The authors acknowledge research funding from a NSERC Discovery Grant (#05573) and the Canada Foundation for Innovation (#222084) for funding the in vivo micro-CT. W.E. Ward is a Canada Research Chair in Bone and Muscle Development.

This study was approved by the Animal Care Committee of Brock University and conducted in accordance with the guidelines established by the Canadian Council on Animal Care 21.
1. Anesthesia Using Isoflurane Gas
<ol>
	<li>Pre-fill the acrylic glass incubation chamber with high-quality O2 at a continuous flow rate of approximately 1-2 L/min from an anesthetic machine (Supplementary Figure 1).</li>
	<li>Transfer the rat to the incubation chamber tail first and close the incubation chamber lid to create an airtight seal.</li>
	<li>Begin to fill the incubation chamber with veterinary-grade isoflurane at 3-4% v/v dissolved in O2 at a continuous flow rate of 1-2 L/min (Supplementary Figure 1). 
	CAUTION: Waste anesthetic gases can adversely affect handlers. A scavenger system (i.e., a charcoal filter or exhaust directly into a fume hood) must always be in place.</li>
	<li>When the rat is no longer able to stand, transfer the rat to a face mask or nose cone receiving 1-3% isoflurane dissolved in O2 at a flow rate of 1-2 L/min. Rats primarily breathe through their nose and so, as long as the nose is covered by the face mask or nose cone, there will be sufficient anesthesia delivery.</li>
	<li>Apply ophthalmic lubrication to the delicate membranes of the eyes to protect them from any escaped isoflurane gas. 
	NOTE: Ensure that ophthalmic lubrication is without antibiotic, as this may affect outcomes from an intervention.</li>
	<li>Measure palpebral (eye blinking response to gentle stimulation of palpebral opening) and pedal (withdrawal of hind limbs in response to pinching) reflexes; with increasing depth of anesthesia, palpebral reflex will be absent before pedal reflexes (Supplementary Figure 2).</li>
	<li>When an appropriate level of anesthesia is reached and the rat has lost both palpebral and pedal reflexes, maintain the rat on 0.5-2% isoflurane dissolved in O2 at a flow rate of 1-2 L/min.</li>
	<li>Continuously monitor the breathing rate of the rat throughout the procedure by keeping a constant visual on the rat either directly with an internal monitoring system or through the live-video feed (Supplementary Figure 3).</li>
</ol>
2. Positioning and Restraint of the Rat Hind Limb
<ol>
	<li>Lay the rat in the supine position on the carbon-fiber scanner bed (Supplementary Figure 4).</li>
	<li>Restrain the right foot in a malleable, foam tube, with the toes extending out of the end of the tube. Apply dental wax to hold the foot tightly within the foam and tape the tube closed tightly. Ensure that the diameter of the tube holding the foot is enough to fit firmly into the plastic tube.</li>
	<li>Slide the plastic tube into the X-ray scanner bed (Supplementary Figure 5).</li>
	<li>Extend the rat hind limb until it is taut. Do not over-extend the leg as to cause any harm to the rat (Supplementary Figure 5) as this may induce involuntary movement in the limbs due to labored respiration.</li>
	<li>Pull the left leg (non-scanned hind limb) along with the tail out of the scanning field of view and toward the torso, away from the extended leg to be scanned.</li>
	<li>Secure the left leg (non-scanned hind limb) and the tail in position using masking tape. Do not use anything more or less sticky (i.e., duct tape or painter&#39;s tape) as these materials will either harm the rat when they are removed (duct tape) or not provide a strong enough hold (painter&#39;s tape) (Supplementary Figure 6).</li>
	<li>Secure the rat body into position at the hips, shoulders, and head with the masking tape. Secure the face mask or nose cone to the rat (Supplementary Figure 6). 
	NOTE: Blot the adhesive side of the masking tape to remove its ability to stick to the rat fur. Do not blot the ends of the masking tape so that it may be firmly secured to the scanning bed.</li>
	<li>Wrap the rat in vet-wrap to limit heat loss (Supplementary Figure 6). 
	NOTE: When under general anesthesia, rats lose heat rapidly due to their large surface to body weight ratio 19,20.</li>
	<li>Continuously monitor the breathing rate of the rat throughout the procedure by keeping a constant visual on the rat (either directly or through a live-video feed). 
	NOTE: Here set up takes 5 min, scan acquisition is acquisition setting-dependent, and recovery time is 60 mins.</li>
	<li>Proceed to acquire the &#181;CT images. 
	NOTE: The exact specifications for scan acquisition are specific to each scanner type, software system and the specific research question, however, several methodological publications exist throughout the literature 1,2,9.</li>
</ol>
3. Recovery from Anesthesia
<ol>
	<li>After in vivo &#181;CT scanning is complete, stop the flow of isoflurane to the rat but maintain a 1-2 L/min flow of O2.</li>
	<li>When the rat regains motor control (1-2 min), remove it from the respirator and allow it to recover individually in a cage placed partially on a general-purpose heating pad at low heat. Rats are known to reduce their body temperature by 1 &#176;C when under general anesthetic19. Do not leave the rat unattended until it has regained sufficient consciousness to maintain sternal recumbency. 
	NOTE: Anecdotal evidence from our research group reports that immediately following recovery from isoflurane anesthesia, rats begin to eat and so it is important to have their food and water available to them during recovery. Although we have observed this behavior, repeated general anesthesia does not cause a significant increase in food intake or body weight 1,9.</li>
</ol>

