The effect of sublethal short-duration exposure of paraoxon on pregnancy and fetuses in mice

A convincing number of epidemiological studies have reported on the exposure to and consequences of organophosphorus compounds (OPCs) in pregnant women. However, there is still a knowledge gap and paucity of systematic literature from animal studies. This study was undertaken with the hypot...

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Main Authors: Nurulain Syed M., Shafiullah Mohamed, Sharma Charu, Ali Mahmoud A., Ojha Shreesh
Format: Article
Language:English
Published: University of Belgrade, University of Novi Sad 2015-01-01
Series:Archives of Biological Sciences
Subjects:
Online Access:http://www.doiserbia.nb.rs/img/doi/0354-4664/2015/0354-46641500045N.pdf
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author Nurulain Syed M.
Shafiullah Mohamed
Sharma Charu
Ali Mahmoud A.
Ojha Shreesh
author_facet Nurulain Syed M.
Shafiullah Mohamed
Sharma Charu
Ali Mahmoud A.
Ojha Shreesh
author_sort Nurulain Syed M.
collection DOAJ
description A convincing number of epidemiological studies have reported on the exposure to and consequences of organophosphorus compounds (OPCs) in pregnant women. However, there is still a knowledge gap and paucity of systematic literature from animal studies. This study was undertaken with the hypothesis that short-duration sublethal exposure to OPCs can produce maternal and fetal lethal effects as chronic exposure. This study examineses the teratogenicity and embryotoxicity of paraoxon (POX) in mice at a dose that is non-lethal to non-pregnant mothers. Pregnant mice were injected intraperitoneally (i.p.) with paraoxon (50 nmol/mouse) on the 4th and 5th days of gestation, and the effect of the treatment was assessed on day 18 of gestation. This dose was fatal to pregnant mice in 21% of instances as compared to non-pregnant animals in which 0% mortality was detected, even after daily injection of a similar dose for five days. Significant inhibition of red blood cell acetylcholinesterase (RBC-AChE) was observed in pregnant mice as compared to non-pregnant ones; however, no apparent neuronal effect was detected. Of note were fetal weight decrement, pregnancy termination, intrauterine growth retardation and maternal death. We concluded that exposure to even a non-toxic dose might be critical for pregnant mothers, the pregnancy as well as fetuses. In addition, even exposure of short duration can be detrimental and capable of producing profound and fatal effects.
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spelling doaj.art-fc9f5e5d6034447ca26df4cb4b1120922022-12-21T21:03:29ZengUniversity of Belgrade, University of Novi SadArchives of Biological Sciences0354-46641821-43392015-01-0167386186710.2298/ABS141114045N0354-46641500045NThe effect of sublethal short-duration exposure of paraoxon on pregnancy and fetuses in miceNurulain Syed M.0Shafiullah Mohamed1Sharma Charu2Ali Mahmoud A.3Ojha Shreesh4United Arab Emirates University, Faculty of Medicine and Health Sciences, Department of Pharmacology and Therapeutics, Al Ain, Abu Dhabi, UAEUnited Arab Emirates University, Faculty of Medicine and Health Sciences, Department of Pharmacology and Therapeutics, Al Ain, Abu Dhabi, UAEUnited Arab Emirates University, Faculty of Medicine and Health Sciences, Department of Internal Medicine, Al Ain, Abu Dhabi, UAEUnited Arab Emirates University, Faculty of Medicine and Health Sciences, Department of Pharmacology and Therapeutics, Al Ain, Abu Dhabi, UAEUnited Arab Emirates University, Faculty of Medicine and Health Sciences, Department of Pharmacology and Therapeutics, Al Ain, Abu Dhabi, UAEA convincing number of epidemiological studies have reported on the exposure to and consequences of organophosphorus compounds (OPCs) in pregnant women. However, there is still a knowledge gap and paucity of systematic literature from animal studies. This study was undertaken with the hypothesis that short-duration sublethal exposure to OPCs can produce maternal and fetal lethal effects as chronic exposure. This study examineses the teratogenicity and embryotoxicity of paraoxon (POX) in mice at a dose that is non-lethal to non-pregnant mothers. Pregnant mice were injected intraperitoneally (i.p.) with paraoxon (50 nmol/mouse) on the 4th and 5th days of gestation, and the effect of the treatment was assessed on day 18 of gestation. This dose was fatal to pregnant mice in 21% of instances as compared to non-pregnant animals in which 0% mortality was detected, even after daily injection of a similar dose for five days. Significant inhibition of red blood cell acetylcholinesterase (RBC-AChE) was observed in pregnant mice as compared to non-pregnant ones; however, no apparent neuronal effect was detected. Of note were fetal weight decrement, pregnancy termination, intrauterine growth retardation and maternal death. We concluded that exposure to even a non-toxic dose might be critical for pregnant mothers, the pregnancy as well as fetuses. In addition, even exposure of short duration can be detrimental and capable of producing profound and fatal effects.http://www.doiserbia.nb.rs/img/doi/0354-4664/2015/0354-46641500045N.pdfIntrauterine growth restriction (IUGR)gestation day (GD)RBC-AChEorganophosphorous compound (OPC)paraoxon (POX)
spellingShingle Nurulain Syed M.
Shafiullah Mohamed
Sharma Charu
Ali Mahmoud A.
Ojha Shreesh
The effect of sublethal short-duration exposure of paraoxon on pregnancy and fetuses in mice
Archives of Biological Sciences
Intrauterine growth restriction (IUGR)
gestation day (GD)
RBC-AChE
organophosphorous compound (OPC)
paraoxon (POX)
title The effect of sublethal short-duration exposure of paraoxon on pregnancy and fetuses in mice
title_full The effect of sublethal short-duration exposure of paraoxon on pregnancy and fetuses in mice
title_fullStr The effect of sublethal short-duration exposure of paraoxon on pregnancy and fetuses in mice
title_full_unstemmed The effect of sublethal short-duration exposure of paraoxon on pregnancy and fetuses in mice
title_short The effect of sublethal short-duration exposure of paraoxon on pregnancy and fetuses in mice
title_sort effect of sublethal short duration exposure of paraoxon on pregnancy and fetuses in mice
topic Intrauterine growth restriction (IUGR)
gestation day (GD)
RBC-AChE
organophosphorous compound (OPC)
paraoxon (POX)
url http://www.doiserbia.nb.rs/img/doi/0354-4664/2015/0354-46641500045N.pdf
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