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In vivo Assessment of Antioxidant and Wound Healing Improvement of a New Schiff Base Derived Co (II) Complex in Rats
Co (II) complex (CMLA) was investigated to evaluate the rate of wound healing in rats. Animals were placed into four groups: gum acacia, Intrasite gel, 10 and 20 mg/ml of CMLA. Wounds were made on the dorsal neck area, then treated with Intrasite gel or CMLA; both of these treatments led to faster h...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5153835/ https://www.ncbi.nlm.nih.gov/pubmed/27958299 http://dx.doi.org/10.1038/srep38748 |
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author | El-Ferjani, Rashd. M. Ahmad, Musa Dhiyaaldeen, Summaya M. Harun, Farah Wahida Ibrahim, Mohamed Yousif Adam, Hoyam Mohd. Yamin, Bohari Al-Obaidi, Mazen M. Jamil Batran, Rami Al |
author_facet | El-Ferjani, Rashd. M. Ahmad, Musa Dhiyaaldeen, Summaya M. Harun, Farah Wahida Ibrahim, Mohamed Yousif Adam, Hoyam Mohd. Yamin, Bohari Al-Obaidi, Mazen M. Jamil Batran, Rami Al |
author_sort | El-Ferjani, Rashd. M. |
collection | PubMed |
description | Co (II) complex (CMLA) was investigated to evaluate the rate of wound healing in rats. Animals were placed into four groups: gum acacia, Intrasite gel, 10 and 20 mg/ml of CMLA. Wounds were made on the dorsal neck area, then treated with Intrasite gel or CMLA; both of these treatments led to faster healing than with gum acacia. Histology of the wounds dressed with CMLA or Intrasite gel displayed a smaller scar width, required less time to heal and showed more collagen staining and fewer inflammatory cells in comparison to wounds dressed with the vehicle. Immunohistochemistry for Hsp70 and TGF-β showed greater staining intensity in the treated groups compared to the vehicle group. Bax staining was less intense in treated groups compared to the vehicle group, suggesting that CMLA and Intrasite gel provoked apoptosis, responsible for the development of granulation tissue into a scar. CD31 protein analysis showed that the treated groups enhanced angiogenesis and increased vascularization compared to the control group. Furthermore, a significant increase in the levels of GPx and SOD and a decrease in MDA were also observed in the treated groups. This results suggest that CMLA is a potentially promising agent for the wounds treatment. |
format | Online Article Text |
id | pubmed-5153835 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-51538352016-12-28 In vivo Assessment of Antioxidant and Wound Healing Improvement of a New Schiff Base Derived Co (II) Complex in Rats El-Ferjani, Rashd. M. Ahmad, Musa Dhiyaaldeen, Summaya M. Harun, Farah Wahida Ibrahim, Mohamed Yousif Adam, Hoyam Mohd. Yamin, Bohari Al-Obaidi, Mazen M. Jamil Batran, Rami Al Sci Rep Article Co (II) complex (CMLA) was investigated to evaluate the rate of wound healing in rats. Animals were placed into four groups: gum acacia, Intrasite gel, 10 and 20 mg/ml of CMLA. Wounds were made on the dorsal neck area, then treated with Intrasite gel or CMLA; both of these treatments led to faster healing than with gum acacia. Histology of the wounds dressed with CMLA or Intrasite gel displayed a smaller scar width, required less time to heal and showed more collagen staining and fewer inflammatory cells in comparison to wounds dressed with the vehicle. Immunohistochemistry for Hsp70 and TGF-β showed greater staining intensity in the treated groups compared to the vehicle group. Bax staining was less intense in treated groups compared to the vehicle group, suggesting that CMLA and Intrasite gel provoked apoptosis, responsible for the development of granulation tissue into a scar. CD31 protein analysis showed that the treated groups enhanced angiogenesis and increased vascularization compared to the control group. Furthermore, a significant increase in the levels of GPx and SOD and a decrease in MDA were also observed in the treated groups. This results suggest that CMLA is a potentially promising agent for the wounds treatment. Nature Publishing Group 2016-12-13 /pmc/articles/PMC5153835/ /pubmed/27958299 http://dx.doi.org/10.1038/srep38748 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article El-Ferjani, Rashd. M. Ahmad, Musa Dhiyaaldeen, Summaya M. Harun, Farah Wahida Ibrahim, Mohamed Yousif Adam, Hoyam Mohd. Yamin, Bohari Al-Obaidi, Mazen M. Jamil Batran, Rami Al In vivo Assessment of Antioxidant and Wound Healing Improvement of a New Schiff Base Derived Co (II) Complex in Rats |
title | In vivo Assessment of Antioxidant and Wound Healing Improvement of a New Schiff Base Derived Co (II) Complex in Rats |
title_full | In vivo Assessment of Antioxidant and Wound Healing Improvement of a New Schiff Base Derived Co (II) Complex in Rats |
title_fullStr | In vivo Assessment of Antioxidant and Wound Healing Improvement of a New Schiff Base Derived Co (II) Complex in Rats |
title_full_unstemmed | In vivo Assessment of Antioxidant and Wound Healing Improvement of a New Schiff Base Derived Co (II) Complex in Rats |
title_short | In vivo Assessment of Antioxidant and Wound Healing Improvement of a New Schiff Base Derived Co (II) Complex in Rats |
title_sort | in vivo assessment of antioxidant and wound healing improvement of a new schiff base derived co (ii) complex in rats |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5153835/ https://www.ncbi.nlm.nih.gov/pubmed/27958299 http://dx.doi.org/10.1038/srep38748 |
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