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Platelet-rich plasma can release nutrient factors to promote facial nerve crush injury recovery in rats
OBJECTIVES: To evaluate the effects of platelet-rich plasma (PRP) on promoting neural repair after facial nerve compression in rats and the mechanism by which this occurs. METHODS: Adult Wistar rats (n=100) were divided into 3 groups: healthy controls, surgery-only, and surgery+PRP groups. The rats...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Saudi Medical Journal
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6969627/ https://www.ncbi.nlm.nih.gov/pubmed/31828272 http://dx.doi.org/10.15537/smj.2019.12.24747 |
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author | Li, Liheng Cai, Jing Yuan, Yang Mao, Yanyan Xu, Lei Han, Yuechen Li, Jianfeng Wang, Haibo |
author_facet | Li, Liheng Cai, Jing Yuan, Yang Mao, Yanyan Xu, Lei Han, Yuechen Li, Jianfeng Wang, Haibo |
author_sort | Li, Liheng |
collection | PubMed |
description | OBJECTIVES: To evaluate the effects of platelet-rich plasma (PRP) on promoting neural repair after facial nerve compression in rats and the mechanism by which this occurs. METHODS: Adult Wistar rats (n=100) were divided into 3 groups: healthy controls, surgery-only, and surgery+PRP groups. The rats underwent nerve crush injury to establish a facial palsy model. The blood from the rats was used to prepare the PRP for application to the injury site. The evaluation methods included vibrissae movement, eyelid closure, and electrophysiology. Electron microscopy, immunohistochemistry, and real-time polymerase chain reaction (PCR) were used to detect nutrient factor expression in the brain and nerve sections. This study was conducted in Shandong Provincial ENT Hospital Affiliated to Shandong University, Shandong, China between January and November 2018. RESULTS: Platelet-rich plasma promotes the recovery of vibrissae movement, eyelid closure, and electrophysiological function in a rat model of nerve crush injury. Hematoxylin and eosin staining, toluidine blue staining, and electron microscopy showed significant recovery of Schwann cells and axons in the PRP group. Polymerase chain reaction results showed that PRP releases growth factors, which include nerve growth factor and brain-derived neurotrophic factor. Immunohistochemistry also demonstrated higher levels of S-100 protein expression in the PRP group compared to the other groups. CONCLUSIONS: Platelet-rich plasma releases nutrient factors in the brainstem, and the use of PRP can promote injury recovery. |
format | Online Article Text |
id | pubmed-6969627 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Saudi Medical Journal |
record_format | MEDLINE/PubMed |
spelling | pubmed-69696272021-02-26 Platelet-rich plasma can release nutrient factors to promote facial nerve crush injury recovery in rats Li, Liheng Cai, Jing Yuan, Yang Mao, Yanyan Xu, Lei Han, Yuechen Li, Jianfeng Wang, Haibo Saudi Med J Original Article OBJECTIVES: To evaluate the effects of platelet-rich plasma (PRP) on promoting neural repair after facial nerve compression in rats and the mechanism by which this occurs. METHODS: Adult Wistar rats (n=100) were divided into 3 groups: healthy controls, surgery-only, and surgery+PRP groups. The rats underwent nerve crush injury to establish a facial palsy model. The blood from the rats was used to prepare the PRP for application to the injury site. The evaluation methods included vibrissae movement, eyelid closure, and electrophysiology. Electron microscopy, immunohistochemistry, and real-time polymerase chain reaction (PCR) were used to detect nutrient factor expression in the brain and nerve sections. This study was conducted in Shandong Provincial ENT Hospital Affiliated to Shandong University, Shandong, China between January and November 2018. RESULTS: Platelet-rich plasma promotes the recovery of vibrissae movement, eyelid closure, and electrophysiological function in a rat model of nerve crush injury. Hematoxylin and eosin staining, toluidine blue staining, and electron microscopy showed significant recovery of Schwann cells and axons in the PRP group. Polymerase chain reaction results showed that PRP releases growth factors, which include nerve growth factor and brain-derived neurotrophic factor. Immunohistochemistry also demonstrated higher levels of S-100 protein expression in the PRP group compared to the other groups. CONCLUSIONS: Platelet-rich plasma releases nutrient factors in the brainstem, and the use of PRP can promote injury recovery. Saudi Medical Journal 2019-12 /pmc/articles/PMC6969627/ /pubmed/31828272 http://dx.doi.org/10.15537/smj.2019.12.24747 Text en Copyright: © Saudi Medical Journal http://creativecommons.org/licenses/by-nc This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial License (CC BY-NC),which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Li, Liheng Cai, Jing Yuan, Yang Mao, Yanyan Xu, Lei Han, Yuechen Li, Jianfeng Wang, Haibo Platelet-rich plasma can release nutrient factors to promote facial nerve crush injury recovery in rats |
title | Platelet-rich plasma can release nutrient factors to promote facial nerve crush injury recovery in rats |
title_full | Platelet-rich plasma can release nutrient factors to promote facial nerve crush injury recovery in rats |
title_fullStr | Platelet-rich plasma can release nutrient factors to promote facial nerve crush injury recovery in rats |
title_full_unstemmed | Platelet-rich plasma can release nutrient factors to promote facial nerve crush injury recovery in rats |
title_short | Platelet-rich plasma can release nutrient factors to promote facial nerve crush injury recovery in rats |
title_sort | platelet-rich plasma can release nutrient factors to promote facial nerve crush injury recovery in rats |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6969627/ https://www.ncbi.nlm.nih.gov/pubmed/31828272 http://dx.doi.org/10.15537/smj.2019.12.24747 |
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