$$\rightleftharpoonup{xx}$$
$$\longleftharp{xx}$$,
$$\longrightharp{xx}$$,
1. Pre-requisites for Biomechanical Locomotion Analyses
Prior to embarking upon purchasing expensive locomotor analysis equipment, and planning experiments where kinematics and/or kinetic locomotor assessment will be performed, it is imperative that the experimenter be familiar with the technical and practical aspects of biomechanical analyses, sensorimotor behavior, operant conditioning of animals, and handling/storing/managing large amounts of digitized data. Though these pre-requisites seem obvious to many, it is only after embarking upon these types of experiments where trainees realize the technical and practical complexities of performing relatively detailed locomotor analysis. The authors recommend that experimenters enroll in a course dealing with introductory biomechanics, be familiar with or hire someone familiar with a programming language required for data management, and of equal importance, spend substantial time interacting, handling, and working with laboratory animals. For understanding locomotion analysis and sensorimotor behavioral analysis in the neurosciences, experimenters are referred to several important references (see 1, 4-7).
2. Kinematic and Kinetic Testing Apparatus
A kinematic and kinetic testing apparatus, useful for collecting bilateral data, is comprised of the following components (see "Table of Specific Reagents and Equipment" for more detail):
- Quiet and sufficiently-sized room (not necessarily sound-proofed, though located in a low-traffic area)
- Radio to supply background "noise" to limit distracting noises from outside the room to animals
- Clear plexiglass, enclosed, flat-surface runway (180 cm long X 20 cm wide X 60 cm high) with a square hole (11 cm X 11 cm) located within the centre of the runway equidistant from either end
- Piece of plexi-glass (10.5 cm X 10.5 cm)
- Double-sided adhesive scotch tape
- 3M reflective adhesive tape for skin markers
- Hole punch for creating skin markers
- Isofluorane anesthesia machine required for anesthetizing animals for shaving prior to placement of skin markers
- Cheerios for encouraging movement of the animal along the length of the runway
- AMTI HE6X6 forceplate
- Vicon Motus customized system (software, computer, etc)
- 4 video cameras (at least 60 Hz sampling) and tripods with appropriate connector cables
- 4 camera-mounted halogen lights provides optimal lighting for illumination of the animal subject and the reflective skin markers
- Appropriate sized calibration frame or volume necessary for Vicon Motus system to calibrate x, y, z positions into meaningful distance measures
3. Animal Training
Prior to collecting data, each animal must be trained to cross a flat-surface, enclosed runway. Upon receiving rats from an appropriate animal supplier, animals should be acclimated to their new home for 1 week. During this acclimation time, several cheerios are placed daily into the rat's cage. Animals are food restricted to their maintenance energy requirements to prevent obesity and ensure motivation to perform this task. Thereafter, each animal is handled by the experimenter for 10-15 minutes daily for 1 week. During this same time period, each animal is placed into the runway with cheerios located at either end. Once the animal becomes familiar with their environment, they will begin eating the cheerios. Once the animal is comfortable and eating cheerios within the runway, the experimenter must then operantly condition the animal to run the length of the runway for a food reward. This is accomplished by tossing ¼ cheerio to the opposite end of the runway where the rat is positioned. Once the rat eats this cheerio, another ¼ cheerio is placed at the other end of the runway. This is done for 15-20 minutes daily until the rat consistently (>90% of tosses) moves along the runway at a constant velocity (i.e. without starting, stopping, exploring, or without changing gait) to eat the cheerio without galloping/bounding. The rat should only be employing a trotting gait. Over-conditioning of the animals to this task can lead to animals galloping and bounding these gaits are indicative of animals traveling >90 cm/s. Bounding and galloping gaits, biomechanically, are more difficult to interpret for a variety of reasons (e.g. leg lead inclusion criteria, etc). In our experience, once rats consistently employ galloping or bounding gaits, it is difficult, if not impossible to have them use a trotting gait while locomoting in the runway. Velocities >90 cm/s are rarely seen after an animal has suffered from peripheral or central nervous system injury. Time to reach successful training is variable between strains and sexes of rats. Wistar, Lewis, Long-Evans, and Sprague-Dawley strains are able to consistently traverse the runway within 2 weeks from the onset of training 8. In our experience, Fischer (F-344) rats tend to take upwards of 4-6 weeks to learn this task 8.
