conduct statistical analyses for micro-CT and quantitative histologic evaluations using the independent sample t-test. Consider a p-value &#60; 0.05 as statistically significant.</li>
</ol>

Elastic Tape Rat Model of Steroid-Induced Femoral Head Osteonecrosis Enhancement

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D., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=A+field+study+of+histologic+and+bacteriologic+characterization+of+femoral+head+separation+and+femoral+head+necrosis.">A field study of histologic and bacteriologic characterization of femoral head separation and femoral head necrosis.</a> Avian Dis. 64 (4), 571-581 (2020).</li><li>Fan, M., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Comparisons+of+emu+necrotic+femoral+head+micro+structure+repaired+in+two+different+methods.">Comparisons of emu necrotic femoral head micro structure repaired in two different methods.</a> Acta Acad Med Sinicae. 38 (1), 16-21 (2016).</li><li>Naito, S., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Femoral+head+necrosis+and+osteopenia+in+stroke-prone+spontaneously+hypertensive+rats+(SHRSPs).">Femoral head necrosis and osteopenia in stroke-prone spontaneously hypertensive rats (SHRSPs).</a> Bone. 14 (5), 745-753 (1993).</li><li>Omokawa, S., Tamai, S., Ohneda, Y., Mizumoto, S., Yamamoto, S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=A+histopathological+study+on+the+femoral+head+necrosis+in+spontaneously+hypertensive+rats+(SHR).">A histopathological study on the femoral head necrosis in spontaneously hypertensive rats (SHR).</a> Nihon Seikeigeka Gakkai Zasshi. 66 (1), 69-82 (1992).</li></ol>

The author declares no conflicts of interest, affiliations, or collaborations that could potentially influence the objectivity or outcomes of this research.

Currently, various animals, such as rabbits25, rats26, mice27, pigs28, broilers29, ostriches8, and emus30 can be used to establish models of femoral head necrosis. Among them, rats, mice, and rabbits are the most commonly used species. The rat, as a model for femoral head necrosis, offers numerous advantages. Rats are easy to feed and breed, grow rapidly, ...

The administration of glucocorticoids is the most common risk factor for non-traumatic osteonecrosis of the femoral head (ONFH)1. Numerous pieces of evidence suggest that, in addition to glucocorticoids, the pressure load on the hip joint in patients is also associated with the occurrence of ONFH. Factors such as body weight and physical labor intensity are recognized as risk factors for ONFH2. Multiple clinical studies have demonstrated a close relationship between hip joint loading conditions and the timing and incidence of joint replacement3,4,5,6. Therefore, establishing a model that reflects the relationship between load bearing and steroid-induced osteonecrosis of the femoral head (SONFH) is important for a comprehensive investigation of this condition.
Large bipedal birds, such as ostriches and emus, serve as good models to simulate hip joint stress, resembling human leg loads7,8. However, maintaining large bird species is challenging, and the associated research costs are high. Spontaneously hypertensive rat models9,10 can exhibit higher rates of ONFH, but the compartment pressure load in the marrow generated by spontaneous hypertension differs significantly from mechanical pressure and is unsuitable for studying the impact of mechanical pressure on SONFH.
Small animal models are commonly used in research on SONFH. However, quadrupedal reptiles have lower hip joint stress, and their hip models cannot simulate the biomechanical environment of human hip joints during bipedal walking. Single limb immobilization models11 and partial unloading models12 are common, but both reduce limb loading. As humans are bipedal organisms with substantial lower limb loads while standing and walking, reducing the load in these models diminishes the connection between animal models and human diseases.
This study aims to establish a simple and cost-effective model for weight-bearing training to investigate the impact of weight-bearing training on steroid-induced osteonecrosis of the femoral head in rats. Currently, rat models have been used to study steroid-induced osteonecrosis of the femoral head13,14, but there is still no model that can provide long-term, safe fixation with minimal disruption to movement, which is also relatively simple and inexpensive. In this study, a high-adhesive fixation material is applied, adopting tension-free fixation, which maintains the rats&#39; mobility and reduces the suffering and even death caused by improper fixation.

