This study was supported by DoD Peer Reviewed Medical Research Program - Investigator-Initiated Research Award W81XWH-20-1-0304 from the U.S. ARMY MEDICAL RESEARCH ACQUISITION ACTIVITY, by NIH NIAMS R01AR076477 and a Comprehensive Musculoskeletal T32 Training Program from the NIH (AR065971) and by NIH NIAMS Grant R01 AR069657. The authors would like to thank Kevin Carr for providing his expertise in machining and fabrication to this project, and Drew Brown and the Indiana Center for Musculoskeletal Health Bone Histology Core for aiding with histology.

The following procedure was performed with approval from the Indiana University School of Medicine Institutional Animal Care and Use Committee (IACUC). All survival surgeries were performed under sterile conditions, as outlined by the NIH guidelines. Pain and infection risks were managed with proper analgesics and antibiotics to optimize successful outcomes. Skeletally mature male New Zealand White rabbits, weighing 3.0-4.0 kg, were used for the present study.
1. Drop tower fabrication
<ol>
	<li>Generate CAD drawings for components of the drop tower, base platform, and mechanism to secure the Steinman pin (Supplementary Figures 1-14).</li>
	<li>Purchase commercially available components (See Table of Materials).</li>
	<li>Procure the machine parts of the device or give CAD drawings to a machinist for fabrication. 
	NOTE: A high-precision machinist with toolmaking capability is required to fabricate the 3 mm diameter impactor tip (Supplementary Figure 1, part 20&#160;and Supplementary Figures 13,14). The impacting face of the impactor head had curvatures of 7.14 mm and 5.56 mm in the sagittal and coronal planes, respectively, to conform to the curvature of the medial rabbit condyle35(Supplementary Figures 13,14).</li>
	<li>Assemble parts such that the drop tower consists of a carriage traveling on two vertical rods via fixed-alignment linear ball bearings, and the base platform supports the rabbit and secures the Steinman pin (Figure 1 and Figure 2). 
	&#8203;NOTE: The carriage crossbeam of this design has a bending stiffness equal to that of a previous drop tower38 with an acceptable vibration level.</li>
</ol>
2. Animal preparation
<ol>
	<li>Weigh the rabbit and anesthetize it using 2.5 mg/kg alfaxalone and 0.15 mg/kg midazolam IM (see Table of Materials). Apply eye ointment to both eyes after induction. Maintain anesthesia using ~2%-3% isoflurane. Give buprenorphine SR (0.1 mg/kg) SQ for analgesia and perioperative enrofloxacin (10 mg/kg) SQ.&#160;In place of Buprenorphine, NSAIDs such as Carprofen, 4mg/kg or Meloxicam, 0.2 &#8211; 0.3mg/kg or Ketoprofen, 3mg/kg can be given as SQ injections.</li>
	<li>Shave the rabbit&#39;s hind limb from the ankle to the hindquarters.&#160;Extra caution is urged in rabbit hair removal to prevent contamination of the incision. Using a set of dedicated, sharp rabbit hair clippers is important.</li>
	<li>Place the stainless steel front leg block (Supplementary Figure 1, part No. 2,&#160;and Supplementary Figure 4) under the end of the impact platform and cover the platform with a heating pad. Place the rabbit sternal (i.e., prone) on the heating pad. Place a padded bump under the contralateral hip.
	<ol>
		<li>Ensure the operative extremity has the knee centered and resting on the polyethylene block (Figure 2A1). Use silk tape to gently retract the tail superior and contralateral to the operative extremity.</li>
	</ol>
	</li>
	<li>Wipe down the surgical site with chlorohexidine and 70% alcohol-soaked sterile gauze. Scrub the surgical site, starting at the posterior knee, with a circular sweep outward. Repeat at least 3 times with fresh scrubs, ending with 70% alcohol.</li>
	<li>Place a sterile glove over the operative foot up to the ankle and wrap it with a sterile cohesive wrap.</li>
	<li>Sterilely drape out the surgical site with three drapes: one directly under the operative extremity and the other two to cover the rest of the body. Secure the drapes with towel clamps.</li>
</ol>
3. Surgical exposure
NOTE: Prior to the surgery and impact, the weight and the drop height that deliver visible cartilage damage without subchondral bone fracture should be empirically determined for the specific strain, age, and sex of the rabbit.
<ol>
	<li>Palpate the position of the patella anteriorly to estimate the position of the knee joint, which is located distal to the patella. Using a 15-blade, make a 3-4 cm incision along the posterior aspect of the extended knee from the level of the superior pole of the patella distally.</li>
	<li>Perform blunt and sharp dissections through the underlying superficial fascia. Develop the interval between the skin medially and the medial gastrocnemius laterally. Place a self-retaining Weitlaner retractor in this interval (see Table of Materials).
	<ol>
		<li>A secondary fascial layer will become visible just overlying the saphenous artery and vein. Dissect lateral to the saphenous and retract the vasculature medially and the posterior gastrocsoleus complex laterally. 
		NOTE: Take care not to cut this vasculature. If this artery is damaged, ensure proper ligation, as post-operative hemorrhagic shock can occur.</li>
	</ol>
	</li>
	<li>Dissect distally until a small mobile fabella is identified over the posterior medial femoral condyle. Perform an arthrotomy to mobilize the fabella superolateral, exposing the underlying medial femoral condyle. Gently remove soft tissue by blunt and sharp dissection to expose the posterior aspect of the medial femoral condyle. Use a Freer and Cricket self-retainer (see Table of Materials) to retract soft tissues at this level.</li>
	<li>While keeping the condyle exposed, advance a 0.062 inch Steinman pin (see Table of Materials) across the distal femur, beginning at the superior aspect of the medial femoral condyle and centered in the anterior-posterior direction of the medial femoral condyle, roughly 5 mm from the posterior aspect of the condyle.
	<ol>
		<li>Drive the wire laterally through the bone and lateral skin parallel to the joint surface using a battery-powered Steinman pin driver. Palpation of the lateral epicondyle will ensure the appropriate trajectory of the Steinman pin.</li>
	</ol>
	</li>
	<li>Remove the retractors and close the skin with a 3-0 polysorb suture (see Table of Materials) in a running fashion. Cover the incision with sterile gauze.</li>
</ol>
4. Impact of the femoral condyle
<ol>
	<li>Remove the drape under the operative limb and secure the Steinman pin to a customizable and adjustable height impact platform. First, place the height-adjustable, lower aspect of the Steinman pin securing apparatus under the pin (Figure 2A2). Ensure the wire is parallel with the ground on this platform by adjusting the screw heights as needed.
	<ol>
		<li>After ensuring the Steinman pin is parallel to the ground, place the top screw-based aspect of the secure platform (Figure 2A3) onto the lower screw-based aspect of the height-adjustable piece. Ensure the Steinman pin is tightly secured by screwing the top bar into the lower height adjustable portion of the pin-holding platform (Figure 2A2).</li>
	</ol>
	</li>
