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Effects of Autologous Platelet-Rich Plasma on Regeneration of Damaged Endometrium in Female Rats

PURPOSE: To investigate whether autologous platelet-rich plasma (PRP) treatment can improve regeneration of the endometrium in an experimental model of ethanol-induced damage. MATERIALS AND METHODS: Sixty female Sprague-Dawley rats were randomly assigned into three groups: control group, ethanol gro...

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Autores principales: Jang, Hang-Yong, Myoung, Soo Min, Choe, Jeong Min, Kim, Tak, Cheon, Yong-Pil, Kim, Yong Min, Park, Hyuntae
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Yonsei University College of Medicine 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5653485/
https://www.ncbi.nlm.nih.gov/pubmed/29047244
http://dx.doi.org/10.3349/ymj.2017.58.6.1195
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author Jang, Hang-Yong
Myoung, Soo Min
Choe, Jeong Min
Kim, Tak
Cheon, Yong-Pil
Kim, Yong Min
Park, Hyuntae
author_facet Jang, Hang-Yong
Myoung, Soo Min
Choe, Jeong Min
Kim, Tak
Cheon, Yong-Pil
Kim, Yong Min
Park, Hyuntae
author_sort Jang, Hang-Yong
collection PubMed
description PURPOSE: To investigate whether autologous platelet-rich plasma (PRP) treatment can improve regeneration of the endometrium in an experimental model of ethanol-induced damage. MATERIALS AND METHODS: Sixty female Sprague-Dawley rats were randomly assigned into three groups: control group, ethanol group, and PRP-treated group (administration of 0.25 mL of PRP into both uterine cavities 72 hours after ethanol injection). After 15 days of endometrial damage, all the animals were sacrificed during the estrous cycle, and samples were taken from the mid-uterine horn. Functional and structural recovery of the endometrium was analyzed by hematoxylin-eosin (H&E) and Masson trichrome (MT) staining, real-time polymerase chain reaction (PCR) assay, and immuno-histochemical (IHC) analyses. RESULTS: H&E and MT staining confirmed significantly decreased fibrosis and increased cellular proliferation in the PRP-treated group, compared to the ethanol group. The endometrial areas in the ethanol and PRP-treated groups were 212.83±15.84 µm(2) and 262.34±12.33 µm(2) (p=0.065). Significantly stronger IHC expression of cytokeratin, homeobox A10 (HOXA10), vascular endothelial growth factor (VEGF), and Ki-67 was found in the PRP-treated group, compared to the ethanol group. In real-time PCR analyses, interleukin-1β mRNA was down-regulated, while c-Kit mRNA was up-regulated, in the PRP-treated group, compared to the ethanol group. CONCLUSION: Intrauterine administration of autologous PRP stimulated and accelerated regeneration of the endometrium and also decreased fibrosis in a murine model of damaged endometrium.
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spelling pubmed-56534852017-11-01 Effects of Autologous Platelet-Rich Plasma on Regeneration of Damaged Endometrium in Female Rats Jang, Hang-Yong Myoung, Soo Min Choe, Jeong Min Kim, Tak Cheon, Yong-Pil Kim, Yong Min Park, Hyuntae Yonsei Med J Original Article PURPOSE: To investigate whether autologous platelet-rich plasma (PRP) treatment can improve regeneration of the endometrium in an experimental model of ethanol-induced damage. MATERIALS AND METHODS: Sixty female Sprague-Dawley rats were randomly assigned into three groups: control group, ethanol group, and PRP-treated group (administration of 0.25 mL of PRP into both uterine cavities 72 hours after ethanol injection). After 15 days of endometrial damage, all the animals were sacrificed during the estrous cycle, and samples were taken from the mid-uterine horn. Functional and structural recovery of the endometrium was analyzed by hematoxylin-eosin (H&E) and Masson trichrome (MT) staining, real-time polymerase chain reaction (PCR) assay, and immuno-histochemical (IHC) analyses. RESULTS: H&E and MT staining confirmed significantly decreased fibrosis and increased cellular proliferation in the PRP-treated group, compared to the ethanol group. The endometrial areas in the ethanol and PRP-treated groups were 212.83±15.84 µm(2) and 262.34±12.33 µm(2) (p=0.065). Significantly stronger IHC expression of cytokeratin, homeobox A10 (HOXA10), vascular endothelial growth factor (VEGF), and Ki-67 was found in the PRP-treated group, compared to the ethanol group. In real-time PCR analyses, interleukin-1β mRNA was down-regulated, while c-Kit mRNA was up-regulated, in the PRP-treated group, compared to the ethanol group. CONCLUSION: Intrauterine administration of autologous PRP stimulated and accelerated regeneration of the endometrium and also decreased fibrosis in a murine model of damaged endometrium. Yonsei University College of Medicine 2017-11-01 2017-09-28 /pmc/articles/PMC5653485/ /pubmed/29047244 http://dx.doi.org/10.3349/ymj.2017.58.6.1195 Text en © Copyright: Yonsei University College of Medicine 2017 http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Jang, Hang-Yong
Myoung, Soo Min
Choe, Jeong Min
Kim, Tak
Cheon, Yong-Pil
Kim, Yong Min
Park, Hyuntae
Effects of Autologous Platelet-Rich Plasma on Regeneration of Damaged Endometrium in Female Rats
title Effects of Autologous Platelet-Rich Plasma on Regeneration of Damaged Endometrium in Female Rats
title_full Effects of Autologous Platelet-Rich Plasma on Regeneration of Damaged Endometrium in Female Rats
title_fullStr Effects of Autologous Platelet-Rich Plasma on Regeneration of Damaged Endometrium in Female Rats
title_full_unstemmed Effects of Autologous Platelet-Rich Plasma on Regeneration of Damaged Endometrium in Female Rats
title_short Effects of Autologous Platelet-Rich Plasma on Regeneration of Damaged Endometrium in Female Rats
title_sort effects of autologous platelet-rich plasma on regeneration of damaged endometrium in female rats
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5653485/
https://www.ncbi.nlm.nih.gov/pubmed/29047244
http://dx.doi.org/10.3349/ymj.2017.58.6.1195
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