Table of Contents Author Guidelines Submit a Manuscript
Evidence-Based Complementary and Alternative Medicine
Volume 2013, Article ID 290675, 8 pages
http://dx.doi.org/10.1155/2013/290675
Research Article

Propolis Induces Chondroitin/Dermatan Sulphate and Hyaluronic Acid Accumulation in the Skin of Burned Wound

1Department of Community Pharmacy, Medical University of Silesia, ul. Kasztanowa 3, 41-200 Sosnowiec, Poland
2Department of Clinical Chemistry and Laboratory Diagnostics, Medical University of Silesia, ul. Kasztanowa 3, 41-200 Sosnowiec, Poland
3Center of Experimental Medicine, Medical University of Silesia, ul. Kasztanowa 3, 41-200 Sosnowiec, Poland
4Department of Statistics, Medical University of Silesia, ul. Kasztanowa 3, 41-200 Sosnowiec, Poland

Received 7 January 2013; Accepted 9 February 2013

Academic Editor: Ewelina Szliszka

Copyright © 2013 Pawel Olczyk 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. K. Gunjan, Ch. Shobha, Ch. Sheetal, H. Nanda, C. Vikrant, and D. S. Chitnis, “A comparative study of the effect of different topical agents on burn wound infections,” Indian Journal of Plastic Surgery, vol. 45, no. 2, pp. 374–378, 2012. View at Google Scholar
  2. K. Arslan, Ö. Karahan, A. Okuş et al., “Comparison of topical zinc oxide and silver sulfadiazine in burn wounds: an experimental study,” Turkish Journal of Trauma & Emergency Surgery, vol. 18, no. 5, pp. 376–383, 2012. View at Google Scholar
  3. P. Olczyk, I. Wroblewska-Adamek, J. Stojko, K. Komosinska-Vassev, and K. Olczyk, “Histopathological evaluation of Propol-T and silver sulfadiazine therapeutic efficacy in burn healing,” Polish Pharmacy, vol. 63, pp. 1108–1116, 2007. View at Google Scholar
  4. S. Guo and L. A. DiPietro, “Factors affecting wound healing,” Critical Reviews in Oral Biology & Medicine, vol. 89, no. 3, pp. 219–229, 2010. View at Google Scholar
  5. R. J. Mendonça and J. Coutinho-Netto, “Cellular aspects of wound healing,” Anais Brasileiros De Dermatologia, vol. 84, no. 3, pp. 257–262, 2009. View at Google Scholar
  6. A. Siméon, Y. Wegrowski, Y. Bontemps, and F. X. Maquart, “Expression of glycosaminoglycans and small proteoglycans in wounds: modulation by the tripeptide-copper complex glycyl-L-histidyl-L-lysine-Cu2+,” Journal of Investigative Dermatology, vol. 115, no. 6, pp. 962–968, 2000. View at Publisher · View at Google Scholar · View at Scopus
  7. N. Afratis, Ch. Gialeli, D. Nikitovic et al., “Glycosaminoglycans: key players in cancer cell biology,” FEBS Journal, vol. 279, no. 7, pp. 1177–1197, 2012. View at Google Scholar
  8. A. Im and Y. S. Kim, “Role of glycosaminoglycans in wound healing,” Archives of Pharmaceutical Sciences and Research, vol. 1, no. 2, pp. 106–114, 2009. View at Google Scholar
  9. M. J. Hoekstra, P. Hupkens, R. P. Dutrieux, M. M. C. Bosch, T. A. Brans, and R. W. Kreis, “A comparative burn wound model in the New Yorkshire pig for the histopathological evaluation of local therapeutic regimens: silver sulfadiazine cream as a standard,” British Journal of Plastic Surgery, vol. 46, no. 7, pp. 585–589, 1993. View at Publisher · View at Google Scholar · View at Scopus
  10. J. J. Vranckx, F. Yao, N. Petrie et al., “In vivo gene delivery of Ad-VEGF121 to full-thickness wounds in aged pigs results in high levels of VEGF expression but not in accelerated healing,” Wound Repair and Regeneration, vol. 13, no. 1, pp. 51–60, 2005. View at Publisher · View at Google Scholar · View at Scopus
  11. J. E. Scott, “Aliphatic ammonium salts in the assay of acidic polysaccharides from tissues,” in Methods of Biochemical Analysis, D. Glick, Ed., pp. 145–197, Wiley, New York, NY, USA, 1960. View at Google Scholar
  12. J. P. Van Amerongen, A. G. Lemmens, and G. J. M. Tonino, “Glycosaminoglycans in dental pulp,” in Dynamic Aspects of Dental Pulp: Molecular Biology, Pharmacology and Pathophysiology, I. K. Olgart, Ed., pp. 259–276, Chapman and Hall, London, UK, 1990. View at Google Scholar
  13. N. Blumenkrantz and G. Asboe Hansen, “New method for quantitative determination of uronic acids,” Analytical Biochemistry, vol. 54, no. 2, pp. 484–489, 1973. View at Google Scholar · View at Scopus
