» Articles » PMID: 37185735

Effects of Whole-Body Vibration and Manually Assisted Locomotor Therapy on Neurotrophin-3 Expression and Microglia/Macrophage Mobilization Following Thoracic Spinal Cord Injury in Rats

Overview
Publisher MDPI
Specialty Molecular Biology
Date 2023 May 15
PMID 37185735
Authors
Affiliations
Soon will be listed here.
Abstract

Microglial cells play an important role in neuroinflammation and secondary damages after spinal cord injury (SCI). Progressive microglia/macrophage inflammation along the entire spinal axis follows SCI, and various factors may determine the microglial activation profile. Neurotrophin-3 (NT-3) is known to control the survival of neurons, the function of synapses, and the release of neurotransmitters, while also stimulating axon plasticity and growth. We examined the effects of whole-body vibration (WBV) and forms of assisted locomotor therapy, such as passive flexion-extension (PFE) therapy, at the neuronal level after SCI, with a focus on changes in NT-3 expression and on microglia/macrophage reaction, as they play a major role in the reconstitution of CNS integrity after injury and they may critically account for the observed structural and functional benefits of physical therapy. More specifically, the WBV therapy resulted in the best overall functional recovery when initiated at day 14, while inducing a decrease in Iba1 and the highest increase in NT-3. Therefore, the WBV therapy at the 14th day appeared to be superior to the PFE therapy in terms of recovery. Functional deficits and subsequent rehabilitation depend heavily upon the inflammatory processes occurring caudally to the injury site; thus, we propose that increased expression of NT-3, especially in the dorsal horn, could potentially be the mediator of this favorable outcome.

Citing Articles

The effects of whole-body vibration therapy on immune and brain functioning: current insights in the underlying cellular and molecular mechanisms.

Ahuja G, Arenales Arauz Y, van Heuvelen M, Kortholt A, Oroszi T, van der Zee E Front Neurol. 2024; 15:1422152.

PMID: 39144715 PMC: 11323691. DOI: 10.3389/fneur.2024.1422152.

References
1.
Elliott Donaghue I, Tator C, Shoichet M . Sustained delivery of bioactive neurotrophin-3 to the injured spinal cord. Biomater Sci. 2015; 3(1):65-72. DOI: 10.1039/c4bm00311j. View

2.
Zhou Y, Li N, Zhu L, Lin Y, Cheng H . The microglial activation profile and associated factors after experimental spinal cord injury in rats. Neuropsychiatr Dis Treat. 2018; 14:2401-2413. PMC: 6157579. DOI: 10.2147/NDT.S169940. View

3.
Mautes A, Weinzierl M, Donovan F, Noble L . Vascular events after spinal cord injury: contribution to secondary pathogenesis. Phys Ther. 2000; 80(7):673-87. View

4.
Chadi G, Andrade M, Leme R, Gomide V . Experimental models of partial lesion of rat spinal cord to investigate neurodegeneration, glial activation, and behavior impairments. Int J Neurosci. 2002; 111(3-4):137-65. DOI: 10.3109/00207450108994227. View

5.
Bove M, Nardone A, Schieppati M . Effects of leg muscle tendon vibration on group Ia and group II reflex responses to stance perturbation in humans. J Physiol. 2003; 550(Pt 2):617-30. PMC: 2343054. DOI: 10.1113/jphysiol.2003.043331. View