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Mediators of Inflammation
Volume 2016, Article ID 4567343, 14 pages
http://dx.doi.org/10.1155/2016/4567343
Research Article

Kinin Peptides Enhance Inflammatory and Oxidative Responses Promoting Apoptosis in a Parkinson’s Disease Cellular Model

Department of Analytical Biochemistry, Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University in Krakow, Krakow, Poland

Received 12 May 2016; Revised 6 August 2016; Accepted 9 August 2016

Academic Editor: Sandra Helena Penha Oliveira

Copyright © 2016 Anna Niewiarowska-Sendo et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Linked References

  1. C. A. Davie, “A review of Parkinson's disease,” British Medical Bulletin, vol. 86, no. 1, pp. 109–127, 2008. View at Publisher · View at Google Scholar
  2. E. C. Hirsch, S. Vyas, and S. Hunot, “Neuroinflammation in Parkinson's disease,” Parkinsonism and Related Disorders, vol. 18, supplement 1, pp. S210–S212, 2012. View at Publisher · View at Google Scholar
  3. P. J. Khandelwal, A. M. Herman, and C. E.-H. Moussa, “Inflammation in the early stages of neurodegenerative pathology,” Journal of Neuroimmunology, vol. 238, no. 1-2, pp. 1–11, 2011. View at Publisher · View at Google Scholar · View at Scopus
  4. J. Emerit, M. Edeas, and F. Bricaire, “Neurodegenerative diseases and oxidative stress,” Biomedicine & Pharmacotherapy, vol. 58, no. 1, pp. 39–46, 2004. View at Publisher · View at Google Scholar · View at Scopus
  5. H. Akiyama, S. Barger, S. Barnum, B. Bradt et al., “Inflammation and Alzheimer's disease,” Neurobiology of Aging, vol. 21, no. 3, pp. 383–421, 2000. View at Publisher · View at Google Scholar
  6. I. Guevara-Lora, M. Majkucinska, A. Barbasz, A. Faussner, and A. Kozik, “Kinin generation from exogenous kininogens at the surface of retinoic acid-differentiated human neuroblastoma IMR-32 cells after stimulation with interferon-γ,” Peptides, vol. 32, no. 6, pp. 1193–1200, 2011. View at Publisher · View at Google Scholar · View at Scopus
  7. L. Bergamaschini, L. Parnetti, D. Pareyson, S. Canziani, M. Cugno, and A. Agostoni, “Activation of the contact system in cerebrospinal fluid of patients with Alzheimer disease,” Alzheimer Disease and Associated Disorders, vol. 12, no. 2, pp. 102–108, 1998. View at Publisher · View at Google Scholar · View at Scopus
  8. L. P. Fernando, S. Natesan, K. Joseph, and A. P. Kaplan, “High molecular weight kininogen and factor XII binding to endothelial cells and astrocytes,” Thrombosis and Haemostasis, vol. 90, no. 5, pp. 787–795, 2003. View at Google Scholar · View at Scopus
  9. J. B. Calixto, D. A. Cabrini, J. Ferreira, and M. M. Campos, “Kinins in pain and inflammation,” Pain, vol. 87, no. 1, pp. 1–5, 2000. View at Publisher · View at Google Scholar
  10. A. Levant, E. Levy, M. Argaman, and S. Fleisher-Berkovich, “Kinins and neuroinflammation: dual effect on prostaglandin synthesis,” European Journal of Pharmacology, vol. 546, no. 1–3, pp. 197–200, 2006. View at Publisher · View at Google Scholar · View at Scopus
  11. I. Guevara-Lora, “Kinin-mediated inflammation in neurodegenerative disorders,” Neurochemistry International, vol. 61, no. 1, pp. 72–78, 2012. View at Publisher · View at Google Scholar · View at Scopus
  12. D. M. Raidoo and K. D. Bhoola, “Pathophysiology of the kallikrein-kinin system in mammalian nervous tissue,” Pharmacology & Therapeutics, vol. 79, no. 2, pp. 105–127, 1998. View at Publisher · View at Google Scholar · View at Scopus
  13. L. M. F. Leeb-Lundberg, F. Marceau, W. Müller-Esterl, D. J. Pettibone, and B. L. Zuraw, “International union of pharmacology. XLV. Classification of the kinin receptor family: from molecular mechanisms to pathophysiological consequences,” Pharmacological Reviews, vol. 57, no. 1, pp. 27–77, 2005. View at Publisher · View at Google Scholar · View at Scopus