	<li>Once the Steinman pin is secured to the platform, remove the suture, and reopen the incision. Expose the medial femoral condyle with self-retaining Weitlaner and cricket retractors. An additional Freer may be needed to retract additional soft tissue out of the path of the impactor tip (Figure 2B).</li>
	<li>Wipe down the drop tower with an approved disinfectant. Attach the sterile 3 mm impactor head (Figure 2A4) to the drop tower carriage. Bring the drop tower over the operative extremity and place its base (Figure 2A6) underneath the impacting platform (Figure 3A).</li>
	<li>Gently lower the impactor (Supplementary Figure 2, part 20, and Supplementary Figure 13) onto the center of the posterior medial femoral condyle. Ensure no soft tissue is in the path of the impactor.
	<ol>
		<li>Move the rabbit or tower as needed to ensure the impactor head is centered over the posterior medial femoral condyle (Figure 3B).&#160;Any time the rabbit is moved or re-positioned that surgical site should be assessed for any possible breaks to sterility and the area re-sterilized if needed.&#160;</li>
	</ol>
	</li>
	<li>Once appropriate trajectory is ensured, clamp the tower onto the platform with the toggle clamps (Figure 2A5,&#160;see Table of Materials).</li>
	<li>Administer one dose of intravenous alfaxalone (0.5-0.7 mg/kg) 5-10 min prior to impact for deeper anesthesia without increasing inhalant anesthesia. 
	NOTE: A lack of palpebral reflex, pedal withdrawal, and pinna reflex evidences deeper anesthetization. This deeper anesthesia helps prevent possible limb reactions during placement in the apparatus and during impact. 
	CAUTION: If given too quickly, alfaxalone can cause transient apnea and hypoxia in rabbits and should be given slowly over 1-2 min. If hypoxia does occur, ensure adequate oxygenation and restoration of vitals before proceeding.</li>
	<li>Set the impactor on the drop tower at the desired height above the medial femoral condyle. For the current carriage assembly, including the bearings, with a mass of 1.41 kg, this is a height of 7 cm. 
	NOTE: Drop tower height was determined from pilot studies on cadaver tissue. This height generated visible cartilage damage but not subchondral bone fracture for the rabbits in this study.</li>
	<li>Click on the Start button on the LabVIEW data acquisition software (Supplementary Coding File 1) just before freeing the spindle stop (Supplementary Figure 2, item No. 14) to release the carriage and allow it to drop under the force of gravity. 
	NOTE: The data acquisition software will collect the data from a load cell (Figure 1, 6) positioned between the impactor and carriage and an accelerometer (Figure 1, 7) during the impact at 100 kHz using a laptop connected to a data acquisition module.</li>
	<li>Place the txt file generated by the data acquisition software in the same folder with the Matlab data analysis code (Supplementary Coding File 2) and run the data analysis code to filter raw data and calculate impact parameters.</li>
	<li>Ensure that the maximum load is identified. The associated time point is considered the time of maximum deformation and zero velocity. 
	NOTE: Data analysis code will analyze all txt files in the folder and report the results for each file. The code will determine the beginning and end of impact based on changes in the load-time data. Data from the accelerometer will be integrated numerically to calculate velocity and integrated again to calculate displacement. Data analysis code will numerically calculate the impulse, work, and kinetic energy from the following formulas: 
	<img alt="Equation 1" src="/files/ftp_upload/64450/64450eq01.jpg" style="margin: auto;" /> 
	<img alt="Equation 2" src="/files/ftp_upload/64450/64450eq02.jpg" style="margin: auto;" /> 
	<img alt="Equation 3" src="/files/ftp_upload/64450/64450eq03.jpg" style="margin: auto;" /> 
	where F is the force measured by the load sensor, x0 and t0 are the displacement and time at the beginning of the impact, and x, and tf&#160;are the displacement and time at the end of the impact. The loading rate will be numerically calculated as the average of d&#963;/dt in the loading phase of impact. Peak stress will be calculated by dividing the peak load by the contact area of the impactor head.</li>
	<li>Perform visualization of the cartilage surface to determine whether appropriate cartilage damage has occurred (Figure 4A).</li>
</ol>
5. Surgical site closure
<ol>
	<li>Remove the drop tower from over the operative extremity. Place all used surgical tools aside and change into new sterile gloves. 
	NOTE: Given that the drop tower is not sterile, all tools used up to the impact should now be considered contaminated.</li>
	<li>Reapply a sterile drape to the lower extremity and obtain unused sterile self-retractors.</li>
	<li>Re-expose the medial femoral condyle and thoroughly irrigate the surgical site with 50-60 mL of sterile saline.</li>
	<li>Close the posterior capsule with a 5-0 polysorb suture, followed by skin closure with a 4-0 monosorb suture (see Table of Materials).</li>
	<li>Inject 2 mL of lidocaine/bupivacaine for local analgesia around the incision intradermally.</li>
	<li>Remove the Steinman pin with a power driver set (see Table of Materials) by&#160;oscillating&#160;to minimize soft tissue injury.</li>
	<li>Dress the wound with a non-adhesive dressing, followed by adhesive tape. Perform an x-ray of the operative extremity to ensure no fracture occurred and appropriate pin placement (Figure 4B).</li>
</ol>
6. Post-operative management
<ol>
	<li>Return the rabbit to its cage and monitor it on heated blankets until it recovers from anesthesia (~25 min).</li>
	<li>Continue closely monitoring the rabbits for several days after the surgery to ensure they heal properly and regain mobility. Administer enrofloxacin (10 mg/kg) for 2 days post-operatively for infection prophylaxis. Administer buprenorphine SR analgesia (0.1 mg/kg) subcutaneously every 2-3 days after the surgery and as needed.&#160;In place of Buprenorphine, NSAIDs such as Carprofen, 4mg/kg SQ daily, Meloxicam, 0.2 &#8211; 0.3mg/kg SQ daily up to 3 days or Ketoprofen, 3mg/kg SQ daily can be administered 3-5 days after surgery and as needed. 
	&#8203;NOTE: We have succeeded in preventing postoperative&#160;wound dehiscence, due to rabbit licking or chewing, with the placement of human neonatal pants over the&#160; hindlimbs39. If the rabbit chews through the pants, an Elizabethan collar (see Table of Materials) may be placed to prevent chewing of the incision.</li>
</ol>
7. Histological evaluation
<ol>
	<li>At 16 weeks post-injury, harvest knees from euthanized rabbits, fix them in 10% neutral buffered formalin for 48 h, followed by paraffin embedding and sectioning into 5 &#181;m thick slices.</li>
	<li>After de-paraffinization and rehydration, stain the sections with safranin O fast green per standard protocols40,41.</li>
	<li>Perform the terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay on the sections using TUNEL Chromogenic Apoptosis Detection kit following the manufacturer&#39;s instructions, counterstained with Hematoxylin42 (see Table of Materials).</li>
</ol>

