Name: "avatar", a modified ex vivo work loop experiments using in vivo strain and activation
Uploaded: 2023-08-18T12:20:00.000+00:00
Duration: 7 min 3 s
Description: Watch this Scientific Journal Video about Bridging the Gap Between In Vivo and Ex Vivo Studies with the "Avatar" Technique to Advance Muscle Mechanics Research at JoVE.com

We thank Dr. Nicolai Konow for providing the data used in this study. Funded by NSF IOS-2016049 and NSF DBI-2021832.

"Avatar"- Optimized Ex Vivo Work Loop Experiment to Emulate In Vivo Muscle Force

<ol>
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All authors acknowledge there is no conflict of interest.

While organisms move seamlessly across landscapes, the underlying loads and strains that the muscles experience vary drastically1,6,23. During both in vivo locomotion1,24 and in &#34;avatar&#34; experiments, muscles are stimulated submaximally under cyclical, non-steady conditions. The isometric force-length and isotonic force-velocity relationships are not well suited for predicting muscle force under these conditions2. Understanding the effects of non-steady strain (i.e., transients) and loading is essential for predicting force production during in vivo movement, and therefore is the main rationale for developing these &#34;avatar&#34; experiments2. &#34;Avatar&#34; experiments allow us to control muscle loading and strain trajectories while measuring force output. The &#34;avatar&#34; technique investigates the force response of muscles under in vivo-like conditions, without confounding factors of neural control and tendon compliance. To perform the &#34;avatar&#34; experiments, researchers will need a program that allows a muscle to go through prescribed length changes with the ability to stimulate at different starting lengths and for varying durations (see Supplementary Figure 3 for the program the authors use). Researchers need to specify starting muscle length (mm), length of excursion (mm), onset of stimulation (% of cycle duration) and duration of stimulation (ms) before doing experiments (see steps 1.3-1.4to obtain values for these parameters). In general, it is often desirable to select strides that are representative of all strides in the trial (e.g., start and end at a similar length, reach a similar peak force, have average EMG activity, etc.). Determining whether EMG/activation and force data from a selected stride is representative of other strides in the same trial can be helpful for &#34;tuning&#34; later, which can be done by plotting work loops (force versus length) of the entire trial using the target animal&#39;s muscle. During bipedal and quadrupedal locomotion, the shortest length to shortest length generally demarcates an entire stride (toe-off to toe-off), but EMG activation can vary. In some animals and muscles, EMG activation is closely correlated to foot contact, such as the rat MG shown here22. In other animals, such as the guinea fowl lateral gastrocnemius, EMG activation generally occurs at the longest length to achieve more stability during unknown terrain25. 
To perform &#34;avatar&#34; experiments, it is important to minimize the noise in the ex vivo force data. Force measurements are sensitive to several issues, including but not limited to tearing of the muscles during surgery, compliance of the sutures if the loop-knots are too long, improper scaling of the length inputs and excursion, and muscle fatigue. Tearing of the muscles often occurs when &#34;dissecting the pocket&#34; (step 2.2.3) and tying the loop-knot around the proximal portion of the tendon (step 2.2.4). While &#34;dissecting the pocket&#34;, keeping the dissection scissors flat and horizontal to the muscle will prevent the tips from nicking the EDL. Additionally, pulling the dissection scissors away and distally while blunt dissecting will also limit contact between the dissection scissors and the EDL muscles. Additionally, muscles should be kept damp with Krebs-Henseliet solution during the surgery preparation and when being used on the rig.
Properly scaling length inputs is more complicated. Muscle passive and active force can be affected if the starting length and/or excursion are not scaled properly. The ex vivo rise in passive tension should match the in vivo rise in passive tension (see Figure 1). One scaling issue that has been observed in previous experiments is that both passive and active tension can be affected if the length excursion (starting length to longest length) is too small or too large. Theoretically, muscles should reach peak force near their optimal length (L0)26, which is why we use optimal length (L0) to scale in vivo muscle lengths in ex vivo &#34;avatar&#34; experiments to accurately replicate in vivo force production. Architectural differences between muscles will play a role in determining the starting length and length excursion parameters. Although optimal length (L0) is found during supramaximally stimulated isotonic and isometric conditions, using it as a scaling metric in &#34;avatar&#34; experiments can potentially highlight limitations of the force-length and force-velocity relationships during cyclical movement that need more investigation. In most steady-state conditions, muscle&#39;s instantaneous length, velocity, and activation (i.e., force-length and force-velocity properties) can be used to predict force and work output with reasonable accuracy12,24,27. Under dynamic conditions with variable loading, the force increases as a function of velocity28 and has a complex relationship with strain and activation29,30. This contradicts the isotonic force-velocity and isometric force-length properties of muscles28. In the rat MG, strain and velocity transients are evidence of loading, such as foot contact or interaction with the environment (i.e., rough terrain, wind, sudden change in direction for predation avoidance) (Figure 9). These rat MG strain trajectories, like most realistic conditions, have sudden changes in the applied load, force production, and work output2,28. This experimental method aims to highlight these complex interactions among strain, velocity, and activation dynamics under in vivo conditions that are not well explained by traditional force-length and force-velocity relationships.
Other issues can occur when the muscle starting length is too short or long. A too-short starting length will result in a reduced rate of rise in tension during the passive and active stretch (not shown), whereas a too-long starting length will result in an increased rate of rise in passive tension (see Figure 1B). Using the ratio of active to passive tension can be helpful. For example, in rat MG, passive tension (N) is generally around half the active tension (Figure 2). If a muscle starts at too long a length and/or is stretched to a length that is too long, the passive tension may be too high relative to the active tension (see Figure 1B), and the force may decrease quickly due to overstretching. Also, stretching to a length that is too long will potentially damage the muscle and can cause the muscle to fatigue more quickly. Additionally, active tension may appear unfused if the starting length is too short and/or the muscle is not stretched to a long enough length.
Preliminary experiments are necessary to determine starting length and excursion based on L0. Additional preliminary experiments may be needed to adjust the duration of stimulation if the activation dynamics of the muscles used are different. These optimizations are needed because the fiber type composition and/or activation dynamics of in vivo and ex vivo muscles may be different. In our representative results (Figure 4 and Figure 5), we used two stimulation protocols for mouse EDL during ex vivo experiments to replicate in vivo rat MG force production. To optimize force production in the mouse EDL to best fit in vivo rat MG, stimulation duration was increased (Figure 2 and Figure 3). Rat MG is comprised of slower fiber types than mouse EDL31,32,33. This was evident in &#34;avatar&#34; experiments because ex vivo mouse EDL muscles produced force faster after excitation, and force decreased at a faster rate after deactivation than observed in vivo in rat MG15 (Figure 2), even after accounting for excitation-contraction delay differences between in vivo and ex vivo conditions34. Depending on the ex vivo and in vivo target muscles, optimization of stimulation might be needed in other &#34;avatar&#34; experiments as well. Either the mouse EDL or soleus (SOL) muscles may be used in this ex vivo work loop technique. EDL was chosen as an &#34;avatar&#34; for the rat MG due to the similarities in muscle fiber type and pennation structure. It is possible that some muscles may have a complex structure and cannot be emulated using muscles from laboratory rodents as an &#34;avatar&#34;.
While &#34;avatar&#34; experiments do need some manual optimization to best replicate in vivo force production, the technique is applicable to a variety of different animals and locomotor modes. The &#34;avatar&#34; technique can be especially useful to understand in vivo force production in animals whose muscles are too large or otherwise inaccessible for ex vivo experiments. While only preliminary work has been done on larger animals35, this work has shown potential for the applicability of this technique across animals, muscles, and locomotor gait using laboratory mice as &#34;avatars&#34;. The usefulness of &#34;avatar&#34; experiments depends on how accurately a convenient, inexpensive, readily available, and well-characterized laboratory rodent model (i.e., mouse EDL) can be used for understanding in vivo mechanics of different muscles from varying species of vertebrates. Results from preliminary &#34;avatar&#34; experiments presented here (rat MG) and elsewhere (guinea fowl LG19), suggest this technique can be used to accurately predict in vivo forces and could be applied to other animals. Future applications of this method should expand the types of muscles and animals that have been used as both targets and &#34;avatar&#34; during ex vivo and in vitro experiments. &#34;Avatar&#34; experiments allow us to examine factors that affect muscle force and work output during in vivo locomotion when muscle loading and strain vary abruptly1,2,19. Specifically, the &#34;avatar&#34; method allows us to examine the effects of strain and velocity transients on muscle force that are not captured by traditional muscle models or sinusoidal work loop experiments.