<ol><li>Longo, A. B., Sacco, S. M., Salmon, P. L., Ward, W. E. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Longitudinal+use+of+micro-computed+tomography+does+not+alter+microarchitecture+of+the+proximal+tibia+in+sham+or+ovariectomized+sprague-dawley+rats%5BTitle%5D)+AND+%22Calcif+Tissue+Int%22%5BJournal%5D)">Longitudinal use of micro-computed tomography does not alter microarchitecture of the proximal tibia in sham or ovariectomized sprague-dawley rats.</a> Calcif Tissue Int. 98 (6), 631-641 (2016).</li>
<li>Sacco, S. M., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Repeated+irradiation+from+micro-computed+tomography+scanning+at+2%2C+4+and+6+months+of+age+does+not+induce+damage+to+tibial+bone+microstructure+in+male+and+female+CD-1+mice%5BTitle%5D)+AND+%22Bonekey+Rep%22%5BJournal%5D)">Repeated irradiation from micro-computed tomography scanning at 2, 4 and 6 months of age does not induce damage to tibial bone microstructure in male and female CD-1 mice.</a> Bonekey Rep. 6, 855(2017).</li>
<li>Waarsing, J. H., Day, J. S., Verhaar, J. A., Ederveen, A. G., Weinans, H. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Bone+loss+dynamics+result+in+trabecular+alignment+in+aging+and+ovariectomized+rats%5BTitle%5D)+AND+%22J+Orthop+Res%22%5BJournal%5D)">Bone loss dynamics result in trabecular alignment in aging and ovariectomized rats.</a> J Orthop Res. 24 (5), 926-935 (2006).</li>
<li>Klinck, R. J., Campbell, G. M., Boyd, S. K. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Radiation+effects+on+bone+architecture+in+mice+and+rats+resulting+from+in+vivo+micro-computed+tomography+scanning%5BTitle%5D)+AND+%22Med+Eng+Phys%22%5BJournal%5D)">Radiation effects on bone architecture in mice and rats resulting from in vivo micro-computed tomography scanning.</a> Med Eng Phys. 30 (7), 888-895 (2008).</li>
<li>Laperre, K., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Development+of+micro-CT+protocols+for+in+vivo+follow-up+of+mouse+bone+architecture+without+major+radiation+side+effects%5BTitle%5D)+AND+%22Bone%22%5BJournal%5D)">Development of micro-CT protocols for in vivo follow-up of mouse bone architecture without major radiation side effects.</a> Bone. 49 (4), 613-622 (2011).</li>
<li>Brouwers, J. E., van Rietbergen, B., Huiskes, R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((No+effects+of+in+vivo+micro-CT+radiation+on+structural+parameters+and+bone+marrow+cells+in+proximal+tibia+of+wistar+rats+detected+after+eight+weekly+scans%5BTitle%5D)+AND+%22J+Orthop+Res%22%5BJournal%5D)">No effects of in vivo micro-CT radiation on structural parameters and bone marrow cells in proximal tibia of wistar rats detected after eight weekly scans.</a> J Orthop Res. 25 (10), 1325-1332 (2007).</li>
<li>Francisco, J. I., Yu, Y., Oliver, R. A., Walsh, W. R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Relationship+between+age%2C+skeletal+site%2C+and+time+post-ovariectomy+on+bone+mineral+and+trabecular+microarchitecture+in+rats%5BTitle%5D)+AND+%22J+Orthop+Res%22%5BJournal%5D)">Relationship between age, skeletal site, and time post-ovariectomy on bone mineral and trabecular microarchitecture in rats.</a> J Orthop Res. 29 (2), 189-196 (2011).</li>
<li>Altman, A. R., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Quantification+of+skeletal+growth%2C+modeling%2C+and+remodeling+by+in+vivo+micro+computed+tomography%5BTitle%5D)+AND+%22Bone%22%5BJournal%5D)">Quantification of skeletal growth, modeling, and remodeling by in vivo micro computed tomography.</a> Bone. 81, 370-379 (2015).</li>
<li>Longo, A. B., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Lifelong+intake+of+flaxseed+or+menhaden+oil+to+provide+varying+n-6+to+n-3+PUFA+ratios+modulate+bone+microarchitecture+during+growth%2C+but+not+after+OVX+in+Sprague-Dawley+rats%5BTitle%5D)+AND+%22Mol+Nutr+Food+Res%22%5BJournal%5D)">Lifelong intake of flaxseed or menhaden oil to provide varying n-6 to n-3 PUFA ratios modulate bone microarchitecture during growth, but not after OVX in Sprague-Dawley rats.</a> Mol Nutr Food Res. 61 (8), (2017).</li>
<li>Sacco, S. M., Saint, C., LeBlanc, P. J., Ward, W. E. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Maternal+consumption+of+hesperidin+and+naringin+flavanones+exerts+transient+effects+to+tibia+bone+structure+in+female+CD-1+offspring%5BTitle%5D)+AND+%22Nutrients%22%5BJournal%5D)">Maternal consumption of hesperidin and naringin flavanones exerts transient effects to tibia bone structure in female CD-1 offspring.</a> Nutrients. 9 (3), 250(2017).</li>
<li>Campbell, G. M., Buie, H. R., Boyd, S. K. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Signs+of+irreversible+architectural+changes+occur+early+in+the+development+of+experimental+osteoporosis+as+assessed+by+in+vivo+micro-CT%5BTitle%5D)+AND+%22Osteoporos+Int%22%5BJournal%5D)">Signs of irreversible architectural changes occur early in the development of experimental osteoporosis as assessed by in vivo micro-CT.</a> Osteoporos Int. 19 (10), 1409-1419 (2008).</li>