Roman Natoli delivers lectures for AO Trauma North America, is a section editor for Current Osteoporosis Reports, and received textbook royalties from Morgan and Claypool. Todd McKinley receives royalties from Innomed. The remaining authors have nothing to disclose.

This surgical procedure aims to generate consistent cartilage damage to the weight-bearing surface of the rabbit medial femoral condyle in a model of PTOA. An advantage of this procedure is that the posterior approach to the knee allows for direct visualization of the complete posterior medial femoral condyle, and it can be performed in approximately 37 min (Table 2). It should also be noted that this is an open injury model and may lead to acute inflammatory changes beyond just the impact due to potenti...

Post-traumatic osteoarthritis (PTOA) is a leading cause of disability worldwide, and accounts for 12%-16% of symptomatic osteoarthritis (OA)1. The current gold standard for end-stage OA management is total knee and hip arthroplasty2 or arthrodesis, as in the case of end-stage tibiotalar or subtalar arthritis. Although largely successful, arthroplasty can have costly and morbid complications3. In addition, arthroplasty is less desirable in patients under 50 years, given the low revision-free implant survivorship of 77%-83%4,5. Currently, there are no FDA-approved treatments to prevent or mitigate the progression of PTOA.
PTOA affects the whole joint, including the synovial tissue, subchondral bone, and articular cartilage. It is characterized by articular cartilage degeneration, synovial inflammation, subchondral bone remodeling, and osteophyte formation6,7. The phenotype of PTOA develops via a complex process of interplay between cartilage, synovium, and subchondral bone. The current understanding is that cartilage injury leads to the liberation of extra-cellular matrix (ECM) components such as type 2 collagen (COL2) and aggrecan (ACAN). These ECM component fragments are pro-inflammatory and cause increased production of IL-6, IL-1&#946;, and reactive oxygen species. These mediators act on chondrocytes, causing upregulation of matrix metalloproteinases (MMPs), such as MMP-13, which degrade articular cartilage while also decreasing matrix synthesis, leading to an overall catabolic environment for the articular cartilage8. In addition, there is evidence of increased chondrocyte apoptosis in primary osteoarthritis and PTOA9,10. Mitochondrial dysfunction occurs after supraphysiological loading of cartilage11,12,13,14, which can lead to increased chondrocyte apoptosis12,15. Enhanced chondrocyte apoptosis has been associated with increased proteoglycan depletion and cartilage catabolism and has been shown to precede changes in cartilage and subchondral bone remodeling16,17,18.
As with most human diseases, reliable and translational models of PTOA are needed to further understand the pathophysiology of the disease and test novel therapeutics. Large animals such as swine and canines have been used in intra-articular fracture and impact models of PTOA17,19, but they are costly. Smaller animal models, such as mice, rats, and rabbits&#160;are less expensive and are used to study PTOA generated through joint destabilization, which typically involves surgical transection of the anterior cruciate ligament (ACL) and/or disruption of the medial meniscus20,21,22,23,24,25. Although joint trauma can lead to various consequences, including ligamentous injury26, mechanical overload of the cartilage occurs in nearly all cases.
There is emerging evidence that the pathology behind the development of PTOA after ligamentous instability (as in ACL transection) and acute chondral injury is due to distinct mechanisms27. Therefore, developing models of direct injury to cartilage is important. There are currently a limited number of impact models generating osteochondral or chondral injury in rats and mice28,29. However, murine cartilage is not well-suited for generating isolated chondral defects. This is because murine articular cartilage is only 3-5 cell layers thick and lacks organized superficial, radial, and transitional cartilage zones, as well as the thick calcified cartilage layer found in humans and larger animals. Murine models also display spontaneous resolution of partial cartilage defects30,31. Hence, we chose the rabbit for this impact model as its cartilage thickness and organization are similar to those of humans, and it is the smallest animal model that will allow for the delivery of a consistent chondral impact that results in PTOA. Prior open surgical models of femoral condyle impact in the rabbit have employed a pendulum32, a hand-held spring-loaded cartilage impaction device33, and a drop tower that allowed rabbit-specific impactor creation34. However, these studies lacked in vivo data. Others have reported in vivo data with pendulum-based35, pneumatic36, and spring-loaded37 impact devices10, and these studies show a high rate of variability in peak stress and loading rates between the methods. Still, the field lacks a consistent approach to reliably model acute cartilage trauma in vivo.
The current protocol employs a drop-tower-based system to deliver a consistent impact to the posterior medial condyle of the rabbit knee. A posterior approach to the knee is employed to expose the posterior medial femoral condyle. A Steinman pin is then placed across the femoral condyles from medial to lateral in line with the joint surface and secured to the platform. Once secured, a load is delivered to the posterior medial femoral condyle. This method allows for consistent cartilage damage to be delivered to the weight-bearing surface of the rabbit distal&#160;femur.

