Prangos ferulacea (L.) ameliorates behavioral alterations, hippocampal oxidative stress markers, and apoptotic deficits in a rat model of autism induced by valproic acid

Abstract Background Prenatal exposure to valproic acid (VPA) may enhance the risk of autism spectrum disorder (ASD) in children. This study investigated the effect of Prangos ferulacea (L.) on behavioral alterations, hippocampal oxidative stress markers, and apoptotic deficits in a rat model of auti...

Full description

Bibliographic Details
Main Authors: Maryam Saadat, Abbas Ali Taherian, Mohammad Reza Aldaghi, Payman Raise‐Abdullahi, Hamid Reza Sameni, Abbas Ali Vafaei
Format: Article
Language:English
Published: Wiley 2023-11-01
Series:Brain and Behavior
Subjects:
Online Access:https://doi.org/10.1002/brb3.3224
_version_ 1797632562475040768
author Maryam Saadat
Abbas Ali Taherian
Mohammad Reza Aldaghi
Payman Raise‐Abdullahi
Hamid Reza Sameni
Abbas Ali Vafaei
author_facet Maryam Saadat
Abbas Ali Taherian
Mohammad Reza Aldaghi
Payman Raise‐Abdullahi
Hamid Reza Sameni
Abbas Ali Vafaei
author_sort Maryam Saadat
collection DOAJ
description Abstract Background Prenatal exposure to valproic acid (VPA) may enhance the risk of autism spectrum disorder (ASD) in children. This study investigated the effect of Prangos ferulacea (L.) on behavioral alterations, hippocampal oxidative stress markers, and apoptotic deficits in a rat model of autism induced by valproic acid. Methods Pregnant rats received VPA (600 mg/kg, intraperitoneally [i.p.]) or saline on gestational day 12.5 (E 12.5). Starting from the 30th postnatal day (PND 30), the pups were i.p. administered Prangos ferulacea (PF, 100 and 200 mg/kg), or the vehicle, daily until PND 58. On PND 30 and 58, various behavioral tasks were used to evaluate pups, including the open field, elevated plus‐maze, hot‐plate, and rotarod test. On PND 65, the animals were euthanized, and their brains were removed for histopathological and biochemical assay. Results Prenatal exposure to VPA caused significant behavioral changes in the offspring, reversed by administering an extract of Prangos ferulacea (L.). Additionally, prenatal VPA administration resulted in increased levels of malondialdehyde and deficits in antioxidant enzyme activities in the hippocampus, including catalase and glutathione, ameliorated by PF. Likewise, postnatal treatment with PF improved VPA‐induced dysregulation of Bax and Blc2 in the hippocampus and reduced neuronal death in CA1, CA3, and dentate gyrus. Conclusion The findings of this study suggest that postnatal administration of PF can prevent VPA‐induced ASD‐like behaviors by exhibiting antiapoptotic and antioxidant properties. Therefore, PF may have the potential as an adjunct in the management of ASD.
first_indexed 2024-03-11T11:39:42Z
format Article
id doaj.art-96b129302b6c4201b8b642c2c256f0fd
institution Directory Open Access Journal
issn 2162-3279
language English
last_indexed 2024-03-11T11:39:42Z
publishDate 2023-11-01
publisher Wiley
record_format Article
series Brain and Behavior
spelling doaj.art-96b129302b6c4201b8b642c2c256f0fd2023-11-10T06:53:59ZengWileyBrain and Behavior2162-32792023-11-011311n/an/a10.1002/brb3.3224Prangos ferulacea (L.) ameliorates behavioral alterations, hippocampal oxidative stress markers, and apoptotic deficits in a rat model of autism induced by valproic acidMaryam Saadat0Abbas Ali Taherian1Mohammad Reza Aldaghi2Payman Raise‐Abdullahi3Hamid Reza Sameni4Abbas Ali Vafaei5Department of Anatomical Sciences, School of Medicine Semnan University of Medical Sciences Semnan IranDepartment of Anatomical Sciences, School of Medicine Semnan University of Medical Sciences Semnan IranNervous System Stem Cells Research Center Semnan University of Medical Sciences Semnan IranResearch Center of Physiology Semnan University of Medical Sciences Semnan IranNervous System Stem Cells Research Center Semnan University of Medical Sciences Semnan IranResearch Center of Physiology Semnan University of Medical Sciences Semnan IranAbstract Background Prenatal exposure to valproic acid (VPA) may enhance the risk of autism spectrum disorder (ASD) in children. This study investigated