Moving animals achieve impressive athletic feats of endurance, speed, and agility in complex environments. Animal locomotion is particularly impressive in contrast to human-engineered machines-the stability and agility of current-legged robots, prostheses, and exoskeletons remain poor compared to animals. Legged locomotion in natural terrain requires precise control and rapid adjustments to alter the speed and maneuver environmental features that act as unexpected perturbations1,2,3,4. Yet, understanding non-steady locomotion is inherently challenging because the dynamics depend on complex interactions between the physical environment, musculoskeletal mechanics, and sensorimotor control1,2. Legged locomotion requires responding to unexpected perturbations with rapid multi-modal processing of sensory information and coordinated actuation of limbs and joints1,5. Ultimately, movement is made possible by muscles producing force via intrinsic mechanical properties of the musculoskeletal system as well as from neural control1,5,6,7. An outstanding question of neuromechanics is how these factors interact to produce coordinated movement in response to unexpected perturbations. The following technique utilizes muscle&#39;s intrinsic mechanical response to deformation using in vivo strain trajectories during controllable ex vivo experiments with an &#34;avatar&#34; muscle.
The muscle work loop technique has provided an important framework for understanding intrinsic muscle mechanics during cyclical movements8,9,10. The traditional work loop technique drives muscles through predefined, typically sinusoidal, strain trajectories using frequencies and activation patterns measured during in vivo experiments2,8,9,11. Using sinusoidal length trajectories can realistically estimate work and power output during flight12 and swimming2 under conditions where animals do not undergo rapid changes in strain trajectories due to interaction with the environment and musculoskeletal kinematics. However, in vivo muscle strain trajectories during legged locomotion arise dynamically from interactions among neural activation, musculoskeletal kinematics, and loads applied by the environment5,7,13,14. A more realistic work loop technique is needed to emulate loads, strain trajectories, and force production that corresponds to in vivo muscle-tendon dynamics and provides insight into how intrinsic muscle mechanics and neural control interact to produce coordinated movement in the face of perturbations.
Here, we present a novel way to emulate in vivo muscle forces during treadmill locomotion by using an &#34;avatar&#34; muscle from a laboratory rodent during controlled ex vivo experiments with in vivo strain trajectories that represent time-varying in vivo loads. Using the measured in vivo strain trajectories from a target muscle on muscles from a laboratory animal during controlled ex vivo experiments will emulate loads experienced during locomotion. In the experiments described here, the ex vivo mouse extensor digitorum longus (EDL) muscle is used as an &#34;avatar&#34; for the in vivo rat medial gastrocnemius (MG) muscle during walking, trotting, and galloping on a treadmill13. This approach is similar to the work-loop technique, except that in vivo strain trajectories are scaled appropriately and imposed on ex vivo mouse muscles attached to a servo motor. While mouse EDL muscles differ in size, fiber type, and architecture compared to the rat MG, it is possible to control for these differences. The &#34;avatar&#34; technique allows one to: (1) emulate in vivo strain, activation, stride frequency, and work-loop patterns; (2) vary these patterns to match in vivo force responses most accurately; and (3) vary specific features of strain and/or activation in controlled combinations to test mechanistic hypotheses.

