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Combined therapy of photobiomodulation and adipose-derived stem cells synergistically improve healing in an ischemic, infected and delayed healing wound model in rats with type 1 diabetes mellitus

OBJECTIVE: We assessed the therapeutic effects of photobiomodulation (PBM) and adipose-derived stem cell (ADS) treatments individually and together on the maturation step of repairing of a delayed healing wound model in rats with type 1 diabetes mellitus (DM1). RESEARCH DESIGN AND METHODS: We random...

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Autores principales: Ebrahimpour-Malekshah, Roohollah, Amini, Abdollah, Zare, Fatemeh, Mostafavinia, Atarodsadat, Davoody, Samin, Deravi, Niloofar, Rahmanian, Mohammad, Hashemi, Seyed Mahmoud, Habibi, Malihe, Ghoreishi, Seyed Kamran, Chien, Sufan, Shafikhani, Sasha, Ahmadi, Houssein, Bayat, Sahar, Bayat, Mohammad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7206914/
https://www.ncbi.nlm.nih.gov/pubmed/32098898
http://dx.doi.org/10.1136/bmjdrc-2019-001033
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author Ebrahimpour-Malekshah, Roohollah
Amini, Abdollah
Zare, Fatemeh
Mostafavinia, Atarodsadat
Davoody, Samin
Deravi, Niloofar
Rahmanian, Mohammad
Hashemi, Seyed Mahmoud
Habibi, Malihe
Ghoreishi, Seyed Kamran
Chien, Sufan
Shafikhani, Sasha
Ahmadi, Houssein
Bayat, Sahar
Bayat, Mohammad
author_facet Ebrahimpour-Malekshah, Roohollah
Amini, Abdollah
Zare, Fatemeh
Mostafavinia, Atarodsadat
Davoody, Samin
Deravi, Niloofar
Rahmanian, Mohammad
Hashemi, Seyed Mahmoud
Habibi, Malihe
Ghoreishi, Seyed Kamran
Chien, Sufan
Shafikhani, Sasha
Ahmadi, Houssein
Bayat, Sahar
Bayat, Mohammad
author_sort Ebrahimpour-Malekshah, Roohollah
collection PubMed
description OBJECTIVE: We assessed the therapeutic effects of photobiomodulation (PBM) and adipose-derived stem cell (ADS) treatments individually and together on the maturation step of repairing of a delayed healing wound model in rats with type 1 diabetes mellitus (DM1). RESEARCH DESIGN AND METHODS: We randomly assigned 24 rats with DM1 to four groups (n=6 per group). Group 1 was the control (placebo) group. In group 2, allograft human ADSs were transplanted. Group 3 was subjected to PBM (wavelength: 890 nm, peak power output: 80 W, pulse frequency: 80 Hz, pulsed duration: 180 ns, duration of exposure for each point: 200 s, power density: 0.001 W/cm(2), energy density: 0.2 J/cm(2)) immediately after surgery, which continued for 6 days per week for 16 days. Group 4 received both the human ADS and PBM. In addition, we inflicted an ischemic, delayed healing, and infected wound simulation in all of the rats. The wounds were infected with methicillin-resistant Staphylococcus aureus (MRSA). RESULTS: All three treatment regimens significantly decreased the amount of microbial flora, significantly increased wound strength and significantly modulated inflammatory response and significantly increased angiogenesis on day 16. Microbiological analysis showed that PBM+ADS was significantly better than PBM and ADS alone. In terms of wound closure rate and angiogenesis, PBM+ADS was significantly better than the PBM, ADS and control groups. CONCLUSIONS: Combination therapy of PBM+ADS is more effective that either PBM or ADS in stimulating skin injury repair, and modulating inflammatory response in an MRSA-infected wound model of rats with DM1.