<li>De Schaepdrijver, L., Delille, P., Geys, H., Boehringer-Shahidi, C., Vanhove, C. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((In+vivo+longitudinal+micro-CT+study+of+bent+long+limb+bones+in+rat+offspring%5BTitle%5D)+AND+%22Reprod+Toxicol%22%5BJournal%5D)">In vivo longitudinal micro-CT study of bent long limb bones in rat offspring.</a> Reprod Toxicol. 46, 91-97 (2014).</li>
<li>Perilli, E., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Detecting+early+bone+changes+using+in+vivo+micro-CT+in+ovariectomized%2C+zoledronic+acid-treated%2C+and+sham-operated+rats%5BTitle%5D)+AND+%22Osteoporos+Int%22%5BJournal%5D)">Detecting early bone changes using in vivo micro-CT in ovariectomized, zoledronic acid-treated, and sham-operated rats.</a> Osteoporos Int. 21 (8), 1371-1382 (2010).</li>
<li>Bouxsein, M. L., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Guidelines+for+assessment+of+bone+microstructure+in+rodents+using+micro-computed+tomography%5BTitle%5D)+AND+%22J+Bone+Miner+Res%22%5BJournal%5D)">Guidelines for assessment of bone microstructure in rodents using micro-computed tomography.</a> J Bone Miner Res. 25 (7), 1468-1486 (2010).</li>
<li>Li, H., Zhang, H., Tang, Z., Hu, G. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Micro-computed+tomography+for+small+animal+imaging%3A+Technological+details%5BTitle%5D)+AND+%22Progress+in+Natural+Science%22%5BJournal%5D)">Micro-computed tomography for small animal imaging: Technological details.</a> Progress in Natural Science. 18 (5), 513-521 (2008).</li>
<li>Campbell, G. M., Sophocleous, A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Quantitative+analysis+of+bone+and+soft+tissue+by+micro-computed+tomography%3A+applications+to+ex+vivo+and+in+vivo+studies%5BTitle%5D)+AND+%22Bonekey+Rep%22%5BJournal%5D)">Quantitative analysis of bone and soft tissue by micro-computed tomography: applications to ex vivo and in vivo studies.</a> Bonekey Rep. 3, 564(2014).</li>
<li>Meganck, J. A., Kozloff, K. M., Thornton, M. M., Broski, S. M., Goldstein, S. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Beam+hardening+artifacts+in+micro-computed+tomography+scanning+can+be+reduced+by+X-ray+beam+filtration+and+the+resulting+images+can+be+used+to+accurately+measure+BMD%5BTitle%5D)+AND+%22Bone%22%5BJournal%5D)">Beam hardening artifacts in micro-computed tomography scanning can be reduced by X-ray beam filtration and the resulting images can be used to accurately measure BMD.</a> Bone. 45 (6), 1104-1116 (2009).</li>
<li>Vazquez, C. M., Molina, M. T., Ilundain, A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Role+of+rat+large+intestine+in+reducing+diarrhea+after+50%25+or+80%25+distal+small+bowel+resection%5BTitle%5D)+AND+%22Dig+Dis+Sci%22%5BJournal%5D)">Role of rat large intestine in reducing diarrhea after 50% or 80% distal small bowel resection.</a> Dig Dis Sci. 34 (11), 1713-1719 (1989).</li>
<li>Albrecht, M., Henke, J., Tacke, S., Markert, M., Guth, B. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Effects+of+isoflurane%2C+ketamine-xylazine+and+a+combination+of+medetomidine%2C+midazolam+and+fentanyl+on+physiological+variables+continuously+measured+by+telemetry+in+Wistar+rats%5BTitle%5D)+AND+%22BMC+Vet+Res%22%5BJournal%5D)">Effects of isoflurane, ketamine-xylazine and a combination of medetomidine, midazolam and fentanyl on physiological variables continuously measured by telemetry in Wistar rats.</a> BMC Vet Res. 10, 198(2014).</li>
<li>Schmitz, S., Tacke, S., Guth, B., Henke, J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Comparison+of+physiological+parameters+and+anaesthesia+specific+observations+during+isoflurane%2C+ketamine-xylazine+or+medetomidine-midazolam-fentanyl+anaesthesia+in+male+guinea+pigs%5BTitle%5D)+AND+%22PLoS+One%22%5BJournal%5D)">Comparison of physiological parameters and anaesthesia specific observations during isoflurane, ketamine-xylazine or medetomidine-midazolam-fentanyl anaesthesia in male guinea pigs.</a> PLoS One. 11 (9), e0161258(2016).</li>
<li>Canadian Council on Animal Care. Guide to the care and use of experimental animals. , Available from:
 <a target="_blank" href="http://www.ccac.ca/Documents/Standards/Guidelines/Experimental_Animals_Vol1.pdf">http://www.ccac.ca/Documents/Standards/Guidelines/Experimental_Animals_Vol1.pdf</a> (1993).</li>
<li>Stevens, W. C., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Comparative+toxicities+of+halothane%2C+isoflurane%2C+and+diethyl+ether+at+subanesthetic+concentrations+in+laboratory+animals%5BTitle%5D)+AND+%22Anesthesiology%22%5BJournal%5D)">Comparative toxicities of halothane, isoflurane, and diethyl ether at subanesthetic concentrations in laboratory animals.</a> Anesthesiology. 42 (4), 408-419 (1975).</li>
</ol>