<table><tbody><tr><td>Braided Non-Absorbable Silk Suture 4-0&amp;nbsp;</td><td>Mersilk&amp;nbsp;</td><td>734H</td><td></td></tr><tr><td>Calcium Chloride Dihydrate (CaCl&lt;sub&gt;2&lt;/sub&gt;)</td><td>Sigma-Aldrich</td><td>1086436</td><td>Krebs-Henseleit&amp;nbsp;solution</td></tr><tr><td>Dextrose&amp;nbsp;</td><td>Sigma-Aldrich</td><td>D9434</td><td>Krebs-Henseleit&amp;nbsp;solution</td></tr><tr><td>HEPES</td><td>Sigma-Aldrich</td><td>PHR1428</td><td>Krebs-Henseleit&amp;nbsp;solution</td></tr><tr><td>Hydorchloric Acid (HCl)&amp;nbsp;</td><td>Sigma-Aldrich</td><td>1.37055</td><td>Krebs-Henseleit&amp;nbsp;solution</td></tr><tr><td>LabView Data Collection&amp;nbsp;</td><td>Lab-View</td><td></td><td></td></tr><tr><td>Magnesium Sulfate (MgSO&lt;sub&gt;4&lt;/sub&gt;)</td><td>Sigma-Aldrich</td><td>M7506</td><td>Krebs-Henseleit&amp;nbsp;solution</td></tr><tr><td>Potassium Chloride (KCl)&amp;nbsp;</td><td>Sigma-Aldrich</td><td>P3911</td><td>Krebs-Henseleit&amp;nbsp;solution</td></tr><tr><td>Potassium Phosphate Monobasic (KH&lt;sub&gt;2&lt;/sub&gt;PO&lt;sub&gt;4&lt;/sub&gt;)</td><td>Sigma-Aldrich</td><td>5.43841</td><td>Krebs-Henseleit&amp;nbsp;solution</td></tr><tr><td>S88 Stimulator</td><td>Grass</td><td>M643H05</td><td>Available for purchase on Ebay</td></tr><tr><td>Series 300B Lever System</td><td>Aurora</td><td>1200A</td><td>includes water-jacket tissue bath</td></tr><tr><td>Sodium Bicarbonate (NaHCO&lt;sub&gt;3&lt;/sub&gt;)</td><td>Sigma-Aldrich</td><td>S5761</td><td>Krebs-Henseleit&amp;nbsp;solution</td></tr><tr><td>Sodium Chloride (NaCl)&amp;nbsp;</td><td>Sigma-Aldrich</td><td>S9888</td><td>Krebs-Henseleit&amp;nbsp;solution</td></tr><tr><td>Sodium Hydroxide (NaOH)</td><td>Sigma-Aldrich</td><td>S5881</td><td>Krebs-Henseleit&amp;nbsp;solution</td></tr><tr><td>Wild Type Mice</td><td>Jackson Laboratory</td><td>B6C3Fe a/a Ttn mdm/J</td><td></td></tr></tbody></table>

"avatar", a modified ex vivo work loop experiments using in vivo strain and activation

Movement behaviors are emergent features of dynamic systems that result from muscle force production and work output. The interplay between neural and mechanical systems occurs at all levels of biological organization concurrently, from the tuning of leg muscle properties while running to the dynamics of the limbs interacting with the ground. Understanding the conditions under which animals shift their neural control strategies toward intrinsic muscle mechanics (&#39;preflexes&#39;) in the control hierarchy would allow muscle models to predict in vivo muscle force and work more accurately. To understand in vivo muscle mechanics, ex vivo investigation of muscle force and work under dynamically varying strain and loading conditions similar to in vivo locomotion is required. In vivo strain trajectories typically exhibit abrupt changes (i.e., strain and velocity transients) that arise from interactions among neural activation, musculoskeletal kinematics, and loads applied by the environment. The principal goal of our &#34;avatar&#34; technique is to investigate how muscles function during abrupt changes in strain rate and loading when the contribution of intrinsic mechanical properties to muscle force production may be highest. In the &#34;avatar&#34; technique, the traditional work-loop approach is modified using measured in vivo strain trajectories and electromyographic (EMG) signals from animals during dynamic movements to drive ex vivo muscles through multiple stretch-shortening cycles. This approach is similar to the work-loop technique, except that in vivo strain trajectories are scaled appropriately and imposed on ex vivo mouse muscles attached to a servo motor. This technique allows one to: (1) emulate in vivo strain, activation, stride frequency, and work-loop patterns; (2) vary these patterns to match in vivo force responses most accurately; and (3) vary specific features of strain and/or activation in controlled combinations to test mechanistic hypotheses.

