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Effect of prenatal administration of venlafaxine on postnatal development of rat offspring

About 3% of pregnant women are treated with antidepressant drugs during gestation. After delivery the number of treated women increases to 5 to 7%. Most prescribed antidepressants in pregnancy are selective serotonin re-uptake inhibitors and/or serotonin and noradrenaline re-uptake inhibitors, such...

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Autores principales: Dubovický, Michal, Császárová, Eszter, Brnoliaková, Zuzana, Ujházy, Eduard, Navarová, Jana, Mach, Mojmír
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Slovak Toxicology Society SETOX 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3485660/
https://www.ncbi.nlm.nih.gov/pubmed/23118594
http://dx.doi.org/10.2478/v10102-012-0016-3
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author Dubovický, Michal
Császárová, Eszter
Brnoliaková, Zuzana
Ujházy, Eduard
Navarová, Jana
Mach, Mojmír
author_facet Dubovický, Michal
Császárová, Eszter
Brnoliaková, Zuzana
Ujházy, Eduard
Navarová, Jana
Mach, Mojmír
author_sort Dubovický, Michal
collection PubMed
description About 3% of pregnant women are treated with antidepressant drugs during gestation. After delivery the number of treated women increases to 5 to 7%. Most prescribed antidepressants in pregnancy are selective serotonin re-uptake inhibitors and/or serotonin and noradrenaline re-uptake inhibitors, such as fluoxetine, paroxetine, sertraline, citalopram and venlafaxine (VENF). Despite the fact that VENF has been assigned to pregnancy category C by the FDA, experimental studies with this drug are rare. The aim of this pilot study was to investigate the effect of prenatal administration of VENF on early postnatal development of rat offspring and selected biochemical variables at weaning of pups. Pregnant female Wistar rats were treated with VENF from day 15 to 20 of gestation at the doses of 7.5, 37.5 and 70 mg/kg. Females were allowed to spontaneously deliver their pups. After delivery the pups were inspected for viability, gross malformation and they were weighed on day 0, 4 and 21 post partum. On day 21 post partum, the pups were killed, brains were removed from the skulls and blood samples were collected for biochemical assay (proteins, glucose-GOD, glucose-HEX, lactate dehydrogenase, aspartate aminotransferase, alanine aminotransferase and total antioxidant status). The study showed that prenatal VENF administration resulted in a mild maternal intoxication manifested by decreased body weight gain of pregnant females. There was no effect of the drug tested on the body and brain weights of offspring. No obvious morphological alterations were observed in the delivered pups. Similarly, there were no changes in the selected biochemical variables determined.
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spelling pubmed-34856602012-11-01 Effect of prenatal administration of venlafaxine on postnatal development of rat offspring Dubovický, Michal Császárová, Eszter Brnoliaková, Zuzana Ujházy, Eduard Navarová, Jana Mach, Mojmír Interdiscip Toxicol Original Article About 3% of pregnant women are treated with antidepressant drugs during gestation. After delivery the number of treated women increases to 5 to 7%. Most prescribed antidepressants in pregnancy are selective serotonin re-uptake inhibitors and/or serotonin and noradrenaline re-uptake inhibitors, such as fluoxetine, paroxetine, sertraline, citalopram and venlafaxine (VENF). Despite the fact that VENF has been assigned to pregnancy category C by the FDA, experimental studies with this drug are rare. The aim of this pilot study was to investigate the effect of prenatal administration of VENF on early postnatal development of rat offspring and selected biochemical variables at weaning of pups. Pregnant female Wistar rats were treated with VENF from day 15 to 20 of gestation at the doses of 7.5, 37.5 and 70 mg/kg. Females were allowed to spontaneously deliver their pups. After delivery the pups were inspected for viability, gross malformation and they were weighed on day 0, 4 and 21 post partum. On day 21 post partum, the pups were killed, brains were removed from the skulls and blood samples were collected for biochemical assay (proteins, glucose-GOD, glucose-HEX, lactate dehydrogenase, aspartate aminotransferase, alanine aminotransferase and total antioxidant status). The study showed that prenatal VENF administration resulted in a mild maternal intoxication manifested by decreased body weight gain of pregnant females. There was no effect of the drug tested on the body and brain weights of offspring. No obvious morphological alterations were observed in the delivered pups. Similarly, there were no changes in the selected biochemical variables determined. Slovak Toxicology Society SETOX 2012-06 2012-06 /pmc/articles/PMC3485660/ /pubmed/23118594 http://dx.doi.org/10.2478/v10102-012-0016-3 Text en Copyright © 2012 Slovak Toxicology Society SETOX http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Dubovický, Michal
Császárová, Eszter
Brnoliaková, Zuzana
Ujházy, Eduard
Navarová, Jana
Mach, Mojmír
Effect of prenatal administration of venlafaxine on postnatal development of rat offspring
title Effect of prenatal administration of venlafaxine on postnatal development of rat offspring
title_full Effect of prenatal administration of venlafaxine on postnatal development of rat offspring
title_fullStr Effect of prenatal administration of venlafaxine on postnatal development of rat offspring
title_full_unstemmed Effect of prenatal administration of venlafaxine on postnatal development of rat offspring
title_short Effect of prenatal administration of venlafaxine on postnatal development of rat offspring
title_sort effect of prenatal administration of venlafaxine on postnatal development of rat offspring
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3485660/
https://www.ncbi.nlm.nih.gov/pubmed/23118594
http://dx.doi.org/10.2478/v10102-012-0016-3
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