4. Joint Position Marking
Forelimb kinematic analysis is unreliable due to skin movement artifact imposed by placing skin markers on the forelimbs which is exacerbated in species, like rats, that have a crouched posture 9. Instead, kinematics of the forelimbs must be achieved using x-ray cinematography or fluoroscopy 10-13. As such, hind limb joint position marker placement is only described herein.
Prior to data collection, each rat must be anesthetized at least 24 hours in advance of data collection using an appropriate inhalational anesthetic (e.g. isofluorane, 1.5-2% dialed on a precision vaporizor) and administered in oxygen via face mask, and key topographic anatomical landmarks must be marked. Given the brevity of the procedure, and because long-acting anesthetic agents are not used, use of an animal warming device need not be used to maintain the animal's body temperature. Once the animal is anesthetized, the hind limbs and the dorsum, to the level of the iliac crests are shaven. The animal is then placed in sternal recumbency and its hindlimbs are placed in an approximate standing position using firm packing foam to support it. The skin overlying the cranial-most portions of the iliac crests, the greater trochanter of the femur, the lateral tibial tuberosity, the tarsal joint, and the distal and lateral aspect of the 5th metatarsal is marked with a non-toxic permanent marker. The animal is recovered from anesthesia. For temporal studies, periodic anesthesia may be required to shave the hindlimbs thereby permitting subsequent reflective marker placement (see below). Also, daily highlighting of the previously marked anatomical landmarks (using the same non-toxic marker) will be required as rats will slowly remove the markers through natural grooming behavior.
5. Data Recording
All camera views are examined to ensure that their position is appropriate and capturing the same field of view. Each camera should be placed at approximately 60-80 degrees to each other. The field of view should include the forceplate in the centre and a length of runway sufficient to capture two strides.
The calibration volume is placed within the pre-determined area of the runway. A single frame of the calibration volume within the runway, from each of the cameras, is captured. All calibrated marks along the length of each of the poles are digitized. Only once a satisfactory error in digitizing is accomplished, can the experimenter proceed to collecting locomotor data. This calibration step is critical prior to collecting data. If calibration is not performed accurately, or if calibration does not occur immediately prior to a recording session, all resulting data will be inaccurate and unusable. Importantly, if any of the cameras are touched or moved, it is safest to assume that calibration of the system needs to be repeated.
Immediately prior to placing the animal in the runway, its weight is recorded and pre-made conical reflective skin markers (using 3M reflective tape, see table) are adhered to the pre-determined felt marks made on the hind limb topographical landmarks. Recording the animal's weight will permit retrospective normalization of ground reaction forces to body weight - an important aspect if one wishes to make comparisons between groups. Additionally, body weight measurement facilitates monitoring of the animal's overall health for the duration of the experiment. Marker placement only requires appropriate animal handling and does not require anesthesia of the animal. If the adhesive on the reflective tape is insufficient to adhere to the animal's skin, a very small amount of non-toxic glue (e.g. 3M VetBond Tissue Adhesive) can be used to facilitate adherence of the marker on the animal's body. Once the markers are placed on the hindlimbs, the experimenter should be positioned comfortably near the keyboard of the computer and have in-hand the event marker attached through the Vicon Motus system. Using the calibrated file as a template, several files are made in advance of recording. Typically, 25 to 30 files need to be saved. Each file should be named uniquely. Each file will represent one recorded run of the animal being recorded. Twenty-five to 30 files are required to ensure that sufficient numbers of runs meeting the inclusion criterion velocity (i.e. 60-90 cm/s) are collected. After sufficient numbers of files are created the experimenter can begin collecting data. The experimenter must prompt the rat to shuttle within the runway by throwing ¼ pieces of cheerios at either end of the runway. With careful coordination and timing, the event marker is triggered at initiation and just prior to completion of the rat successfully completing a pass along the runway. After examining the crude ground reaction force tracing, and after recording whether the left or the right limbs hit the force plate, the file is saved and closed. Equal numbers of left and right limb forceplate hits should be recorded. The process of recording the data from a given run is repeated until sufficient numbers of runs have been recorded.
