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The Protective Effect of Hydralazine against Hydrogen Peroxide (H2O2)-Induced Oxidative Damage in C6 Glial Cell Line

Year 2021, Volume: 2 Issue: 1, 8 - 15, 29.01.2021

Abstract

Purpose: Recent studies have shown that hydralazine has positive effects on nervous system. However, its effect on hydrogen peroxide-induced oxidative damage in glial cells is still unclear. The current experiment was designed to examine the effect of hydralazine on glial damage after hydrogen peroxide-induced oxidative damage in C6 glial cells involving proinflammatory cytokines.
Material and Methods: In this study, the C6 glioma cell line was used. Four cell groups were prepared to evaluate the effect of hydralazine on glial cell death after hydrogen peroxide-induced oxidative damage. The control group was without any treatment. Cells in the H2O2 group were treated with 0.5 mM H2O2 for 24 hours. Cells in the hydralazine group were treated with various concentrations (12.5, 25, 50, and 100 µM/mL) of hydralazine for 24 hours. Cells in the hydralazine + H2O2 group were pre-treated with various concentrations (12.5, 25 50, and 100 µM/mL) of hydralazine for 1 hour and then exposed to 0.5 mM H2O2 for 24 hours. After completing oxidative damage induction, the cell viability was evaluated XTT assay. Total antioxidant status (TAS), total oxidant status (TOS), tumor necrosis factor alpha (TNF-α), and interleukin-1 beta (IL-1 β) levels in the cells were measured by commercial kits.
Results: Hydralazine at the concentrations of 50 and 100 µM/mL significantly increased the cell viability in C6 cells after hydrogen peroxide-induced oxidative damage (p < 0.001). It also significantly decreased the levels of TOS (p < 0.001) whereas rising TAS levels (p < 0.01) after hydrogen peroxide-induced oxidative damage. Moreover, hydralazine reduced TNF-α and IL-1 β levels in C6 cells after hydrogen peroxide-induced oxidative damage (P < 0.001).
Conclusion: Hydralazine decreases glial cell death after hydrogen peroxide-induced oxidative damage in C6 cells by activating antioxidant system and inhibiting proinflammatory cytokines.

References

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  • Dringen, R., Kussmaul, L., and Hamprecht, B. (1998). Detoxification of exogenous hydrogen peroxide and organic hydroperoxides by cultured astroglial cells assessed by microtiter plate assay. Brain Research Protocols, 2(3), 223–228. https://doi.org/10.1016/S1385-299X(97)00047-0
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  • Lu, T., Aron, L., Zullo, J., Pan, Y., Kim, H., Chen, Y., … Yankner, B. A. (2014). REST and stress resistance in ageing and Alzheimer’s disease. Nature, 507(7493), 448–454. https://doi.org/10.1038/nature13163
  • Magee, L. A. (2003). Hydralazine for treatment of severe hypertension in pregnancy: meta-analysis. BMJ, 327(7421), 955–0. https://doi.org/10.1136/bmj.327.7421.955
  • Maheshwari, M., Roberts, J. K., DeSutter, B., Duong, K. T., Tingling, J., Fawver, J. N., … Murray, I. V. J. (2010). Hydralazine Modifies Aβ Fibril Formation and Prevents Modification by Lipids in Vitro. Biochemistry, 49(49), 10371–10380. https://doi.org/10.1021/bi101249p
  • Mehrabani, M., Nematollahi, M. H., Tarzi, M. E., Juybari, K. B., Abolhassani, M., Sharifi, A. M., … Mirzamohammadi, S. (2020). Protective effect of hydralazine on a cellular model of Parkinson’s disease: a possible role of hypoxia-inducible factor (HIF)-1α. Biochemistry and Cell Biology, 98(3), 405–414. https://doi.org/10.1139/bcb-2019-0117
  • Ransohoff, R. M. (2016). How neuroinflammation contributes to neurodegeneration. Science (New York, N.Y.), 353(6301), 777–783. https://doi.org/10.1126/science.aag2590
  • Ray, P. D., Huang, B.-W., and Tsuji, Y. (2012). Reactive oxygen species (ROS) homeostasis and redox regulation in cellular signaling. Cellular Signalling, 24(5), 981–990. https://doi.org/10.1016/j.cellsig.2012.01.008
Year 2021, Volume: 2 Issue: 1, 8 - 15, 29.01.2021

