Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2023 Feb 28:11:tkac054.
doi: 10.1093/burnst/tkac054. eCollection 2023.

Role of inflammation in neurological damage and regeneration following spinal cord injury and its therapeutic implications

Affiliations
Review

Role of inflammation in neurological damage and regeneration following spinal cord injury and its therapeutic implications

Yan Jin et al. Burns Trauma. .

Abstract

Spinal cord injury (SCI) is an incurable trauma that frequently results in partial or complete loss of motor and sensory function. Massive neurons are damaged after the initial mechanical insult. Secondary injuries, which are triggered by immunological and inflammatory responses, also result in neuronal loss and axon retraction. This results in defects in the neural circuit and a deficiency in the processing of information. Although inflammatory responses are necessary for spinal cord recovery, conflicting evidence of their contributions to specific biological processes have made it difficult to define the specific role of inflammation in SCI. This review summarizes our understanding of the complex role of inflammation in neural circuit events following SCI, such as cell death, axon regeneration and neural remodeling. We also review the drugs that regulate immune responses and inflammation in the treatment of SCI and discuss the roles of these drugs in the modulation of neural circuits. Finally, we provide evidence about the critical role of inflammation in facilitating spinal cord neural circuit regeneration in zebrafish, an animal model with robust regenerative capacity, to provide insights into the regeneration of the mammalian central nervous system.

Keywords: Axon regeneration; Cell death; Immune response; Inflammation; Inflammatory drugs; Neurological damage; Spinal cord injury; Trauma; Zebrafish.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Cellular events following SCI over time. Damage and cellular events, as well as immune cell activation, are revealed. Primary injury triggers a pathophysiological cascade, including the secondary injury stage. Secondary injury begins as early as a few minutes after the initial trauma and is divided into three stages: acute, subacute and chronic injury. The changes of various cells (neutrophils, microglia, monocytes/macrophages, lymphocytes and NK cells) in the process of SCI are marked. This Figure is modified from [11,99] with permission. SCI spinal cord injury, NK cells natural killer cells

References

    1. Bracken MB, Shepard MJ, Collins WF, Holford TR, Young W, Baskin DS, et al. A randomized, controlled trial of methylprednisolone or naloxone in the treatment of acute spinal-cord injury. Results of the second national acute spinal cord injury study. N Engl J Med. 1990;322:1405–11. - PubMed
    1. Afshary K, Chamanara M, Talari B, Rezaei P, Nassireslami E. Therapeutic effects of minocycline pretreatment in the locomotor and sensory complications of spinal cord injury in an animal model. J Mol Neurosci. 2020;70:1064–72. - PubMed
    1. Stirling DP, Cummins K, Mishra M, Teo W, Yong VW, Stys P. Toll-like receptor 2-mediated alternative activation of microglia is protective after spinal cord injury. Brain. 2014;137:707–23. - PubMed
    1. El-Daher F, Becker CG. Neural circuit reorganisation after spinal cord injury in zebrafish. Curr Opin Genet Dev. 2020;64:44–51. - PubMed
    1. Ahuja CS, Wilson JR, Nori S, Kotter MRN, Druschel C, Curt A, et al. Traumatic spinal cord injury. Nat Rev Dis Primers. 2017;3:17018. - PubMed