The authors have nothing to disclose.

This protocol provides viewers with the first detailed guideline for the proper anesthesia, placement, and restraint of the rat during in vivo &#181;CT scanning of the hind limb. These guidelines enable users of in vivo &#181;CT scanning systems to obtain high resolution and high quality images of the tibia that can be processed for the quantification of 3-dimensional bone micro-architecture. Critical steps in the protocol necessary to ensure proper positioning and restraint involve the proper anesthesia of the rat as well as extending the hind limb away from all other critical structures until it is taut, but not in an unnatural position. For optimal imaging outcomes, it is imperative that the rat be anesthetized to a level of complete relaxation, and that palpebral and pedal reflexes are lost. In addition, the scanning leg should be extended and the entire foot and ankle should be restrained in foam. The methods described above to achieve optimal positioning of the scanning leg will ensure that: 1) hind limbs of rats within a study are consistently oriented in the same direction, thus permitting the x-ray beam to pass through the same area of each leg as it rotates around the sample; 2) both voluntary and involuntary movement of the hind limb will not occur, thus minimizing the potential for movement artifacts to interfere with the quality of acquired images; 3) obstructions from objects (i.e., the tail) are prevented, thus minimizing the potential for partial volume effects to produce inaccurate BMD and TMD measurements. These guidelines may be modified for each individual rat, as the rate of isoflurane metabolism and positioning can vary depending on strain and body size 22. The most common in vivo scanning machines are designed for small animal models (i.e., mice, rats, rabbits, guinea pigs) and will have interchangeable animal stages to permit the scanning of different animal sizes. Therefore, they can accommodate a wide range of body weights.
Although in vivo &#181;CT scanning permits for the rat to be repositioned and rescanned if the images acquired from the initial scan are poor quality, repeated scanning will expose the rat to additional doses of radiation and isoflurane anesthesia for a prolonged period of time. Monthly repeated radiation exposure of 600 mGy focused to the rat tibia over four months does not cause adverse effects to bone micro-architecture compared to the contralateral hind limb 1, but this does not ascertain the safety of two scans repeated in immediate succession. Further limitations of the technique described include the need to extend the hind limb taut with forces applied to it to keep it still, which may invoke some changes in bone structure. While the severity of restraint of the hind limb during scanning will depend on each research objective, previous research from our lab involving monthly repeated in vivo &#181;CT imaging of one hind limb resulted in a difference in the cortical micro-architectural parameter, eccentricity, compared to the contralateral hind limb that did not undergo repeated extension, stabilization and scanning 1. Eccentricity is a measure of the elliptical shape of the cortical bone and changes in response to altered load-bearing. Therefore, when using this method of positioning and restraining of the hind limb for repeated in vivo &#181;CT imaging, consideration should be made when assessing and interpreting changes to load-bearing micro-architectural parameters.
While the above guidelines have been provided for the imaging and analysis of bone tissue, slight adjustments to the protocol must be made when imaging soft tissue of the hind limb. Specifically, the way in which the hind limb is extended from the torso and restrained must be taken into account, as the current procedure misshapes the orientation of the soft tissue (muscle, adipose tissue) into abnormal positioning for the duration of the scan. Therefore, when extrapolating this model for the use in imaging of soft tissue of the hind limb, some adjustments should be made to the restraint technique to reduce or eliminate the changes in the positioning of the tissues in relation to one another.
Furthermore, the guidelines have been written specifically based on the experiences of our research group, however, they can be modified to accommodate other commercially-available in vivo &#181;CT scanners. Other suggested methods to position and restrain the hind limb may be available by the manufacturer of the in vivo &#181;CT scanning system. Most commercially available in vivo &#181;CT units list polypropylene, expanded polystyrene, and plastic tubes with dental wax to hold a protruding foot as acceptable materials and methods for restraining the scanning leg. However, the method presented in this protocol provide more controlled and consistent positioning and restraint of the scanned leg and, consistently produces high-quality images. The guidelines presented in the present method require specialized equipment necessary for the anesthesia of the rat, such as a vaporizer, tubes, masks, induction chambers, and oxygen. Although the equipment is associated with a somewhat higher cost compared to injectable anesthetics, it allows researchers the ability to rapidly and precisely induce anesthesia at specific depths of consciousness, which provides an advantage over alternative methods.
Using the guidelines outlined in the present method video, researchers utilizing high resolution in vivo &#181;CT technologies to investigate their intervention of interest will be able to properly and consistently orient and restrain a rat hind limb for high quality X-ray imaging. This will provide a continuum in the field of in vivo &#181;CT image acquisition and serve as a step towards optimizing the consistency and accuracy within studies and enable comparisons across studies in the literature. Similarly, these protocols and methods can be expanded for use in other rodent species, including mice, although some changes will be required 2,10. For example, the restraint of the foot in the foam tube can include the ankle to minimize the possibility of leg movement during the scan. In addition, the full foot will fit into the foam holder. Thus, the toes do not extend out of the end of the holder as they do when securing the foot of a rat. In addition, the body of the mouse does not require the same restraint with tape as the rat. A smaller nose cone can be used for maintaining anesthesia in mice during the scan. If a smaller nose cone is not available, one can secure a nitrile glove over the available nose cone and make a small incision in the glove to provide a space that can fit the nose of the mouse to provide anesthesia while maintaining a seal around the nose.
While the proximal tibia is the main site of investigation of changes to bone micro-structure in the rat, guidelines for the proper and consistent positioning of other skeletal sites such as the femur and lumbar vertebrae should be investigated and established for consistency in the literature. However, when undertaking future research involving the imaging of the lumbar vertebrae, considerations must be made as imaging of the spine provides radiation exposure to the surrounding organs and tissues.

