Have a personal or library account? Click to login
Antioxidative role of propolis on LPS induced renal damage Cover

Antioxidative role of propolis on LPS induced renal damage

Open Access
|Jul 2020

References

  1. Rietschel ET, Brade H, Holst O, Brade L, Müller-Loennies S, Mamat U, Zahringer U, Schumann RR. Bacterial endotoxin: chemical constitution, biological recognition, host response, and immunological detoxification. In: Rietschel ET, Wagner H, ed. Pathology of Septic Shock. Current Topics in Microbiology and Immunology, vol 216.Springer, Berlin, Heidelberg; 1996: 39-81.
  2. Iskit AB. Sepsiste Deneysel Modeller. Hacettepe University Faculty of Medicine, Department of Medical Pharmacology. Turkish Journal of Intensive Care 2005; 5(2): 133-136.
  3. Otero-Anton E, Gonzalez-Quintela A, Lopez-Soto A, Lopez-Soto A, Lopez-Ben S, Llovo J and Perez LF. Cecal ligation and puncture as a model of sepsis in the rat: influence of the puncture size on mortality, bacteremia, endotoxemia and tumor necrosis factor alpha levels. European Surgical Research 2001; 33(2): 77-79.
  4. Bone RC. Gram-negative sepsis. Background, clinical features, and intervention. Chest 1991;100(3): 802-8
  5. Powell RJ, Machiedo GW, Rush BF, Jr & Dikdan GS. Effect of oxygen-free radical scavengers on survival in sepsis. American Surgery 1991; 57: 86-88.
  6. Doganyigit Z, Kup FO, Silici S, Deniz K, Yakan B and Atayoglu T. Protective effects of propolis on female rats’ histopathological, biochemical and genotoxic changes during LPS induced endotoxemia. Phytomedicine 2013; 20(7): 632– 639.
  7. Búfalo MC, Ferreira I, Costa G, Francisco V, Liberal J, Cruz MT, Lopes MC and Sforcin JM. Propolis and its constituent caffeic acid suppress LPS-stimulated pro-inflammatory response by blocking NF-κB and MAPK activation in macrophages. Journal of Ethnopharmacology 2013; 149 (1): 84-92.
  8. Basnet P, Matsushige K, Hase K, Kadota S and Namba T. Four di-O-caffeoyl quinic acid derivatives from propolis. Potent hepatoprotective activity in experimental liver injury models. Biological and Pharmaceutical Bulletin 1996; 19(11): 1479-84.
  9. Rossi A, Longo R, Russo A, Borrelli F and Sautebin L. The role of the phenethyl ester of caffeic acid (CAPE) in the inhibition of rat lung cyclooxygenase activity by propolis. Fitoterapia 2002; 73: 30-37.
  10. Finkel T and Holbrook NJ. Oxidants, oxidative stress and the biology of ageing. Nature 2000; 408 (6809): 239-247.
  11. Randerath K, Randerath E, Smith CV and Chang J. Structural origins of bulky oxidative DNA adducts (type II I-compounds) as deduced by oxidation of oligonucleotides of known sequence. Chemical Research in Toxicology 1996; 9(1): 247-254.
  12. Mallis RJ, Buss JE and Thomas JA. Oxidative modification of Hras: S-thiolation and S-nitrosylation of reactive cysteines. Biochemical Journal 2001; 355: 145-153.
  13. Sugino K, Dhi K, Yamada K and Kawasaki T. The role of lipid peroxidation in endotoxin-induced hepatic damage and the protective effect of antioxidants. Surgery 1987; 101(6): 746752.
  14. Baykara M, Silici S, Ozcelik M, Guler O, Erdogan N and Bilgen M. In vivo nephroprotective efficcay of propolis against contrast-induced nephropathy. Diagnostic and Interventional Radiology 2015;21(4): 317-21.
  15. Ulusoy HB, Ozturk I and Sonmez MF. Protective effect of propolis on methotrexate-induced kidney injury in the rat. Renal Failure 2016; 38(5): 744-750.
  16. Silici S and Kutluca S. Chemical composition and antibacterial activity of propolis collected by three different races of honeybees in the same region. Journal of Ethnopharmacology 2005; 99 (1): 69-73.
  17. Bancroft JD, Stevens A and Turner DR. Theory and Practice of Histological Techniques. 3rd ed. Churchill Livingstone, Philadelphia; 1990, 167: 43-49.