<table><tbody><tr><td>15ml centrifuge tube</td><td>Corning,USA</td><td>430791</td><td></td></tr><tr><td>5mm stainless steel bead</td><td>Gelisen,China</td><td>5mm</td><td></td></tr><tr><td>Acetic acid</td><td>Merck KGaA, Germany</td><td>64-19-7</td><td></td></tr><tr><td>Anhydrous alcohol</td><td>Merck KGaA, Germany</td><td>64-17-5</td><td></td></tr><tr><td>clay</td><td>Mincai stationery,China</td><td>102</td><td></td></tr><tr><td>Coverslip</td><td>Servicebio,China</td><td>WMWD-1818</td><td></td></tr><tr><td>Flat pressure bottle 10ml</td><td>BEHNCKE,China</td><td>MD10ml</td><td></td></tr><tr><td>Formic acid</td><td>Macklin Biochemical&amp;nbsp;,China</td><td>64-18-6</td><td></td></tr><tr><td>HE staining kit</td><td>Solarbio,China</td><td>G1120</td><td></td></tr><tr><td>HistoCore AUTOCUT</td><td>Leica, Germany</td><td>149AUTO00C1</td><td></td></tr><tr><td>Kinesio tape (elastic therapeutic tape)</td><td>Fuluo medicine,China</td><td>CL1819</td><td></td></tr><tr><td>Lipopolysaccharide</td><td>Solarbio,China</td><td>L8880</td><td></td></tr><tr><td>Lipopolysaccharides (LPS)</td><td>Selleck,USA</td><td>S7850&amp;nbsp;</td><td></td></tr><tr><td>Manual carbon dioxide euthanasia box</td><td>Yuyan,China</td><td>LC-500-S1</td><td></td></tr><tr><td>Methylprednisolone&amp;nbsp;sodium succinate,MPS</td><td>AbMole,China</td><td>M25573</td><td></td></tr><tr><td>MicroCT</td><td>&amp;nbsp;Hiscan,China</td><td>&amp;nbsp;Hiscan VM Pro</td><td></td></tr><tr><td>Neutral resin</td><td>Beijing Zhongshan Golden Bridge Biotechnology l&amp;nbsp;,China</td><td>ZLI-9555</td><td></td></tr><tr><td>Paraffin</td><td>Servicebio,China</td><td>WGHB-319213129</td><td></td></tr><tr><td>Paraformaldehyde</td><td>Servicebio,China</td><td>G1101-500ML</td><td></td></tr><tr><td>Potassium chloride</td><td>Macklin Biochemical&amp;nbsp;,China</td><td>&amp;nbsp;7447-40-7</td><td></td></tr><tr><td>Slide</td><td>Servicebio,China</td><td>WG6012</td><td></td></tr><tr><td>Treadmill for Rats and&amp;nbsp; mice</td><td>Litc Life Science,USA</td><td>801</td><td></td></tr><tr><td>Xylene</td><td>Macklin Biochemical&amp;nbsp;,China</td><td>&amp;nbsp;1330-20-7</td><td></td></tr></tbody></table>

tension-free weight-bearing model of steroid-induced osteonecrosis of femoral head in rats

Unlike humans, rats are animals that walk on all fours, while humans are bipedal animals that stand, and the hips are subjected to tremendous pressure when walking and standing. In rat steroid-induced femoral head necrosis models, the biomechanical characteristics of the human hip under higher pressure often need to be simulated. Some scholars try to emulate the state of human hip pressure by making rats bear a certain weight, but fixing the weight-bearing object on the rat is tough. Rats can easily break free of immobilization, and sticking the weight on the rats with adhesive tape will cause the rats to suffocate or die from intestinal obstruction. Our research group used elastic therapeutic tape to perform tension-free immobilization of weight-bearing objects in rats so that the rats could breathe freely and not break away from the immobilization under weight-bearing conditions. Compared to the usual steroid-induced femoral head necrosis rat model, we found that this weight-bearing intervention can aggravate the progression of femoral head necrosis in rats.