  14. K. Gu, R. J. Linhardt, M. Laliberte, K. Gu, and J. Zimmermann, “Purification, characterization and specificity of chondroitin lyases and glycuronidase from Flavobacterium heparinum,” Biochemical Journal, vol. 312, no. 2, pp. 569–577, 1995. View at Google Scholar · View at Scopus
  15. K. B. Komosinska-Vassev, K. Winsz-Szczotka, K. Kuznik-Trocha, P. Olczyk, and K. Olczyk, “Age-related changes of plasma glycosaminoglycans,” Clinical Chemistry and Laboratory Medicine, vol. 46, no. 2, pp. 219–224, 2008. View at Publisher · View at Google Scholar · View at Scopus
  16. J. A. Deakin and M. Lyon, “A simplified and sensitive fluorescent method for disaccharide analysis of both heparan sulfate and chondroitin/dermatan sulfates from biological samples,” Glycobiology, vol. 18, no. 6, pp. 483–491, 2008. View at Publisher · View at Google Scholar · View at Scopus
  17. P. Olczyk, K. Komosinska-Vassev, K. Winsz-Szczotka et al., “Propolis modulates vitronectin, laminin, and heparan sulfate/heparin expression during experimental burn healing,” Journal of Zhejiang University Science B, vol. 13, no. 11, pp. 932–941, 2012. View at Google Scholar
  18. M. David-Raoudi, F. Tranchepain, B. Deschrevel et al., “Differential effects of hyaluronan and its fragments on fibroblasts: relation to wound healing,” Wound Repair and Regeneration, vol. 16, pp. 274–287, 2008. View at Google Scholar
  19. E. T. Ahmed, O. M. Abo-Salem, and A. Osman, “The influence of egyptian propolis on induced burn wound healing in diabetic rats, antibacterial mechanism,” Science Journal of Medicines and Clinical Trials, vol. 11, no. 3, p. 21, 2011. View at Google Scholar
  20. A. Mertas, E. Szliszka, J. Bronikowska, A. Herman, and W. Krol, “Antibacterial and anti-imflammatory properthies of ethanolic extract of propolis (EEP) in prevention and treatment of parodonthis,” Inżynieria Stomatologiczna, vol. 7, no. 1, pp. 40–44, 2010. View at Google Scholar
  21. P. Dudko, “Influence of cow's udder infusion of propolis and antimycotic preparations on activity of mammary gland in cows,” Postępy Fitoterapii, vol. 1, pp. 12–18, 2009. View at Google Scholar
  22. E. Szliszka, Z. P. Czuba, J. Bronikowska, A. Mertas, A. Paradysz, and W. Krol, “Ethanolic extract of propolis augments TRAIL-induced apoptotic death in prostate cancer cells,” Evidence-Based Complementary and Alternative Medicine, vol. 2011, Article ID 535172, 11 pages, 2011. View at Publisher · View at Google Scholar
  23. J. P. Bentley, “Rate of chondroitin sulfate formation in wound healing,” Annals of Surgery, vol. 165, no. 2, pp. 186–191, 1967. View at Google Scholar · View at Scopus
  24. M. Hoffman, A. Harger, A. Lenkowski, U. Hedner, H. R. Roberts, and D. M. Monroe, “Cutaneous wound healing is impaired in hemophilia B,” Blood, vol. 108, no. 9, pp. 3053–3060, 2006. View at Publisher · View at Google Scholar · View at Scopus
  25. A. A. Berretta, A. P. Nascimento, P. C. Bueno, M. M. Vaz, and J. M. Marchetti, “Propolis standardized extract (EPP-AF), an innovative chemically and biologically reproducible pharmaceutical compound for treating wounds,” International Journal of Biological Sciences, vol. 8, no. 4, pp. 512–521, 2012. View at Google Scholar
  26. P. S. Murphy and G. R. D. Evans, “Advances in wound healing: a review of current wound healing products,” Plastic Surgery International, vol. 2012, Article ID 190436, 8 pages, 2012. View at Publisher · View at Google Scholar
  27. E. Vassal-Stermann, A. Duranton, A. F. Black et al., “A new C-Xyloside induces modifications of GAG expression, structure and functional properties,” PLoS One, vol. 7, no. 10, Article ID e47933, 2012. View at Google Scholar
  28. J. Muto, N. N. Naidu, K. Yamasaki, N. Pineau, L. Breton, and R. L. Gallo, “Exogenous addition of a c-xylopyranoside derivative stimulates keratinocyte dermatan sulfate synthesis and promotes migration,” PLoS ONE, vol. 6, no. 10, Article ID e25480, 2011. View at Google Scholar
  29. J. K. Plichta and K. A. Radek, “Sugar-coating wound repair: a review of FGF-10 and dermatan sulfate in wound healing and their potential application in burn wounds,” Journal of Burn Care Research, vol. 33, no. 3, pp. 299–310, 2012. View at Google Scholar