The goal of the &#34;avatar&#34; experiments is to replicate in vivo force production and work output as closely as possible during ex vivo work loop experiments. This study chose to use mouse EDL as an &#34;avatar&#34; for rat MG because mouse EDL and rat MG are both comprised of mostly of fast-twitch muscles20,21. Both muscles are primary movers of the ankle joint (EDL ankle dorsiflexor, MG ankle plantarflexor) with similar pennation angles (mouse EDL 12.4 + 2.12&#176;22, rat MG 20&#176; used in this study15). Scaled representative work loops of rat MG15 were compared to ex vivo &#34;avatar&#34; experiments (Figure 4) using two different stimulation protocols (one from measured EMG activity and one optimized as in step 3.3). R2 values presented here were calculated using the entire scaled stretch-shortening cycle (2 cycles/condition), with each cycle having more than 2000 points corresponding to the locomotor speed (walk = 5521 points, trot = 5002, gallop = 2502 points). Work loops were scaled to account for differences in muscle size, P0, and PCSA. Scaling was done by linearly mapping force and strain onto a similar scale (0-1) to compare rat MG and mouse EDL. Visually, it is apparent that optimizing the stimulation protocol (Figure 4B) to account for different activation dynamics of the mouse EDL and rat MG muscles improves the fit to the in vivo rat MG force compared to the EMG-based activation (see Discussion section). For the mouse EDL, approximately doubling the stimulation duration for slower strain trajectories (walk and trot) increased the R2 by 62% in walking and 109% in trot. For the faster strain trajectory (gallop), increasing stimulation time by half the observed time increased the R2 by 22%.
<img alt="Figure 4" class="xfigimg" src="/files/ftp_upload/65610/65610fig04.jpg" /> 
Figure 4: Comparison of in vivo and ex vivo work loops. Work loops of in vivo rat MG (black) and ex vivo mouse EDL (green) during walking (2.9Hz) using in vivo strain trajectories. The thicker line indicates stimulation in both in vivo and ex vivo work loops. (A) Work loop of in vivo rat MG (black) and ex vivo mouse EDL (dashed green) during walking using EMG-based stimulation protocol. (B) Work loop of in vivo rat MG (black) and ex vivo mouse EDL (solid green) during walking (2.9Hz) using optimized stimulation. <a href="https://www-jove-com.remotexs.ntu.edu.sg/files/ftp_upload/65610/65610fig04large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
High R2 between mouse EDL ex vivo force production and in vivo force production of rat medial gastrocnemius (MG)15 indicates good replication (Figure 5). In EMG-based stimulation experiments, average R2 values were 0.535, 0.428, and 0.77 for walk, trot, and gallop, respectively. In optimized stimulation experiments, average R2 values were 0.872, 0.895, and 0.936 in walk, trot, and gallop, respectively. As previously discussed (step 3.3, Figure 5), depending on the activation dynamics of the muscles used, the stimulation protocol may also need to be optimized. Prediction of in vivo MG force using ex vivo mouse EDL was improved across all locomotor speeds by optimizing stimulation, increasing R2 (Figure 5A,B), and decreasing root mean square error (RMSE). RMSE decreased after optimization for all speeds (Figure 6). Averaged RMSE for EMG-based stimulation was 0.31, 0.43, and 0.158 for walk, trot, and gallop. Averaged RMSE for optimized stimulation was 0.181, 0.116, 0.101 for walk, trot, and gallop.
<img alt="Figure 5" class="xfigimg" src="/files/ftp_upload/65610/65610fig05.jpg" /> 
Figure 5: R2 Values for in vivo and ex vivo force production: Box and whisker plot of R2 values for in vivo and ex vivo force comparisons. Individual observations plotted, median, 25th, and 75th percentile indicated. (A) R2 values for in vivo and ex vivo force production using stimulation protocol based on measured in vivo EMG signal during walking at 2.9 Hz (green), trotting at 3.2 Hz (magenta), and galloping at 6.2 Hz (cyan). (B) R2 values for in vivo and ex vivo force production using optimized stimulation (see Figure 2). Optimizing the stimulation onset and duration increased R2 for all gaits. EMG-based stimulation: walk R2 = 0.50-0.55, trot R2 = 0.37-0.47, gallop R2= 0.62-0.90; optimized stimulation: walk R2 = 0.74-0.93, trot R2 = 0.85-0.92, gallop R2 = 0.87-0.97. <a href="https://www-jove-com.remotexs.ntu.edu.sg/files/ftp_upload/65610/65610fig05large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 6" class="xfigimg" src="/files/ftp_upload/65610/65610fig06.jpg" /> 
Figure 6: Root-mean square error (RMSE) for in vivo and ex vivo force production. Box and whisker plot of RMSE values for in vivo and ex vivo force comparisons. Individual observations plotted, median, 25th, and 75th percentile indicated. (A) RMSE values for in vivo and ex vivo force production using EMG-based stimulation protocol. (B) RMSE values for in vivo and ex vivo using optimized stimulation protocol. Optimizing the stimulation onset and duration reduced RMSE for all gaits. Walking at 2.9 Hz (green), trot at 3.2 Hz (magenta), and gallop at 6.4 Hz (cyan). <a href="https://www-jove-com.remotexs.ntu.edu.sg/files/ftp_upload/65610/65610fig06large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