<table><tbody><tr><td>Flat head screw</td><td>McMaster-Carr</td><td>92210A194</td><td>Stainless steel hex drive flat head screw, 8-32, 1/2&quot;</td></tr><tr><td>#15 scalpel blades</td><td>McKesson</td><td>1029066</td><td>Scalpel McKesson No. 15 Stainless Steel / Plastic Classic Grip Handle Sterile Disposable</td></tr><tr><td>1/2&amp;rdquo;-20 threaded rod</td><td>McMaster-Carr</td><td>99065A120</td><td>1/2&amp;rdquo;-20 threaded rod</td></tr><tr><td>10 mL syringe</td><td>McKesson</td><td>1031801</td><td>For irrigation; General Purpose Syringe McKesson 10 mL Blister Pack Luer Lock Tip Without Safety</td></tr><tr><td>3 mL syringe</td><td>McKesson</td><td>1031804</td><td>For lidocaine/bupiviacaine injection; General Purpose Syringe McKesson 3 mL Blister Pack Luer Lock Tip Without Safety.</td></tr><tr><td>3-0 polysorb</td><td>Ethicon</td><td>J332H</td><td>3-0 Vircryl, CT-2, 1/2 circle, 26 mm, tapered</td></tr><tr><td>4-0 monosorb</td><td>Ethicon</td><td>Z397H</td><td>4-0 PDS 2, FS-2, 3/8 circle, 19mm, cutting edge</td></tr><tr><td>5-0 polysorb</td><td>Med Vet International</td><td>NC9335902</td><td>Med Vet International 5-0 ETHICON COATED VICRYL C-3</td></tr><tr><td>Accelerometer</td><td>Kistler</td><td>8743A5</td><td>Accelerometer</td></tr><tr><td>Adson-Browns Forceps</td><td>World precision tools</td><td>500177</td><td>Adson-Brown Forceps, 12 cm, Straight, TC Jaws, 7 x 7 Teeth</td></tr><tr><td>Alfaxalone</td><td>Jurox</td><td>49480-002-01</td><td>Alfaxan Multidose by Jurox : 10 mg/mL</td></tr><tr><td>Buprenorphine</td><td>Par Pharmaceuticals</td><td>42023-0179-05</td><td>Buprenorphine HCL injection: 0.3 mg/mL</td></tr><tr><td>Butorphanol&amp;nbsp;</td><td>Zoetis</td><td>54771-2033</td><td>Butorphanol tartrate&amp;nbsp;10mg/ml by Zoetis</td></tr><tr><td>Chlorhexidine Hand Scrub</td><td>BD</td><td>371073</td><td>BD E-Z Scrub 107 Surgical Scrub Brush/Sponge, 4% CHG, Red</td></tr><tr><td>Collet</td><td>STRYKER</td><td>14023</td><td>Stryker 4100-62 wire Collet 0.28-0.71&#039;&#039;</td></tr><tr><td>Cordless Driver handpiece</td><td>STRYKER</td><td>OR-S4300</td><td>Stryker 4300 CD3 Cordless Driver 3 handpiece</td></tr><tr><td>Cricket Retractors</td><td>Novosurgical</td><td>G3510 21</td><td>2x Heiss (Holzheimer) Cross Action Retractor</td></tr><tr><td>Dissector Scissors</td><td>Jorvet labs</td><td>J0662</td><td>Aesculap AG, Metzenbaum, Scissors, Straight 5 3/4&amp;Prime;</td></tr><tr><td>Elizabethian Collar</td><td>ElizaSoft</td><td>62054</td><td>ElizaSoft Elizabethan Recovery Collar</td></tr><tr><td>Enrofloxacin</td><td>Custom Meds</td><td></td><td>Enrofloxacin compounded by Custom Meds</td></tr><tr><td>Eye Ointment</td><td>Pivetal&amp;nbsp;</td><td>46066-753-55</td><td>Pivetal Articifical Tears- recently recalled</td></tr><tr><td>Face-mount shaft collar</td><td>McMaster-Carr</td><td>5631T11</td><td>Face-mount shaft collar</td></tr><tr><td>Fast green</td><td>Millipore Sigma</td><td>F7258</td><td>Fast green</td></tr><tr><td>Freer</td><td>Jorvet labs</td><td>J0226Q</td><td>Freer elevator</td></tr><tr><td>Head screw -1</td><td>McMaster-Carr</td><td>91251A197</td><td>Black-oxide alloy steel socket head screw, 8-32, 3/4&quot;</td></tr><tr><td>Head screw -2</td><td>McMaster-Carr</td><td>92196A194</td><td>Stainless steel socket head screw, 8-32, 1/2&quot;</td></tr><tr><td>Head screw -3</td><td>McMaster-Carr</td><td>92196A146</td><td>Stainless steel socket head screw, 8-32, 1/2&quot;</td></tr><tr><td>Head screw -4</td><td>McMaster-Carr</td><td>92196A151</td><td>Stainless steel socket head screw, 6-32, 3/4&quot;</td></tr><tr><td>Hematoxylin Solution, Gill No. 1</td><td>Millipore Sigma</td><td>GHS132-1L</td><td>Hematoxylin Solution, Gill No. 1</td></tr><tr><td>Hex nut</td><td>McMaster-Carr</td><td>91841A007</td><td>Stainless steel hex nut, 6-32</td></tr><tr><td>Hold-down toggle clamp</td><td>McMaster-Carr</td><td>5126A71</td><td>Hold-down toggle clamp</td></tr><tr><td>Impact device</td><td>n/a</td><td>n/a</td><td>custom made</td></tr><tr><td>Impact platform</td><td>n/a</td><td>n/a</td><td>custom made</td></tr><tr><td>K-wires</td><td>Jorvet Labs</td><td>J0250A</td><td>JorVet Intramedullary Steinman Pins, Trocar-Trocar 1/16&quot; x 7&quot;</td></tr><tr><td>Lab View</td><td>National Instruments</td><td>n/a</td><td>n/a</td></tr><tr><td>Load cell</td><td>Kistler</td><td>9712B5000</td><td>Load cell</td></tr><tr><td>MATLAB</td><td>The MathWorks Inc.</td><td>n/a</td><td>n/a</td></tr><tr><td>Microscope</td><td>Leica</td><td>DMi-8</td><td>Leica DMi8 microscope with LAS-X software</td></tr><tr><td>Midazolam</td><td>Almaject</td><td>72611-749-10</td><td>Midazolam Hydrochloride injection: 5mg/ml by Almaject</td></tr><tr><td>milling machine depth stops</td><td>McMaster-Carr</td><td>2949A71</td><td>Clamp-on milling machine depth stops</td></tr><tr><td>Mobile C-arm</td><td>Philips</td><td>718095</td><td>BV&amp;nbsp;Pulsera, Mobile C-arm</td></tr><tr><td>Mounted linear ball bearing</td><td>McMaster-Carr</td><td>9338T7</td><td>Mounted linear ball bearing</td></tr><tr><td>Needle Driver</td><td>A2Z Scilab</td><td>A2ZTCIN39</td><td>TC Webster Needle Holder Smooth Jaws 5&quot;, Premium</td></tr><tr><td>Pentobarbital</td><td>Vortech</td><td>0298-9373-68</td><td>Pentobarbital 390 mg/mL by Vortech</td></tr><tr><td>Safranin O</td><td>Millipore Sigma</td><td>HT90432</td><td>Safranin O</td></tr><tr><td>Small Battery pack</td><td>STRYKER</td><td>NS014036</td><td>6212 Small Battery pack- 9.6 V</td></tr><tr><td>Steel rod, 2&amp;rsquo;</td><td>McMaster-Carr</td><td>89535K25</td><td>Steel rod, 2&amp;rsquo;</td></tr><tr><td>Sterile Saline</td><td>ICU Medical</td><td>6139-22</td><td>AquaLite Solution Pour Bottles, 250 mL</td></tr><tr><td>Stryker 6110-120 System 6 Battery Charger</td><td>STRYKER</td><td>OR-S6110-120</td><td></td></tr><tr><td>Surgical gloves</td><td>McKesson</td><td>1044729</td><td>Surgical Glove McKesson Perry Size 6.5 Sterile Pair Latex Extended Cuff Length Smooth Brown Not Chemo Approved</td></tr><tr><td>Surgical gown</td><td>McKesson</td><td>1104452</td><td>Non-Reinforced Surgical Gown with Towel McKesson Large Blue Sterile AAMI Level 3 Disposable</td></tr><tr><td>Suture scissors</td><td>Jorvet Labs</td><td>J0910SA</td><td>Super Cut Scissors, Mayo, Straight, 5 1/2&amp;Prime;</td></tr><tr><td>TUNEL staining kit</td><td>ABP Bioscience</td><td>A049</td><td>TUNEL Chromogenic Apoptosis Detection Kit</td></tr><tr><td>Weitlaner Retractors</td><td>Fine Science Tools</td><td>17012-11</td><td>2x Weitlaner-Locktite Retractors</td></tr></tbody></table>

