Force Measurement During Contraction to Assess Muscle Function in Zebrafish Larvae

Summary

Force measurements can be used to demonstrate changes in muscle function due to development, injury, disease, treatment or chemical toxicity. In this video, we demonstrate a method to measure force during a maximal contraction of zebrafish larval trunk muscle.

Abstract

Zebrafish larvae provide models of muscle development, muscle disease and muscle-related chemical toxicity, but related studies often lack functional measures of muscle health. In this video article, we demonstrate a method to measure force generation during contraction of zebrafish larval trunk muscle. Force measurements are accomplished by placing an anesthetized larva into a chamber filled with a salt solution. The anterior end of the larva is tied to a force transducer and the posterior end of the larva is tied to a length controller. An isometric twitch contraction is elicited by electric field stimulation and the force response is recorded for analysis. Force generation during contraction provides a measure of overall muscle health and specifically provides a measure of muscle function. Although we describe this technique for use with wild-type larvae, this method can be used with genetically modified larvae or with larvae treated with drugs or toxicants, to characterize muscle disease models and evaluate treatments, or to study muscle development, injury, or chemical toxicity.

Introduction

Young zebrafish (Danio rerio) larvae, 3-7 days post-fertilization (dpf), are increasingly recognized as a useful organism for skeletal muscle research. Young larvae are used to model human muscle disease^1-9, evaluate drugs and therapeutic strategies^10-11, study muscle injury¹², understand muscle development^13-16, and investigate muscle-related chemical toxicity^17-19. Typical studies in these areas examine the degree to which healthy muscle is rendered abnormal by genetic manipulation or exposure to toxicants, and some studies examine the degree to which abnormal muscle responds to treatment. Critical to the success of these studies is the ability to accurately assess muscle health.

While there are a variety of methods available to assess muscle health in zebrafish larvae, few provide direct information about muscle function. Muscle health is usually evaluated by appearance, as assessed by histological staining^6,8,11, immunostaining^9,15,16,18, light microscopy^3,13, electron microscopy^3,4,14,16, or birefringence^7,9,11, but these techniques provide morphological information only. Trunk and tail displacements and swimming speed^4,17 evaluate motor function, but these are not direct measures of muscle function since they also reflect neural input, energy metabolism, and other processes.

In contrast, measuring force generation during contraction provides a direct assessment of muscle function and represents a measure of overall muscle health. Added benefits of this approach include straightforward data analysis and quantitative results. In this video article, we provide a detailed procedure for measuring force generation by larval muscles, in the hope that more researchers will use this method to complement existing measures of muscle health in their research.

The overall goal of this method is to measure force generation during contraction of zebrafish larval trunk muscle. To accomplish this goal, a zebrafish larva is anesthetized and placed into a chamber filled with a salt solution. The anterior end of the larva is tied to a force transducer and the posterior end of the larva is tied to a length controller. Muscle activation is accomplished by electric field stimulation, and the stimulation current and the length of the larva are adjusted to produce maximum twitch force. An isometric twitch contraction is elicited and the force response is recorded for analysis.

To be clear, this technique does not measure forces generated by larval muscles during swimming. Because both ends of the larva are tied to equipment and because the larva remains anesthetized, it cannot initiate movement during testing. Furthermore, field stimulation activates all the muscle fibers at the same time to induce a bilateral contraction, which is not what naturally occurs²⁰. Therefore, rather than measuring actual forces generated during swimming, this technique determines the force generating capability of the larval muscles.

We have used this technique to demonstrate muscle weakness in a zebrafish model of nemaline myopathy²¹, as well as to evaluate the effect of antioxidant treatment on muscle function in a zebrafish model of multi-minicore disease²². Others have used a similar technique²³ to examine the effects of an environmental pollutant on muscle function¹⁹.

Protocol

Note: all procedures involving zebrafish should be performed in accordance with relevant guidelines, regulations, and regulatory agencies. All animal use procedures shown in this article were approved by the University of Michigan Committee on the Use and Care of Animals (UCUCA).

1. Make Suture Loops

1. Use forceps to separate non-sterile suture (USP 10/0 monofilament nylon, 3 ply) into three strands.
2. Begin to tie a double overhand knot in one of the strands. Stop before tightening the knot completely to make a small (~1 mm diameter) loop instead of a knot.
3. Use scissors to cut excess suture from the loop tails. An example of a finished loop is shown in Figure 1.
4. Place the loop on the sticky side of a Post-it Note for later use. The suture loops will be used to hold the larvae in place during force testing.
5. Repeat steps 1.1-1.4 as necessary. Make two suture loops for each larva that will be tested.