  18. Nangaku M, Alpers CE, Pippin J, Shankland SJ, Adler S, Kurokawa K, Couser WG and Johnson RJ. A new model of renal microvascular endothelial injury. Kidney International 1997; 52 (1): 182-94.
  19. Yoshioka T, Kawada K, Shimada T and Mori M. Lipid peroxidation in maternal and cord blood and protective mechanism against activated-oxygen toxicity in the blood. American Journal of Obstetrics & Gynecology 1979;135(3): 372-376.
  20. Eraslan G, Kanbur M, Silici S, Altınordulu S and Karabacak M. Effects of cypermetrin on some biochemical changes in rats: the protective role of propolis. Experimental Animals 2008; 57(5): 453460.
  21. Niki E, Yamamoto Y, Komuro E and Sato K. Membrane damage due to lipid oxidation. American Jounal of Clinical Nutrition 1991; 53: 201-205.
  22. Wu QJ, Wang YQ and Qi YX. The protective effect of procyanidin against LPS-induced acute gut injury by the regulations of oxidative state. Springerplus 2016; 5(1): 1645.
  23. Qi T, Li H and Shuai L. Indirubin improves antioxidant and anti-infalmmatory functions in lipopolysaccharide-challenged mice. Oncotarget 2017; 8(22): 36658-36662.
  24. Garoui El M, Hamadi F, Soudani N, Boudawara T and Zeghal N. Propolis attenuates cobalt induced nephrotoxicity in adult rats and their progeny. Experimental and Toxicological Pathology 2012; 64 (7-8): 837-846.
  25. Keun Ha S, Moon E and Kim YS. Chrysin suppresses LPS-stimulated proinflammatory responses by blocking NF-KB and JNK activations in microglia cells. Neuroscience Letters 2010; 485 (3): 143–147.
  26. Napal DNG, Carpinella CM and Palacios MS. Antifeedant activity of ethanolic extract from Flourensia oolepis and isolation of pinocembrin as its active principle compound. Bioresource Technology 2009; 100(14): 3669–3673.
  27. Heo YM, Sohn JS and Au WW. Anti-genotoxicity of galangin as a cancer chemopreventive agent candidate. Mutation Research 2001;488(2): 135–150.
  28. Ozen S, Akyol O, Iraz M, Sogut S, Ozugurlu F, Ozyurt H, Odaci E and Yildirim Z. Role of caffeic acid phenethyl ester, an active component of propolis, against cisplatin-induced nephrotoxicity in rats. Journal of Applied Toxicology 2004; 24(1): 27–35.
  29. Irmak MK, Koltuksuz U, Kutlu NO, Yagmurca M, Ozyurt H, Karaman A and Akyol O. The effect of caffeic acid phenethyl ester on ischemia-reperfusion injury in comparison with α-tocopherol in rat kidneys. Urological Research 2001; 29(3): 190–193.
  30. Ozyurt H, Irmak MK, Akyol O, Sogut S. Caffeic acid phenethyl ester changes the indices of oxidative stress in serum of rats with renal ischaemia-reperfusion injury. Cell Biochemistry and Function 2001; 19: 259–263.
  31. Gurel A, Armutcu F, Sahin S, Sogut S, Ozyurt H, Gulec M, Kutlu NO and Akyol O. Protective role of a-tocopherol and caffeic acid phenethyl ester on ischemia–reperfusion injury via nitric oxide and myeloperoxidase in rat kidneys. Clinica Chimica Acta 2004; 339 (1-2): 33–41.
  32. Ogeturk M, Kus I, Colakoglu N, Zararsiz I, Ilhan N and Sarsılmaz M. Caffeic acid phenethyl ester protects kidneys against carbon tetrachloride toxicity in rats. Journal of Ethnopharmacology 2005; 97(2): 273–280.
  33. Zhang C, Walker LM and Mayeux PR. Role of nitric oxide in lipopolysaccharide-induced oxidant stress in the rat kidney. Biochemical Pharmacology 2000; 59: 203–209.
Language: English
Page range: 156 - 160
Published on: Jul 19, 2020
Published by: European Biotechnology Thematic Network Association
In partnership with: Paradigm Publishing Services
Publication frequency: 4 issues per year

© 2020 Züleyha Doğanyiğit, Birkan Yakan, Aslı Okan, Sibel Silici, published by European Biotechnology Thematic Network Association
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License.