Xinchen Huang1 and Bo He1
1The First Affiliated Hospital of Kunming Medical University, kunming, China
Synopsis
Keywords: Muscle, Aging
Motivation: The evaluation of extracellular matrix levels in skeletal muscle often requires tissue biopsy, which is difficult for patients to accept in clinical practice
Goal(s): We evaluated the extracellular matrix level of skeletal muscle using non-invasive magnetic resonance imaging technology and conducted pathological verification using skeletal muscle samples from rats with sarcopenia
Approach: We constructed a classic sarcopenic rat model , scanned the lumbar paravertebral muscles with a 3.0T MRI-based DTI sequence, and validated through histological experiments
Results: FA and CSA of sarcopenic rats were significantly reduced compared to the normal control group, and there was a strong correlation between them and pathological related parameters
Impact: Our study provides
a non-invasive tool for evaluating the extracellular matrix levels of skeletal
muscles in sarcopenia
Abstract
Introduction: Extracellular
matrix remodeling in skeletal muscle is one of the important reasons leading to
the development of sarcopenia. The aim of this study was to evaluate
alterations in extracellular matrix remodeling in lumbar paravertebral muscles
of sarcopenic rats by diffusion-tensor magnetic resonance imaging((DT-MRI).
Methods: Twenty
6-month-old female Sprague Dawley rats were randomly divided into dexamethasone
(DEX) group and normal saline control group. Rats in both groups were subjected
to 3.0T magnetic resonance imaging scanning included Mensa, T2WI, and DT-MRI sequences.
Observe the changes in muscle fibers and extracellular matrix of the erector
spinal muscle using hematoxylin eosin and Sirius red staining. The expressions
of chollagen I, III and fibronectin in erector spinae were detected by western
blot. Pearson correlation analysis was used to evaluate the correlation
strength between MRI quantitative parameters and corresponding histopathology
markers.
Results: The cross-sectional
area and fractional anisotropy values of erector spinae in DEX group rats were
significantly decreased compared with those in the control group (p < 0.05). Hematoxylin eosin staining showed atrophy and
disordered arrangement of muscle fibers in the DEX group; Sirius red staining
showed a significant increase in collagen volume fraction in the DEX group. The
results of western blot showed that the expression of collagen I, collagen III,
and fibronectin was significantly increased in the dexamethasone group (p < 0.001 for all). The correlation
coefficients between fractional anisotropy values and collagen volume fraction,
collagen I, collagen III, fibronectin were -0.71, -0.94, -0.85, -0.88,
respectively (p < 0.05 for
all).
Discussion:In our study, compared with the
control group, the CSA value of the erector spinalis muscle in the DEX group
rats was significantly reduced, while the CSA value of the multifidus muscle
did not show significant changes. From the perspective of muscle fiber types,
this is because the erector spinalis muscle is mainly composed of type II
muscle fibers, while the multifidus muscle is mainly composed of type I muscle
fibers[1]. In our results, the skeletal muscles of dexamethasone
group rats showed an increase in interstitial fibrous connective tissue, with
significant increases in Collagen I and Collagen III contents. Mahdy et al.'s
research suggests that the accumulation of fibrous tissue increases the
stiffness of skeletal muscles, limits their extension and contraction, and
reduces the body's motor ability[2].
Conclusion: The fractional anisotropy value strongly correlates
with pathological collagen volume fraction, collagen I, collagen III, and fibronectin, indicating that DT-MRI can non-invasive
evaluate the changes of extracellular matrix remodeling in the erector spinal
muscle of sarcopenia, providing a potential imaging biomarker for diagnosis of
sarcopenia.Acknowledgements
Not ApplicableReferences
[1] AGTEN A, STEVENS S, VERBRUGGHE
J, et al. The lumbar multifidus is characterised by larger type I muscle fibres
compared to the erector spinae [J]. Anatomy & cell biology, 2020, 53(2):
143-50.
[2] MAHDY M A A. Skeletal muscle
fibrosis: an overview [J]. Cell and tissue research, 2019, 375(3): 575-88.