  14. T. A. Viel, A. Lima Caetano, A. G. Nasello et al., “Increases of kinin B1 and B2 receptors binding sites after brain infusion of amyloid-beta 1–40 peptide in rats,” Neurobiology of Aging, vol. 29, no. 12, pp. 1805–1814, 2008. View at Publisher · View at Google Scholar · View at Scopus
  15. C. M. Costa-Neto, P. Dillenburg-Pilla, T. A. Heinrich et al., “Participation of kallikrein–kinin system in different pathologies,” International Immunopharmacology, vol. 8, no. 2, pp. 135–142, 2008. View at Publisher · View at Google Scholar · View at Scopus
  16. M. Murakami, T. Ohta, and S. Ito, “Interleukin-1β enhances the action of bradykinin in rat myenteric neurons through up-regulation of glial B1 receptor expression,” Neuroscience, vol. 151, no. 1, pp. 222–231, 2008. View at Publisher · View at Google Scholar · View at Scopus
  17. M. Noda, Y. Kariura, T. Amano et al., “Expression and function of bradykinin receptors in microglia,” Life Sciences, vol. 72, no. 14, pp. 1573–1581, 2003. View at Publisher · View at Google Scholar · View at Scopus
  18. Y. B. Wang, C. Peng, and Y. H. Liu, “Low dose of bradykinin selectively increases intracellular calcium in glioma cells,” Journal of the Neurological Sciences, vol. 258, no. 1-2, pp. 44–51, 2007. View at Publisher · View at Google Scholar
  19. L. Qian, P. M. Flood, and J.-S. Hong, “Neuroinflammation is a key player in Parkinson's disease and a prime target for therapy,” Journal of Neural Transmission, vol. 117, no. 8, pp. 971–979, 2010. View at Publisher · View at Google Scholar · View at Scopus
  20. A. Niewiarowska-Sendo, K. Patrzalek, A. Kozik, and I. Guevara-Lora, “The effect of differentiation agents on inflammatory and oxidative responses of the human neuroblastoma cell line SK-N-SH,” Acta Biochimica Polonica, vol. 62, no. 3, pp. 435–443, 2015. View at Publisher · View at Google Scholar · View at Scopus
  21. H. Wang and J. A. Joseph, “Quantifying cellular oxidative stress by dichlorofluorescein assay using microplate reader,” Free Radical Biology & Medicine, vol. 27, no. 5-6, pp. 612–616, 1999. View at Publisher · View at Google Scholar · View at Scopus
  22. T. P. Misko, R. J. Schilling, D. Salvemini, W. M. Moore, and M. G. Currie, “A fluorometric assay for the measurement of nitrite in biological samples,” Analytical Biochemistry, vol. 214, no. 1, pp. 11–16, 1993. View at Publisher · View at Google Scholar · View at Scopus
  23. S.-M. Lucas, N. J. Rothwell, and R. M. Gibson, “The role of inflammation in CNS injury and disease,” British Journal of Pharmacology, vol. 147, no. 1, pp. S232–S240, 2006. View at Publisher · View at Google Scholar · View at Scopus
  24. M. D. G. Naffah-Mazzacoratti, T. L. Furtado Gouveia, P. S. Rodrigues Simoes, and S. R. Perosa, “What have we learned about the kallikrein-kinin and renin-angiotensin systems in neurological disorders?” World Journal of Biological Chemistry, vol. 5, no. 2, pp. 130–140, 2014. View at Publisher · View at Google Scholar
  25. P. H. Black, “Stress and the inflammatory response: a review of neurogenic inflammation,” Brain, Behavior, and Immunity, vol. 16, no. 6, pp. 622–653, 2002. View at Publisher · View at Google Scholar
  26. S. Baratchi, R. K. Kanwar, and J. R. Kanwar, “Survivin mutant protects differentiated dopaminergic SK-N-SH cells against oxidative stress,” PLoS ONE, vol. 6, article e15865, 2011. View at Publisher · View at Google Scholar · View at Scopus
  27. J. S. Kim-Han, J. A. Antenor-Dorsey, and K. L. O'Malley, “The parkinsonian mimetic, MPP+, specifically impairs mitochondrial transport in dopamine axons,” The Journal of Neuroscience, vol. 31, no. 19, pp. 7212–7221, 2011. View at Publisher · View at Google Scholar · View at Scopus
  28. D. R. McIlwain, T. Berger, and T. W. Mak, “Caspase functions in cell death and disease,” Cold Spring Harbor perspectives in biology, vol. 5, no. 4, Article ID a008656, 2013. View at Publisher · View at Google Scholar · View at Scopus
