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Involvement of NADPH oxidase in high-dose phenolic acid-induced pro-oxidant activity on rat mesenteric venules

  • Authors:
    • Wen-Yuan Du
    • Ying Xiao
    • Jian-Jing Yao
    • Zhe Hao
    • Yu-Bin Zhao
  • View Affiliations / Copyright

    Affiliations: Medical and Electronic Experimental Center, The Traditional Chinese Medicine Hospital of Shijiazhuang Affiliated to Hebei University of Chinese Medicine, Shijiazhuang, Hebei 050051, P.R. China, School of Chemical Engineering, Shijiazhuang University, Shijiazhuang, Hebei 050035, P.R. China, The Third Hospital of Shijiazhuang, Shijiazhuang, Hebei 050011, P.R. China
    Copyright: © Du et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
  • Pages: 17-22
    |
    Published online on: November 22, 2016
       https://doi.org/10.3892/etm.2016.3923
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Abstract

In the present study, we investigated the potential role of phenolic acids in initiating oxidative damage to microvascular endothelial cells and the underlying mechanism mediating the pro-oxidant action. Male Wistar rats received high doses of phenolic acid [caffeic acid (CA), salvianolic acid B (SAB), chlorogenic acid (ChA) or ferulic acid (FA)]. The creation of reactive oxygen species in mesenteric microcirculation endothelial cells and adherent leukocytes along with venules were assessed using intravital microscopy. The expression levels of NADPH oxidase subunits (Nox4 and p22phox) in terminal ileum tissues were determined by western blot analysis. Intravenous injection of high-dose ChA or CA (7 mg/kg) markedly increased the peroxide production in the venular walls and upregulated the protein expression levels of Nox4 and p22phox in the ileum tissues, while the same dose of CA and SAB made no difference within the observation period. No changes were observed in the number of leukocytes adhering to the venular walls. High-dose ChA and FA led to an imbalance between the oxidant and antioxidant mechanism by boosting the expression levels of NADPH oxidase. Thus, we clarified the rationale behind the adverse effects of a herbal injection containing high levels of phenolic acid compounds.
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Copy and paste a formatted citation
Spandidos Publications style
Du W, Xiao Y, Yao J, Hao Z and Zhao Y: Involvement of NADPH oxidase in high-dose phenolic acid-induced pro-oxidant activity on rat mesenteric venules. Exp Ther Med 13: 17-22, 2017.
APA
Du, W., Xiao, Y., Yao, J., Hao, Z., & Zhao, Y. (2017). Involvement of NADPH oxidase in high-dose phenolic acid-induced pro-oxidant activity on rat mesenteric venules. Experimental and Therapeutic Medicine, 13, 17-22. https://doi.org/10.3892/etm.2016.3923
MLA
Du, W., Xiao, Y., Yao, J., Hao, Z., Zhao, Y."Involvement of NADPH oxidase in high-dose phenolic acid-induced pro-oxidant activity on rat mesenteric venules". Experimental and Therapeutic Medicine 13.1 (2017): 17-22.
Chicago
Du, W., Xiao, Y., Yao, J., Hao, Z., Zhao, Y."Involvement of NADPH oxidase in high-dose phenolic acid-induced pro-oxidant activity on rat mesenteric venules". Experimental and Therapeutic Medicine 13, no. 1 (2017): 17-22. https://doi.org/10.3892/etm.2016.3923
Copy and paste a formatted citation
x
Spandidos Publications style
Du W, Xiao Y, Yao J, Hao Z and Zhao Y: Involvement of NADPH oxidase in high-dose phenolic acid-induced pro-oxidant activity on rat mesenteric venules. Exp Ther Med 13: 17-22, 2017.
APA
Du, W., Xiao, Y., Yao, J., Hao, Z., & Zhao, Y. (2017). Involvement of NADPH oxidase in high-dose phenolic acid-induced pro-oxidant activity on rat mesenteric venules. Experimental and Therapeutic Medicine, 13, 17-22. https://doi.org/10.3892/etm.2016.3923
MLA
Du, W., Xiao, Y., Yao, J., Hao, Z., Zhao, Y."Involvement of NADPH oxidase in high-dose phenolic acid-induced pro-oxidant activity on rat mesenteric venules". Experimental and Therapeutic Medicine 13.1 (2017): 17-22.
Chicago
Du, W., Xiao, Y., Yao, J., Hao, Z., Zhao, Y."Involvement of NADPH oxidase in high-dose phenolic acid-induced pro-oxidant activity on rat mesenteric venules". Experimental and Therapeutic Medicine 13, no. 1 (2017): 17-22. https://doi.org/10.3892/etm.2016.3923
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