To test the performance of traditional work loop methods at predicting in vivo muscle forces, sinusoidal work loops were also performed for the mouse EDL at the same frequency, length excursion, starting length, stimulation onset, and duration as for the &#34;avatar&#34; experiments using in vivo rat MG strain trajectories. R2 values were significantly lower than for the in vivo strain trajectories for both EMG-based and optimized stimulation protocols (Figure 7). Averaged R2 values for EMG-based stimulation using sinusoidal length trajectories were 0.062, 0.067, and 0.141 at walk, trot, and gallop frequencies. Averaged R2 values for optimized stimulation using sinusoidal length trajectories were 0.09, 0.067, and 0.141 at walk, trot, and gallop frequencies.
<img alt="Figure 7" class="xfigimg" src="/files/ftp_upload/65610/65610fig07.jpg" /> 
Figure 7: R2 Values for in vivo and ex vivo force production using sinusoidal length changes. Box and whisker plot of RMSE values for in vivo and ex vivo force comparisons. Individual observations plotted, median, 25th, and 75th percentile indicated. R2 values for walk (green, 2.9 Hz), trot (magenta, 3.2 Hz), and gallop (cyan, 6.2 Hz) using sinusoidal length changes with EMG-based (translucent) and optimized (opaque) stimulation protocols. For both EMG-based and optimized stimulation, the R2 values were lower for the sinusoidal length changes than for in vivo length changes. EMG-based stimulation: walk R2 = 0.00 - 0.30, trot R2 = 0.00 - 0.02, gallop R2= 0.03 - 0.07; optimized stimulation: walk R2 = 0.02 - 0.21, trot R2 = 0.02 - 0.12, gallop R2 = 0.12 - 0.17. <a href="https://www-jove-com.remotexs.ntu.edu.sg/files/ftp_upload/65610/65610fig07large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
Work loops produced by the ex vivo mouse EDL muscle using sinusoidal length trajectories do not as accurately emulate in vivo rat MG force compared to in vivo strain trajectories (Figure 8). The change in work produced by sinusoidal vs. in vivo strain trajectories can be explained by the absence of strain and velocity transients in the sinusoidal trajectory (Figure 9). While the muscles were stimulated at similar lengths during the active shortening phase of the contractions in both sinusoidal trajectories and in vivo-based strain trajectories, the onset of stimulation occurred at different phases of the cycle (e.g., stimulation onset occurred at a phase of 74% for trot EMG-based stimulation, but at a phase of 43% for walking EMG-based stimulation; see Discussion section).
<img alt="Figure 8" class="xfigimg" src="/files/ftp_upload/65610/65610fig08.jpg" /> 
Figure 8: Comparing in vivo and ex vivo sinusoidal&#160;work loops. (A) In vivo work loop (black) from rat MG and ex vivo work loop (dashed magenta) from mouse EDL using sinusoidal strain trajectory and EMG-based stimulation. (B) In vivo work loop (black) from rat MG and ex vivo work loop (solid magenta) from mouse EDL using sinusoidal strain trajectory and optimized stimulation. Note that the sinusoidal work loops overestimate the in vivo work due to the absence of strain and velocity transients in the sinusoidal trajectory. EMG-based stimulation R2 = 0.0003, optimized stimulation R2 = 0.084. <a href="https://www-jove-com.remotexs.ntu.edu.sg/files/ftp_upload/65610/65610fig08large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 9" class="xfigimg" src="/files/ftp_upload/65610/65610fig09v2.jpg" /> 
Figure 9:&#160;Comparison of in vivo strain and ex vivo sinusoidal length trajectories. Comparison of in vivo strain and ex vivo sinusoidal length trajectories at walk (green), trot (magenta), and gallop (blue). The solid line is in vivo strain trajectory. Dashed line ex vivo sinusoidal length trajectory. The highlighted portion is stimulation. Stimulation started at the same length during the shortening phase of the stride. Arrows indicating strain and velocity transients. Deviations from sinusoidal are impedance from outside forces on muscle. <a href="https://www-jove-com.remotexs.ntu.edu.sg/files/ftp_upload/65610/65610fig09largev2.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
Supplementary Figure 1: Program used to collect isometric maximal force at optimal length. The program used to determine optimal length during supramaximal and submaximal twitch and tetanic stimulation. <a href="https://www-jove-com.remotexs.ntu.edu.sg/files/ftp_upload/65610/NewFigure2.pdf" target="_blank">Please click here to download this File.</a>
Supplementary Figure 2: Viable twitch response. Twitch response of mouse EDL. Twitch force rises and falls quickly and should reach active tension of ~1 V. &#34;Noise&#34; should be minimal after the peak active tension has been reached. <a href="https://www-jove-com.remotexs.ntu.edu.sg/files/ftp_upload/65610/NewFigure3.pdf" target="_blank">Please click here to download this File.</a>
Supplementary Figure 3: Program used to collect work loop data. The program used to control muscle length of and timing of stimulation in ex vivo work loops. <a href="https://www-jove-com.remotexs.ntu.edu.sg/files/ftp_upload/65610/NewFigure4.pdf" target="_blank">Please click here to download this File.</a>
Supplementary Coding File 1: MATLab code used to segment and create an experimental protocol for the work loop. MATLab code that was used to segment target step information (length, EMG activation, and force) into individual strides. Code includes scaling and interpolating target animal steps into lengths that ex vivo mouse EDL can stretch. Additionally, includes code to smooth EMG signal and compare activation to select onset and duration of stimulation in ex vivo work loop experiments. <a href="https://www-jove-com.remotexs.ntu.edu.sg/files/ftp_upload/65610/NewFigure1.pdf" target="_blank">Please click here to download this File.</a>

