» Articles » PMID: 34718779

Genomic and Epigenomic Evaluation of Electrically Induced Exercise in People With Spinal Cord Injury: Application to Precision Rehabilitation

Overview
Journal Phys Ther
Date 2021 Oct 31
PMID 34718779
Citations 7
Authors
Affiliations
Soon will be listed here.
Abstract

Objective: Physical therapists develop patient-centered exercise prescriptions to help overcome the physical, emotional, psychosocial, and environmental stressors that undermine a person's health. Optimally prescribing muscle activity for people with disability, such as a spinal cord injury, is challenging because of their loss of volitional movement control and the deterioration of their underlying skeletal systems. This report summarizes spinal cord injury-specific factors that should be considered in patient-centered, precision prescription of muscle activity for people with spinal cord injury. This report also presents a muscle genomic and epigenomic analysis to examine the regulation of the proliferator-activated receptor γ coactivator 1α (PGC-1α) (oxidative) and myostatin (hypertrophy) signaling pathways in skeletal muscle during low-frequency (lower-force) electrically induced exercise versus higher-frequency (higher-force) electrically induced exercise under constant muscle recruitment (intensity).

Methods: Seventeen people with spinal cord injury participated in 1 or more unilateral electrically induced exercise sessions using a lower-force (1-, 3-, or 5-Hz) or higher-force (20-Hz) protocol. Three hours after the exercise session, percutaneous muscle biopsies were performed on exercised and nonexercised muscles for genomic and epigenomic analysis.

Results: We found that low-frequency (low-force) electrically induced exercise significantly increased the expression of PGC-1α and decreased the expression of myostatin, consistent with the expression changes observed with high-frequency (higher-force) electrically induced exercise. Further, we found that low-frequency (lower-force) electrically induced exercise significantly demethylated, or epigenetically promoted, the PGC-1α signaling pathway. A global epigenetic analysis showed that >70 pathways were regulated with low-frequency (lower-force) electrically induced exercise.

Conclusion: These novel results support the notion that low-frequency (low-force) electrically induced exercise may offer a more precise rehabilitation strategy for people with chronic paralysis and severe osteoporosis. Future clinical trials are warranted to explore whether low-frequency (lower-force) electrically induced exercise training affects the overall health of people with chronic spinal cord injury.

Citing Articles

Rehabilomics Strategies Enabled by Cloud-Based Rehabilitation: Scoping Review.

Oh S, Lee S J Med Internet Res. 2025; 27:e54790.

PMID: 39874565 PMC: 11815311. DOI: 10.2196/54790.


Distinct Genomic Expression Signatures after Low-Force Electrically Induced Exercises in Persons with Spinal Cord Injury.

Petrie M, Suneja M, Shields R Int J Mol Sci. 2024; 25(18).

PMID: 39337673 PMC: 11432617. DOI: 10.3390/ijms251810189.


Low-frequency electrically induced exercise after spinal cord injury: Physiologic challenge to skeletal muscle and feasibility for long-term use.

Petrie M, Dudley-Javoroski S, Johnson K, Lee J, Dubey O, Shields R J Spinal Cord Med. 2024; 47(6):1026-1032.

PMID: 38619192 PMC: 11533229. DOI: 10.1080/10790268.2024.2338295.


Impaired Glucose Tolerance and Visceral Adipose Tissue Thickness among Lean and Non-Lean People with and without Spinal Cord Injury.

Kimball A, Petrie M, McCue P, Johnson K, Shields R J Funct Morphol Kinesiol. 2023; 8(3).

PMID: 37606417 PMC: 10443282. DOI: 10.3390/jfmk8030123.


Optimal neuromuscular electrical stimulation parameters after spinal cord injury.

Bickel C, Lein Jr D, Yuen H J Spinal Cord Med. 2023; 47(6):968-976.

PMID: 37428446 PMC: 11537308. DOI: 10.1080/10790268.2023.2231674.


References
1.
Song X, Kawano Y, Krook A, Ryder J, Efendic S, Roth R . Muscle fiber type-specific defects in insulin signal transduction to glucose transport in diabetic GK rats. Diabetes. 1999; 48(3):664-70. DOI: 10.2337/diabetes.48.3.664. View

2.
Johnson R, Gerhart K, McCray J, Menconi J, Whiteneck G . Secondary conditions following spinal cord injury in a population-based sample. Spinal Cord. 1998; 36(1):45-50. DOI: 10.1038/sj.sc.3100494. View

3.
Petrie M, Sharma A, Taylor E, Suneja M, Shields R . Impact of short- and long-term electrically induced muscle exercise on gene signaling pathways, gene expression, and PGC1a methylation in men with spinal cord injury. Physiol Genomics. 2019; 52(2):71-80. PMC: 7052569. DOI: 10.1152/physiolgenomics.00064.2019. View

4.
Lee M, Myers J, Hayes A, Madan S, Froelicher V, Perkash I . C-reactive protein, metabolic syndrome, and insulin resistance in individuals with spinal cord injury. J Spinal Cord Med. 2005; 28(1):20-5. DOI: 10.1080/10790268.2005.11753794. View

5.
Banerjea R, Sambamoorthi U, Weaver F, Maney M, Pogach L, Findley T . Risk of stroke, heart attack, and diabetes complications among veterans with spinal cord injury. Arch Phys Med Rehabil. 2008; 89(8):1448-53. DOI: 10.1016/j.apmr.2007.12.047. View