The use of in vivo micro-computed tomography (&#181;CT) is a powerful tool which involves the non-destructive imaging of internal structures at high resolutions using rodent models. The non-destructive nature of in vivo &#181;CT allows for repeated imaging of the same rodent over time. This feature not only reduces the total number of rodents required in an experimental design and thereby reduces the inter-subject variation that can arise, but also allows researchers to understand long-term responses to an intervention. With the use of repeated in vivo &#181;CT, experiments in mice and rats have elucidated developmental changes to bone micro-architecture and bone mineral density (BMD) throughout periods of the lifespan 1,2,3,4,5,6,7,8 as well as the response of bone health to interventions such as diet 9,10, ovariectomy 7,11 and pharmacologic agents 8,12,13. BMD and bone micro-architecture at specific skeletal sites, namely the proximal tibia, femur and lumbar vertebrae, are indicative of overall bone health and of the risk of sustaining a fracture and so are the primary measures when quantifying responses to an intervention.
In vivo &#181;CT image acquisition involves two-dimensional X-ray projections being acquired at multiple angles as the X-ray source and detector rotate around the animal under investigation 14,15. The quality of the resulting image is dependent on many factors including, but not limited to: selected acquisition parameters (i.e., spatial resolution, X-ray voltage, amperage, rotation step, applied filter, exposure time), limitations of the &#181;CT scanner (i.e., scanner-based artifacts such as ring artifacts or dust that cause streaking or partial volume effects) and proper positioning and restraint of the animal. The former two of these factors can be manipulated to some degree by the user, depending on the specific scanning machine, study objectives and the corrections that are needed to optimize the function of the scanner or the processing of acquired images. The latter of these factors, the proper positioning of the rodent prior to scanning, can be achieved regardless of the scanner-based limitations or the acquisition parameters that are selected to achieve a specific study objective. While many publications involving in vivo imaging have been published in the literature 14,15,16,17, classic manuscript style is such that detailed &#34;how to&#34; information cannot be included. Therefore, the aim of this article and video guide is to fill this void. Here we aim to instruct users of in vivo &#181;CT scanners how to anesthetize a rat, and position and restrain the hind limb to produce high quality images that can be analyzed to more accurately quantify outcomes of bone micro-architecture.
Preventing obstructions of the x-ray beam through objects other than the hind limb are imperative for quantifying the most accurate BMD and bone micro-architecture values. As the X-rays pass through objects and tissues of varying thickness and densities, some of the X-rays are absorbed (i.e. attenuated) by the materials they pass through. Since the measured mass density of a sample is affected by its thickness, and the presence and thicknesses of surrounding tissues, it is imperative that calibration phantoms used to determine BMD are scanned in the same manner. Therefore, if the X-ray beam is to pass through objects (i.e., the tail) before or after passing through the region of interest, those objects will absorb some of the X-ray energies and will interfere with the transmission image acquired. In addition, these scans would be very difficult to simulate when scanning the phantoms that must closely resemble sample scans. As a result, these attenuation differences lead to inaccuracy in the evaluation of BMD measurements of the bone. Thus, for ease and accuracy, it is best to limit the number of obstructions between the x-ray source, region of interest and x-ray detector.
Longitudinal assessment of bone structure from an intervention in pre-clinical models involve the repeated anesthesia of the animal to limit their movement during scanning protocols. Several methods of general anesthesia exist in order to subdue the animals undergoing a &#181;CT scan, including injectable and inhalant anesthesia 1,2,4,5,6,12. Unlike inhalant anesthetics such as isoflurane, repeated general anesthesia using injectable anesthetics cause a reduction in body weight, surgical tolerance and significant changes to other physiological parameters in rodents, specifically rats and guinea pigs, suggesting significant contraindications for repeated use 18,19,20. While isoflurane is highly volatile and allows for rapid induction and recovery, injectable anesthetic agents produce varying levels of anesthesia and time under anesthesia depends on the strain, sex, body composition, fasted state, and circadian cycle of the animal. Injectable anesthetics also pose additional barriers to their use as they are highly regulated by national governing bodies. Inhalation anesthesia however, involves the direct delivery into the respiratory system; this method allows for faster induction and recovery time and better control over the length and depth of anesthesia19,20. Limitations to the inhalation anesthesia method involve its requirement for specialized vaporizing equipment and some changes to heart rate and blood pressure during induction, maintenance and recovery 18,19.

<table><tbody><tr><td>Isoflurane</td><td>Fresenius Kabi Animal Health</td><td>108737</td><td></td></tr><tr><td>Vaporizer</td><td>Dispomed</td><td>990-1091-3SINEWA</td><td></td></tr><tr><td>Scavengers/Charcoal Filters</td><td>Dispomed</td><td>985-1005-000</td><td></td></tr><tr><td>Micro-CT Scanner</td><td>Bruker microCT</td><td>SkyScan 1176</td><td></td></tr><tr><td>Dental wax</td><td>Kerr Dental Laboratory</td><td>623</td><td></td></tr><tr><td>Foam (Backer Rod)</td><td>Rona</td><td>CF12086</td><td>1&amp;rdquo;x10&amp;rsquo;</td></tr><tr><td>Plastic tube</td><td>Bruker microCT</td><td>SP-3010</td><td></td></tr><tr><td>Carbon-fiber bed</td><td>Bruker microCT</td><td>SP-3002</td><td></td></tr><tr><td>Vet Wrap/Bandage</td><td>Dura-Tech</td><td>17473</td><td></td></tr><tr><td>Ophthalmic Gel</td><td>OptixCare</td><td>006CLC-4256</td><td>Antibiotic-free</td></tr><tr><td>Heating pad</td><td>Sunbeam</td><td>000731-500-000</td><td></td></tr></tbody></table>

proper positioning and restraint of a rat hind limb for focused high resolution imaging of bone micro-architecture using in vivo micro-computed tomography

The use of in vivo micro-computed tomography (&#181;CT) is a powerful tool which involves the non-destructive imaging of internal structures at high resolutions in live animal models. This allows for repeated imaging of the same rodent over time. This feature not only reduces the total number of rodents required in an experimental design and thereby reduces the inter-subject variation that can arise, but also allows researchers to assess longitudinal or life-long responses to an intervention. To acquire high quality images that can be processed and analyzed to more accurately quantify outcomes of bone micro-architecture, users of in vivo &#181;CT scanners must properly anesthetize the rat, and position and restrain the hind limb. To do this, it is imperative that the rat be anesthetized to a level of complete relaxation, and that pedal reflexes are lost. These guidelines may be modified for each individual rat, as the rate of isoflurane metabolism can vary depending on strain and body size. Proper technique for in vivo &#181;CT image acquisition enables accurate and consistent measurement of bone micro-architecture within and across studies.

