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Article

Anti‑inflammatory effect of delphinidin on intramedullary spinal pressure in a spinal cord injury rat model

  • Authors:
    • Cheng‑Hu Wang
    • Lin‑Lin Zhu
    • Ke‑Feng Ju
    • Jin‑Long Liu
    • Kun‑Peng Li
  • View Affiliations / Copyright

    Affiliations: Department of Orthopedics, Liaocheng People's Hospital, Liaocheng Clinical School of Taishan Medical University, Liaocheng, Shandong 252000, P.R. China, Department of Orthopedics, Weifang Cancer Hospital The Affiliated Hospital of Weifang Medical University, Weifang, Shandong 261000, P.R. China
  • Pages: 5583-5588
    |
    Published online on: September 27, 2017
       https://doi.org/10.3892/etm.2017.5206
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Abstract

Delphinidin, a flavonoid polyphenolic compound, is widely found in nature and is used as a food supplement due to its pharmacological activity. The aims of the present study were to examine the anti‑inflammatory effect of delphinidin in alleviating spinal cord injury (SCI)‑induced inflammation in a rat model and to determine the underlying mechanisms in SCI. The Basso, Beattie, Bresnahan (BBB) scores of rats were assessed to evaluate the effect of delphinidin on the recovery of motor function. ELISA kits were also used to analyze the activities of tumor necrosis factor‑α (TNF‑α), interleukin (IL)‑6, cyclooxygenase‑2 (COX‑2), prostaglandin E2 (PGE2) and caspase‑3. In addition, the protein expression levels of nuclear factor (NF)‑κB, activator protein 1 (AP‑1) and p38‑MAPK protein expression were measured using western blot analysis. Treatment with delphinidin significantly increased the BBB scores, as well as inhibited the intramedullary spinal pressure in SCI rats. Delphinidin treatment also significantly suppressed the levels of inflammatory factors and NF‑κB protein expression in SCI rats. Finally, treatment with delphinidin significantly inhibited NF‑κB stimulation, COX‑2 activity, PGE2 production, and AP‑1 and p38‑MAPK protein expression in SCI rats. These results suggest that the anti‑inflammatory effect of delphinidin alleviated inflammation in the SCI rat model via alleviation of the intramedullary spinal pressure through the NF‑κB and p38‑MAPK signaling pathways.
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Copy and paste a formatted citation
Spandidos Publications style
Wang CH, Zhu LL, Ju KF, Liu JL and Li KP: Anti‑inflammatory effect of delphinidin on intramedullary spinal pressure in a spinal cord injury rat model. Exp Ther Med 14: 5583-5588, 2017.
APA
Wang, C., Zhu, L., Ju, K., Liu, J., & Li, K. (2017). Anti‑inflammatory effect of delphinidin on intramedullary spinal pressure in a spinal cord injury rat model. Experimental and Therapeutic Medicine, 14, 5583-5588. https://doi.org/10.3892/etm.2017.5206
MLA
Wang, C., Zhu, L., Ju, K., Liu, J., Li, K."Anti‑inflammatory effect of delphinidin on intramedullary spinal pressure in a spinal cord injury rat model". Experimental and Therapeutic Medicine 14.6 (2017): 5583-5588.
Chicago
Wang, C., Zhu, L., Ju, K., Liu, J., Li, K."Anti‑inflammatory effect of delphinidin on intramedullary spinal pressure in a spinal cord injury rat model". Experimental and Therapeutic Medicine 14, no. 6 (2017): 5583-5588. https://doi.org/10.3892/etm.2017.5206
Copy and paste a formatted citation
x
Spandidos Publications style
Wang CH, Zhu LL, Ju KF, Liu JL and Li KP: Anti‑inflammatory effect of delphinidin on intramedullary spinal pressure in a spinal cord injury rat model. Exp Ther Med 14: 5583-5588, 2017.
APA
Wang, C., Zhu, L., Ju, K., Liu, J., & Li, K. (2017). Anti‑inflammatory effect of delphinidin on intramedullary spinal pressure in a spinal cord injury rat model. Experimental and Therapeutic Medicine, 14, 5583-5588. https://doi.org/10.3892/etm.2017.5206
MLA
Wang, C., Zhu, L., Ju, K., Liu, J., Li, K."Anti‑inflammatory effect of delphinidin on intramedullary spinal pressure in a spinal cord injury rat model". Experimental and Therapeutic Medicine 14.6 (2017): 5583-5588.
Chicago
Wang, C., Zhu, L., Ju, K., Liu, J., Li, K."Anti‑inflammatory effect of delphinidin on intramedullary spinal pressure in a spinal cord injury rat model". Experimental and Therapeutic Medicine 14, no. 6 (2017): 5583-5588. https://doi.org/10.3892/etm.2017.5206
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