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bFGF and collagen matrix hydrogel attenuates burn wound inflammation through activation of ERK and TRK pathway

Burn injuries are most challenging to manage since it causes loss of the integrity of large portions of the skin leading to major disability or even death. Over the years, hydrogels are considered as a significant delivery system for wound treatment because of several advantages over other conventio...

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Autores principales: Chakrabarti, Srijita, Mazumder, Bhaskar, Rajkonwar, Jadab, Pathak, Manash Pratim, Patowary, Pompy, Chattopadhyay, Pronobesh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7870886/
https://www.ncbi.nlm.nih.gov/pubmed/33558597
http://dx.doi.org/10.1038/s41598-021-82888-9
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author Chakrabarti, Srijita
Mazumder, Bhaskar
Rajkonwar, Jadab
Pathak, Manash Pratim
Patowary, Pompy
Chattopadhyay, Pronobesh
author_facet Chakrabarti, Srijita
Mazumder, Bhaskar
Rajkonwar, Jadab
Pathak, Manash Pratim
Patowary, Pompy
Chattopadhyay, Pronobesh
author_sort Chakrabarti, Srijita
collection PubMed
description Burn injuries are most challenging to manage since it causes loss of the integrity of large portions of the skin leading to major disability or even death. Over the years, hydrogels are considered as a significant delivery system for wound treatment because of several advantages over other conventional formulations. We hypothesized that the bFGF-collagen-AgSD incorporated hydrogel formulation can accelerate the rate of burn healing in animal model and would promote fibroblast cell proliferation. Neovascularization and re-epithelialization is a hall mark of burn wound healing. In the present study, histopathological investigation and scanning electron microscopy of skin tissue of Wistar rats showed almost complete epithelialisation after 16 days in the treatment group. The developed hydrogel showed significantly accelerated wound closure compared with a standard and control group. The faster wound closure resulted from increased re-epithelialization and granulation tissue formation because of the presence of collagen and growth factor. Expressions of proteins such as TrkA, p- TrkA, ERK1/2, p-ERK1/2, NF-kβ, and p-NF-kβ involved in nerve growth factor (NGF) signalling pathway were analysed by western blot. All the findings obtained from this study indicated that the hydrogel can be considered as a promising delivery system against second degree burn by faster healing.
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spelling pubmed-78708862021-02-10 bFGF and collagen matrix hydrogel attenuates burn wound inflammation through activation of ERK and TRK pathway Chakrabarti, Srijita Mazumder, Bhaskar Rajkonwar, Jadab Pathak, Manash Pratim Patowary, Pompy Chattopadhyay, Pronobesh Sci Rep Article Burn injuries are most challenging to manage since it causes loss of the integrity of large portions of the skin leading to major disability or even death. Over the years, hydrogels are considered as a significant delivery system for wound treatment because of several advantages over other conventional formulations. We hypothesized that the bFGF-collagen-AgSD incorporated hydrogel formulation can accelerate the rate of burn healing in animal model and would promote fibroblast cell proliferation. Neovascularization and re-epithelialization is a hall mark of burn wound healing. In the present study, histopathological investigation and scanning electron microscopy of skin tissue of Wistar rats showed almost complete epithelialisation after 16 days in the treatment group. The developed hydrogel showed significantly accelerated wound closure compared with a standard and control group. The faster wound closure resulted from increased re-epithelialization and granulation tissue formation because of the presence of collagen and growth factor. Expressions of proteins such as TrkA, p- TrkA, ERK1/2, p-ERK1/2, NF-kβ, and p-NF-kβ involved in nerve growth factor (NGF) signalling pathway were analysed by western blot. All the findings obtained from this study indicated that the hydrogel can be considered as a promising delivery system against second degree burn by faster healing. Nature Publishing Group UK 2021-02-08 /pmc/articles/PMC7870886/ /pubmed/33558597 http://dx.doi.org/10.1038/s41598-021-82888-9 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Chakrabarti, Srijita
Mazumder, Bhaskar
Rajkonwar, Jadab
Pathak, Manash Pratim
Patowary, Pompy
Chattopadhyay, Pronobesh
bFGF and collagen matrix hydrogel attenuates burn wound inflammation through activation of ERK and TRK pathway
title bFGF and collagen matrix hydrogel attenuates burn wound inflammation through activation of ERK and TRK pathway
title_full bFGF and collagen matrix hydrogel attenuates burn wound inflammation through activation of ERK and TRK pathway
title_fullStr bFGF and collagen matrix hydrogel attenuates burn wound inflammation through activation of ERK and TRK pathway
title_full_unstemmed bFGF and collagen matrix hydrogel attenuates burn wound inflammation through activation of ERK and TRK pathway
title_short bFGF and collagen matrix hydrogel attenuates burn wound inflammation through activation of ERK and TRK pathway
title_sort bfgf and collagen matrix hydrogel attenuates burn wound inflammation through activation of erk and trk pathway
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7870886/
https://www.ncbi.nlm.nih.gov/pubmed/33558597
http://dx.doi.org/10.1038/s41598-021-82888-9
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