the effect of Prangos ferulacea (L.) on behavioral alterations, hippocampal oxidative stress markers, and apoptotic deficits in a rat model of autism induced by valproic acid. Methods Pregnant rats received VPA (600 mg/kg, intraperitoneally [i.p.]) or saline on gestational day 12.5 (E 12.5). Starting from the 30th postnatal day (PND 30), the pups were i.p. administered Prangos ferulacea (PF, 100 and 200 mg/kg), or the vehicle, daily until PND 58. On PND 30 and 58, various behavioral tasks were used to evaluate pups, including the open field, elevated plus‐maze, hot‐plate, and rotarod test. On PND 65, the animals were euthanized, and their brains were removed for histopathological and biochemical assay. Results Prenatal exposure to VPA caused significant behavioral changes in the offspring, reversed by administering an extract of Prangos ferulacea (L.). Additionally, prenatal VPA administration resulted in increased levels of malondialdehyde and deficits in antioxidant enzyme activities in the hippocampus, including catalase and glutathione, ameliorated by PF. Likewise, postnatal treatment with PF improved VPA‐induced dysregulation of Bax and Blc2 in the hippocampus and reduced neuronal death in CA1, CA3, and dentate gyrus. Conclusion The findings of this study suggest that postnatal administration of PF can prevent VPA‐induced ASD‐like behaviors by exhibiting antiapoptotic and antioxidant properties. Therefore, PF may have the potential as an adjunct in the management of ASD.https://doi.org/10.1002/brb3.3224autismhippocampusoxidative stressPrangos ferulacea (L.)valproic acid
spellingShingle Maryam Saadat
Abbas Ali Taherian
Mohammad Reza Aldaghi
Payman Raise‐Abdullahi
Hamid Reza Sameni
Abbas Ali Vafaei
Prangos ferulacea (L.) ameliorates behavioral alterations, hippocampal oxidative stress markers, and apoptotic deficits in a rat model of autism induced by valproic acid
Brain and Behavior
autism
hippocampus
oxidative stress
Prangos ferulacea (L.)
valproic acid
title Prangos ferulacea (L.) ameliorates behavioral alterations, hippocampal oxidative stress markers, and apoptotic deficits in a rat model of autism induced by valproic acid
title_full Prangos ferulacea (L.) ameliorates behavioral alterations, hippocampal oxidative stress markers, and apoptotic deficits in a rat model of autism induced by valproic acid
title_fullStr Prangos ferulacea (L.) ameliorates behavioral alterations, hippocampal oxidative stress markers, and apoptotic deficits in a rat model of autism induced by valproic acid
title_full_unstemmed Prangos ferulacea (L.) ameliorates behavioral alterations, hippocampal oxidative stress markers, and apoptotic deficits in a rat model of autism induced by valproic acid
title_short Prangos ferulacea (L.) ameliorates behavioral alterations, hippocampal oxidative stress markers, and apoptotic deficits in a rat model of autism induced by valproic acid
title_sort prangos ferulacea l ameliorates behavioral alterations hippocampal oxidative stress markers and apoptotic deficits in a rat model of autism induced by valproic acid
topic autism
hippocampus
oxidative stress
Prangos ferulacea (L.)
valproic acid
url https://doi.org/10.1002/brb3.3224
work_keys_str_mv AT maryamsaadat prangosferulacealamelioratesbehavioralalterationshippocampaloxidativestressmarkersandapoptoticdeficitsinaratmodelofautisminducedbyvalproicacid
AT abbasalitaherian prangosferulacealamelioratesbehavioralalterationshippocampaloxidativestressmarkersandapoptoticdeficitsinaratmodelofautisminducedbyvalproicacid
AT mohammadrezaaldaghi prangosferulacealamelioratesbehavioralalterationshippocampaloxidativestressmarkersandapoptoticdeficitsinaratmodelofautisminducedbyvalproicacid
AT paymanraiseabdullahi prangosferulacealamelioratesbehavioralalterationshippocampaloxidativestressmarkersandapoptoticdeficitsinaratmodelofautisminducedbyvalproicacid
AT hamidrezasameni prangosferulacealamelioratesbehavioralalterationshippocampaloxidativestressmarkersandapoptoticdeficitsinaratmodelofautisminducedbyvalproicacid
AT abbasalivafaei prangosferulacealamelioratesbehavioralalterationshippocampaloxidativestressmarkersandapoptoticdeficitsinaratmodelofautisminducedbyvalproicacid