» Articles » PMID: 708412

The Influence of Passive Stretch on the Growth and Protein Turnover of the Denervated Extensor Digitorum Longus Muscle

Overview
Journal Biochem J
Specialty Biochemistry
Date 1978 Aug 15
PMID 708412
Citations 15
Authors
Affiliations
Soon will be listed here.
Abstract

At 7 days after cutting the sciatic nerve, the extensor digitorum longus muscle was smaller and contained less protein than its innervated control. Correlating with these changes was the finding of elevated rates of protein degradation (measured in vitro) in the denervated tissue. However, at this time, rates of protein synthesis (measured in vitro) and nucleic acid concentrations were also higher in the denervated tissue, changes more usually associated with an active muscle rather than a disused one. These anabolic trends have, at least in part, been explained by the possible greater exposure of the denervated extensor digitorum longus to passive stretch. When immobilized under a maintained influence of stretch the denervated muscle grew to a greater extent. Although this stretch-induced growth appeared to occur predominantly through a stimulation of protein synthesis, it was opposed by smaller increases in degradative rates. Nucleic acids increased at a similar rate to the increase in muscle mass when a continuous influence of stretch was imposed on the denervated tissue. In contrast, immobilization of the denervated extensor digitorum longus in a shortened unstretched state reversed most of the stretch-induced changes; that is, the muscle became even smaller, with protein synthesis decreasing to a greater extent than breakdown after the removal of passive stretch. The present investigation suggests that stretch will promote protein synthesis and hence growth of the extensor digitorum longus even in the absence of an intact nerve supply. However, some factor(s), in addition to passive stretch, must contribute to the anabolic trends in this denervated muscle.

Citing Articles

Tension in fibrils suppresses their enzymatic degradation - A molecular mechanism for 'use it or lose it'.

Saini K, Cho S, Dooling L, Discher D Matrix Biol. 2019; 85-86:34-46.

PMID: 31201857 PMC: 6906264. DOI: 10.1016/j.matbio.2019.06.001.


Agent-based computational model investigates muscle-specific responses to disuse-induced atrophy.

Martin K, Blemker S, Peirce S J Appl Physiol (1985). 2015; 118(10):1299-309.

PMID: 25722379 PMC: 4436981. DOI: 10.1152/japplphysiol.01150.2014.


Use it or lose it: multiscale skeletal muscle adaptation to mechanical stimuli.

Wisdom K, Delp S, Kuhl E Biomech Model Mechanobiol. 2014; 14(2):195-215.

PMID: 25199941 PMC: 4352121. DOI: 10.1007/s10237-014-0607-3.


Changes in REDD1, REDD2, and atrogene mRNA expression are prevented in skeletal muscle fixed in a stretched position during hindlimb immobilization.

Kelleher A, Gordon B, Kimball S, Jefferson L Physiol Rep. 2014; 2(2):e00246.

PMID: 24744910 PMC: 3966240. DOI: 10.1002/phy2.246.


Intra- and intermuscular variation in human quadriceps femoris architecture assessed in vivo.

Blazevich A, Gill N, Zhou S J Anat. 2006; 209(3):289-310.

PMID: 16928199 PMC: 2100333. DOI: 10.1111/j.1469-7580.2006.00619.x.


References
1.
Gutmann E, Zak R . Nervous regulation of nucleic acid level in cross-striated muscle. Changes in denervated muscle. Physiol Bohemoslov (1956). 1961; 10:493-500. View

2.
Waalkes T, UDENFRIEND S . A fluorometric method for the estimation of tyrosine in plasma and tissues. J Lab Clin Med. 1957; 50(5):733-6. View

3.
SOLA O, MARTIN A . Denervation hypertrophy and atrophy of the hemidiaphragm of the rat. Am J Physiol. 1953; 172(2):324-32. DOI: 10.1152/ajplegacy.1953.172.2.324. View

4.
LOWRY O, ROSEBROUGH N, FARR A, RANDALL R . Protein measurement with the Folin phenol reagent. J Biol Chem. 1951; 193(1):265-75. View

5.
Hamosch M, Lesch M, Baron J, Kaufman S . Enhanced protein synthesis in a cell-free system from hypertrophied skeletal muscle. Science. 1967; 157(3791):935-7. DOI: 10.1126/science.157.3791.935. View