Abstract

BackgroundRotator cuff tendon tear is a leading cause for atrophy, fibrosis and fatty infiltration of the rotator cuff muscles. The pathophysiology of fatty muscle infiltration is not well understood. An animal model suited to study cellular and molecular mechanisms would therefore be desirable. While a rat model has been established for chronic rotator cuff tendon pathology, sufficient and easily identifiable fatty infiltration of the muscle has not yet been shown in rats. As younger animals regenerate better, we hypothesized that the absence of a sufficient amount of fatty infiltration in previous experiments was due to the selection of young animals and that older animals would exhibit higher amounts of fatty infiltration after tendon tear.FindingsThe supraspinatus tendon was released using tenotomy in 3 young (6 weeks old) and in 3 aged (24 months old) Sprague Dawley rats (group I and II). Another 3 aged (24 months old) rats underwent sham surgery and served as a control group (group III). In group I and II retraction of the musculotendinous unit was allowed for 6 weeks. All animals were sacrificed 6 weeks after surgery and the supraspinatus muscles were harvested. Each sample was examined for fatty infiltration of the muscle by histological methods and micro-CT. In histology, fat cells were counted with a 10-fold magnification in 6 fields of view twice. An adjusted measurement setup was developed for the use of micro-CT to quantify the absorption coefficient of the muscle as a reciprocal indicator for fatty infiltration, based on the established procedure for quantification of fatty infiltration on CT in humans.Tenotomy resulted in an insignificant increase of fat cells in histological sections in both, aged and young rats. Micro-CT was able to quantify small differences in the absorption coefficients of muscle samples; the absorption coefficient was 8.1% ± 11.3% lower in retracted muscles (group I and II) compared with the control (group III), indicating a tendency towards a higher amount of intra- and/or extracellular fat. Absorption was 4.28% ± 3.2% higher in aged compared with young muscles; however, this difference could not be confirmed by histology.ConclusionsSubstantial fatty muscle infiltration following chronic retraction after supraspinatus tenotomy could be documented histologically neither in young nor aged rats. Although micro-CT was able to reveal minor differences in absorption between the studied groups, the differences were too small to make the rat supraspinatus model interesting to study fatty infiltration of the chronically retracted muscle.

Highlights

  • Rotator cuff tendon tear is a leading cause for atrophy, fibrosis and fatty infiltration of the rotator cuff muscles

  • Rotator cuff tears are a highly prevalent musculoskeletal disorder [1] resulting in deterioration of the musculotendinous unit, characterized by atrophy, fibrosis and fatty infiltration of the muscle [2]

  • Histology Tenotomy resulted in a slight increase in fat cell count in aged rats compared to the sham group (Figure 1)

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Summary

Introduction

Rotator cuff tendon tear is a leading cause for atrophy, fibrosis and fatty infiltration of the rotator cuff muscles. An animal model suited to study cellular and molecular mechanisms would be desirable. While a rat model has been established for chronic rotator cuff tendon pathology, sufficient and identifiable fatty infiltration of the muscle has not yet been shown in rats. A small animal model in which investigations of cellular and molecular mechanism were feasible is desirable. While there have been efforts to establish a rat model for chronic rotator cuff tears [10,11,12,13], development of substantial fatty infiltration as seen in humans, could not yet be established by means of tendon release alone. The effect of age of the animals in a rat rotator cuff model has not been investigated so far and remains unknown. A pilot study with 3 young (6 weeks) and 3 aged (24 months) rats were carried out to investigate whether substantial fatty infiltration can be observed in rodents of different ages

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