The Impact of Treadmill Training on Tissue Integrity, Axon Growth, and Astrocyte Modulation

Spinal cord injury (SCI) presents a complex challenge in neurorehabilitation, demanding innovative therapeutic strategies to facilitate functional recovery. This study investigates the effects of treadmill training on SCI recovery, emphasizing motor function enhancement, neural tissue preservation,...

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Published in:International journal of molecular sciences Vol. 25; no. 7; p. 3772
Main Authors: Ageeva, Tatyana, Sabirov, Davran, Sufianov, Albert, Davletshin, Eldar, Plotnikova, Elizaveta, Shigapova, Rezeda, Sufianova, Galina, Timofeeva, Anna, Chelyshev, Yuri, Rizvanov, Albert, Mukhamedshina, Yana
Format: Journal Article
Language:English
Published: Switzerland MDPI AG 01-04-2024
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Summary:Spinal cord injury (SCI) presents a complex challenge in neurorehabilitation, demanding innovative therapeutic strategies to facilitate functional recovery. This study investigates the effects of treadmill training on SCI recovery, emphasizing motor function enhancement, neural tissue preservation, and axonal growth. Our research, conducted on a rat model, demonstrates that controlled treadmill exercises significantly improve motor functions post-SCI, as evidenced by improved scores on the Basso, Beattie, and Bresnahan (BBB) locomotor rating scale and enhanced electromyography readings. Notably, the training facilitates the preservation of spinal cord tissue, effectively reducing secondary damage and promoting the maintenance of neural fibers in the injured area. A key finding is the significant stimulation of axonal growth around the injury epicenter in trained rats, marked by increased growth-associated protein 43 (GAP43) expression. Despite these advancements, the study notes a limited impact of treadmill training on motoneuron adaptation and highlights minimal changes in the astrocyte and neuron-glial antigen 2 (NG2) response. This suggests that, while treadmill training is instrumental in functional improvements post-SCI, its influence on certain neural cell types and glial populations is constrained.
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ISSN:1422-0067
1661-6596
1422-0067
DOI:10.3390/ijms25073772