Watch this Scientific Journal Video about Bridging the Gap Between In Vivo and Ex Vivo Studies with the "Avatar" Technique to Advance Muscle Mechanics Research at JoVE.com

Author Spotlight: Bridging the Gap Between In Vivo and Ex Vivo Studies with the "Avatar" Technique to Advance Muscle Mechanics Research 

This article details the methodology for emulating in vivo muscle force production during ex vivo work loop experiments using an "avatar" muscle from a laboratory rodent to assess the contributions of strain transients and activation to the muscle force response.

"Avatar", a Modified Ex vivo Work Loop Experiments Using In vivo Strain and Activation

Movement behaviors are emergent features of dynamic systems that result from muscle force production and work output. The interplay between neural and ...

avatar-modified-ex-vivo-work-loop-experiments-using-vivo-strain

Nanyang Technological University

Research

JoVE Journal

Bioengineering

689 조회수.  Northern Arizona University. This article details the methodology for emulating in vivo muscle force production during ex vivo work loop experiments using an "avatar" muscle from a laboratory rodent to assess the contributions of strain transients and activation to the muscle force response. 

비디오: Author Spotlight: Bridging the Gap Between In Vivo and Ex Vivo Studies with the "Avatar" Technique to Advance Muscle Mechanics Research 

Ex Vivo Culture of Patient Tissue &amp; Examination of Gene Delivery

This video describes the use of patient tissue as an ex vivo model for the study of gene delivery. Fresh patient tissue obtained at the time of surgery is sliced and maintained in culture. The ex vivo model system allows for the physical delivery of genes into intact patient tissue and gene expression is analysed by bioluminescence imaging using the IVIS detection system. The bioluminescent detection system demonstrates rapid and accurate quantification of gene expression within individual slices without the need for tissue sacrifice. This slice tissue culture system may be used in a variety of tissue types including normal and malignant tissue and allows us to study the effects of the heterogeneous nature of intact tissue and the high degree of variability between individual patients. This model system could be used in certain situations as an alternative to animal models and as a complementary preclinical mode prior to entering clinical trial.

Ex Vivo Culture of Patient Tissue & Examination of Gene Delivery

This article describes the culture of patient tissue slices for gene delivery studies and subsequent analysis of gene expression using IVIS bioluminescence imaging.

환자 조직 및 유전자 전달의 시험 전의 VIVO 문화

This video describes the use of patient tissue as an ex vivo model for the study of gene delivery.  Fresh patient tissue obtained at the time of surgery ...

연구

의학

Assessing the Viability of a Synthetic Bacterial Consortium on the In Vitro Gut Host-microbe Interface

The interplay between host and microbiota has been long recognized and extensively described. The mouth is similar to other sections of the gastrointestinal tract, as resident microbiota occurs and prevents colonisation by exogenous bacteria. Indeed, more than 600 species of bacteria are found in the oral cavity, and a single individual may carry around 100 different at any time. Oral bacteria possess the ability to adhere to the various niches in the oral ecosystem, thus becoming integrated within the resident microbial communities, and favouring growth and survival. However, the flow of bacteria into the gut during swallowing has been proposed to disturb the balance of the gut microbiota. In fact, oral administration of P. gingivalis shifted bacterial composition in the ileal microflora. We used a synthetic community as a simplified representation of the natural oral ecosystem, to elucidate the survival and viability of oral bacteria subjected to simulated gastrointestinal transit conditions. Fourteen species were selected, subjected to in vitro salivary, gastric, and intestinal digestion processes, and presented to a multicompartment cell model containing Caco-2 and HT29-MTX cells to simulate the gut mucosal epithelium. This model served to unravel the impact of swallowed bacteria on cells involved in the enterohepatic circulation. Using synthetic communities allows for controllability and reproducibility. Thus, this methodology can be adapted to assess pathogen viability and subsequent inflammation-associated changes, colonization capacity of probiotic mixtures, and ultimately, potential bacterial impact on the presystemic circulation.

Assessing the Viability of a Synthetic Bacterial Consortium on the In Vitro Gut Host-microbe Interface

Gut host-microbe interactions were assessed using a novel approach combining a synthetic oral community, in vitro gastrointestinal digestion, and a model of the small intestine epithelium. We present a method that can be adapted to evaluate cell invasion of pathogens and multi-species biofilms, or even to test probiotic formulations&#39; survivability.

생체 외에서 직감 호스트 미생물 인터페이스에 합성 세균 컨소시엄의 생존 능력을 평가

The interplay between host and microbiota has been long recognized and extensively described. The mouth is similar to other sections of the ...

생화학

The Ex Vivo Culture and Pattern Recognition Receptor Stimulation of Mouse Intestinal Organoids

Primary intestinal organoids are a valuable model system that has the potential to significantly impact the field of mucosal immunology. However, the complexities of the organoid growth characteristics carry significant caveats for the investigator. Specifically, the growth patterns of each individual organoid are highly variable and create a heterogeneous population of epithelial cells in culture. With such caveats, common tissue culture practices cannot be simply applied to the organoid system due to the complexity of the cellular structure. Counting and plating based solely on cell number, which is common for individually separated cells, such as cell lines, is not a reliable method for organoids unless some normalization technique is applied. Normalizing to total protein content is made complex due to the resident protein matrix. These characteristics in terms of cell number, shape and cell type should be taken into consideration when evaluating secreted contents from the organoid mass. This protocol has been generated to outline a simple procedure to culture and treat small intestinal organoids with microbial pathogens and pathogen associated molecular patterns (PAMPs). It also emphasizes the normalization techniques that should be applied when protein analysis are conducted after such a challenge.

