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Effect of maternal fluoxetine exposure on lung, heart, and kidney development in rat neonates

OBJECTIVE(S): Depression during pregnancy negatively affects fetal development. Fluoxetine as a selective serotonin reuptake inhibitor (SSRIs) is used for treatment of gestational depression. This study is trying to determine the effects of fluoxetine on the renal, heart and lung development. MATERI...

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Autores principales: Ghavamabadi, Razieh Taghizadeh, Taghipour, Zahra, Hassanipour, Mahsa, Khademi, Marzieh, Shariati, Mehdi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mashhad University of Medical Sciences 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5960760/
https://www.ncbi.nlm.nih.gov/pubmed/29796227
http://dx.doi.org/10.22038/IJBMS.2018.27203.6650
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author Ghavamabadi, Razieh Taghizadeh
Taghipour, Zahra
Hassanipour, Mahsa
Khademi, Marzieh
Shariati, Mehdi
author_facet Ghavamabadi, Razieh Taghizadeh
Taghipour, Zahra
Hassanipour, Mahsa
Khademi, Marzieh
Shariati, Mehdi
author_sort Ghavamabadi, Razieh Taghizadeh
collection PubMed
description OBJECTIVE(S): Depression during pregnancy negatively affects fetal development. Fluoxetine as a selective serotonin reuptake inhibitor (SSRIs) is used for treatment of gestational depression. This study is trying to determine the effects of fluoxetine on the renal, heart and lung development. MATERIALS AND METHODS: Fifteen pregnant rats were treated with fluoxetine at 7 mg/kg from days 0 to 21 of gestation. Immediately after born, heart and kidney samples were evaluated for genes expression and histological assessment. Lung sample were fixed for immunohistochemical study. RESULTS: The gene expression of BMP7 and WNT4 were reduced in the kidney of fluoxetine-treated group (P-value<0.05), but in the heart of both groups no significant difference was found in gene expression (P-value>0.05). Histological assessment showed that the glomeruli of the kidneys in treated group are more primordial compared to control. There was a developmental deficiency in Bowman’s capsule, and the capsular space was not clear. The arrangements of the filaments, the position of the nucleus and cells morphology were normal in the hearts of both groups. Immunohistochemical analysis demonstrated that in the fluoxetine-exposed group HoxB5 is more expressed in the mesenchymal cells, but in the control group the expression is limited to alveolar cells. CONCLUSION: According to developmental changes in kidney, heart and lung, fluoxetine affects neonatal growth during pregnancy, which may lead to delay of some organs growth. So, it is essential to survey the roles of antidepressant drugs on fatal and neonatal development during pregnancy.
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spelling pubmed-59607602018-05-24 Effect of maternal fluoxetine exposure on lung, heart, and kidney development in rat neonates Ghavamabadi, Razieh Taghizadeh Taghipour, Zahra Hassanipour, Mahsa Khademi, Marzieh Shariati, Mehdi Iran J Basic Med Sci Original Article OBJECTIVE(S): Depression during pregnancy negatively affects fetal development. Fluoxetine as a selective serotonin reuptake inhibitor (SSRIs) is used for treatment of gestational depression. This study is trying to determine the effects of fluoxetine on the renal, heart and lung development. MATERIALS AND METHODS: Fifteen pregnant rats were treated with fluoxetine at 7 mg/kg from days 0 to 21 of gestation. Immediately after born, heart and kidney samples were evaluated for genes expression and histological assessment. Lung sample were fixed for immunohistochemical study. RESULTS: The gene expression of BMP7 and WNT4 were reduced in the kidney of fluoxetine-treated group (P-value<0.05), but in the heart of both groups no significant difference was found in gene expression (P-value>0.05). Histological assessment showed that the glomeruli of the kidneys in treated group are more primordial compared to control. There was a developmental deficiency in Bowman’s capsule, and the capsular space was not clear. The arrangements of the filaments, the position of the nucleus and cells morphology were normal in the hearts of both groups. Immunohistochemical analysis demonstrated that in the fluoxetine-exposed group HoxB5 is more expressed in the mesenchymal cells, but in the control group the expression is limited to alveolar cells. CONCLUSION: According to developmental changes in kidney, heart and lung, fluoxetine affects neonatal growth during pregnancy, which may lead to delay of some organs growth. So, it is essential to survey the roles of antidepressant drugs on fatal and neonatal development during pregnancy. Mashhad University of Medical Sciences 2018-04 /pmc/articles/PMC5960760/ /pubmed/29796227 http://dx.doi.org/10.22038/IJBMS.2018.27203.6650 Text en Copyright: © Iranian Journal of Basic Medical Sciences 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-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Ghavamabadi, Razieh Taghizadeh
Taghipour, Zahra
Hassanipour, Mahsa
Khademi, Marzieh
Shariati, Mehdi
Effect of maternal fluoxetine exposure on lung, heart, and kidney development in rat neonates
title Effect of maternal fluoxetine exposure on lung, heart, and kidney development in rat neonates
title_full Effect of maternal fluoxetine exposure on lung, heart, and kidney development in rat neonates
title_fullStr Effect of maternal fluoxetine exposure on lung, heart, and kidney development in rat neonates
title_full_unstemmed Effect of maternal fluoxetine exposure on lung, heart, and kidney development in rat neonates
title_short Effect of maternal fluoxetine exposure on lung, heart, and kidney development in rat neonates
title_sort effect of maternal fluoxetine exposure on lung, heart, and kidney development in rat neonates
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5960760/
https://www.ncbi.nlm.nih.gov/pubmed/29796227
http://dx.doi.org/10.22038/IJBMS.2018.27203.6650
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