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Improvement of Skeletal Muscle Regeneration by Platelet-Rich Plasma in Rats with Experimental Chronic Hyperglycemia

Herein, the structural effect of autologous platelet-rich plasma (PRP) on posttraumatic skeletal muscle regeneration in rats with chronic hyperglycemia (CH) was tested. 130 white laboratory male rats divided into four groups (I—control; II—rats with CH; III—rats with CH and PRP treatment; and IV—rat...

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Autores principales: Rtail, Raed, Maksymova, Olena, Illiashenko, Viacheslav, Gortynska, Olena, Korenkov, Oleksii, Moskalenko, Pavlo, Nasser, Mohamad, Tkach, Gennadii
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7374220/
https://www.ncbi.nlm.nih.gov/pubmed/32766312
http://dx.doi.org/10.1155/2020/6980607
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author Rtail, Raed
Maksymova, Olena
Illiashenko, Viacheslav
Gortynska, Olena
Korenkov, Oleksii
Moskalenko, Pavlo
Nasser, Mohamad
Tkach, Gennadii
author_facet Rtail, Raed
Maksymova, Olena
Illiashenko, Viacheslav
Gortynska, Olena
Korenkov, Oleksii
Moskalenko, Pavlo
Nasser, Mohamad
Tkach, Gennadii
author_sort Rtail, Raed
collection PubMed
description Herein, the structural effect of autologous platelet-rich plasma (PRP) on posttraumatic skeletal muscle regeneration in rats with chronic hyperglycemia (CH) was tested. 130 white laboratory male rats divided into four groups (I—control; II—rats with CH; III—rats with CH and PRP treatment; and IV—rats for CH confirmation) were used for the experiment. CH was simulated by streptozotocin and nicotinic acid administration. Triceps surae muscle injury was reproduced by transverse linear incision. Autologous PRP was used in order to correct the possible negative CH effect on skeletal muscle recovery. On the 28th day after the injury, the regenerating muscle fiber and blood vessel number in the CH+PRP group were higher than those in the CH rats. However, the connective tissue area in the CH group was larger than that in the CH+PRP animals. The amount of agranulocytes in the regenerating muscle of the CH rats was lower compared to that of the CH+PRP group. The histological analysis of skeletal muscle recovery in CH+PRP animals revealed more intensive neoangiogenesis compared to that in the CH group. Herewith, the massive connective tissue development and inflammation signs were observed within the skeletal muscle of CH rats. Obtained results suggest that streptozotocin-induced CH has a negative effect on posttraumatic skeletal muscle regeneration, contributing to massive connective tissue development. The autologous PRP injection promotes muscle recovery process in rats with CH, shifting it away from fibrosis toward the complete muscular organ repair.
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spelling pubmed-73742202020-08-05 Improvement of Skeletal Muscle Regeneration by Platelet-Rich Plasma in Rats with Experimental Chronic Hyperglycemia Rtail, Raed Maksymova, Olena Illiashenko, Viacheslav Gortynska, Olena Korenkov, Oleksii Moskalenko, Pavlo Nasser, Mohamad Tkach, Gennadii Biomed Res Int Research Article Herein, the structural effect of autologous platelet-rich plasma (PRP) on posttraumatic skeletal muscle regeneration in rats with chronic hyperglycemia (CH) was tested. 130 white laboratory male rats divided into four groups (I—control; II—rats with CH; III—rats with CH and PRP treatment; and IV—rats for CH confirmation) were used for the experiment. CH was simulated by streptozotocin and nicotinic acid administration. Triceps surae muscle injury was reproduced by transverse linear incision. Autologous PRP was used in order to correct the possible negative CH effect on skeletal muscle recovery. On the 28th day after the injury, the regenerating muscle fiber and blood vessel number in the CH+PRP group were higher than those in the CH rats. However, the connective tissue area in the CH group was larger than that in the CH+PRP animals. The amount of agranulocytes in the regenerating muscle of the CH rats was lower compared to that of the CH+PRP group. The histological analysis of skeletal muscle recovery in CH+PRP animals revealed more intensive neoangiogenesis compared to that in the CH group. Herewith, the massive connective tissue development and inflammation signs were observed within the skeletal muscle of CH rats. Obtained results suggest that streptozotocin-induced CH has a negative effect on posttraumatic skeletal muscle regeneration, contributing to massive connective tissue development. The autologous PRP injection promotes muscle recovery process in rats with CH, shifting it away from fibrosis toward the complete muscular organ repair. Hindawi 2020-07-11 /pmc/articles/PMC7374220/ /pubmed/32766312 http://dx.doi.org/10.1155/2020/6980607 Text en Copyright © 2020 Raed Rtail et al. http://creativecommons.org/licenses/by/4.0/ 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
Rtail, Raed
Maksymova, Olena
Illiashenko, Viacheslav
Gortynska, Olena
Korenkov, Oleksii
Moskalenko, Pavlo
Nasser, Mohamad
Tkach, Gennadii
Improvement of Skeletal Muscle Regeneration by Platelet-Rich Plasma in Rats with Experimental Chronic Hyperglycemia
title Improvement of Skeletal Muscle Regeneration by Platelet-Rich Plasma in Rats with Experimental Chronic Hyperglycemia
title_full Improvement of Skeletal Muscle Regeneration by Platelet-Rich Plasma in Rats with Experimental Chronic Hyperglycemia
title_fullStr Improvement of Skeletal Muscle Regeneration by Platelet-Rich Plasma in Rats with Experimental Chronic Hyperglycemia
title_full_unstemmed Improvement of Skeletal Muscle Regeneration by Platelet-Rich Plasma in Rats with Experimental Chronic Hyperglycemia
title_short Improvement of Skeletal Muscle Regeneration by Platelet-Rich Plasma in Rats with Experimental Chronic Hyperglycemia
title_sort improvement of skeletal muscle regeneration by platelet-rich plasma in rats with experimental chronic hyperglycemia
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7374220/
https://www.ncbi.nlm.nih.gov/pubmed/32766312
http://dx.doi.org/10.1155/2020/6980607
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