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6,6′-Bieckol Isolated from Ecklonia cava Protects Oxidative Stress Through Inhibiting Expression of ROS and Proinflammatory Enzymes in High-Glucose-Induced Human Umbilical Vein Endothelial Cells

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Abstract

Hyperglycemia-induced oxidative stress accelerates endothelial cell dysfunctions, which cause various complications of diabetes. The protective effects of 6,6′-bieckol (BEK), one of phlorotannin compound purified from Ecklonia cava against high-glucose-induced oxidative stress was investigated using human umbilical vein endothelial cells (HUVECs), which is susceptible to oxidative stress. High glucose (30 mM) treatment induced HUVECs’ cell death, but BEK, at concentration 10 or 50 μg/ml, significantly inhibited the high-glucose-induced cytotoxicity. Furthermore, treatment with BEK dose-dependently decreased thiobarbituric acid reactive substances (TBARS), intracellular reactive oxygen species (ROS) generation, and nitric oxide level increased by high glucose. In addition, high glucose levels induced the overexpressions of inducible nitric oxide synthase (iNOS), cyclooxygenase-2 (COX-2), and nuclear factor-kappa B (NF-κB) proteins in HUVECs, but BEK treatment reduced the overexpressions of these proteins. These findings indicate that BEK is a potential therapeutic agent that will prevent diabetic endothelial dysfunction and related complications.

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References

  1. Zimmet, P., Alberti, K., & Shaw, J. (2001). Nature, 414, 782–787.

    Article  CAS  Google Scholar 

  2. Baron, A. D. (1998). Diabetes Reserch and Clinical Practice, 40, S51–S55.

    Article  CAS  Google Scholar 

  3. Van Dam, P. S., Van Asbeck, B. S., Van Oirschot, J. F., Biessels, G. J., Hamers, F. P., & Marx, J. J. (2001). European Journal of Clinical Investigation, 31, 417–424.

    Article  Google Scholar 

  4. Feldman, E. F. (2003). Journal of Clinical Investigation, 111, 431–433.

    Article  CAS  Google Scholar 

  5. Hiramatsu, K., & Arimori, S. (1998). Diabetes, 37, 832–837.

    Article  Google Scholar 

  6. Dewanjee, S., Das, A. K., Sahu, R., & Gangopadhyay, M. (2009). Food and Chemical Toxicology, 47, 2679–2685.

    Article  CAS  Google Scholar 

  7. Morigi, M., Angioletti, S., Imberti, B., Donatelli, R., Micheletti, G., Figliuzzi, M., et al. (1998). Journal of Clinical Investigation, 101, 1905–1915.

    Article  CAS  Google Scholar 

  8. Yokozawa, T., Kim, Y. A., Kim, H. Y., Lee, Y. A., & Nonaka, G. (2007). Food and Chemical Toxicology, 45, 1979–1987.

    Article  CAS  Google Scholar 

  9. Lee, S. H., Han, J. S., Heo, S. J., Hwang, J. Y., & Jeon, Y. J. (2010). Toxicology In Vitro, 24, 375–381.

    Article  CAS  Google Scholar 

  10. Ahn, G. N., Kim, K. N., Cha, S. H., Song, C. B., Lee, J. H., Heo, M. S., et al. (2007). European Food Research and Technology, 226, 71–79.

    Article  CAS  Google Scholar 

  11. Le, Q. T., Li, Y., Qian, Z. J., Kim, M. M., & Kim, S. K. (2008). Process Biochemistry, 44, 168–176.

    Article  Google Scholar 

  12. Ahn, M. J., Yoon, K. D., Min, S. Y., Lee, J. S., Kim, J. H., Kim, T. G., et al. (2004). Biological & Pharmaceutical Bulletin, 27, 544–547.

    Article  CAS  Google Scholar 

  13. Lee, S. H., Park, M. H., Heo, S. J., Kang, S. M., KO, S. C., Han, J. S., et al. (2010). Food and Chemical Toxicology, 48, 2633–2637.