Histopathology analysis 
Hematoxylin and eosin staining revealed that in the Control group and Control+Load group, bone trabeculae were intact and arranged regularly. Blood vessel endothelial cells were present in bone dimples, and the cell morphology appeared plump. In contrast, the Model group and Model+Load group exhibited fractured and disordered bone trabeculae, along with a significantly higher number of empty lacunae. The Model+Load group had more empty lacunae compared to the Model group. In...

Author Spotlight: Developing a Rat Model for Weight-Bearing Intervention to Investigate Osteonecrosis of the Femoral Head

The protocol shows building a simple and cost-effective rat weight-bearing training model for steroid-induced osteonecrosis of the femoral head using elastic therapeutic tape.

Tension-Free Weight-Bearing Model of Steroid-Induced Osteonecrosis of Femoral Head in Rats

Unlike humans, rats are animals that walk on all fours, while humans are bipedal animals that stand, and the hips are subjected to tremendous pressure ...

tension-free-weight-bearing-model-steroid-induced-osteonecrosis

Research

JoVE Journal

Medicine

466 Views.  Beijing University of Chinese Medicine. The protocol shows building a simple and cost-effective rat weight-bearing training model for steroid-induced osteonecrosis of the femoral head using elastic therapeutic tape.

Video: Author Spotlight: Developing a Rat Model for Weight-Bearing Intervention to Investigate Osteonecrosis of the Femoral Head

A Contusion Model of Severe Spinal Cord Injury in Rats

The translational potential of novel treatments should be investigated in severe spinal cord injury (SCI) contusion models. A detailed methodology is described to obtain a consistent model of severe SCI. Use of a stereotactic frame and computer controlled impactor allows for creation of reproducible injury. Hypothermia and urinary tract infection pose significant challenges in the post-operative period. Careful monitoring of animals with daily weight recording and bladder expression allows for early detection of post-operative complications. The functional results of this contusion model are equivalent to transection models. The contusion model can be utilized to evaluate the efficacy of both neuroprotective and neuroregenerative approaches.

A contusion model of severe spinal cord injury is described. Detailed pre-operative, operative and post-operative steps are described to obtain a consistent model.

The translational potential of novel treatments should be investigated in severe spinal cord injury (SCI) contusion models. A detailed methodology is ...

Femoral Bone Marrow Aspiration in Live Mice

Serial sampling of the cellular composition of bone marrow (BM) is a routine procedure critical to clinical hematology. This protocol describes a detailed step-by-step technical procedure for an analogous procedure in live mice which allows for serial characterization of cells present in the BM. This procedure facilitates studies aimed to detect the presence of exogenously administered cells within the BM of mice as would be done in xenograft studies for instance. Moreover, this procedure allows for the retrieval and characterization of cells enriched in the BM such as hematopoietic stem and progenitor cells (HSPCs) without sacrifice of mice. Given that the cellular composition of peripheral blood is not necessarily reflective of proportions and types of stem and progenitor cells present in the marrow, procedures which provide access to this compartment without requiring termination of the mice are very helpful. The use of femoral bone marrow aspiration is illustrated here for cytological analysis of marrow cells, flow cytometric characterization of the hematopoietic stem/progenitor compartment, and culture of sorted HSPCs obtained by femoral BM aspiration compared with conventional marrow harvest.

This protocol describes a procedure for serial sampling of femoral bone marrow (BM) without requiring the sacrifice of mice. This procedure facilitates longitudinal studies of the BM composition of mice over time and provides serial access to cells within the BM for ex vivo and transplantation studies.

Serial sampling of the cellular composition of bone marrow (BM) is a routine procedure critical to clinical hematology. This protocol describes a detailed ...

