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Article

Neuroprotective effects of vitexin against isoflurane-induced neurotoxicity by targeting the TRPV1 and NR2B signaling pathways

  • Authors:
    • Linlin Chen
    • Bin Zhang
    • Shiqiang Shan
    • Xin Zhao
  • View Affiliations / Copyright

    Affiliations: Department of Anesthesiology, The Cangzhou Central Hospital, Cangzhou, Hebei 061000, P.R. China
  • Pages: 5607-5613
    |
    Published online on: November 16, 2016
       https://doi.org/10.3892/mmr.2016.5948
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Abstract

Vitexin is a bioactive compound extracted from hawthorn leaves, which reduces blood pressure and has anti‑inflammatory and potential anticancer effects. However, the mechanisms underlying the protective effects of vitexin against isoflurane‑induced neurotoxicity remain elusive. Therefore, the aim of the present study was to investigate these mechanisms further. Sprague Dawley rats received 1.4% isoflurane in a 100% oxygen environment for 2 h. Human PC12 pheochromocytoma neurosecretory cells were exposed to 2% isoflurane for 12 h before they were treated with 1, 10 or 100 µM vitexin for a further 24 h. Vitexin inhibited the isoflurane-induced cell cytotoxicity and weakened isoflurane-induced neuroinflammation and oxidative stress pathways in PC12 cells. In addition, treatment with vitexin suppressed isoflurane‑induced caspase‑3 activation and increased β-secretase 1 levels in PC12 cells. Furthermore, vitexin treatment decreased the levels of isoflurane‑induced cytosolic calcium and reactive oxygen species, and downregulated the expression of transient receptor potential cation channel subfamily V member 1 (TRPV1) and glutamate ionotropic receptor NMDA type subunit 2B (NR2B) protein expression in isoflurane-treated PC12 cells. These results suggest that vitexin mediates its protective effects against isoflurane-induced neurotoxicity by targeting the TRPV1 and NR2B signaling pathways.
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Copy and paste a formatted citation
Spandidos Publications style
Chen L, Zhang B, Shan S and Zhao X: Neuroprotective effects of vitexin against isoflurane-induced neurotoxicity by targeting the TRPV1 and NR2B signaling pathways. Mol Med Rep 14: 5607-5613, 2016.
APA
Chen, L., Zhang, B., Shan, S., & Zhao, X. (2016). Neuroprotective effects of vitexin against isoflurane-induced neurotoxicity by targeting the TRPV1 and NR2B signaling pathways. Molecular Medicine Reports, 14, 5607-5613. https://doi.org/10.3892/mmr.2016.5948
MLA
Chen, L., Zhang, B., Shan, S., Zhao, X."Neuroprotective effects of vitexin against isoflurane-induced neurotoxicity by targeting the TRPV1 and NR2B signaling pathways". Molecular Medicine Reports 14.6 (2016): 5607-5613.
Chicago
Chen, L., Zhang, B., Shan, S., Zhao, X."Neuroprotective effects of vitexin against isoflurane-induced neurotoxicity by targeting the TRPV1 and NR2B signaling pathways". Molecular Medicine Reports 14, no. 6 (2016): 5607-5613. https://doi.org/10.3892/mmr.2016.5948
Copy and paste a formatted citation
x
Spandidos Publications style
Chen L, Zhang B, Shan S and Zhao X: Neuroprotective effects of vitexin against isoflurane-induced neurotoxicity by targeting the TRPV1 and NR2B signaling pathways. Mol Med Rep 14: 5607-5613, 2016.
APA
Chen, L., Zhang, B., Shan, S., & Zhao, X. (2016). Neuroprotective effects of vitexin against isoflurane-induced neurotoxicity by targeting the TRPV1 and NR2B signaling pathways. Molecular Medicine Reports, 14, 5607-5613. https://doi.org/10.3892/mmr.2016.5948
MLA
Chen, L., Zhang, B., Shan, S., Zhao, X."Neuroprotective effects of vitexin against isoflurane-induced neurotoxicity by targeting the TRPV1 and NR2B signaling pathways". Molecular Medicine Reports 14.6 (2016): 5607-5613.
Chicago
Chen, L., Zhang, B., Shan, S., Zhao, X."Neuroprotective effects of vitexin against isoflurane-induced neurotoxicity by targeting the TRPV1 and NR2B signaling pathways". Molecular Medicine Reports 14, no. 6 (2016): 5607-5613. https://doi.org/10.3892/mmr.2016.5948
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