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Effect of insulin-like growth factor-1 and hyaluronic acid in experimentally produced osteochondral defects in rats

BACKGROUND: The common purpose of almost all methods used to treat the osteochondral injuries is to produce a normal cartilage matrix. However current methods are not sufficient to provide a normal cartilage matrix. For that reason, researchers have studied to increase the effectiveness of this meth...

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Autores principales: Alemdar, Celil, Yücel, İstemi, Erbil, Barış, Erdem, Havva, Atiç, Ramazan, Özkul, Emin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4964775/
https://www.ncbi.nlm.nih.gov/pubmed/27512224
http://dx.doi.org/10.4103/0019-5413.185607
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author Alemdar, Celil
Yücel, İstemi
Erbil, Barış
Erdem, Havva
Atiç, Ramazan
Özkul, Emin
author_facet Alemdar, Celil
Yücel, İstemi
Erbil, Barış
Erdem, Havva
Atiç, Ramazan
Özkul, Emin
author_sort Alemdar, Celil
collection PubMed
description BACKGROUND: The common purpose of almost all methods used to treat the osteochondral injuries is to produce a normal cartilage matrix. However current methods are not sufficient to provide a normal cartilage matrix. For that reason, researchers have studied to increase the effectiveness of this methods using chondrogenic and chondroprotective molecules in recent experimental studies. Insulin-like growth factor-1 (IGF-1) and hyaluronic acid (HA) are two important agents used in this field. This study compared the effects of IGF-1 and HA in an experimental osteochondral defect in rat femora. MATERIALS AND METHODS: The rats were divided into three groups (n = 15 per group) as follows: The IGF-1 group, HA group, and control group. An osteochondral defect of a diameter of 1.5 mm and a depth of 2 mm was created on the patellar joint side of femoral condyles. The IGF-1 group received an absorbable gelatin sponge soaked with 15 μg/15 μl of IGF-1, and the HA group received an absorbable gelatin sponge soaked with 80 μg HA. The control group received only an absorbable gelatin sponge. Rats were sacrificed at the 6(th) week, and the femur condyles were evaluated histologically. RESULTS: According to the total Mankin scale, there was a statistically significant difference between IGF-1 and HA groups and between IGF-1 and control groups. There was also a significant statistical difference between HA and control groups. CONCLUSION: It was shown histopathologically that IGF-1 is an effective molecule for osteochondral lesions. Although it is weaker than IGF-1, HA also strengthened the repair tissue.
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spelling pubmed-49647752016-08-10 Effect of insulin-like growth factor-1 and hyaluronic acid in experimentally produced osteochondral defects in rats Alemdar, Celil Yücel, İstemi Erbil, Barış Erdem, Havva Atiç, Ramazan Özkul, Emin Indian J Orthop Original Article BACKGROUND: The common purpose of almost all methods used to treat the osteochondral injuries is to produce a normal cartilage matrix. However current methods are not sufficient to provide a normal cartilage matrix. For that reason, researchers have studied to increase the effectiveness of this methods using chondrogenic and chondroprotective molecules in recent experimental studies. Insulin-like growth factor-1 (IGF-1) and hyaluronic acid (HA) are two important agents used in this field. This study compared the effects of IGF-1 and HA in an experimental osteochondral defect in rat femora. MATERIALS AND METHODS: The rats were divided into three groups (n = 15 per group) as follows: The IGF-1 group, HA group, and control group. An osteochondral defect of a diameter of 1.5 mm and a depth of 2 mm was created on the patellar joint side of femoral condyles. The IGF-1 group received an absorbable gelatin sponge soaked with 15 μg/15 μl of IGF-1, and the HA group received an absorbable gelatin sponge soaked with 80 μg HA. The control group received only an absorbable gelatin sponge. Rats were sacrificed at the 6(th) week, and the femur condyles were evaluated histologically. RESULTS: According to the total Mankin scale, there was a statistically significant difference between IGF-1 and HA groups and between IGF-1 and control groups. There was also a significant statistical difference between HA and control groups. CONCLUSION: It was shown histopathologically that IGF-1 is an effective molecule for osteochondral lesions. Although it is weaker than IGF-1, HA also strengthened the repair tissue. Medknow Publications & Media Pvt Ltd 2016 /pmc/articles/PMC4964775/ /pubmed/27512224 http://dx.doi.org/10.4103/0019-5413.185607 Text en Copyright: © Indian Journal of Orthopaedics http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Original Article
Alemdar, Celil
Yücel, İstemi
Erbil, Barış
Erdem, Havva
Atiç, Ramazan
Özkul, Emin
Effect of insulin-like growth factor-1 and hyaluronic acid in experimentally produced osteochondral defects in rats
title Effect of insulin-like growth factor-1 and hyaluronic acid in experimentally produced osteochondral defects in rats
title_full Effect of insulin-like growth factor-1 and hyaluronic acid in experimentally produced osteochondral defects in rats
title_fullStr Effect of insulin-like growth factor-1 and hyaluronic acid in experimentally produced osteochondral defects in rats
title_full_unstemmed Effect of insulin-like growth factor-1 and hyaluronic acid in experimentally produced osteochondral defects in rats
title_short Effect of insulin-like growth factor-1 and hyaluronic acid in experimentally produced osteochondral defects in rats
title_sort effect of insulin-like growth factor-1 and hyaluronic acid in experimentally produced osteochondral defects in rats
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4964775/
https://www.ncbi.nlm.nih.gov/pubmed/27512224
http://dx.doi.org/10.4103/0019-5413.185607
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