    Article  CAS  Google Scholar 

  14. Kang, S. M., Heo, S. J., Kim, K. N., Lee, S. H., & Jeon, Y. J. (2012). Journal of Functional Foods, 4, 158–166.

    Article  CAS  Google Scholar 

  15. Kang, S. M., Lee, S. H., Heo, S. J., Kim, K. N., & Jeon, Y. J. (2011). Nutrition Research Practice, 5, 495–502.

    Article  CAS  Google Scholar 

  16. Fautz, R., Husen, B., & Hechenberger, C. (1991). Mutation Research, 253, 173–179.

    Article  CAS  Google Scholar 

  17. Wang, H., & Joseph, J. A. (1999). Free Radical Biology and Medicine, 27, 612–616.

    Article  CAS  Google Scholar 

  18. Fraga, C. G., Leibovita, R. M., & Roeder, R. G. (1988). Free Radical Biology and Medicine, 4, 155–161.

    Article  CAS  Google Scholar 

  19. Nath, J., & Powledge, A. (1997). Journal of Leukocyte Biology, 62, 805–816.

    CAS  Google Scholar 

  20. Yamabe, N., Kang, K. S., Goto, E., Tanaka, T., & Yokozawa, T. (2007). Biological & Pharmaceutical Bulletin, 30, 520–526.

    Article  CAS  Google Scholar 

  21. Uemura, S., Matsushita, H., Li, W., Glassford, A. J., Asagami, T., Lee, K. H., et al. (2001). Circulation Research, 88, 1291–1298.

    Article  CAS  Google Scholar 

  22. Finkel, T. N., & Holbrook, J. (2000). Nature, 408, 239–247.

    Article  CAS  Google Scholar 

  23. Lee, Y. J., Kang, D. G., Kim, J. S., & Lee, H. S. (2008). Vascular Pharmacology, 48, 38–46.

    Article  CAS  Google Scholar 

  24. Sevanian, A., & Hochstein, P. (1985). Annual Review of Nutrition, 5, 365–390.

    Article  CAS  Google Scholar 

  25. Bucula, R. (1991). Journal of Clinical Investigation, 87, 432–438.

    Article  Google Scholar 

  26. Schmidtmann, S., Muller, M., von Baehr, R., & Precht, K. (1991). Nephrology, Dialysis, Transplantation, 6, 71–74.

    Google Scholar 

  27. Seghrouchni, I., Drai, J., Bannier, E., Riviere, J., Calmard, P., Garcia, I., et al. (2002). Clinica Chimica Acta, 321, 89–96.

    Article  CAS  Google Scholar 

  28. Radi, R., Beckman, J. S., Bush, K. M., & Freeman, B. A. (1991). Archives of Biochemistry and Biophysics, 288, 481–487.

    Article  CAS  Google Scholar 

  29. Moncada, S., Palmer, R. M., & Higgs, E. A. (1991). Pharmacological Reviews, 43, 109–142.

    CAS  Google Scholar 

  30. Beckman, J. S., Beckman, T. W., Chen, J., Marshall, P. A., & Freeman, B. A. (1990). Proceedings of the National Academy Sciences of the United States of America, 87, 1620–1624.

    Article  CAS  Google Scholar 

  31. Spencer, N. F., Poynter, M. E., Im, S. Y., & Daynes, R. A. (1997). International Immunology, 9, 1581–1588.

    Article  CAS  Google Scholar 

  32. Wu, K. K. (1995). Advances in Pharmacology, 33, 179–190.

    Article  CAS  Google Scholar 

  33. Baeuerle, P. A., & Baltimore, D. (1996). Cell, 87, 13–20.

    Article  CAS  Google Scholar 

  34. Han, M., Wen, J. K., Zheng, B., & Zhang, D. Q. (2004). Life Sciences, 75, 675–684.

    Article  CAS  Google Scholar 

  35. Du, X., Stocklauser-Farber, K., & Rosen, P. (1999). Free Radical Biology and Medicine, 27, 752–763.

    Article  CAS  Google Scholar 

  36. Hattori, Y., Hattori, S., Sato, N., & Kasai, K. (2000). Cardiovascular Research, 46, 188–197.

    Article  CAS  Google Scholar 

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Acknowledgments

This research was also supported by the research programs of the Korea Institute of Ocean Science and Technology (PE99214). This research was supported by a grant from Marine Biotechnology Program Funded by Ministry of Oceans and Fisheries, Korea (PM 57770).

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Correspondence to Seung-Hong Lee.

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Mi-Hwa Park and Soo-Jin Heo contributed equally to this work.

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Park, MH., Heo, SJ., Park, PJ. et al. 6,6′-Bieckol Isolated from Ecklonia cava Protects Oxidative Stress Through Inhibiting Expression of ROS and Proinflammatory Enzymes in High-Glucose-Induced Human Umbilical Vein Endothelial Cells. Appl Biochem Biotechnol 174, 632–643 (2014). https://doi.org/10.1007/s12010-014-1099-4

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