The Ex Vivo Culture and Pattern Recognition Receptor Stimulation of Mouse Intestinal Organoids

Here, a protocol to harvest, maintain, and treat mouse small intestinal organoids with pathogen associated molecular patterns (PAMPs) and Listeria monocytogenes is described, as well as emphasis on gene expression and proper normalization techniques for protein.

그만큼<em&gt; 전의 VIVO</em마우스 소장 Organoids의&gt; 문화 및 패턴 인식 수용체 자극

Primary intestinal organoids are a valuable model system that has the potential to significantly impact the field of mucosal immunology. However, the ...

면역학 및 감염병학

The Ex Vivo Colon Organ Culture and Its Use in Antimicrobial Host Defense Studies

The intestine displays an architecture of repetitive crypt structures consisting of different types of epithelial cells, lamina propia containing immune cells, and stroma. All of these heterogeneous cells contribute to intestinal homeostasis and participate in antimicrobial host defense. Therefore, identifying a surrogate model for studying immune response and antimicrobial activity of the intestine in an in vitro setting is extremely challenging. In vitro studies using immortalized intestinal epithelial cell lines or even primary crypt organoid culture do not represent the exact physiology of normal intestine and its microenvironment. Here, we discuss a method of culturing mouse colon tissue in a culture dish and how this ex vivo organ culture system can be implemented in studies related to antimicrobial host defense responses. In representative experiments, we showed that colons in organ culture express antimicrobial peptides in response to exogenous IL-1&#946; and IL-18. Further, the antimicrobial effector molecules produced by the colon tissues in the organ culture efficiently kill Escherichia coli in vitro. This approach, therefore, can be utilized to dissect the role of pathogen- and danger-associated molecular patterns and their cellular receptors in regulating intestinal innate immune responses and antimicrobial host defense responses.

The Ex Vivo Colon Organ Culture and Its Use in Antimicrobial Host Defense Studies

The ex vivo organ culture allows investigation of biological processes in the context of the intact tissue architecture. Here, we introduce a method of ex vivo culture of the mouse colon, which can be used to study innate immunity and antimicrobial host defense in the intestine.

그만큼<em&gt; 전의 VIVO</em항균 호스트 방어 연구에&gt; 콜론 오르간 문화와 그것의 사용

The intestine displays an architecture of repetitive crypt structures consisting of different types of epithelial cells, lamina propia containing immune ...

Adult Mouse DRG Explant and Dissociated Cell Models to Investigate Neuroplasticity and Responses to Environmental Insults Including Viral Infection

This protocol describes an ex vivo model of mouse-derived dorsal root ganglia (DRG) explant and in vitro DRG-derived co-culture of dissociated sensory neurons and glial satellite cells. These are useful and versatile models to investigate a variety of biological responses associated with physiological and pathological conditions of the peripheral nervous system (PNS) ranging from neuron-glial interaction, neuroplasticity, neuroinflammation, and viral infection. The usage of DRG explant is scientifically advantageous compared to simplistic single cells models for multiple reasons. For instance, as an organotypic culture, the DRG explant allows ex vivo transfer of an entire neuronal network including the extracellular microenvironment that play a significant role in all the neuronal and glial functions. Further, DRG explants can also be maintained ex vivo for several days and the culture conditions can be perturbed as desired. In addition, the harvested DRG can be further dissociated into an in vitro co-culture of primary sensory neurons and satellite glial cells to investigate neuronal-glial interaction, neuritogenesis, axonal cone interaction with the extracellular microenvironment, and more general, any aspect associated with the neuronal metabolism. Therefore, the DRG-explant system offers a great deal of flexibility to study a wide array of events related to biological, physiological, and pathological conditions in a cost-effective manner.

In this report, the advantages of organotypic cultures and dissociated primary cultures of mouse-derived dorsal root ganglia are highlighted to investigate a wide range of mechanisms associated with neuron-glial interaction, neuroplasticity, neuroinflammation, and response to viral infection.

성인 마우스 DRG Explant와 해리 셀 모델 Neuroplasticity 바이러스 성 감염을 포함 한 환경 모욕에 대 한 응답을 조사 하

This protocol describes an ex vivo model of mouse-derived dorsal root ganglia (DRG) explant and in vitro DRG-derived co-culture of dissociated sensory ...

신경과학

Ex Vivo Assessment of Contractility, Fatigability and Alternans in Isolated Skeletal Muscles

Described here is a method to measure contractility of isolated skeletal muscles. Parameters such as muscle force, muscle power, contractile kinetics, fatigability, and recovery after fatigue can be obtained to assess specific aspects of the excitation-contraction coupling (ECC) process such as excitability, contractile machinery and Ca2+ handling ability. This method removes the nerve and blood supply and focuses on the isolated skeletal muscle itself. We routinely use this method to identify genetic components that alter the contractile property of skeletal muscle though modulating Ca2+ signaling pathways. Here, we describe a newly identified skeletal muscle phenotype, i.e., mechanic alternans, as an example of the various and rich information that can be obtained using the in vitro muscle contractility assay. Combination of this assay with single cell assays, genetic approaches and biochemistry assays can provide important insights into the mechanisms of ECC in skeletal muscle.

Ex Vivo Assessment of Contractility, Fatigability and Alternans in Isolated Skeletal Muscles

We describe a method to directly measure muscle force, muscle power, contractile kinetics and fatigability of isolated skeletal muscles in an in vitro system using field stimulation. Valuable information on Ca2+ handling properties and contractile machinery of the muscle can be obtained using different stimulating protocols.

절연 골격근의 수축성, Fatigability 및 Alternans의 예 VIVO 평가

 
Described here is a method to measure contractility of isolated skeletal muscles. Parameters such as muscle force, muscle power, contractile kinetics, ...

