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Article

Myricitrin decreases traumatic injury of the spinal cord and exhibits antioxidant and anti‑inflammatory activities in a rat model via inhibition of COX‑2, TGF‑β1, p53 and elevation of Bcl‑2/Bax signaling pathway

  • Authors:
    • Yang Lei
  • View Affiliations / Copyright

    Affiliations: The Third Department of Orthopedics, Cangzhou Central Hospital, Cangzhou, Hebei 061000, P.R. China
  • Pages: 7699-7705
    |
    Published online on: September 21, 2017
       https://doi.org/10.3892/mmr.2017.7567
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Abstract

Myricitrin has multiple effects, including antagonism of platelet activating factor, regulation of blood sugar levels, oxidation resistance, protection of the liver and the relieving of ethylism. The present study evaluated how myricitrin weakens traumatic injury of the spinal cord (TISC), and exhibits antioxidant and anti‑inflammatory activities in a rat model. TISC model rats were injected intraperitoneally with 5, 10 or 30 mg/kg/day of myricitrin for 5 days. Basso‑Beattie‑Bresnahan evaluation of locomotion and water content of spinal cord were used to analyze the effects of myricitrin on TISC. Myricitrin significantly inhibited the TISC‑induced oxidative stress and inflammatory reactions. In addition, cyclooxygenase‑2 (COX‑2), transforming growth factor (TGF)‑β1 and p53 were significantly reduced and Bcl‑2/Bax rate was significantly increased by treatment with myricitrin. The results of the current study suggested that the neuroprotective effect of myricitrin exhibits significant antioxidant and anti‑inflammatory activities, and a remarkable trauma protection activity in TISC rats through inhibition of COX‑2, TGF‑β1, p53 and elevation of Bcl‑2/Bax signaling pathway.
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Copy and paste a formatted citation
Spandidos Publications style
Lei Y: Myricitrin decreases traumatic injury of the spinal cord and exhibits antioxidant and anti‑inflammatory activities in a rat model via inhibition of COX‑2, TGF‑β1, p53 and elevation of Bcl‑2/Bax signaling pathway. Mol Med Rep 16: 7699-7705, 2017.
APA
Lei, Y. (2017). Myricitrin decreases traumatic injury of the spinal cord and exhibits antioxidant and anti‑inflammatory activities in a rat model via inhibition of COX‑2, TGF‑β1, p53 and elevation of Bcl‑2/Bax signaling pathway. Molecular Medicine Reports, 16, 7699-7705. https://doi.org/10.3892/mmr.2017.7567
MLA
Lei, Y."Myricitrin decreases traumatic injury of the spinal cord and exhibits antioxidant and anti‑inflammatory activities in a rat model via inhibition of COX‑2, TGF‑β1, p53 and elevation of Bcl‑2/Bax signaling pathway". Molecular Medicine Reports 16.5 (2017): 7699-7705.
Chicago
Lei, Y."Myricitrin decreases traumatic injury of the spinal cord and exhibits antioxidant and anti‑inflammatory activities in a rat model via inhibition of COX‑2, TGF‑β1, p53 and elevation of Bcl‑2/Bax signaling pathway". Molecular Medicine Reports 16, no. 5 (2017): 7699-7705. https://doi.org/10.3892/mmr.2017.7567
Copy and paste a formatted citation
x
Spandidos Publications style
Lei Y: Myricitrin decreases traumatic injury of the spinal cord and exhibits antioxidant and anti‑inflammatory activities in a rat model via inhibition of COX‑2, TGF‑β1, p53 and elevation of Bcl‑2/Bax signaling pathway. Mol Med Rep 16: 7699-7705, 2017.
APA
Lei, Y. (2017). Myricitrin decreases traumatic injury of the spinal cord and exhibits antioxidant and anti‑inflammatory activities in a rat model via inhibition of COX‑2, TGF‑β1, p53 and elevation of Bcl‑2/Bax signaling pathway. Molecular Medicine Reports, 16, 7699-7705. https://doi.org/10.3892/mmr.2017.7567
MLA
Lei, Y."Myricitrin decreases traumatic injury of the spinal cord and exhibits antioxidant and anti‑inflammatory activities in a rat model via inhibition of COX‑2, TGF‑β1, p53 and elevation of Bcl‑2/Bax signaling pathway". Molecular Medicine Reports 16.5 (2017): 7699-7705.
Chicago
Lei, Y."Myricitrin decreases traumatic injury of the spinal cord and exhibits antioxidant and anti‑inflammatory activities in a rat model via inhibition of COX‑2, TGF‑β1, p53 and elevation of Bcl‑2/Bax signaling pathway". Molecular Medicine Reports 16, no. 5 (2017): 7699-7705. https://doi.org/10.3892/mmr.2017.7567
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