  29. W. Torres-Rivera, D. Pérez, K.-Y. Park et al., “Kinin-B2 receptor exerted neuroprotection after diisopropylfluorophosphate-induced neuronal damage,” Neuroscience, vol. 247, pp. 273–279, 2013. View at Publisher · View at Google Scholar · View at Scopus
  30. A. H. Martins, J. M. Alves, D. Perez et al., “Kinin-B2 receptor mediated neuroprotection after NMDA excitotoxicity is reversed in the presence of kinin-B1 receptor agonists,” PLoS ONE, vol. 7, no. 2, Article ID e30755, 2012. View at Publisher · View at Google Scholar · View at Scopus
  31. K. D. Bhoola, C. D. Figueroa, and K. Worthy, “Bioregulation of kinins: kallikreins, kininogens, and kininases,” Pharmacological Reviews, vol. 44, no. 1, pp. 1–80, 1992. View at Google Scholar · View at Scopus
  32. S. Koppula, H. Kumar, I. S. Kim, and D.-K. Choi, “Reactive oxygen species and inhibitors of inflammatory enzymes, NADPH oxidase, and iNOS in experimental models of parkinsons disease,” Mediators of Inflammation, vol. 2012, Article ID 823902, 16 pages, 2012. View at Publisher · View at Google Scholar · View at Scopus
  33. S. Singh and M. Dikshit, “Apoptotic neuronal death in Parkinson's disease: involvement of nitric oxide,” Brain Research Reviews, vol. 54, no. 2, pp. 233–250, 2007. View at Publisher · View at Google Scholar · View at Scopus
  34. P. Thornton, E. Pinteaux, R. M. Gibson, S. M. Allan, and N. J. Rothwell, “Interleukin-1-induced neurotoxicity is mediated by glia and requires caspase activation and free radical release,” Journal of Neurochemistry, vol. 98, no. 1, pp. 258–266, 2006. View at Publisher · View at Google Scholar · View at Scopus
  35. H. E. De Vries, J. Kuiper, A. G. De Boer, T. J. C. Van Berkel, and D. D. Breimer, “The blood-brain barrier in neuroinflammatory diseases,” Pharmacological Reviews, vol. 49, no. 2, pp. 143–155, 1997. View at Google Scholar · View at Scopus
  36. K. Sriram, J. M. Matheson, S. A. Benkovic, D. B. Miller, M. I. Luster, and J. P. O'Callaghan, “Mice deficient in TNF receptors are protected against dopaminergic neurotoxicity: implications for Parkinson's disease,” The FASEB Journal, vol. 16, no. 11, pp. 1474–1476, 2002. View at Google Scholar · View at Scopus
  37. S. Hisahara and S. Shimohama, “Dopamine receptors and Parkinson's disease,” International Journal of Medicinal Chemistry, vol. 2011, Article ID 403039, 16 pages, 2011. View at Publisher · View at Google Scholar
  38. A. Usiello, J.-H. Baik, F. Rougé-Pont et al., “Distinct functions of the two isoforms of dopamine D2 receptors,” Nature, vol. 408, no. 6809, pp. 199–203, 2000. View at Publisher · View at Google Scholar · View at Scopus
  39. L. Wiemerslage, B. J. Schultz, A. Ganguly, and D. Lee, “Selective degeneration of dopaminergic neurons by MPP+ and its rescue by D2 autoreceptors in Drosophila primary culture,” Journal of Neurochemistry, vol. 126, no. 4, pp. 529–540, 2013. View at Publisher · View at Google Scholar · View at Scopus
  40. D. C. Jones, P. G. Gunasekar, J. L. Borowitz, and G. E. Isom, “Dopamine-induced apoptosis is mediated by oxidative stress and is enhanced by cyanide in differentiated PC12 cells,” Journal of Neurochemistry, vol. 74, no. 6, pp. 2296–2304, 2000. View at Publisher · View at Google Scholar · View at Scopus
  41. I. Guevara-Lora, B. Blonska, A. Faussner, and A. Kozik, “Kinin-generating cellular model obtained from human glioblastoma cell line U-373,” Acta Biochimica Polonica, vol. 60, no. 3, pp. 299–305, 2013. View at Google Scholar · View at Scopus
  42. I. Guevara-Lora, M. Florkowska, and A. Kozik, “Bradykinin-related peptides up-regulate the expression of kinin B1 and B2 receptor genes in human promonocytic cell line U937,” Acta Biochimica Polonica, vol. 56, no. 3, pp. 515–522, 2009. View at Google Scholar · View at Scopus