a reproducible cartilage impact model to generate post-traumatic osteoarthritis in the rabbit

Post-traumatic osteoarthritis (PTOA) is responsible for 12% of all osteoarthritis cases in the United States. PTOA can be initiated by a single traumatic event, such as a high-impact load acting on articular cartilage, or by joint instability, as occurs with anterior cruciate ligament rupture. There are no effective therapeutics to prevent PTOA currently. Developing a reliable animal model of PTOA is necessary to better understand the mechanisms by which cartilage damage proceeds and to investigate novel treatment strategies to alleviate or prevent the progression of PTOA. This protocol describes an open, drop tower-based rabbit femoral condyle impact model to induce cartilage damage. This model delivered peak loads of 579.1 &plusmn; 71.1 N, and peak stresses of 81.9 &plusmn; 10.1 MPa with a time-to-peak load of 2.4 &plusmn; 0.5 ms. Articular cartilage from impacted medial femoral condyles (MFCs) had higher rates of apoptotic cells (p = 0.0058) and possessed higher Osteoarthritis Research Society International (OARSI) scores of 3.38 &plusmn; 1.43 compared to the non-impacted contralateral MFCs (0.56 &plusmn; 0.42), and other cartilage surfaces of the impacted knee (p &lt; 0.0001). No differences in OARSI scores were detected among the non-impacted articular surfaces (p &gt; 0.05).

The success of this procedure was monitored immediately after impact by visualization of the condyle by the surgeon (Figure 4A) and by radiography to ensure no fracture occurred (Figure 4B). There is a risk of impact failure leading to an intra-operative fracture of the condyle. This was typically due to improper Steinman pin placement (Figure 5). Using this model, there was a fracture failure rate secondary to intra-operative fract...

Watch this Scientific Journal Video about A Reproducible Cartilage Impact Model to Generate Post-Traumatic Osteoarthritis in the Rabbit at JoVE.com

A Reproducible Cartilage Impact Model to Generate Post-Traumatic Osteoarthritis in the Rabbit

The open medial femoral condyle impact model in rabbits is reliable for studying post-traumatic osteoarthritis (PTOA) and novel therapeutic strategies to mitigate PTOA progression. This protocol generates an isolated cartilage defect of the posterior medial femoral condyle in rabbits using a carriage-based drop tower with an impactor head.

Post-traumatic osteoarthritis (PTOA) is responsible for 12% of all osteoarthritis cases in the United States. PTOA can be initiated by a single traumatic ...

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Medicine

1.0K Views.  Indiana University School of Medicine. Deze methode veroorzaakt acute kraakbeenschade aan het gewichtdragende oppervlak van de konijnenknie en induceert op betrouwbare wijze posttraumatische artrose. Dit model weerspiegelt gewrichtstrauma dat relevant is voor de klinische praktijk. Het zal de evaluatie mogelijk maken van nieuwe therapieën om posttraumatische artritis te verminderen.De belangrijkste technische hindernis is de plaatsing van de Steinmann-pen in de femurschacht. Verkeerde plaatsing zal resulteren in femurschac...