Semiautomated Longitudinal Microcomputed Tomography-based Quantitative Structural Analysis of a Nude Rat Osteoporosis-related Vertebral Fracture Model

Osteoporosis-related vertebral compression fractures (OVCFs) are a common and clinically unmet need with increasing prevalence as the world population ages. Animal OVCF models are essential to the preclinical development of translational tissue engineering strategies. While a number of models currently exist, this protocol describes an optimized method for inducing multiple highly reproducible vertebral defects in a single nude rat. A novel longitudinal semiautomated microcomputed tomography (&#181;CT)-based quantitative structural analysis of the vertebral defects is also detailed. Briefly, rats were imaged at multiple time points post-op. The day 1 scan was reoriented to a standard position, and a standard volume of interest was defined. Subsequent &#181;CT scans of each rat were automatically registered to the day 1 scan so the same volume of interest was then analyzed to assess for new bone formation. This versatile approach can be adapted to a variety of other models where longitudinal imaging-based analysis could benefit from precise 3D semiautomated alignment. Taken together, this protocol describes a readily quantifiable and easily reproducible system for osteoporosis and bone research. The suggested protocol takes 4 months to induce osteoporosis in nude ovariectomized rats and between 2.7 and 4 h to generate, image, and analyze two vertebral defects, depending on tissue size and equipment.

The goal of this protocol is to generate a nude rat osteoporosis-related vertebral compression fracture model that can be longitudinally evaluated in vivo using a semiautomated microcomputed tomography-based quantitative structural analysis.

Osteoporosis-related vertebral compression fractures (OVCFs) are a common and clinically unmet need with increasing prevalence as the world population ...

Bioengineering

An Efficient and Reproducible Protocol for Distraction Osteogenesis in a Rat Model Leading to a Functional Regenerated Femur

This protocol describes the use of a newly developed external fixator for distraction osteogenesis in a rat femoral model. Distraction osteogenesis (DO) is a surgical technique leading to bone regeneration after an osteotomy. The osteotomized extremities are moved away from each other by gradual distraction to reach the desired elongation. This procedure is widely used in humans for lower and upper limb lengthening, treatment after a bone nonunion, or the regeneration of a bone defect following surgery for bone tumor excision, as well as in maxillofacial reconstruction. Only a few studies clearly demonstrate the efficiency of their protocol in obtaining a functional regenerated bone, i.e., bone that will support physiological weight-bearing without fracture after removal of the external fixator. Moreover, protocols for DO vary and reproducibility is limited by lack of information, making comparison between studies difficult. The aim of this study was to develop a reproducible protocol comprising an appropriate external fixator design for rat limb lengthening, with a detailed surgical technique that permits physiological weight-bearing by the animal after removal of the external fixator.

This study describes a reproducible and detailed protocol using a newly developed external fixator for distraction osteogenesis (DO) in a femoral rat model which permits physiological weight-bearing by the animal after removal of the external fixator.

This protocol describes the use of a newly developed external fixator for distraction osteogenesis in a rat femoral model. Distraction osteogenesis (DO) ...

A Non-Invasive Method for Generating the Cyclic Loading-Induced Intra-Articular Cartilage Lesion Model of the Rat Knee

The pathophysiology of primary osteoarthritis (OA) remains unclear. However, a specific subclassification of OA in relatively younger age groups is likely correlated with a history of articular cartilage damage and ligament avulsion. Surgical animal models of OA of the knee play an important role in understanding the onset and progression of post-traumatic OA and aid in the development of novel therapies for this disease. However, non-surgical models have been recently considered to avoid traumatic inflammation that could affect the evaluation of the intervention. 
In this study, an intra-articular cartilage lesion rat model induced by in vivo cyclic compressive loading was developed, which allowed researchers to (1) determine the optimal magnitude, speed, and duration of load that could cause focal cartilage damage; (2) assess post-traumatic spatiotemporal pathological changes in chondrocyte vitality; and (3) evaluate the histological expression of destructive or protective molecules that are involved in the adaptation and repair mechanisms against joint compressive loads. This report describes the experimental protocol for this novel cartilage lesion in a rat model.

Here, we present the cyclic loading-induced intra-articular cartilage lesion model of the rat knee, generated by 60 cyclic compressions over 20 N, resulting in damage to the femoral condylar cartilage in rats.

The pathophysiology of primary osteoarthritis (OA) remains unclear. However, a specific subclassification of OA in relatively younger age groups is likely ...

