PUBLICATION
Structure and function of skeletal muscle in zebrafish early larvae
- Authors
- Dou, Y., Andersson-Lendahl, M., and Arner, A.
- ID
- ZDB-PUB-080501-8
- Date
- 2008
- Source
- The Journal of general physiology 131(5): 445-453 (Journal)
- Registered Authors
- Lendahl, Monika Andersson
- Keywords
- none
- MeSH Terms
-
- Actin Cytoskeleton/metabolism
- Animals
- Animals, Newborn
- Crystallography, X-Ray
- Electric Stimulation
- Isometric Contraction/drug effects
- Isometric Contraction/physiology
- Larva/anatomy & histology*
- Larva/physiology*
- Muscle Fibers, Fast-Twitch/physiology
- Muscle Fibers, Slow-Twitch/physiology
- Muscle Strength/drug effects
- Muscle Strength/physiology
- Muscle Tonus/drug effects
- Muscle Tonus/physiology
- Muscle, Skeletal/physiology*
- Muscle, Skeletal/ultrastructure*
- Sarcomeres/physiology
- Sarcomeres/ultrastructure
- Sulfonamides/pharmacology
- Toluene/analogs & derivatives
- Toluene/pharmacology
- Zebrafish/anatomy & histology*
- Zebrafish/embryology
- Zebrafish/physiology*
- PubMed
- 18443359 Full text @ J. Gen. Physiol.
Citation
Dou, Y., Andersson-Lendahl, M., and Arner, A. (2008) Structure and function of skeletal muscle in zebrafish early larvae. The Journal of general physiology. 131(5):445-453.
Abstract
Zebrafish muscles were examined at an early developmental stage (larvae 5-7 d). Using aluminum clips, preparations (approximately 1.5 mm length, 150 microm diameter) were mounted for force registration and small angle x-ray diffraction. Sarcomeres were oriented mainly in parallel with the preparation long axis. Electrical stimulation elicited fast and reproducible single twitch contractions. Length-force relations showed an optimal sarcomere length of 2.15 microm. X-ray diffraction revealed clear equatorial 1.1/1.0 reflections, showing that myofilaments are predominantly arranged along the preparation long axis. In contrast, reflections from older (2 mo) zebrafish showed two main filament orientations each at an approximately 25 degrees angle relative to the preparation long axis. Electrical stimulation of larvae muscles increased the 1.1/1.0 intensity ratio, reflecting mass transfer to thin filaments during contraction. The apparent lattice volume was 3.42 x 10(-3) microm(3), which is smaller than that of mammalian striated muscle and more similar to that of frog muscles. The relation between force and stimulation frequency showed fusion of responses at a comparatively high frequency (approximately 186 Hz), reflecting a fast muscle phenotype. Inhibition of fast myosin with N-benzyl-p-toluene sulphonamide (BTS) showed that the later phase of the tetanus was less affected than the initial peak. This suggests that, although the main contractile phenotype is fast, slow twitch fibers can contribute to sustained contraction. A fatigue stimulation protocol with repeated 220 ms/186 Hz tetani showed that tetanic force decreased to 50% at a train rate of 0.1 s(-1). In conclusion, zebrafish larvae muscles can be examined in vitro using mechanical and x-ray methods. The muscles and myofilaments are mainly orientated in parallel with the larvae long axis and exhibit a significant fast contractile component. Sustained contractions can also involve a small contribution from slower muscle types.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping