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

Changes in extracellular matrix glycosaminoglycans during the wound repair allowed us to apply the burn model in which therapeutic efficacy of propolis and silver sulfadiazine was compared. Burns were inflicted on four pigs. Glycosaminoglycans isolated from healthy and burned skin were quantified us...

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Autores principales: Olczyk, Pawel, Komosinska-Vassev, Katarzyna, Winsz-Szczotka, Katarzyna, Stojko, Jerzy, Klimek, Katarzyna, Kozma, Ewa M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3606753/
https://www.ncbi.nlm.nih.gov/pubmed/23533471
http://dx.doi.org/10.1155/2013/290675
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author Olczyk, Pawel
Komosinska-Vassev, Katarzyna
Winsz-Szczotka, Katarzyna
Stojko, Jerzy
Klimek, Katarzyna
Kozma, Ewa M.
author_facet Olczyk, Pawel
Komosinska-Vassev, Katarzyna
Winsz-Szczotka, Katarzyna
Stojko, Jerzy
Klimek, Katarzyna
Kozma, Ewa M.
author_sort Olczyk, Pawel
collection PubMed
description Changes in extracellular matrix glycosaminoglycans during the wound repair allowed us to apply the burn model in which therapeutic efficacy of propolis and silver sulfadiazine was compared. Burns were inflicted on four pigs. Glycosaminoglycans isolated from healthy and burned skin were quantified using a hexuronic acid assay, electrophoretic fractionation, and densitometric analyses. Using the reverse-phase HPLC the profile of sulfated disaccharides released by chondroitinase ABC from chondroitin/dermatan sulfates was estimated. Chondroitin/dermatan sulfates and hyaluronic acid were found in all samples. Propolis stimulated significant changes in the content of particular glycosaminoglycan types during burn healing. Glycosaminoglycans alterations after silver sulfadiazine application were less expressed. Propolis maintained high contribution of 4-O-sulfated disaccharides to chondroitin/dermatan sulfates structure and low level of 6-O-sulfated ones throughout the observed period of healing. Propolis led to preservation of significant contribution of disulfated disaccharides especially 2,4-O-disulfated ones to chondroitin sulfates/dermatan sulfates structure throughout the observed period of healing. Our findings demonstrate that propolis accelerates the burned tissue repair by stimulation of the wound bed glycosaminoglycan accumulation needed for granulation, tissue growth, and wound closure. Moreover, propolis accelerates chondroitin/dermatan sulfates structure modification responsible for binding growth factors playing the crucial role in the tissue repair.
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spelling pubmed-36067532013-03-26 Propolis Induces Chondroitin/Dermatan Sulphate and Hyaluronic Acid Accumulation in the Skin of Burned Wound Olczyk, Pawel Komosinska-Vassev, Katarzyna Winsz-Szczotka, Katarzyna Stojko, Jerzy Klimek, Katarzyna Kozma, Ewa M. Evid Based Complement Alternat Med Research Article Changes in extracellular matrix glycosaminoglycans during the wound repair allowed us to apply the burn model in which therapeutic efficacy of propolis and silver sulfadiazine was compared. Burns were inflicted on four pigs. Glycosaminoglycans isolated from healthy and burned skin were quantified using a hexuronic acid assay, electrophoretic fractionation, and densitometric analyses. Using the reverse-phase HPLC the profile of sulfated disaccharides released by chondroitinase ABC from chondroitin/dermatan sulfates was estimated. Chondroitin/dermatan sulfates and hyaluronic acid were found in all samples. Propolis stimulated significant changes in the content of particular glycosaminoglycan types during burn healing. Glycosaminoglycans alterations after silver sulfadiazine application were less expressed. Propolis maintained high contribution of 4-O-sulfated disaccharides to chondroitin/dermatan sulfates structure and low level of 6-O-sulfated ones throughout the observed period of healing. Propolis led to preservation of significant contribution of disulfated disaccharides especially 2,4-O-disulfated ones to chondroitin sulfates/dermatan sulfates structure throughout the observed period of healing. Our findings demonstrate that propolis accelerates the burned tissue repair by stimulation of the wound bed glycosaminoglycan accumulation needed for granulation, tissue growth, and wound closure. Moreover, propolis accelerates chondroitin/dermatan sulfates structure modification responsible for binding growth factors playing the crucial role in the tissue repair. Hindawi Publishing Corporation 2013 2013-03-07 /pmc/articles/PMC3606753/ /pubmed/23533471 http://dx.doi.org/10.1155/2013/290675 Text en Copyright © 2013 Pawel Olczyk et al. https://creativecommons.org/licenses/by/3.0/ 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.
spellingShingle Research Article
Olczyk, Pawel
Komosinska-Vassev, Katarzyna
Winsz-Szczotka, Katarzyna
Stojko, Jerzy
Klimek, Katarzyna
Kozma, Ewa M.
Propolis Induces Chondroitin/Dermatan Sulphate and Hyaluronic Acid Accumulation in the Skin of Burned Wound
title Propolis Induces Chondroitin/Dermatan Sulphate and Hyaluronic Acid Accumulation in the Skin of Burned Wound
title_full Propolis Induces Chondroitin/Dermatan Sulphate and Hyaluronic Acid Accumulation in the Skin of Burned Wound
title_fullStr Propolis Induces Chondroitin/Dermatan Sulphate and Hyaluronic Acid Accumulation in the Skin of Burned Wound
title_full_unstemmed Propolis Induces Chondroitin/Dermatan Sulphate and Hyaluronic Acid Accumulation in the Skin of Burned Wound
title_short Propolis Induces Chondroitin/Dermatan Sulphate and Hyaluronic Acid Accumulation in the Skin of Burned Wound
title_sort propolis induces chondroitin/dermatan sulphate and hyaluronic acid accumulation in the skin of burned wound
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3606753/
https://www.ncbi.nlm.nih.gov/pubmed/23533471
http://dx.doi.org/10.1155/2013/290675
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