Video: A Reproducible Cartilage Impact Model to Generate Post-Traumatic Osteoarthritis in the Rabbit

Matrix-assisted Autologous Chondrocyte Transplantation for Remodeling and Repair of Chondral Defects in a Rabbit Model

Articular cartilage defects are considered a major health problem because articular cartilage has a limited capacity for self-regeneration 1. Untreated cartilage lesions lead to ongoing pain, negatively affect the quality of life and predispose for osteoarthritis. During the last decades, several surgical techniques have been developed to treat such lesions. However, until now it was not possible to achieve a full repair in terms of covering the defect with hyaline articular cartilage or of providing satisfactory long-term recovery 2-4. Therefore, articular cartilage injuries remain a prime target for regenerative techniques such as Tissue Engineering. In contrast to other surgical techniques, which often lead to the formation of fibrous or fibrocartilaginous tissue, Tissue Engineering aims at fully restoring the complex structure and properties of the original articular cartilage by using the chondrogenic potential of transplanted cells. Recent developments opened up promising possibilities for regenerative cartilage therapies.
The first cell based approach for the treatment of full-thickness cartilage or osteochondral lesions was performed in 1994 by Lars Peterson and Mats Brittberg who pioneered clinical autologous chondrocyte implantation (ACI) 5. Today, the technique is clinically well-established for the treatment of large hyaline cartilage defects of the knee, maintaining good clinical results even 10 to 20 years after implantation 6. In recent years, the implantation of autologous chondrocytes underwent a rapid progression. The use of an artificial three-dimensional collagen-matrix on which cells are subsequently replanted became more and more popular 7-9.
MACT comprises of two surgical procedures: First, in order to collect chondrocytes, a cartilage biopsy needs to be performed from a non weight-bearing cartilage area of the knee joint. Then, chondrocytes are being extracted, purified and expanded to a sufficient cell number in vitro. Chondrocytes are then seeded onto a three-dimensional matrix and can subsequently be re-implanted. When preparing a tissue-engineered implant, proliferation rate and differentiation capacity are crucial for a successful tissue regeneration 10. The use of a three-dimensional matrix as a cell carrier is thought to support these cellular characteristics 11.
The following protocol will summarize and demonstrate a technique for the isolation of chondrocytes from cartilage biopsies, their proliferation in vitro and their seeding onto a 3D-matrix (Chondro-Gide, Geistlich Biomaterials, Wollhusen, Switzerland). Finally, the implantation of the cell-matrix-constructs into artificially created chondral defects of a rabbit's knee joint will be described. This technique can be used as an experimental setting for further experiments of cartilage repair.

An experimental technique for the treatment of chondral defects in the rabbit's knee joint is described. The implantation of autologous chondrocytes seeded on a matrix is a well-accepted method for the remodeling and repair of articular cartilage lesions providing satisfying long-term results. Matrix-assisted autologous chondrocyte transplantation (MACT) offers a standardized and clinically established implantation method.

Articular cartilage defects are considered a major health problem because articular cartilage has a limited capacity for self-regeneration 1. Untreated ...

Treatment of Osteochondral Defects in the Rabbit's Knee Joint by Implantation of Allogeneic Mesenchymal Stem Cells in Fibrin Clots

The treatment of osteochondral articular defects has been challenging physicians for many years. The better understanding of interactions of articular cartilage and subchondral bone in recent years led to increased attention to restoration of the entire osteochondral unit. In comparison to chondral lesions the regeneration of osteochondral defects is much more complex and a far greater surgical and therapeutic challenge. The damaged tissue does not only include the superficial cartilage layer but also the subchondral bone. For deep, osteochondral damage, as it occurs for example with osteochondrosis dissecans, the full thickness of the defect needs to be replaced to restore the joint surface 1. Eligible therapeutic procedures have to consider these two different tissues with their different intrinsic healing potential 2. In the last decades, several surgical treatment options have emerged and have already been clinically established 3-6.
Autologous or allogeneic osteochondral transplants consist of articular cartilage and subchondral bone and allow the replacement of the entire osteochondral unit. The defects are filled with cylindrical osteochondral grafts that aim to provide a congruent hyaline cartilage covered surface 3,7,8. Disadvantages are the limited amount of available grafts, donor site morbidity (for autologous transplants) and the incongruence of the surface; thereby the application of this method is especially limited for large defects.
New approaches in the field of tissue engineering opened up promising possibilities for regenerative osteochondral therapy. The implantation of autologous chondrocytes marked the first cell based biological approach for the treatment of full-thickness cartilage lesions and is now worldwide established with good clinical results even 10 to 20 years after implantation 9,10. However, to date, this technique is not suitable for the treatment of all types of lesions such as deep defects involving the subchondral bone 11.
The sandwich-technique combines bone grafting with current approaches in Tissue Engineering 5,6. This combination seems to be able to overcome the limitations seen in osteochondral grafts alone. After autologous bone grafting to the subchondral defect area, a membrane seeded with autologous chondrocytes is sutured above and facilitates to match the topology of the graft with the injured site. Of course, the previous bone reconstruction needs additional surgical time and often even an additional surgery. Moreover, to date, long-term data is missing 12.
Tissue Engineering without additional bone grafting aims to restore the complex structure and properties of native articular cartilage by chondrogenic and osteogenic potential of the transplanted cells. However, again, it is usually only the cartilage tissue that is more or less regenerated. Additional osteochondral damage needs a specific further treatment. In order to achieve a regeneration of the multilayered structure of osteochondral defects, three-dimensional tissue engineered products seeded with autologous/allogeneic cells might provide a good regeneration capacity 11.
Beside autologous chondrocytes, mesenchymal stem cells (MSC) seem to be an attractive alternative for the development of a full-thickness cartilage tissue. In numerous preclinical in vitro and in vivo studies, mesenchymal stem cells have displayed excellent tissue regeneration potential 13,14. The important advantage of mesenchymal stem cells especially for the treatment of osteochondral defects is that they have the capacity to differentiate in osteocytes as well as chondrocytes. Therefore, they potentially allow a multilayered regeneration of the defect.
In recent years, several scaffolds with osteochondral regenerative potential have therefore been developed and evaluated with promising preliminary results 1,15-18. Furthermore, fibrin glue as a cell carrier became one of the preferred techniques in experimental cartilage repair and has already successfully been used in several animal studies 19-21 and even first human trials 22.
The following protocol will demonstrate an experimental technique for isolating mesenchymal stem cells from a rabbit's bone marrow, for subsequent proliferation in cell culture and for preparing a standardized in vitro-model for fibrin-cell-clots. Finally, a technique for the implantation of pre-established fibrin-cell-clots into artificial osteochondral defects of the rabbit's knee joint will be described.