This method of anesthesia for the rat, and positioning and restraint of the hind limb for in vivo &#181;CT imaging facilitates the acquisition of high quality images appropriate for the analysis of tibia micro-architecture. Proper positioning of the rat hind limb involves the leg being fully extended and the entire foot and ankle restrained in foam (Figure 1A) resulting in an acquired image of sufficient quality for analysis of the trabecular and cortical micro-architecture (Figure 1B). Insufficient placement and restraint of the hind limb (Figure 1C) can result in images with movement artifacts (Figure 1D), while a tail that is not fully removed from the scanning field of view (Figure 1E) will interfere with X-ray attenuation by the scanned samples (Figure 1F) and alter BMD and tissue mineral density (TMD) measurements. Either of these placement errors will result in a poor-quality scan that should not be further analyzed. Attaining images of poor quality will alter the quantification of the fine trabecular network and cortical structure of the hind limb and will produce inappropriate or inconclusive data14.
<img alt="Figure 1" class="xfigimg" src="/files/ftp_upload/56346/56346fig1.jpg" /> 
Figure 1. Representative images of placement of the rat hind limb and corresponding acquired images of the proximal tibia in cross-section. 
(A) Proper placement of the rat hind limb with the ankle fully restrained in foam, leg extended and tail pulled away from the tibia provides sufficient image quality in (B) cross-section of the tibia and its trabecular and cortical micro-architecture. (C) Improper placement of the rat hind limb with the leg not fully extended and ankle not fully restrained in foam may result in (D) movement artifacts, seen as streaking in cross-section. (E) Objects interfering with the field of view, such as the tail not pulled away from the tibia (F) interferes with x-ray attenuation from the tibia and can result in altered BMD and TMD measurements, although not visually evident. The bottom left corner in panel F shows a portion of tail in the field of view, that interfered with the x-ray beam that subsequently passed through the tibia. Red dotted lines in the left panels indicate the cross section presented on the right panels. <a href="https://cloudflare.jove.com/files/ftp_upload/56346/56346fig1large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
Supplementary Figure 1. Isoflurane anesthetic unit. Isoflurane anesthetic unit set up to provide 3-4% isoflurane dissolved in O2 at a continuous flow-rate of 1-2 L/min for induction of general anesthesia. <a href="http://cloudflare.jove.com/files/ftp_upload/56346/Suppl_Fig_1.jpg">Please click here to download this figure.</a>
Supplementary Figure 2. Ensuring depth of anesthesia. Measure pedal reflexes by pinching the toes of the rat receiving continuous inhaled anesthetic through a face mask or nose cone. The pain response is more evident when the leg is slightly extended. Very strong pinches or the use of forceps or clamps can induce tissue damage and therefore should not be used. <a href="http://cloudflare.jove.com/files/ftp_upload/56346/Suppl_Fig_2.jpg">Please click here to download this figure.</a>
Supplementary Figure 3. Screen capture of the live-feed physiological monitoring camera view. <a href="http://cloudflare.jove.com/files/ftp_upload/56346/Suppl_Fig_3.jpg">Please click here to download this figure.</a>
Supplementary Figure 4. Rat laying in the supine position on the carbon-fiber scanner bed. <a href="http://cloudflare.jove.com/files/ftp_upload/56346/Suppl_Fig_4.jpg">Please click here to download this figure.</a>
Supplementary Figure 5. Right foot of the rat restrained in a malleable foam tube. Right foot of the rat is restrained in a malleable foam tube with the toes extending out of the tube (not pictured here). The foam tube is restrained in a plastic holder (please refer to Table of Specific Materials/Equipment for more detailed information). <a href="http://cloudflare.jove.com/files/ftp_upload/56346/Suppl_Fig_5.jpg">Please click here to download this figure.</a>
Supplementary Figure 6. Rat secured in position with the right leg extended straight. The tail and left foot is taped away from the right leg (toward the torso), the hips are secured and the rat torso is wrapped in vet-wrap (blue) to limit heat loss. <a href="http://cloudflare.jove.com/files/ftp_upload/56346/Suppl_Fig_6.jpg">Please click here to download this figure.</a>

Watch this Scientific Journal Video about Proper Positioning and Restraint of a Rat Hind Limb for Focused High Resolution Imaging of Bone Micro-architecture Using In Vivo Micro-computed Tomography at 

Proper Positioning and Restraint of a Rat Hind Limb for Focused High Resolution Imaging of Bone Micro-architecture Using In Vivo Micro-computed Tomography

This paper instructs users of in vivo micro-computed tomography (&#181;CT) scanners how to anesthetize, correctly position and restrain the hind limb of a rat for minimal movement during high-resolution imaging of the tibia. The result is high quality images that can be processed to accurately quantify bone micro-architecture.

Proper Positioning and Restraint of a Rat Hind Limb for Focused High Resolution Imaging of Bone Micro-architecture Using In Vivo Micro-computed Tomography

The use of in vivo micro-computed tomography (&#181;CT) is a powerful tool which involves the non-destructive imaging of internal structures at high ...

proper-positioning-restraint-rat-hind-limb-for-focused-high

Research

JoVE Journal

Bioengineering

9.9K Views.  Brock University. This paper instructs users of in vivo micro-computed tomography (µCT) scanners how to anesthetize, correctly position and restrain the hind limb of a rat for minimal movement during high-resolution imaging of the tibia. The result is high quality images that can be processed to accurately quantify bone micro-architecture.

Video: Proper Positioning and Restraint of a Rat Hind Limb for Focused High Resolution Imaging of Bone Micro-architecture Using In Vivo Micro-computed Tomography

High Resolution 3D Imaging of Ex-Vivo Biological Samples by Micro CT

Non-destructive volume visualization can be achieved only by tomographic techniques, of which the most efficient is the x-ray micro computerized tomography (&mu;CT).
High resolution &mu;CT is a very versatile yet accurate (1-2 microns of resolution) technique for 3D examination of ex-vivo biological samples1, 2. As opposed to electron tomography, the &mu;CT allows the examination of up to 4 cm thick samples. This technique requires only few hours of measurement as compared to weeks in histology. In addition, &mu;CT does not rely on 2D stereologic models, thus it may complement and in some cases can even replace histological methods3, 4, which are both time consuming and destructive. Sample conditioning and positioning in &mu;CT is straightforward and does not require high vacuum or low temperatures, which may adversely affect the structure. The sample is positioned and rotated 180&deg; or 360&deg;between a microfocused x-ray source and a detector, which includes a scintillator and an accurate CCD camera, For each angle a 2D image is taken, and then the entire volume is reconstructed using one of the different available algorithms5-7. The 3D resolution increases with the decrease of the rotation step. The present video protocol shows the main steps in preparation, immobilization and positioning of the sample followed by imaging at high resolution.

High Resolution 3D Imaging of Ex-Vivo Biological Samples by Micro CT

Non-destructive volume visualization can be achieved only by tomographic techniques, of which the most efficient is the x-ray micro computerized tomography ( CT).

