Skeletal muscle activity affects the deformity of long bone morphology in lathyritic chick embryo

Author:

Yuguchi Maki123ORCID,Yamazaki Yosuke123ORCID,Honjo Bin13,Isokawa Keitaro123ORCID

Affiliation:

1. Department of Anatomy Nihon University School of Dentistry Tokyo Japan

2. Division of Functional Morphology, Dental Research Center Nihon University School of Dentistry Tokyo Japan

3. Division of Oral Structural and Functional Biology Nihon University Graduate School of Dentistry Tokyo Japan

Abstract

AbstractEmbryonic muscle activity is involved in various aspects of bone morphogenesis and growth. Normal mechanical stimuli of muscle contraction are important in most cases, and when the muscles are immobilized, the developing bones are abnormally shaped. In chick embryos, a characteristic curved deformity is reproducibly induced in the developing tibiotarsus using the bone‐weakening agent, beta‐aminopropionitrile (bAPN). In this study, we applied decamethonium bromide (DMB), a well‐established neuromuscular blocking agent, to embryos treated with bAPN, to test the hypothesis that the deformity is triggered and formed depending on the balance between the decrease in stiffness of the bAPN‐affected tibiotarsus and the normal physiological increase in embryonic skeletal muscle activity. The occurrence of curved morphology induced by bAPN administered at 4 or 8 days of incubation (embryonic day [ED]) was temporally consistent with the posterior displacement of the leg muscles, which occurred just before ED8. The displaced muscles were assumed to exert a contraction force comparable to that of untreated normal muscles. When treated with DMB at ED8, the muscles atrophied and exhibited degenerative changes, and the degree of curved morphology was alleviated and reduced to 50% or more in the morphometric evaluation at ED10. These findings indicated that the coordinated development of skeletal element stiffness and muscle activity must be temporally regulated, particularly during the early stages of skeletogenesis.

Publisher

Wiley

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