Protocol for Developing a Femur Osteotomy Model in Wistar Albino Rats

Fracture healing is a physiological process resulting in the regeneration of bone defects by the coordinated action of osteoblasts and osteoclasts. Osteoanabolic drugs have the potential to augment the repair of fractures but have constraints like high costs or undesirable side effects. The bone healing potential of a drug can initially be determined by in vitro studies, but in vivo studies are needed for the final proof of concept. Our objective was to develop a femur osteotomy rodent model that could help researchers understand the development of callus formation following fracture of the shaft of the femur and that could help establish whether a potential drug has bone healing properties. Adult male Wistar albino rats were used after Institutional Animal Ethics Committee clearance. The rodents were anesthetized, and under aseptic conditions, complete transverse fractures at the middle one-third of the shafts of the femurs were created using open osteotomy. The fractures were reduced and internally fixed using intramedullary K-wires, and secondary fracture healing was allowed to take place. After surgery, intraperitoneal analgesics and antibiotics were given for 5 days. Sequential weekly x-rays assessed callus formation. The rats were sacrificed based on radiologically pre-determined time points, and the development of the fracture callus was analyzed radiologically and using immunohistochemistry.

Here, we present a protocol to iatrogenically fracture the shaft of the femur of Wistar albino rats and follow up on the development of the callus. This femur osteotomy model can help researchers evaluate the process of fracture healing and to study how a drug could influence fracture healing.

Fracture healing is a physiological process resulting in the regeneration of bone defects by the coordinated action of osteoblasts and osteoclasts. ...

Estrogen-Like Effect of Bazi Bushen Capsule in Ovariectomized Rats

This study aims to show the estrogen-like effect of Bazi Bushen capsule (BZBS), a Chinese herbal compound, in ovariectomized mice. Female Sprague-Dawley (SD) rats were randomly divided into six groups: a sham-operated group, a model group (OVX), a progynova group, and BZBS groups (1, 2, and 4 d/kg/d). An ovariectomy was performed on all rats except those in the sham-operated group. Micro-computed tomography (micro-CT) scanning, hematoxylin and eosin (H&amp;E) staining, immunohistochemistry, and enzyme-linked immunosorbent assay (ELISA) detection were performed after 4 months of BZBS treatment. As a result, compared with the OVX group, rats treated with BZBS showed an increased number and area of trabecular bone and bone marrow cells, and a decreased number of adipose cells. The bone volume, trabecular number, and trabecular thickness of the right tibia in the medication groups increased and the trabecular space decreased. The 17&#946;-estradiol and serum calcium levels in the medication groups were elevated, but the levels of serum phosphorus, sclerostin, &#946;-CTX, and TRACP-5b were decreased. In the medication groups, the RANKL and sclerostin levels were decreased, while the osteoprotegerin (OPG) level was increased. In conclusion, this protocol systematically evaluated the therapeutic effects and potential molecular mechanisms of Chinese herbal compounds in ovariectomized rats with a variety of techniques.

Presented here is a protocol to show that Bazi Bushen capsule (BZBS) can regulate the RANKL/OPG signaling pathway in the ovariectomized rodent model through its estrogen-like effect.

This study aims to show the estrogen-like effect of Bazi Bushen capsule (BZBS), a Chinese herbal compound, in ovariectomized mice. Female Sprague-Dawley ...

Osteoporosis Management in Rats Through Lingnan Fire-Needle Therapy

Operation Procedure and Precautions of Lingnan Fire-Needle Therapy in Osteoporosis Model Rats

Compared to filiform needle therapy, fire-needle therapy has both the stimulation of needles and the warming effect of heat, making it have unexpected effects on some chronic diseases and incurable diseases. Osteoporosis (OP) has a high incidence in postmenopausal women and middle-aged and elderly men, and the treatment cycle is long. According to Traditional Chinese Medicine (TCM), Lingnan fire-needle therapy has shown potential in treating osteoporosis. However, there is still a long way to go before it can be widely used. This article focuses on the application of Lingnan fire-needle therapy in the intervention of OP in rats. It covers the selection of needle tools, acupuncture point selection, positioning of rats' bodies, and fixation methods. We also outline the steps and precautions to be taken during and after needling with fire needles. The experiment was done with three groups: a normal group, a model group, and a fire-needle group, each containing 10 rats. The rats in the fire-needle group were treated with fire-needle intervention for six sessions. After the intervention period, we collected femoral specimens and performed micro-CT scans. The results suggest that fire needling can enhance bone morphology and mineral density in OP rats. This information can serve as a methodological basis for conducting basic research on fire-needle therapy.

