Teratogenic Effects of Coadministration of Fluoxetine and Olanzapine on Rat Fetuses

Objective. Depression during pregnancy is a relatively common problem. Since little is known about the teratogenic effects of concomitant administration of fluoxetine and olanzapine during the organogenesis period, the aim of the present study was to evaluate the teratogenic effects of coadministrat...

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Main Authors: Azam Bakhtiarian, Nasrin Takzare, Mehdi Sheykhi, Narges Sistany, Farahnaz Jazaeri, Mario Giorgi, Vahid Nikoui
Format: Article
Language:English
Published: Wiley 2014-01-01
Series:Advances in Pharmacological Sciences
Online Access:http://dx.doi.org/10.1155/2014/132034
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author Azam Bakhtiarian
Nasrin Takzare
Mehdi Sheykhi
Narges Sistany
Farahnaz Jazaeri
Mario Giorgi
Vahid Nikoui
author_facet Azam Bakhtiarian
Nasrin Takzare
Mehdi Sheykhi
Narges Sistany
Farahnaz Jazaeri
Mario Giorgi
Vahid Nikoui
author_sort Azam Bakhtiarian
collection DOAJ
description Objective. Depression during pregnancy is a relatively common problem. Since little is known about the teratogenic effects of concomitant administration of fluoxetine and olanzapine during the organogenesis period, the aim of the present study was to evaluate the teratogenic effects of coadministration of fluoxetine and olanzapine on rat fetuses. Method. Forty-two pregnant rats were divided into seven groups, randomly. The first group received 0.5 mL of normal saline as the control. The second and third groups received fluoxetine at doses of 9 mg/kg and 18 mg/kg, respectively. Olanzapine was injected at 3 mg/kg and 6 mg/kg to the fourth and fifth groups, respectively. The sixth group received 9 mg/kg fluoxetine and 3 mg/kg olanzapine. Finally, the seventh group was administrated with fluoxetine and olanzapine at 18 mg/kg and 6 mg/kg, respectively. Drugs were injected intraperitoneally between day eight and day 15 of the pregnancy. On the 17th day of pregnancy, the fetuses were removed and micro-/macroscopically studied. Results. Fetuses of rats receiving high doses of these drugs showed a significant rate of cleft palate development, premature eyelid opening and torsion anomalies, compared to the control group (P≤0.01). It is concluded that these drugs can lead to teratogenicity, so their concomitant use during pregnancy should be avoided, or if necessary their doses must be decreased.
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spelling doaj-art-a892ba61819740f4b4aa15557cdec1cf2025-02-03T06:44:41ZengWileyAdvances in Pharmacological Sciences1687-63341687-63422014-01-01201410.1155/2014/132034132034Teratogenic Effects of Coadministration of Fluoxetine and Olanzapine on Rat FetusesAzam Bakhtiarian0Nasrin Takzare1Mehdi Sheykhi2Narges Sistany3Farahnaz Jazaeri4Mario Giorgi5Vahid Nikoui6Department of Pharmacology, School of Medicine, Tehran University of Medical Sciences, Pour Sina Street, Qods Street, Keshavarz Boulevard, Tehran 1417613151, IranDepartment of Anatomy, School of Medicine, Tehran University of Medical Sciences, Tehran 1417613146, IranSchool of Medicine, Tehran University of Medical Sciences, Tehran 1417613110, IranDepartment of Neurosurgery, Shariati Hospital, Tehran University of Medical Sciences, Tehran, IranDepartment of Pharmacology, School of Medicine, Tehran University of Medical Sciences, Pour Sina Street, Qods Street, Keshavarz Boulevard, Tehran 1417613151, IranDepartment of Veterinary Sciences, University of Pisa, San Piero a Grado, Pisa 56122, ItalyDepartment of Pharmacology, School of Medicine, Tehran University of Medical Sciences, Pour Sina Street, Qods Street, Keshavarz Boulevard, Tehran 1417613151, IranObjective. Depression during pregnancy is a relatively common problem. Since little is known about the teratogenic effects of concomitant administration of fluoxetine and olanzapine during the organogenesis period, the aim of the present study was to evaluate the teratogenic effects of coadministration of fluoxetine and olanzapine on rat fetuses. Method. Forty-two pregnant rats were divided into seven groups, randomly. The first group received 0.5 mL of normal saline as the control. The second and third groups received fluoxetine at doses of 9 mg/kg and 18 mg/kg, respectively. Olanzapine was injected at 3 mg/kg and 6 mg/kg to the fourth and fifth groups, respectively. The sixth group received 9 mg/kg fluoxetine and 3 mg/kg olanzapine. Finally, the seventh group was administrated with fluoxetine and olanzapine at 18 mg/kg and 6 mg/kg, respectively. Drugs were injected intraperitoneally between day eight and day 15 of the pregnancy. On the 17th day of pregnancy, the fetuses were removed and micro-/macroscopically studied. Results. Fetuses of rats receiving high doses of these drugs showed a significant rate of cleft palate development, premature eyelid opening and torsion anomalies, compared to the control group (P≤0.01). It is concluded that these drugs can lead to teratogenicity, so their concomitant use during pregnancy should be avoided, or if necessary their doses must be decreased.http://dx.doi.org/10.1155/2014/132034
spellingShingle Azam Bakhtiarian
Nasrin Takzare
Mehdi Sheykhi
Narges Sistany
Farahnaz Jazaeri
Mario Giorgi
Vahid Nikoui
Teratogenic Effects of Coadministration of Fluoxetine and Olanzapine on Rat Fetuses
Advances in Pharmacological Sciences
title Teratogenic Effects of Coadministration of Fluoxetine and Olanzapine on Rat Fetuses
title_full Teratogenic Effects of Coadministration of Fluoxetine and Olanzapine on Rat Fetuses
title_fullStr Teratogenic Effects of Coadministration of Fluoxetine and Olanzapine on Rat Fetuses
title_full_unstemmed Teratogenic Effects of Coadministration of Fluoxetine and Olanzapine on Rat Fetuses
title_short Teratogenic Effects of Coadministration of Fluoxetine and Olanzapine on Rat Fetuses
title_sort teratogenic effects of coadministration of fluoxetine and olanzapine on rat fetuses
url http://dx.doi.org/10.1155/2014/132034
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