  30. D. Matsukura, Y. Yokoyama, K. Tanaka, T. Ozaki, and H. Mizunuma, “Changes of proteoglycan expression and glycosaminoglycan constituents in the intervillous space of the pregnancy-induced hypertension placenta,” The Hirosaki Medical Journal, vol. 59, no. 2-4, pp. 128–135, 2008. View at Google Scholar · View at Scopus
  31. J. A. Deakin, B. S. Blaum, J. T. Gallagher, D. Uhrín, and M. Lyo, “The binding properties of minimal oligosaccharides reveal a common heparan sulfate/dermatan sulfate-binding site in hepatocyte growth factor/scatter factor that can accommodate a wide variety of sulfation patterns,” The Journal of Biological Chemistry, vol. 284, no. 10, pp. 6311–6321, 2009. View at Publisher · View at Google Scholar · View at Scopus
  32. D. G. Seidler, J. Peter-Katalinić, and A. D. Zamfir, “Galactosaminoglycan function and oligosaccharide structure determination,” The Scientific World Journal, vol. 7, pp. 233–241, 2007. View at Google Scholar
  33. F. Maccari and N. Volpi, “Structural characterization of the skin glycosaminoglycans in patients with pseudoxanthoma elasticum,” International Journal of Dermatology, vol. 47, no. 10, pp. 1024–1027, 2008. View at Publisher · View at Google Scholar · View at Scopus
  34. K. C. George, L. Jia, M. M. Shabbir, B. Boon-Huat, and W. Y. George, “Pathology of wound healing: chondroitin sulfate synthase 1 regulates the expression and activity of caspase 1,” in Proceedings of the World Medical Conference, pp. 222–226, 2011.
  35. C. D. Nandini, N. Itoh, and K. Sugahara, “Novel 70-kDa chondroitin sulfate/dermatan sulfate hybrid chains with a unique heterogenous sulfation pattern from shark skin, which exhibit neuritogenic activity and binding activities for growth factors and neurotrophic factors,” The Journal of Biological Chemistry, vol. 280, no. 6, pp. 4058–4069, 2005. View at Publisher · View at Google Scholar · View at Scopus
  36. E. M. Koźma, G. Wisowski, and K. Olczyk, “Platelet derived growth factor BB is a ligand for dermatan sulfate chain(s) of small matrix proteoglycans from normal and fibrosis affected fascia,” Biochimie, vol. 91, no. 11-12, pp. 1394–1404, 2009. View at Publisher · View at Google Scholar · View at Scopus
  37. J. M. Trowbridge and R. L. Gallo, “Dermatan sulfate: new functions from an old glycosaminoglycan,” Glycobiology, vol. 12, no. 9, pp. 117R–125R, 2002. View at Google Scholar
  38. K. K. Taylor, J. A. Rudisill, and R. L. Gallo, “Structural and sequence motifs in dermatan sulfate for promoting fibroblast growth factor-2 (FGF-2) and FGF-7 activity,” The Journal of Biological Chemistry, vol. 280, no. 7, pp. 5300–5306, 2005. View at Publisher · View at Google Scholar · View at Scopus
  39. N. Ganapathy, S. S. Venkataraman, R. Daniel, R. J. Aravind, and V. B. Kumarakrishnan, “Molecular biology of wound healing,” Journal of Pharmacy and Bio Allied Sciences, vol. 4, supplement 2, pp. S334–S337, 2012. View at Google Scholar
  40. T. A. Dechert, A. E. Ducale, S. I. Ward, and D. R. Yager, “Hyaluronan in human acute and chronic dermal wounds,” Wound Repair and Regeneration, vol. 14, no. 3, pp. 252–258, 2006. View at Publisher · View at Google Scholar · View at Scopus
  41. S. Ansorge, D. Reinhold, and U. Lendeckel, “Propolis and some of its constituents down-regulate DNA synthesis and inflammatory cytokine production but induce TGF-β1 production of human immune cells,” Zeitschrift fur Naturforschung C, vol. 58, no. 7-8, pp. 580–589, 2003. View at Google Scholar · View at Scopus
  42. G. S. Schultz, J. M. Davidson, R. S. Kirsner, P. Bornstein, and I. M. Herman, “Dynamic reciprocity in the wound microenvironment,” Wound Repair and Regeneration, vol. 19, no. 2, pp. 134–148, 2011. View at Publisher · View at Google Scholar · View at Scopus
  43. K. Brudzynski and R. Carlone, “Stage-dependent modulation of limb regeneration by Caffeic Acid Phenethyl Ester (CAPE)—immunocytochemical evidence of a CAPE-evoked delay in mesenchyme formation and limb regeneration,” Journal of Experimental Zoology A, vol. 301, no. 5, pp. 389–400, 2004. View at Google Scholar · View at Scopus
  44. P. Olczyk, R. Wojtyczka, J. Stojko et al., “Comparison of the mechanisms of antibacterial action of silver sulfadizine and propolis applied in topical burn treatment,” Scientific Review in Pharmacy, vol. 6, pp. 36–43, 2007. View at Google Scholar