2. Make Testing Solution

1. Make Tyrodes solution by adding 7.977 g sodium chloride, 0.373 g potassium chloride, 0.265 g calcium chloride dihydrate, 0.102 g magnesium chloride hexahydrate, 0.048 g sodium phosphate monobasic, 1.000 g sodium bicarbonate, and 0.037 g ethylenediaminetetraacetic acid disodium salt dihydrate to 1,000 ml of purified water.
2. Stir the solution until the salts are completely dissolved. This solution can be stored for a month at 4 °C.
3. Add 2.1 ml of 4 mg/ml tricaine, prepared according to The Zebrafish Book²⁴, to 47.9 ml Tyrodes solution and mix. Protect this solution from light by storing it in a dark glass bottle or in a glass bottle covered with aluminum foil. This solution should be stored at room temperature and made fresh each day.

3. Tie Aanesthetized Larva into Experimental Chamber

1. Place the testing apparatus (Figure 2) on the stage of a stereo microscope.
2. Connect the force transducer and length controller cables to the testing apparatus. Turn on the force transducer. Turn on the length controller so that it remains rigid. (Note: the length controller provides the ability to stretch or shorten a muscle preparation during a contraction. However, this feature of the length controller is not used in the method described herein. Therefore, the length controller can be thought of as a rigid attachment point mounted to an XYZ positioning system).
3. With a disposable transfer pipette, fill the experimental chamber with testing solution.
4. Use forceps to pick up a suture loop by one of the tails and hang it on the force transducer tube. Hang a second suture loop on the tube attached to the length controller. (Note: gripping a suture loop on the curved part can kink the suture and cause it to break during subsequent steps).
5. With a disposable transfer pipette, transfer a zebrafish larva to a small Petri dish filled with testing solution. Wait for the anesthetic in the testing solution (tricaine) to take effect (~1 min). With a forceps, gently nudge the tail and verify that the larva is anesthetized by a lack of touch-evoked swimming.
6. Use a glass pipette to transfer the larva to the experimental chamber.
7. By gently nudging the larva with closed forceps, guide the anterior portion of the larva through the suture loop on the force transducer tube. Guide the anterior portion of the larva through the suture loop on the tube. Grasp both suture loop tails with forceps and pull them simultaneously to tighten the suture loop posterior to the yolk sac or swimbladder (Figure 3A).
8. With a forceps, hold one suture loop tail and pull, causing the larva to swivel 90° around the tube until the lateral side of the larva faces up (Figure 3B). If the loop was tightened enough, there will be some resistance to the pull; the larva should not swivel easily. If the loop was tightened too much, the larva will not swivel around the tube.
9. Using the XYZ positioning device attached to the length controller, move the length controller tube along the X-axis (axis definitions in Figure 2A) and under the trunk and tail of the larva. Leave space between the ends of the length controller tube and the force transducer tube.
10. Guide the suture loop over the tail of the larva and tighten the suture loop as previously described (Figure 3C). You may need to swivel the posterior part of the larva so that the lateral side faces up. Trim the suture loop tails (Figure 3D).

4. Position Larva in Experimental Chamber

1. Move the larva to an appropriate distance from the chamber bottom to ensure the larva will be within "working distance" of an inverted microscope objective during subsequent steps. To accomplish this, use the XYZ positioning devices to slowly lower the tubes (with attached larva) along the Z-axis until the tubes just touch the bottom of the chamber. Then, raise the tubes until the larva is an appropriate distance from the chamber bottom (~100 μm).
2. Using the XYZ positioning device attached to the length controller, adjust the length controller tube along the Y-axis to align the long axis of the larva with the long axis of the force transducer tube.