An experimental technique for the treatment of osteochondral defects in the rabbit's knee joint is described. The implantation of allogeneic mesenchymal stem cells into osteochondral defects provides a promising development in the field of tissue engineering. The preparation of fibrin-cell-clots in vitro offers a standardized method for implantation.

The treatment of osteochondral articular defects has been challenging physicians for many years. The better understanding of interactions of articular ...

Standardized Histomorphometric Evaluation of Osteoarthritis in a Surgical Mouse Model

One of the most prevalent joint disorders in the United States, osteoarthritis (OA) is characterized by progressive degeneration of articular cartilage, primarily in the hip and knee joints, which results in significant impacts on patient mobility and quality of life. To date, there are no existing curative therapies for OA able to slow down or inhibit cartilage degeneration. Presently, there is an extensive body of ongoing research to understand OA pathology and discover novel therapeutic approaches or agents that can efficiently slow down, stop, or even reverse OA. Thus, it is crucial to have a quantitative and reproducible approach to accurately evaluate OA-associated pathological changes in the joint cartilage, synovium, and subchondral bone. Currently, OA severity and progression are primarily assessed using the Osteoarthritis Research Society International (OARSI) or Mankin scoring systems. In spite of the importance of these scoring systems, they are semiquantitative and can be influenced by user subjectivity. More importantly, they fail to accurately evaluate subtle, yet important, changes in the cartilage during the early disease states or early treatment phases. The protocol we describe here uses a computerized and semiautomated histomorphometric software system to establish a standardized, rigorous, and reproducible quantitative methodology for the evaluation of joint changes in OA. This protocol presents a powerful addition to the existing systems and allows for more efficient detection of pathological changes in the joint.

The current protocol establishes a rigorous and reproducible method for quantification of morphological joint changes that accompany osteoarthritis. Application of this protocol can be valuable in monitoring disease progression and evaluating therapeutic interventions in osteoarthritis.

One of the most prevalent joint disorders in the United States, osteoarthritis (OA) is characterized by progressive degeneration of articular cartilage, ...

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 ...

Destabilization of the Medial Meniscus and Cartilage Scratch Murine Model of Accelerated Osteoarthritis

Osteoarthritis is the most prevalent musculoskeletal disease in people over 45, leading to an increasing economic and societal cost. Animal models are used to mimic many aspects of the disease. The present protocol describes the destabilization and cartilage scratch model (DCS) of post-traumatic osteoarthritis. Based on the widely used destabilization of the medial meniscus (DMM) model, DCS introduces three scratches on the cartilage surface. The current article highlights the steps to destabilize the knee by transecting the medial meniscotibial ligament followed by three intentional superficial scratches on the articular cartilage. The possible analysis methods by dynamic weight-bearing, microcomputed tomography, and histology are also demonstrated. While the DCS model is not recommended for studies that focus on the effect of osteoarthritis on the cartilage, it enables the study of osteoarthritis development in a shorter time window, with special focus on (1) osteophyte formation, (2) osteoarthritic and injury pain, and (3) the effect of cartilage damage in the whole joint.

The present protocol describes the controlled microblade scratches on the surface of the articular cartilage after destabilizing the mouse knee by cutting the medial miniscotibial ligament. This animal model presents an accelerated form of osteoarthritis (OA) suitable for studying osteophyte formation, osteosclerosis, and early-stage pain.

Osteoarthritis is the most prevalent musculoskeletal disease in people over 45, leading to an increasing economic and societal cost. Animal models are ...

Development and Evaluation of a Rat Model of Full-Thickness Cartilage Defects

Cartilage defects of the knee joint caused by trauma are a common sports joint injury in the clinic, and these defects result in joint pain, impaired movement, and eventually, knee osteoarthritis (kOA). However, there is little effective treatment for cartilage defects or even kOA. Animal models are important for developing therapeutic drugs, but the existing models for cartilage defects are unsatisfactory. This work established a full-thickness cartilage defects (FTCD) model by drilling holes in the femoral trochlear groove of rats, and the subsequent pain behavior and histopathological changes were used as readout experiments. After surgery, the mechanical withdrawal threshold was decreased, chondrocytes at the injured site were lost, matrix metalloproteinase MMP13 expression was increased, and type II collagen expression decreased, consistent with the pathological changes observed in human cartilage defects. This methodology is easy and simple to perform and enables gross observation immediately after the injury. Furthermore, this model can successfully mimic clinical cartilage defects, thus providing a platform for studying the pathological process of cartilage defects and developing corresponding therapeutic drugs.

This protocol establishes a full-thickness cartilage defects (FTCD) model by drilling holes in the femoral trochlear groove of rats and measuring the subsequent pain behavior and histopathological changes.

Cartilage defects of the knee joint caused by trauma are a common sports joint injury in the clinic, and these defects result in joint pain, impaired ...

Treating Knee Osteoarthritis with Tuina in a Rabbit Model

Tuina Intervention in Rabbit Model of Knee Osteoarthritis

Knee osteoarthritis (KOA) is mainly characterized by degenerative changes in the knee joint's cartilage and surrounding soft tissues. The efficacy of Tuina in treating KOA has been confirmed, but the underlying mechanism needs to be investigated. This study aims to establish a scientifically feasible KOA rabbit model treated with Tuina to reveal the underlying mechanisms. For this, 18, 6-month-old normal-grade male New Zealand rabbits were randomly divided into sham, model, and Tuina groups, with 6 rabbits in each group. The KOA model was established by injecting 4% papain solution into the knee joint cavity. The Tuina group was intervened with Tuina combined with the knee joint rotary correction method for 4 weeks. Only the standard grasping and fixation were performed in sham and model groups. At the end of the 1-week intervention, the knee joint range of motion (ROM) was observed, and cartilage hematoxylin-eosin (HE) staining was done. The study shows that Tuina could inhibit chondrocyte apoptosis, repair cartilage tissue, and restore knee joint ROM. In conclusion, this study demonstrates the scientific feasibility of Tuina treatment for KOA model rabbits, highlighting its potential application in the study of KOA and similar knee joint-related conditions.