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spelling pubmed-72069142020-05-12 Combined therapy of photobiomodulation and adipose-derived stem cells synergistically improve healing in an ischemic, infected and delayed healing wound model in rats with type 1 diabetes mellitus Ebrahimpour-Malekshah, Roohollah Amini, Abdollah Zare, Fatemeh Mostafavinia, Atarodsadat Davoody, Samin Deravi, Niloofar Rahmanian, Mohammad Hashemi, Seyed Mahmoud Habibi, Malihe Ghoreishi, Seyed Kamran Chien, Sufan Shafikhani, Sasha Ahmadi, Houssein Bayat, Sahar Bayat, Mohammad BMJ Open Diabetes Res Care Clinical Care/Education/Nutrition OBJECTIVE: We assessed the therapeutic effects of photobiomodulation (PBM) and adipose-derived stem cell (ADS) treatments individually and together on the maturation step of repairing of a delayed healing wound model in rats with type 1 diabetes mellitus (DM1). RESEARCH DESIGN AND METHODS: We randomly assigned 24 rats with DM1 to four groups (n=6 per group). Group 1 was the control (placebo) group. In group 2, allograft human ADSs were transplanted. Group 3 was subjected to PBM (wavelength: 890 nm, peak power output: 80 W, pulse frequency: 80 Hz, pulsed duration: 180 ns, duration of exposure for each point: 200 s, power density: 0.001 W/cm(2), energy density: 0.2 J/cm(2)) immediately after surgery, which continued for 6 days per week for 16 days. Group 4 received both the human ADS and PBM. In addition, we inflicted an ischemic, delayed healing, and infected wound simulation in all of the rats. The wounds were infected with methicillin-resistant Staphylococcus aureus (MRSA). RESULTS: All three treatment regimens significantly decreased the amount of microbial flora, significantly increased wound strength and significantly modulated inflammatory response and significantly increased angiogenesis on day 16. Microbiological analysis showed that PBM+ADS was significantly better than PBM and ADS alone. In terms of wound closure rate and angiogenesis, PBM+ADS was significantly better than the PBM, ADS and control groups. CONCLUSIONS: Combination therapy of PBM+ADS is more effective that either PBM or ADS in stimulating skin injury repair, and modulating inflammatory response in an MRSA-infected wound model of rats with DM1. BMJ Publishing Group 2020-02-24 /pmc/articles/PMC7206914/ /pubmed/32098898 http://dx.doi.org/10.1136/bmjdrc-2019-001033 Text en © Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Clinical Care/Education/Nutrition
Ebrahimpour-Malekshah, Roohollah
Amini, Abdollah
Zare, Fatemeh
Mostafavinia, Atarodsadat
Davoody, Samin
Deravi, Niloofar
Rahmanian, Mohammad
Hashemi, Seyed Mahmoud
Habibi, Malihe
Ghoreishi, Seyed Kamran
Chien, Sufan
Shafikhani, Sasha
Ahmadi, Houssein
Bayat, Sahar
Bayat, Mohammad
Combined therapy of photobiomodulation and adipose-derived stem cells synergistically improve healing in an ischemic, infected and delayed healing wound model in rats with type 1 diabetes mellitus
title Combined therapy of photobiomodulation and adipose-derived stem cells synergistically improve healing in an ischemic, infected and delayed healing wound model in rats with type 1 diabetes mellitus
title_full Combined therapy of photobiomodulation and adipose-derived stem cells synergistically improve healing in an ischemic, infected and delayed healing wound model in rats with type 1 diabetes mellitus
title_fullStr Combined therapy of photobiomodulation and adipose-derived stem cells synergistically improve healing in an ischemic, infected and delayed healing wound model in rats with type 1 diabetes mellitus
title_full_unstemmed Combined therapy of photobiomodulation and adipose-derived stem cells synergistically improve healing in an ischemic, infected and delayed healing wound model in rats with type 1 diabetes mellitus
title_short Combined therapy of photobiomodulation and adipose-derived stem cells synergistically improve healing in an ischemic, infected and delayed healing wound model in rats with type 1 diabetes mellitus
title_sort combined therapy of photobiomodulation and adipose-derived stem cells synergistically improve healing in an ischemic, infected and delayed healing wound model in rats with type 1 diabetes mellitus
topic Clinical Care/Education/Nutrition
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7206914/
https://www.ncbi.nlm.nih.gov/pubmed/32098898
http://dx.doi.org/10.1136/bmjdrc-2019-001033
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