5. Record Force During a Maximal Twitch Contraction

1. Move the testing apparatus to the stage of an inverted microscope.
2. Adjust the chamber temperature to a desired value. To begin, connect the water bath circulator, thermometer, and temperature controller to the testing apparatus. Turn on the necessary components and adjust the setting on the temperature controller until the thermometer reports the desired value. Data included in this article were collected at 25 °C, but measurements may also be made at RT or at 28.5 °C.
3. Connect cables from the stimulator to the testing apparatus. Turn on the power to the stimulator but do not stimulate the larva until step 5.6.
4. Make sure the larva is parallel to the chamber bottom. Through a 40X objective, view the portion of the larva between the ends of the tubes. If parallel to the bottom, both ends of the larva will be in focus. If needed, adjust the force transducer tube along the Z-axis until both ends are in focus.
5. Verify that the larva length is shorter than optimal. Turn on the video sarcomere length system and rotate the video camera such that the striations are parallel to the sides of the video frame. This system monitors striation spacing by analyzing variations in pixel intensity along each horizontal row of pixels within a user-defined region of interest (ROI). The results for all rows within the ROI are averaged and reported with a frequency equivalent to the video frame-rate (≥80 sec^-1). The striation spacing is used as an indicator of sarcomere length.
6. Adjust the microscope to focus on peripheral fibers and note the indicated sarcomere length. If necessary, use the XYZ positioning device attached to the length controller to adjust length of the larva (X-axis) until the sarcomere length is less than optimal (e.g. 1.90 μm).
7. Adjust the stimulation current to optimize twitch force. To begin, set the output current on the stimulator to a low magnitude (e.g. 100 mA). The stimulator can be triggered manually or by a computer running a custom LabVIEW program. Elicit a twitch of the larval muscles with a current pulse of 0.2 msec in duration.
8. Use an oscilloscope to record the force output and measure the peak twitch force using the oscilloscope's cursors. Increase the current by 50 mA increments and measure the peak twitch force at each current level. Wait 30 sec between twitches to prevent fatigue. As stimulation current increases, peak twitch force typically increases to a maximum and then gradually decreases. The current at which the larva generates the greatest force is the optimal stimulation current. Set the current amplitude to the optimal stimulation current.
9. Using the XYZ positioning device, adjust the length of the larva (and thus, sarcomere length) in order to elicit maximum twitch force. Wild-type zebrafish larvae (3-7 dpf) generate maximum twitch force at sarcomere lengths of 2.10 μm or 2.15 μm. However, the sarcomere length can be set to 2.08 μm to avoid excess strain on the larva.
10. Elicit a twitch of the larval muscles. Use the oscilloscope to record the force response and save the record for subsequent analysis.

6. Measure Musculature Dimensions with Larva at Optimal Length

1. Move the testing apparatus back to the stereo microscope.
2. Using the eyepiece scale, measure the height of the musculature as viewed from the side. Then, taking care not to change the length of the larva, swivel the larva by 90° using the suture loop tails in order to view the larva from the bottom. Measure the width of the musculature as viewed from the bottom. Take the measurements at an anatomical landmark (e.g. urogenital opening) (Figure 4).
3. Cut the suture loops with a microblade to release the larva from the testing equipment.

Discussion

This method measures force generation during a twitch to assess muscle function in trunk muscles of zebrafish larvae. Although tetanic contractions can be elicited in zebrafish larvae (e.g. by 200 stimulation pulses/sec for a duration of 0.2 sec), the maximum tetanic force is only 10-15% greater than the maximum twitch force. Therefore, the force generated during a twitch is a reasonable measure of force generating capability. Twitches are preferred over tetanic contractions because twitches are less likely to cause ripping or slipping at the suture ties.

In order to generate meaningful data with this technique, maximum twitch force should be achieved for each larva and the variability between experimental groups should be minimized. With these goals in mind, we offer the following suggestions. First, take care when tying the larva to the force transducer and the length controller tubes. If the suture loops are tightened too much, the suture will cut through the muscle tissue. If the suture loops are not tightened enough, the force generated by the larva will not be fully transmitted to the force transducer. Both situations, but especially the latter, underestimate maximum twitch force. Second, since testing multiple experimental groups can take several hours (20-30 min/larva), alternate between groups because larvae will continue to develop during the testing period.

While some of the mentioned equipment is essential for measurement of maximum twitch force (e.g. force transducer, current stimulator), other items are not absolutely necessary. The video sarcomere length system is desirable but not required. As an alternative, a series of twitches can be used to find optimal length, during which the length of the larva is adjusted until maximum twitch force is achieved. A temperature control system is also not absolutely necessary. Temperature control is critical when measuring twitch kinetics, which are highly sensitive to temperature, whereas maximum twitch force is not particularly sensitive to small changes in temperature and could be measured at room temperature. Note that regardless of the temperature in the chamber during force testing, the larvae should be maintained at the optimal growth temperature of 28.5 °C²⁴ prior to force testing for accurate staging.

