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Can a cyclooxygenase inhibitor be an option for treatment of ovarian hyperstimulation syndrome?

PURPOSE: This study aimed to investigate the role of a cyclooxygenase inhibitor in ovarian hyperstimulation syndrome (OHSS) treatment and compare it with cabergoline. MATERIALS AND METHODS: A total of 32 immature female Wistar albino rats were randomly divided into four groups, with each group consi...

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Autor principal: Çilgin, Hasan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6454993/
https://www.ncbi.nlm.nih.gov/pubmed/31040646
http://dx.doi.org/10.2147/DDDT.S188583
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author Çilgin, Hasan
author_facet Çilgin, Hasan
author_sort Çilgin, Hasan
collection PubMed
description PURPOSE: This study aimed to investigate the role of a cyclooxygenase inhibitor in ovarian hyperstimulation syndrome (OHSS) treatment and compare it with cabergoline. MATERIALS AND METHODS: A total of 32 immature female Wistar albino rats were randomly divided into four groups, with each group consisting of eight rats. The first group received only saline for 6 consecutive days, and the remaining 24 rats were given 10 IU of recombinant follicle stimulating hormone subcutaneously on 5 consecutive days. On day 6, 30 IU of human chorionic gonadotropin was administered for OHSS induction. After the development of OHSS, while the second group had no further intervention, the third and fourth groups were given cabergoline and celecoxib daily for 6 days, respectively. Besides weight and hematocrit values, vascular endothelial growth factor (VEGF), IL-2, and endothelin-1 (ET-1) levels were evaluated. RESULTS: Initially, no significant differences were observed between the groups with respect to the evaluated parameters. Although there were no differences between the weight and hema-tocrit values at the end of treatment (P=0.158, P=0.674), the difference between group 1 and the other groups was statistically significant after OHSS was established (P=0.001, P=0.004). Comparison of the groups in terms of VEGF, ET-1, and IL-2 levels revealed that the difference between group 1 and the other groups was significant after OHSS was formed (P=0.012, P=0.018, P=0.015). After treatment, however, a significant difference was observed only between group 2 and the other groups (P=0.001, P=0.002, P=0.038). CONCLUSION: According to these results, celecoxib significantly decreased VEGF, IL-2, and ET-1 levels as much as cabergoline and could reduce the extent of OHSS development.
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spelling pubmed-64549932019-04-30 Can a cyclooxygenase inhibitor be an option for treatment of ovarian hyperstimulation syndrome? Çilgin, Hasan Drug Des Devel Ther Original Research PURPOSE: This study aimed to investigate the role of a cyclooxygenase inhibitor in ovarian hyperstimulation syndrome (OHSS) treatment and compare it with cabergoline. MATERIALS AND METHODS: A total of 32 immature female Wistar albino rats were randomly divided into four groups, with each group consisting of eight rats. The first group received only saline for 6 consecutive days, and the remaining 24 rats were given 10 IU of recombinant follicle stimulating hormone subcutaneously on 5 consecutive days. On day 6, 30 IU of human chorionic gonadotropin was administered for OHSS induction. After the development of OHSS, while the second group had no further intervention, the third and fourth groups were given cabergoline and celecoxib daily for 6 days, respectively. Besides weight and hematocrit values, vascular endothelial growth factor (VEGF), IL-2, and endothelin-1 (ET-1) levels were evaluated. RESULTS: Initially, no significant differences were observed between the groups with respect to the evaluated parameters. Although there were no differences between the weight and hema-tocrit values at the end of treatment (P=0.158, P=0.674), the difference between group 1 and the other groups was statistically significant after OHSS was established (P=0.001, P=0.004). Comparison of the groups in terms of VEGF, ET-1, and IL-2 levels revealed that the difference between group 1 and the other groups was significant after OHSS was formed (P=0.012, P=0.018, P=0.015). After treatment, however, a significant difference was observed only between group 2 and the other groups (P=0.001, P=0.002, P=0.038). CONCLUSION: According to these results, celecoxib significantly decreased VEGF, IL-2, and ET-1 levels as much as cabergoline and could reduce the extent of OHSS development. Dove Medical Press 2019-04-05 /pmc/articles/PMC6454993/ /pubmed/31040646 http://dx.doi.org/10.2147/DDDT.S188583 Text en © 2019 Çilgin. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Çilgin, Hasan
Can a cyclooxygenase inhibitor be an option for treatment of ovarian hyperstimulation syndrome?
title Can a cyclooxygenase inhibitor be an option for treatment of ovarian hyperstimulation syndrome?
title_full Can a cyclooxygenase inhibitor be an option for treatment of ovarian hyperstimulation syndrome?
title_fullStr Can a cyclooxygenase inhibitor be an option for treatment of ovarian hyperstimulation syndrome?
title_full_unstemmed Can a cyclooxygenase inhibitor be an option for treatment of ovarian hyperstimulation syndrome?
title_short Can a cyclooxygenase inhibitor be an option for treatment of ovarian hyperstimulation syndrome?
title_sort can a cyclooxygenase inhibitor be an option for treatment of ovarian hyperstimulation syndrome?
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6454993/
https://www.ncbi.nlm.nih.gov/pubmed/31040646
http://dx.doi.org/10.2147/DDDT.S188583
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