Non-destructive volume visualization can be achieved only by tomographic techniques, of which the most efficient is the x-ray micro computerized ...

Computed Tomography and Optical Imaging of Osteogenesis-angiogenesis Coupling to Assess Integration of Cranial Bone Autografts and Allografts

A major parameter determining the success of a bone-grafting procedure is vascularization of the area surrounding the graft. We hypothesized that implantation of a bone autograft would induce greater bone regeneration by abundant blood vessel formation. To investigate the effect of the graft on neovascularization at the defect site, we developed a micro&#8211;computed tomography (&#181;CT) approach to characterize newly forming blood vessels, which involves systemic perfusion of the animal with a polymerizing contrast agent. This method enables detailed vascular analysis of an organ in its entirety. Additionally, blood perfusion was assessed using fluorescence imaging (FLI) of a blood-borne fluorescent agent. Bone formation was quantified by FLI using a hydroxyapatite-targeted probe and &#181;CT analysis. Stem cell recruitment was monitored by bioluminescence imaging (BLI) of transgenic mice that express luciferase under the control of the osteocalcin promoter. Here we describe and demonstrate preparation of the allograft, calvarial defect surgery, &#181;CT scanning protocols for the neovascularization study and bone formation analysis (including the in vivo perfusion of contrast agent), and the protocol for data analysis.
The 3D high-resolution analysis of vasculature demonstrated significantly greater angiogenesis in animals with implanted autografts, especially with respect to arteriole formation. Accordingly, blood perfusion was significantly higher in the autograft group by the 7th day after surgery. We observed superior bone mineralization and measured greater bone formation in animals that received autografts. Autograft implantation induced resident stem cell recruitment to the graft-host bone suture, where the cells differentiated into bone-forming cells between the 7th and 10th postoperative day. This finding means that enhanced bone formation may be attributed to the augmented vascular feeding that characterizes autograft implantation. The methods depicted may serve as an optimal tool to study bone regeneration in terms of tightly bounded bone formation and neovascularization.

Implantation of autologous and allogeneic bone grafts constitute accepted approaches to treat major craniofacial bone loss. Yet the effect of graft composition on the interplay among neovascularization, cell differentiation and bone formation is unclear. We present a multimodal imaging protocol aimed to elucidate the angiogenesis-osteogenesis interdependence at the graft proximity.

A major parameter determining the success of a bone-grafting procedure is vascularization of the area surrounding the graft. We hypothesized that ...

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 ...

Direct Mouse Trauma/Burn Model of Heterotopic Ossification

Heterotopic ossification (HO) is the formation of bone outside of the skeleton which forms following major trauma, burn injuries, and orthopaedic surgical procedures. The majority of animal models used to study HO rely on the application of exogenous substances, such as bone morphogenetic protein (BMP), exogenous cell constructs, or genetic mutations in BMP signaling. While these models are useful they do not accurately reproduce the inflammatory states that cause the majority of cases of HO. Here we describe a burn/tenotomy model in mice that reliably produces focused HO. This protocol involves creating a 30% total body surface area partial thickness contact burn on the dorsal skin as well as division of the Achilles tendon at its midpoint. Relying solely on traumatic injury to induce HO at a predictable location allows for time-course study of endochondral heterotopic bone formation from intrinsic physiologic processes and environment only. This method could prove instrumental in understanding the inflammatory and osteogenic pathways involved in trauma-induced HO. Furthermore, because HO develops in a predictable location and time-course in this model, it allows for research to improve early imaging strategies and treatment modalities to prevent HO formation.

An Achilles tenotomy and burn injury model of heterotopic ossification allows for the reliable study of trauma induced ectopic bone formation without the application of exogenous factors.

Heterotopic ossification (HO) is the formation of bone outside of the skeleton which forms following major trauma, burn injuries, and orthopaedic surgical ...

Medicine

A Reliable and Reproducible Critical-Sized Segmental Femoral Defect Model in Rats Stabilized with a Custom External Fixator

Orthopedic research relies heavily on animal models to study mechanisms of bone healing in vivo as well as investigate the new treatment techniques. Critical-sized segmental defects are challenging to treat clinically, and research efforts could benefit from a reliable, ambulatory small animal model of a segmental femoral defect. In this study, we present an optimized surgical protocol for the consistent and reproducible creation of a 5 mm critical diaphyseal defect in a rat femur stabilized with an external fixator. The diaphyseal ostectomy was performed using a custom jig to place 4 Kirschner wires bicortically, which were stabilized with an adapted external fixator device. An oscillating bone saw was used to create the defect. Either a collagen sponge alone or a collagen sponge soaked in rhBMP-2 was implanted into the defect, and the bone healing was monitored over 12 weeks using radiographs. After 12 weeks, rats were sacrificed, and histological analysis was performed on the excised control and treated femurs. Bone defects containing only collagen sponge resulted in non-union, while rhBMP-2 treatment yielded the formation of a periosteal callous and new bone remodeling. Animals recovered well after implantation, and external fixation proved successful in stabilizing the femoral defects over 12 weeks. This streamlined surgical model could be readily applied to study bone healing and test new orthopedic biomaterials and regenerative therapies in vivo.

In vivo mammalian models of critical-sized bone defects are essential for researchers studying healing mechanisms and orthopedic therapies. Here, we introduce a protocol for the creation of reproducible, segmental, femoral defects in rats stabilized using external fixation.

Orthopedic research relies heavily on animal models to study mechanisms of bone healing in vivo as well as investigate the new treatment techniques. ...

Principles and Protocols of Mechanical Testing for Bone Fracture Susceptibility

Practical Considerations for the Design, Execution, and Interpretation of Studies Involving Whole-Bone Bending Tests of Rodent Bones

Skeletal fragility leading to fracture is an American public health crisis resulting in 1.5 million fractures each year and $18 billion in direct care costs. The ability to understand the mechanisms underlying bone disease and the response to treatment is not only desired, but critical. Mechanical testing of bone serves as a valuable technique for understanding and quantifying a bone&#39;s susceptibility to fracture. While this method appears simple to perform, inappropriate and inaccurate conclusions may be reached if governing assumptions and key steps are disregarded by the user. This has been observed across disciplines as studies continue to be published with misuse of methods and incorrect interpretation of results. This protocol will serve as a primer for the principles associated with mechanical testing along with the application of these techniques-from considerations of sample size through tissue harvesting and storage, to data analysis and interpretation. With this in hand, valuable information regarding a bone&#39;s susceptibility to fracture may be obtained, furthering understanding for both academic research and clinical solutions.

Author Spotlight: Enhancing Accuracy and Reproducibility in Whole Bone Bending Tests 

Mechanical testing of rodent bones is a valuable method for extracting information regarding a bone's susceptibility to fracture. Lacking proper practical understanding, the results may be overinterpreted or lack validity. This protocol will serve as a guide to ensure mechanical tests are performed accurately to provide valid and functional data.

Skeletal fragility leading to fracture is an American public health crisis resulting in 1.5 million fractures each year and $18 billion in direct care ...

HE Staining and Micro-CT to Evaluate Murine Trabecular Bone Microarchitecture

Trabecular Bone Microarchitecture Evaluation in an Osteoporosis Mouse Model

Bone microstructure refers to the arrangement and quality of bone tissue at the microscopic level. Understanding the bone microstructure of the skeleton is crucial for gaining insight into the pathophysiology of osteoporosis and improving its treatment. However, handling bone samples can be complex due to their hard and dense properties. Secondly, specialized software makes image processing and analysis difficult. In this protocol, we present a cost-effective and easy-to-use solution for trabecular bone microstructure analysis. Detailed steps and precautions are provided. Micro-CT is a non-destructive three-dimensional (3D) imaging technique that provides high-resolution images of trabecular bone structure. It allows for the objective and quantitative evaluation of bone quality, which is why it is widely regarded as the gold standard method for bone quality assessment. However, histomorphometry remains indispensable as it offers crucial cellular-level parameters, bridging the gap between two-dimensional (2D) and 3D assessments of bone specimens. As for the histologic techniques, we chose to decalcify the bone tissue and then perform traditional paraffin embedding. In summary, combining these two methods can provide more comprehensive and accurate information on bone microstructure.

Author Spotlight: An Economic and Efficient Method for Quantitative Evaluation of Bone Microarchitecture in a Murine Osteoporosis Model 

This protocol presents an economical and efficient method for quantitative evaluation of bone microarchitecture in a mouse model of osteoporosis by combining Hematoxylin-Eosin (HE) staining and micro-computed tomography (Micro-CT) techniques.

Bone microstructure refers to the arrangement and quality of bone tissue at the microscopic level. Understanding the bone microstructure of the skeleton ...

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 ...

Assessment of Bone Fracture Healing Using Micro-Computed Tomography

Micro-computed tomography (&#181;CT) is the most common imaging modality to characterize the three-dimensional (3D) morphology of bone and newly formed bone during fracture healing in translational science investigations. Studies of long bone fracture healing in rodents typically involve secondary healing and the formation of a mineralized callus. The shape of the callus formed and the density of the newly formed bone may vary substantially between timepoints and treatments. Whereas standard methodologies for quantifying parameters of intact cortical and trabecular bone are widely used and embedded in commercially available software, there is a lack of consensus on procedures for analyzing the healing callus. The purpose of this work is to describe a standardized protocol that quantitates bone volume fraction and callus mineral density in the healing callus. The protocol describes different parameters that should be considered during imaging and analysis, including sample alignment during imaging, the size of the volume of interest, and the number of slices that are contoured to define the callus.

Micro-computed tomography (&#181;CT) is a non-destructive imaging tool that is instrumental in assessing bone structure in preclinical studies, however there is a lack of consensus on &#181;CT procedures for analyzing the bone healing callus. This study provides a step-by-step &#181;CT protocol that allows the monitoring of fracture healing.

Micro-computed tomography (&#181;CT) is the most common imaging modality to characterize the three-dimensional (3D) morphology of bone and newly formed ...

Biology

Non-invasive Skeletal Muscle Quantification in Small Animals Using Micro-computed Tomography

Skeletal muscle size, mass, and composition are critical properties for studying metabolic and muscle-related diseases, as they directly impact the understanding of disease progression and treatment outcomes. Quantifying a live animal's lean, adipose, and skeletal mass is important in metabolic, physiology, pharmacologic, and geroscience studies. However, obtaining accurate body composition measurements, especially of lean mass, remains challenging due to the inherent limitations of conventional assessment techniques. Micro-computed tomography (micro-CT) is a non-invasive radiological technique that enables high-resolution visualization of internal structures in small animal models. A standardized micro-CT method can significantly enhance translational research with more reliable and impactful results, particularly during aging studies or at different time points within the same animal. Despite its potential, the lack of standardization in image acquisition and analysis methods significantly hinders the comparability of results across different studies. Herein, we present a comprehensive and detailed low-cost protocol for lean mass analysis using micro-CT to address these challenges and promote consistency in research involving small animal models.

This protocol uses micro-computed tomography to enable the cost-effective quantification of lean mass, including skeletal muscle and visceral tissue, adipose tissue, and skeletal tissue in small animals. It distinguishes between lean and adipose tissue, which offers significant advantages for biomedical research, particularly in translational research in small animals.

Skeletal muscle size, mass, and composition are critical properties for studying metabolic and muscle-related diseases, as they directly impact the ...

Proper Positioning and Restraint of a Rat Hind Limb for Focused High Resolution Imaging of Bone Micro-architecture Using In Vivo Micro-computed Tomography

Summary

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High Resolution 3D Imaging of Ex-Vivo Biological Samples by Micro CT

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

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A Reliable and Reproducible Critical-Sized Segmental Femoral Defect Model in Rats Stabilized with a Custom External Fixator

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