The larvae are tested in a Tyrodes solution containing tricaine. We use 0.02% (w/v) tricaine, the concentration recommended for anesthesia²⁴, to eliminate spontaneous contractions evoked by the nervous system and thus prevent fatigue during force testing. Tricaine also facilitates the tie-on step and reduces overall testing time. However, we observe that including tricaine in the testing solution consistently reduces the maximum twitch force by approximately 30%. A similar effect has also been observed in tadpole tail muscle, where tricaine reduced force generation after neuromuscular transmission was blocked, suggesting that tricaine has a direct effect on muscle²⁵. Tricaine may reduce muscle cell excitability by reducing sodium conductance across the cell membrane, as it does in nerve cells²⁶. Other options for blocking activation by motoneurons are d-tubocurarine and α-bungarotoxin but, unlike tricaine, these compounds are not skin-permeable and must be injected directly into the head, spinal cord, or heart²⁷. Individual investigators will need to assess whether or not tricaine is desirable for their specific application. If tricaine is included in the testing solution, the concentration should be consistent between experiments and researchers should verify that the effect of the tricaine does not vary between experimental groups.

We describe this method for larvae as young as 3 dpf and as old as 7 dpf. Although muscle fibers appear to be functional as early as 17 hr post-fertilization, when spontaneous tail movements begin²⁷, the short length of the tail before 3 dpf hinders tying the larva to the testing equipment. We typically do not test larva after 7 dpf since many disease models do not survive much longer than this time. If testing larvae beyond 5 dpf, the larvae should be fed. We have observed that unfed larvae have smaller muscles and generate less maximum twitch force than fed larvae, likely due to the diminishing yolk sac. Thus it may be desirable to test larvae between 3-5 dpf, to avoid the additional variable of external feeding.

In summary, we describe a quantitative and reliable method for measuring force generation during a maximal twitch contraction of zebrafish larval trunk muscle. This method can be used to assess the overall health of zebrafish larval muscle and specifically provides information about muscle function. In addition to providing information about the magnitude of force generation, this technique can be used to study the kinetics of force generation or be adapted to study muscle fatigue²². Although we describe this technique for use with wild-type larvae, this method can be used for genetically modified larvae or for larvae treated with drugs or toxicants, to characterize muscle disease models and evaluate treatments, or to study muscle development, muscle injury, or muscle-related chemical toxicity.

Materials

Name	Company	Catalog Number	Comments
			REAGENTS
Tricaine powder	Sigma-Aldrich	A5040
Sodium chloride	Sigma-Aldrich	S7653
Potassium chloride	Sigma-Aldrich	P9541
Calcium chloride dihydrate	Sigma-Aldrich	223506
Magnesium chloride hexahydrate	Sigma-Aldrich	M2670
Sodium phosphate monobasic	Sigma-Aldrich	S0751
Sodium bicarbonate	Sigma-Aldrich	S6297
Ethylenediaminetetraacetic acid disodium salt dihydrate	Sigma-Aldrich	E5134
			EQUIPMENT
Nonsterile-suture	Ashaway Line & Twine	S30002	USP 10/0 monofilament nylon (3 ply)
Forceps	Fine Science Tools	11251-20	Dumont #5
Spring scissors	Fine Science Tools	15000-08	Vannas
Stereo microscope	Leica Microsystems	MZ8	Illuminated with Fostec EKE ACE I light source
Force transducer	Aurora Scientific	400A
Length controller	Aurora Scientific	318B
XYZ positioning devices	Parker Hannifin	3936M
Thermometer	Physitemp	BAT-12
Disposable transfer pipette	Fisher Scientific	13-711-9AM	Cut end to widen opening and facilitate larva transfer
Petri dish	Fisher Scientific	08-757-11YZ
Glass pipette	Fisher Scientific	13-678-8B	Cut end (and fire-polish) to widen opening and facilitate larva transfer
Inverted microscope	Carl Zeiss Microscopy	Axiovert 100
Water bath circulator	Neslab Instruments	RTE-111
Temperature controller	Alpha Omega Instruments	Series 800
Stimulator	Aurora Scientific	701C	High-power, follow stimulator
Video sarcomere length system	Aurora Scientific	900B-5A
LabVIEW software	National Instruments
Oscilloscope	Nicolet Technologies	ACCURA 100
Microblade	Fine Science Tools	10050-00
Microblade holder	Fine Science Tools	10053-13
Data analysis software (Signo)	Alameda Applied Sciences