Abstract

References

  • Andersen, J. K. (2004). Oxidative stress in neurodegeneration: cause or consequence? Nature Medicine, 10(S7), S18–S25. https://doi.org/10.1038/nrn1434
  • Blesa, J., Trigo-Damas, I., Quiroga-Varela, A., and Jackson-Lewis, V. R. (2015). Oxidative stress and Parkinson’s disease. Frontiers in Neuroanatomy, 9. https://doi.org/10.3389/fnana.2015.00091
  • Coyle, J., and Puttfarcken, P. (1993). Oxidative stress, glutamate, and neurodegenerative disorders. Science, 262(5134), 689–695. https://doi.org/10.1126/science.7901908
  • Daiber, A., Mülsch, A., Hink, U., Mollnau, H., Warnholtz, A., Oelze, M., and Münzel, T. (2005). The Oxidative Stress Concept of Nitrate Tolerance and the Antioxidant Properties of Hydralazine. The American Journal of Cardiology, 96(7), 25–36. https://doi.org/10.1016/j.amjcard.2005.07.030
  • DiSabato, D. J., Quan, N., and Godbout, J. P. (2016). Neuroinflammation: the devil is in the details. Journal of Neurochemistry, 139, 136–153. https://doi.org/10.1111/jnc.13607
  • Dringen, R., Kussmaul, L., and Hamprecht, B. (1998). Detoxification of exogenous hydrogen peroxide and organic hydroperoxides by cultured astroglial cells assessed by microtiter plate assay. Brain Research Protocols, 2(3), 223–228. https://doi.org/10.1016/S1385-299X(97)00047-0
  • Dulce, R. A., Yiginer, O., Gonzalez, D. R., Goss, G., Feng, N., Zheng, M., and Hare, J. M. (2013). Hydralazine and Organic Nitrates Restore Impaired Excitation-Contraction Coupling by Reducing Calcium Leak Associated with Nitroso-Redox Imbalance. Journal of Biological Chemistry, 288(9), 6522–6533. https://doi.org/10.1074/jbc.M112.412130
  • Erel, O. (2004). A novel automated method to measure total antioxidant response against potent free radical reactions. Clinical Biochemistry, 37(2), 112–119. https://doi.org/10.1016/j.clinbiochem.2003.10.014
  • Erel, O. (2005). A new automated colorimetric method for measuring total oxidant status. Clinical Biochemistry, 38(12), 1103–1111. https://doi.org/10.1016/j.clinbiochem.2005.08.008
  • Forman, H. J. (2007). Use and abuse of exogenous H2O2 in studies of signal transduction. Free Radical Biology and Medicine, 42(7), 926–932. https://doi.org/10.1016/j.freeradbiomed.2007.01.011
  • Galvani, S., Coatrieux, C., Elbaz, M., Grazide, M.-H., Thiers, J.-C., Parini, A., … Nègre-Salvayre, A. (2008). Carbonyl scavenger and antiatherogenic effects of hydrazine derivatives. Free Radical Biology and Medicine, 45(10), 1457–1467. https://doi.org/10.1016/j.freeradbiomed.2008.08.026
  • Gandhi, S., and Abramov, A. Y. (2012). Mechanism of oxidative stress in neurodegeneration. Oxidative Medicine and Cellular Longevity, 2012, 428010. https://doi.org/10.1155/2012/428010
  • Hamann, K., Nehrt, G., Ouyang, H., Duerstock, B., and Shi, R. (2007). Hydralazine inhibits compression and acrolein-mediated injuries in ex vivo spinal cord. Journal of Neurochemistry, 071108171001006-??? https://doi.org/10.1111/j.1471-4159.2007.05002.x
  • Jessen, K. R. (2004). Glial cells. The International Journal of Biochemistry & Cell Biology, 36(10), 1861–1867. https://doi.org/10.1016/j.biocel.2004.02.023
