Targeted multifidus muscle activation reduces fibrosis of multifidus muscle following intervertebral disc injury
European Spine Journal, ISSN: 1432-0932, Vol: 33, Issue: 6, Page: 2166-2178
2024
- 4Citations
- 10Captures
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Article Description
Purpose: Aerobic exercise produces beneficial outcomes in patients with low back pain and partially attenuates the fibrotic changes to the multifidus in a model of intervertebral disc (IVD) degeneration. More targeted exercise might be required to fully attenuate these fibrotic alterations. This study aimed to investigate whether activation of the multifidus induced by neurostimulation could reduce fibrosis of the multifidus in a model of IVD degeneration in sheep. Methods: IVD degeneration was induced in 18 merino sheep via a partial thickness unilateral annulus fibrosus lesion to the L1/2 and L3/4 IVDs. All sheep received an implantable neurostimulation device that provides stimulation of the L2 medial branch of the dorsal ramus. Three months after surgery, the animals were assigned to Injury or Activated groups. Activated animals received neurostimulation and the Injury group received no stimulation. Six months after surgery, the multifidus was harvested at L2 and L4. Van Gieson’s, Sirius Red and immunofluorescence staining for Collagen-I and -III and quantitative PCR was used to examine fibrosis. Muscle harvested from a previous study without IVD injury was used as a control. Results: Neurostimulation of the multifidus attenuated IVD degeneration dependent increases in the connective tissue, including Collagen-I but not Collagen-III, compared to the Injury group at L4. No measures of the multifidus muscle at L2, which received no stimulation, differed between the Injury and Activated groups. Conclusions: These data reveal that targeted activation of the multifidus muscle attenuates IVD degeneration dependent fibrotic alterations to the multifidus.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85190116862&origin=inward; http://dx.doi.org/10.1007/s00586-024-08234-5; http://www.ncbi.nlm.nih.gov/pubmed/38607406; https://link.springer.com/10.1007/s00586-024-08234-5; https://dx.doi.org/10.1007/s00586-024-08234-5; https://link.springer.com/article/10.1007/s00586-024-08234-5
Springer Science and Business Media LLC
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