생물학

질병의 세포 상호 작용을 연구하기 위해 쥐 힘줄 집합체를 제작합니다.

Engineering Tendon Assembloids to Probe Cellular Crosstalk in Disease and Repair

Tendons enable locomotion by transferring muscle forces to bones. They rely on a tough tendon core comprising collagen fibers and stromal cell populations. This load-bearing core is encompassed, nourished, and repaired by a synovial-like tissue layer comprising the extrinsic tendon compartment. Despite this sophisticated design, tendon injuries are common, and clinical treatment still relies on physiotherapy and surgery. The limitations of available experimental model systems have slowed the development of novel disease-modifying treatments and relapse-preventing clinical regimes. 
In vivo human studies are limited to comparing healthy tendons to end-stage diseased or ruptured tissues sampled during repair surgery and do not allow the longitudinal study of the underlying tendon disease. In vivo animal models also present important limits regarding opaque physiological complexity, the ethical burden on the animals, and large economic costs associated with their use. Further, in vivo animal models are poorly suited to systematic probing of drugs and multicellular, multi-tissue interaction pathways. Simpler in vitro model systems have also fallen short. One major reason is a failure to adequately replicate the three-dimensional mechanical loading necessary to meaningfully study tendon cells and their function. 
The new 3D model system presented here alleviates some of these issues by exploiting murine tail tendon core explants. Importantly, these explants are easily accessible in large numbers from a single mouse, retain 3D in situ loading patterns at the cellular level, and feature an in vivo-like extracellular matrix. In this protocol, step-by-step instructions are given on how to augment tendon core explants with collagen hydrogels laden with muscle-derived endothelial cells, tendon-derived fibroblasts, and bone marrow-derived macrophages to substitute disease- and injury-activated cell populations within the extrinsic tendon compartment. It is demonstrated how the resulting tendon assembloids can be challenged mechanically or through defined microenvironmental stimuli to investigate emerging multicellular crosstalk during disease and injury.

저자 스포트라이트: 세포 메커니즘을 이해하기 위한 마우스 조립체를 개발하여 힘줄 연구 발전

Here, we present an assembloid model system to mimic tendon cellular crosstalk between the load-bearing tendon core tissue and an extrinsic compartment containing cell populations activated by disease and injury. As an important use case, we demonstrate how the system can be deployed to probe disease-relevant activation of extrinsic endothelial cells.

질병 및 복구에서 세포 누화를 조사하기 위한 힘줄 집합체 엔지니어링

Tendons enable locomotion by transferring muscle forces to bones. They rely on a tough tendon core comprising collagen fibers and stromal cell ...

생체공학

A Novel High-Throughput Ex Vivo Ovine Skin Wound Model for Testing Emerging Antibiotics

The development of antimicrobials is an expensive process with increasingly low success rates, which makes further investment in antimicrobial discovery research less attractive. Antimicrobial drug discovery and subsequent commercialization can be made more lucrative if a fail-fast-and-fail-cheap approach can be implemented within the lead optimization stages where researchers have greater control over drug design and formulation. In this article, the setup of an ex vivo ovine wounded skin model infected with Staphylococcus aureus&#160;is described, which is simple, cost-effective, high throughput, and reproducible. The bacterial physiology in the model mimics that during infection as bacterial proliferation is dependent on the pathogen&#39;s ability to damage the tissue. The establishment of wound infection is verified by an increase in viable bacterial counts compared to the inoculum. This model can be used as a platform to test the efficacy of emerging antimicrobials in the lead optimization stage. It can be contended that the availability of this model will provide researchers developing antimicrobials with a fail-fast-and-fail-cheap model, which will help increase success rates in subsequent animal trials. The model will also facilitate the reduction and refinement of animal use for research and ultimately enable faster and more cost-effective translation of novel antimicrobials for skin and soft tissue infections to the clinic.

A Novel High-Throughput Ex Vivo Ovine Skin Wound Model for Testing Emerging Antibiotics

The protocol describes a step-by-step method to set up an ex vivo ovine wounded skin model infected with Staphylococcus aureus. This high-throughput model better simulates infections in vivo compared with conventional microbiology techniques and presents researchers with a physiologically relevant platform to test the efficacy of emerging antimicrobials.

새로운 항생제 테스트를 위한 새로운 고처리량 생체 외 난소 피부 상처 모델

The development of antimicrobials is an expensive process with increasingly low success rates, which makes further investment in antimicrobial discovery ...

"Avatar", a Modified Ex vivo Work Loop Experiments Using In vivo Strain and Activation

요약

더 많은 비디오 탐색

환자 조직 및 유전자 전달의 시험 전의 VIVO 문화

생체 외에서 직감 호스트 미생물 인터페이스에 합성 세균 컨소시엄의 생존 능력을 평가

그만큼

그만큼

성인 마우스 DRG Explant와 해리 셀 모델 Neuroplasticity 바이러스 성 감염을 포함 한 환경 모욕에 대 한 응답을 조사 하

절연 골격근의 수축성, Fatigability 및 Alternans의 예 VIVO 평가

질병 및 복구에서 세포 누화를 조사하기 위한 힘줄 집합체 엔지니어링

질병 및 복구에서 세포 누화를 조사하기 위한 힘줄 집합체 엔지니어링

질병 및 복구에서 세포 누화를 조사하기 위한 힘줄 집합체 엔지니어링

새로운 항생제 테스트를 위한 새로운 고처리량 생체 외 난소 피부 상처 모델