Journal
NEUROPEPTIDES
Volume 92, Issue -, Pages -Publisher
CHURCHILL LIVINGSTONE
DOI: 10.1016/j.npep.2022.102228
Keywords
Spinal cord injury; Ac-SDKP; Contusion; Inflammation; In vivo; Treatment
Categories
Funding
- Brain and Spinal Cord Injury Research Centre, Neuroscience Institute, TUMS [3880]
Ask authors/readers for more resources
Damage to the spinal cord leads to inflammation and motor impairments. Inhibiting pro-inflammatory cells and activating anti-inflammatory cells may provide a potential treatment strategy. Ac-SDKP has protective effects, improving motor recovery, rescuing motor neurons, reducing inflammatory cytokine levels, and increasing anti-inflammatory gene expression.
Damage to the spinal cord triggers a local complex inflammatory reaction that results in irreversible impairments or complete loss of motor function. The evidence suggested that inhibiting the pro-inflammatory macrophage/ microglia (M1 subsets) and stimulating the anti-inflammatory macrophage/microglia (M2 subsets) are potential strategies for the treatment of neuroinflammation-related diseases. We evaluated the potentially protective effect of Ac-SDKP as an endogenous tetrapeptide on rat spinal cord injury (SCI). Wistar rats were subjected to a weight drop contusion model and were treated with Ac-SDKP (0.8 mg/kg) given subcutaneously once a day for 7 days starting at two clinically relevant times, at 2 h or 6 h post-injury. The effect of Ac-SDKP was assessed by motor functional analysis, real-time PCR (CD86 and CD206 mRNA), western blot (caspase-3), ELISA (TNF-a, IL-10), and histological analysis (toluidine blue staining). Ac-SDKP improved locomotor recovery and rescue motor neuron loss after SCI. Moreover, a decreased in TNF-a level as well as caspase 3 protein levels occurred in the lesion epicenter of the spinal cord following treatment. In addition, CD206 mRNA expression level increased significantly in Ac-SDKP treated rats compared with SCI. Together these data suggest that Ac-SDKP might be a novel immunomodulatory drug. It may be beneficial for the treatment of SCI with regards to increasing CD206 gene expression and suppress inflammatory cytokine to improve motor function and reducing histopathological lesion.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available