» Articles » PMID: 39754210

Spatially Ordered Recruitment of Fast Muscles in Accordance with Movement Strengths in Larval Zebrafish

Overview
Journal Zoological Lett
Publisher Biomed Central
Date 2025 Jan 3
PMID 39754210
Authors
Affiliations
Soon will be listed here.
Abstract

In vertebrates, skeletal muscle comprises fast and slow fibers. Slow and fast muscle cells in fish are spatially segregated; slow muscle cells are located only in a superficial region, and comprise a small fraction of the total muscle cell mass. Slow muscles support low-speed, low-force movements, while fast muscles are responsible for high-speed, high-force movements. However, speed and strength of movement are not binary states, but rather fall on a continuum. This raises the question of whether any recruitment patterns exist within fast muscles, which constitute the majority of muscle cell mass. In the present study, we investigated activation patterns of trunk fast muscles during movements of varying speeds and strengths using larval zebrafish. We employed two complementary methods: calcium imaging and electrophysiology. The results obtained from both methods supported the conclusion that there are spatially-ordered recruitment patterns in fast muscle cells. During weaker/slower movements, only the lateral portion of fast muscle cells is recruited. As the speed or strength of the movements increases, more fast muscle cells are recruited in a spatially-ordered manner, progressively from lateral to medial. We also conducted anatomical studies to examine muscle fiber size. The results of those experiments indicated that muscle fiber size increases systematically from lateral to medial. Therefore, the spatially ordered recruitment of fast muscle fibers, progressing from lateral to medial, correlates with an increase in fiber size. These findings provide significant insights into the organization and function of fast muscles in larval zebrafish, illustrating how spatial recruitment and fiber size interact to optimize movement performance.

References
1.
Kimura Y, Okamura Y, Higashijima S . alx, a zebrafish homolog of Chx10, marks ipsilateral descending excitatory interneurons that participate in the regulation of spinal locomotor circuits. J Neurosci. 2006; 26(21):5684-97. PMC: 6675258. DOI: 10.1523/JNEUROSCI.4993-05.2006. View

2.
Zhou W, Saint-Amant L, Hirata H, Cui W, Sprague S, Kuwada J . Non-sense mutations in the dihydropyridine receptor beta1 gene, CACNB1, paralyze zebrafish relaxed mutants. Cell Calcium. 2005; 39(3):227-36. DOI: 10.1016/j.ceca.2005.10.015. View

3.
McLean D, Masino M, Koh I, Lindquist W, Fetcho J . Continuous shifts in the active set of spinal interneurons during changes in locomotor speed. Nat Neurosci. 2008; 11(12):1419-29. PMC: 2735137. DOI: 10.1038/nn.2225. View

4.
Gong Y, Huang C, Li J, Grewe B, Zhang Y, Eismann S . High-speed recording of neural spikes in awake mice and flies with a fluorescent voltage sensor. Science. 2015; 350(6266):1361-6. PMC: 4904846. DOI: 10.1126/science.aab0810. View

5.
Zajac F, Faden J . Relationship among recruitment order, axonal conduction velocity, and muscle-unit properties of type-identified motor units in cat plantaris muscle. J Neurophysiol. 1985; 53(5):1303-22. DOI: 10.1152/jn.1985.53.5.1303. View