6. Data Analysis
Upon completing data collection for kinematics and ground reaction forces, each run from every animal needs to be evaluated for speed. Using two relatively fixed markers (e.g. wings of the iliums) one can evaluate a virtual point between the markers (done prior when creating a Vicon Motus file template). Before calculating the speed of this "virtual" point, markers for the iliac markers must be digitized. Using Vicon motus software, velocity of this virtual point in the X-direction (horizontal direction of movement) is calculated. In so doing, only runs within a given range speeds (determined a priori) are used in the final analyses. We find that animals moving between 60-90 cm/s are using consistent trotting gaits. A minimum of 10 runs (5 runs where the left limb makes contact with the force platform and 5 runs where the right limb makes contact with the force platform) are required. Once the acceptable runs are identified for each animal, digitization of the remaining skin markers must be completed.
To compensate for skin movement artifact over the knee, estimation of the knee position is calculated using triangulation (intersection between two circles 2D kinematics; or intersection between 2 spheres 3D kinematics), as has been previously described. Hip, knee, and hock joint angles, velocities, and accelerations can now be determined. Stance and swing times can also be evaluated, though their accuracy is limited based upon the sampling speed of the cameras being employed. These and other calculations can be performed directly (i.e. without export) using Vicon Motus KineCalc software, or data can be exported as ASCII data and analyzed using customizable routines in software such as MatLab.
Ground reaction force data is measured and amplified by the AMTI force platform and collected at 1200 Hz by Vicon Motus. As such, once the ground reaction force data is collected, an appropriate digital filter is applied to the data using Vicon Motus. Given that the experimenter has already determined the speed of travel and identified acceptable runs after digitizing appropriate skin markers, ground reaction force data that was collected simultaneously as the kinematic data, can be analyzed using Vicon Motus KineCalc directly, or indirectly using some other customizable software routine. A variety of variables for forces, in each of the three orthogonal directions, can be calculated. Such variables include peak force, area und the curve (i.e. impulse), etc. Importantly, however, the experimenter must keep right and left limb data for each run of each animal separate. Data extracted from right or left limbs is averaged for each animal and used as the representative data for that animal. Data is then analyzed using appropriate statistical procedures.
7. Representative Results
To represent the utility of this form of locomotor analysis, kinematics and ground reaction forces were determined for young, middle-aged, and geriatric female Wistar rats. From this analysis, age-related differences were found for female Wistar rats. In particular, ground reaction force analysis demonstrates that geriatric rats have reduced forelimb braking ability and tend to use their hindlimbs more for lateral stabilization compared to the other groups of animals (Figure 1). Kinematic analysis did not reveal any statistical differences between each group, though demonstrates that kinematics can be readily recorded from virtually any age of rat (Figure 2).

Figure 1. Ground reaction force tracing taken from the left limbs of young (4 month old; n=7), middle-aged (13-14 months old; n=7), and geriatric (24 months old; n=5) female Wistar rats. Right limbs were similar. It is readily apparent that geriatric rats use their forelimbs less for braking (* = p<0.05) compared to young and middle-aged rats, and geriatric rats tend to use their hindlimbs more for lateral stabilization compared to young rats (**). Solid lines represent mean, dotted lines represent mean + SE; dashed lines represent mean SE.Please click here to see a larger figure.

Figure 2. Kinematic stick figures for the left limb of young, middle-aged, and geriatric rats. Stick figures represent the mean movement of the left limb for each of the groups. There were no significant differences between the groups of animals for joint angle during the step cycle.Please click here to see a larger figure.