  • Kaminskas, L. M., Pyke, S. M., and Burcham, P. C. (2004). Strong Protein Adduct Trapping Accompanies Abolition of Acrolein-Mediated Hepatotoxicity by Hydralazine in Mice. Journal of Pharmacology and Experimental Therapeutics, 310(3), 1003–1010. https://doi.org/10.1124/jpet.104.067330
  • Kruger, N. J. (1994). The Bradford Method for Protein Quantitation. In Protein Protocols Handbook, The (pp. 15–22). New Jersey: Humana Press. https://doi.org/10.1385/1-59259-169-8:15
  • Leiro, J. M., Álvarez, E., Arranz, J. A., Cano, E., and Orallo, F. (2004). Antioxidant activity and inhibitory effects of hydralazine on inducible NOS/COX-2 gene and protein expression in rat peritoneal macrophages. International Immunopharmacology, 4(2), 163–177. https://doi.org/10.1016/j.intimp.2003.10.004
  • Li, Y., Hou, D., Chen, X., Zhu, J., Zhang, R., Sun, W., … Kong, X. (2019). Hydralazine protects against renal ischemia-reperfusion injury in rats. European Journal of Pharmacology, 843, 199–209. https://doi.org/10.1016/j.ejphar.2018.11.015
  • Lu, T., Aron, L., Zullo, J., Pan, Y., Kim, H., Chen, Y., … Yankner, B. A. (2014). REST and stress resistance in ageing and Alzheimer’s disease. Nature, 507(7493), 448–454. https://doi.org/10.1038/nature13163
  • Magee, L. A. (2003). Hydralazine for treatment of severe hypertension in pregnancy: meta-analysis. BMJ, 327(7421), 955–0. https://doi.org/10.1136/bmj.327.7421.955
  • Maheshwari, M., Roberts, J. K., DeSutter, B., Duong, K. T., Tingling, J., Fawver, J. N., … Murray, I. V. J. (2010). Hydralazine Modifies Aβ Fibril Formation and Prevents Modification by Lipids in Vitro. Biochemistry, 49(49), 10371–10380. https://doi.org/10.1021/bi101249p
  • Mehrabani, M., Nematollahi, M. H., Tarzi, M. E., Juybari, K. B., Abolhassani, M., Sharifi, A. M., … Mirzamohammadi, S. (2020). Protective effect of hydralazine on a cellular model of Parkinson’s disease: a possible role of hypoxia-inducible factor (HIF)-1α. Biochemistry and Cell Biology, 98(3), 405–414. https://doi.org/10.1139/bcb-2019-0117
  • Ransohoff, R. M. (2016). How neuroinflammation contributes to neurodegeneration. Science (New York, N.Y.), 353(6301), 777–783. https://doi.org/10.1126/science.aag2590
  • Ray, P. D., Huang, B.-W., and Tsuji, Y. (2012). Reactive oxygen species (ROS) homeostasis and redox regulation in cellular signaling. Cellular Signalling, 24(5), 981–990. https://doi.org/10.1016/j.cellsig.2012.01.008
There are 24 citations in total.

Details

Primary Language English
Subjects Biochemistry and Cell Biology (Other)
Journal Section Articles
Authors

Ahmet Şevki Taşkıran 0000-0002-5810-8415

Mustafa Ergül

Publication Date January 29, 2021
Submission Date September 3, 2020
Acceptance Date November 12, 2020
Published in Issue Year 2021 Volume: 2 Issue: 1

Cite

APA Taşkıran, A. Ş., & Ergül, M. (2021). The Protective Effect of Hydralazine against Hydrogen Peroxide (H2O2)-Induced Oxidative Damage in C6 Glial Cell Line. Turkish Journal of Science and Health, 2(1), 8-15.








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