Author Spotlight: Using a Rabbit Model to Explore the Efficacy of Tuina in Treating Knee Osteoarthritis 

The protocol describes a method for Tuina intervention in a rabbit model of knee osteoarthritis.

Knee osteoarthritis (KOA) is mainly characterized by degenerative changes in the knee joint's cartilage and surrounding soft tissues. The efficacy of ...

Impact of Non-Invasive ACL Injury and Surgery on Protease Activity in Mice

Non-Invasive Compression-Induced Anterior Cruciate Ligament (ACL) Injury and In Vivo Imaging of Protease Activity in Mice

Traumatic joint injuries such as anterior cruciate ligament (ACL) rupture or meniscus tears commonly lead to post-traumatic osteoarthritis (PTOA) within 10-20 years following injury. Understanding the early biological processes initiated by joint injuries (e.g., inflammation, matrix metalloproteinases (MMPs), cathepsin proteases, bone resorption) is crucial for understanding the etiology of PTOA. However, there are few options for in vivo measurement of these biological processes, and the early biological responses may be confounded if invasive surgical techniques or injections are used to initiate OA. In our studies of PTOA, we have used commercially available near-infrared protease activatable probes combined with fluorescence reflectance imaging (FRI) to quantify protease activity in vivo following non-invasive compression-induced ACL injury in mice. This non-invasive ACL injury method closely recapitulates clinically relevant injury conditions and is completely aseptic since it does not involve disrupting the skin or the joint capsule. The combination of these injury and imaging methods allows us to study the time course of protease activity at multiple time points following a traumatic joint injury.

Author Spotlight: Investigating Early Events and Long-Term Effects of ACL Injuries for Osteoarthritis Progression

Non-invasive ACL injury is a reliable and clinically relevant method for initiating post-traumatic osteoarthritis (PTOA) in mice. This injury method also allows for in vivo quantification of protease activity in the joint at early time points post-injury using protease-activatable near infrared probes and fluorescence reflectance imaging.

Traumatic joint injuries such as anterior cruciate ligament (ACL) rupture or meniscus tears commonly lead to post-traumatic osteoarthritis (PTOA) within ...

Establishment of the KOA Model in Rabbits Using the Modified Videman Method

Application of Acupotomy in a Knee Osteoarthritis Model in Rabbit

Knee osteoarthritis (KOA) is one of the most frequently encountered diseases in the orthopedic department, which seriously reduces the quality of life of people with KOA. Among several pathogenic factors, the biomechanical imbalance of the knee joint is one of the main causes of KOA. Acupotomology believes that restoring the mechanical balance of the knee joint is the key to treating KOA. Clinical studies have shown that acupotomy can effectively reduce pain and improve knee mobility by reducing adhesion, contracture of soft tissues, and stress concentration points in muscles and tendons around the knee joint. 
In this protocol, we used the modified Videman method to establish a KOA model by immobilizing the left hindlimb in a straight position. We have outlined the method of operation and the precautions related to acupotomy in detail and evaluated the efficacy of acupotomy in conjunction with the theory of "Modulating Muscles and Tendons to Treat Bone Disorders" through the detection of the mechanical properties of quadriceps femoris and tendon, as well as cartilage mechanics and morphology. The results show that acupotomy has a protective effect on cartilage by adjusting the mechanical properties of the soft tissues around the knee joint, improving the cartilage stress environment, and delaying cartilage degeneration.

Author Spotlight: Investigating the Mechanism of Action of Acupotomy in Treating Knee Osteoarthritis

In this protocol, a knee osteoarthritis model was prepared using the modified Videman method, and the operation procedures and precautions of acupotomy are detailed. The effectiveness of acupotomy has been demonstrated by testing the mechanical properties of quadriceps femoris and tendon and the mechanical and morphological properties of cartilage.

Knee osteoarthritis (KOA) is one of the most frequently encountered diseases in the orthopedic department, which seriously reduces the quality of life of ...

Development of a Rabbit Chronic-Like Rotator Cuff Injury Model for Study of Fibrosis and Muscular Fatty Degeneration

Rabbit rotator cuff (RC) pathophysiology can lead to progressive and highly degenerative changes in its associated musculature and tendons, which negatively influences clinically relevant parameters, such as strength and retraction of the muscle-tendon/myotendinous unit, ultimately causing loss of shoulder function and negatively affecting RC repair outcomes. Animal models that mimic aspects of human RC anatomy and pathophysiology are crucial for advancing the conceptual understanding of injury progression and developing effective tissue engineering and regenerative medicine-based therapeutics.
Within this context, a rabbit subscapularis (SSC) model is suitable due to (i) its anatomical similarity to the human supraspinatus (SSP) bone-tendon-muscle unit, which is the most frequently injured RC site; (ii) its pathophysiological similarity to humans in terms of fibrosis and muscle fatty degeneration (FD); and (iii) its amenability to surgical procedures. Therefore, the goal of this study is to describe the surgical techniques for inducing SSC RC injury. Briefly, the procedure involves the isolation of the SSC by identifying the coracobrachialis muscle followed by a full-thickness transection at the muscle-tendon junction and wrapping the free end of the muscle-tendon junction with a silicone-based penrose tubing to prevent spontaneous reattachment. Histologic evaluations are performed to monitor the progression of muscle FD at 4 weeks post-surgery using hematoxylin and eosin (H&#38;E) as well as Masson&#39;s trichrome staining.
Loss of muscle and FD were evident 4 weeks after transection of the SSC muscle-tendon junction, similar to human RC pathophysiological conditions. This protocol demonstrates the steps for successfully establishing a chronic-like rabbit SSC RC injury model, which can serve as a powerful tool to study skeletal muscle changes associated with RC pathophysiology and aid the development of novel therapeutic strategies for chronic-like RC tears.

This study details procedures for establishing a chronic-like rabbit rotator cuff (RC) injury. Specifically, the injury is created in the subscapularis (SSC) muscle-tendon/myotendinous unit to mimic human RC anatomy and pathophysiology, including severe muscle fatty degeneration (FD). This protocol can be applied to study RC injuries and assess regenerative therapies.

A Reproducible Cartilage Impact Model to Generate Post-Traumatic Osteoarthritis in the Rabbit

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