Author Spotlight: Exploring the Impact of Lingnan Fire-Needle Therapy in Osteoporosis Intervention

Here, we present a protocol for the application of Lingnan Fire-Needle therapy in the intervention of osteoporosis model rats.

Compared to filiform needle therapy, fire-needle therapy has both the stimulation of needles and the warming effect of heat, making it have unexpected ...

Surgical Bone Implantation Technique for Rat Tibia Models of Diabetes and Osteoporosis

The rat has long served as a valuable animal model in implant dentistry and orthopedics, particularly in studying the interactions between biomaterials and bone tissue. The rat's tibia is frequently chosen due to its easy surgical access through thin tissue layers (skin and muscle) and the flattened shape of its medial face, facilitating the surgical insertion of intraosseous devices. Additionally, this model enables the induction of specific diseases, mimicking various clinical conditions to assess biological responses to different implant conditions like geometry, surface texture, or biological cues. However, despite its robust cortical structure, certain intraosseous devices may require adaptations in design and size for successful implantation. Therefore, establishing standardized surgical methods for manipulating both soft and hard tissues in the implantation region is essential for ensuring proper implant or screw device placement, particularly in fields like implant dentistry and orthopedics. This study included eighty Sprague Dawley rats divided into two groups based on their respective diseases: Group 1 with osteoporosis and Group 2 with Type 2 Diabetes. Implantations were performed at 4 weeks and 12 weeks, with the same surgeon following a consistent surgical technique. A positive biological response was observed, indicating complete osseointegration of all implants placed. These results validate the success of the surgical protocol, which can be replicated for other studies and serve as a benchmark for the biomaterials community. Notably, osseointegration values remained stable at both 4 weeks and 12 weeks for both disease models, demonstrating a durable integration of the implant over time and emphasizing the establishment of an intimate bone connection as early as 4 weeks.

The placement of implants in a rat model is an essential experimental procedure for clinical research. This study presents a comprehensive surgical protocol for implanting titanium implants into the tibia of rat models with diabetes and osteoporosis.

The rat has long served as a valuable animal model in implant dentistry and orthopedics, particularly in studying the interactions between biomaterials ...

The Creation of a Rat Model for Osteosarcopenia via Ovariectomy

Osteosarcopenia (OS), a complex degenerative disorder, is characterized by the concurrent decline in skeletal muscle mass and bone mineral density (BMD), posing an enormous health hazard for the elderly population. Despite its clinical relevance, the pathophysiological mechanisms underlying OS are not fully understood, underscoring the necessity for a deeper comprehension of its etiology to facilitate effective treatment strategies. The development of a reliable animal model is pivotal in this endeavor. This study presents a refined protocol for the induction of postmenopausal osteosarcopenia in rats through bilateral ovariectomy, a method known to accelerate the onset of age-related muscle and bone loss. In this study, rats aged 12 weeks were stratified by body weight and randomly assigned to either a sham operation group or an ovariectomized (OVX) group. Tissue samples from the quadriceps and triceps muscles of the left hind limb, as well as the left femur, were systematically collected at 4, 8, and 12 weeks post-surgery. This methodical approach ensures a comprehensive evaluation of the effects of ovariectomy on muscle and bone health. Histological evaluation of muscle fiber atrophy and femoral morphology was conducted using hematoxylin and eosin (HE) staining, while bone mineral density was quantified using dual-energy X-ray absorptiometry (DXA). The temporal progression of OS was meticulously monitored at the aforementioned intervals, providing insights into the dynamic interplay between muscle and bone degeneration. This model not only accurately reflects the clinical manifestations of OS but also serves as a robust platform for investigating novel therapeutic approaches and their underlying mechanisms.

This current protocol outlines a procedure for creating a rat model of osteosarcopenia using ovariectomy.

Osteosarcopenia (OS), a complex degenerative disorder, is characterized by the concurrent decline in skeletal muscle mass and bone mineral density (BMD), ...