Prenatal Exposure to Lamotrigine: Effects on Postnatal Development and Behaviour in Rat Offspring
Use of antiepileptic drugs (AEDs) in pregnancy warrants various side effects and also deleterious effects on fetal development. The present study was carried out to assess the effects of prenatal exposure to lamotrigine (LTG) on postnatal development and behavioural alterations of offspring. Adult m...
Gespeichert in:
Veröffentlicht in: | ISRN neuroscience 2014-04, Vol.2014, p.163459-8 |
---|---|
Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 8 |
---|---|
container_issue | |
container_start_page | 163459 |
container_title | ISRN neuroscience |
container_volume | 2014 |
creator | Sathiya, Sekar Ganesh, Murugan Kalaivani, Periyathambi Ranju, Vijayan Janani, Srinivasan Pramila, Bakthavachalam Saravana Babu, Chidambaram |
description | Use of antiepileptic drugs (AEDs) in pregnancy warrants various side effects and also deleterious effects on fetal development. The present study was carried out to assess the effects of prenatal exposure to lamotrigine (LTG) on postnatal development and behavioural alterations of offspring. Adult male and female Sprague Dawley rats weighing 150–180 g b. wt. were allowed to copulate and pregnancy was confirmed by vaginal cytology. Pregnant rats were treated with LTG (11.5, 23, and 46 mg/kg, p.o) from gestational day 3 (GND 3) and this treatment continued till postnatal day 11 (PND 11). Offspring were separated from their dam on day 21 following parturition. LTG, at 46 mg/kg, p.o, produced severe clinical signs of toxicity leading to death of dam between GND 15 and 17. LTG, at 11.5 and 23 mg/kg, p.o, showed significant alterations in offspring’s incisors eruption and vaginal opening when compared to age matched controls. LTG (23 mg/kg, p.o) exposed female offspring expressed hyperactive behaviour and decreased GABA-A receptor expression when compared to control rats. These results reveal that prenatal exposure to LTG may impart differential postnatal behavioural alterations between male and female rats which paves way for further investigations. |
doi_str_mv | 10.1155/2014/163459 |
format | Article |
fullrecord | <record><control><sourceid>pubmed_cross</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4045557</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>24967313</sourcerecordid><originalsourceid>FETCH-LOGICAL-c2619-a830ea7a5c44a7ddc71598cd4d1efe236020302f149fd0a8b5821be928a95a103</originalsourceid><addsrcrecordid>eNp9kN9LwzAQx4MoTuaefJc8K3VJmrSND4LO-QMGG6LP5dYmW6RNRtJN_e_tqI754j3cHdznvnd8ETqj5IpSIYaMUD6kScyFPEAnLKY84klCD_f6HhqE8E7akJwyLo9Rr81JGtP4BMHMKwsNVHj8uXJh7RVuHJ5A7RpvFsaqazzWWhVNwM7imQtNR9-rjarcqla2wWBLfKeWsDFu7bGx-AUaPNU6rLyxi1N0pKEKavBT--jtYfw6eoom08fn0e0kKlhCZQRZTBSkIArOIS3LIqVCZkXJS6q0YnFCGIkJ05RLXRLI5iJjdK4ky0AKoCTuo5tOd7We16os2s88VHn7Qw3-K3dg8r8Ta5b5wm1yTrgQIm0FLjuBwrsQvNK7XUryrdn51uy8M7ulz_fP7dhfa1vgogOWxpbwYf5V-wbNbIfk</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Prenatal Exposure to Lamotrigine: Effects on Postnatal Development and Behaviour in Rat Offspring</title><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central</source><source>PubMed Central Open Access</source><creator>Sathiya, Sekar ; Ganesh, Murugan ; Kalaivani, Periyathambi ; Ranju, Vijayan ; Janani, Srinivasan ; Pramila, Bakthavachalam ; Saravana Babu, Chidambaram</creator><contributor>Depino, A. M. ; Berger, I. ; Kulesza, R.</contributor><creatorcontrib>Sathiya, Sekar ; Ganesh, Murugan ; Kalaivani, Periyathambi ; Ranju, Vijayan ; Janani, Srinivasan ; Pramila, Bakthavachalam ; Saravana Babu, Chidambaram ; Depino, A. M. ; Berger, I. ; Kulesza, R.</creatorcontrib><description>Use of antiepileptic drugs (AEDs) in pregnancy warrants various side effects and also deleterious effects on fetal development. The present study was carried out to assess the effects of prenatal exposure to lamotrigine (LTG) on postnatal development and behavioural alterations of offspring. Adult male and female Sprague Dawley rats weighing 150–180 g b. wt. were allowed to copulate and pregnancy was confirmed by vaginal cytology. Pregnant rats were treated with LTG (11.5, 23, and 46 mg/kg, p.o) from gestational day 3 (GND 3) and this treatment continued till postnatal day 11 (PND 11). Offspring were separated from their dam on day 21 following parturition. LTG, at 46 mg/kg, p.o, produced severe clinical signs of toxicity leading to death of dam between GND 15 and 17. LTG, at 11.5 and 23 mg/kg, p.o, showed significant alterations in offspring’s incisors eruption and vaginal opening when compared to age matched controls. LTG (23 mg/kg, p.o) exposed female offspring expressed hyperactive behaviour and decreased GABA-A receptor expression when compared to control rats. These results reveal that prenatal exposure to LTG may impart differential postnatal behavioural alterations between male and female rats which paves way for further investigations.</description><identifier>ISSN: 2314-4661</identifier><identifier>EISSN: 2314-4661</identifier><identifier>DOI: 10.1155/2014/163459</identifier><identifier>PMID: 24967313</identifier><language>eng</language><publisher>United States: Hindawi Publishing Corporation</publisher><ispartof>ISRN neuroscience, 2014-04, Vol.2014, p.163459-8</ispartof><rights>Copyright © 2014 Sekar Sathiya et al.</rights><rights>Copyright © 2014 Sekar Sathiya et al. 2014</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2619-a830ea7a5c44a7ddc71598cd4d1efe236020302f149fd0a8b5821be928a95a103</citedby><cites>FETCH-LOGICAL-c2619-a830ea7a5c44a7ddc71598cd4d1efe236020302f149fd0a8b5821be928a95a103</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4045557/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4045557/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24967313$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Depino, A. M.</contributor><contributor>Berger, I.</contributor><contributor>Kulesza, R.</contributor><creatorcontrib>Sathiya, Sekar</creatorcontrib><creatorcontrib>Ganesh, Murugan</creatorcontrib><creatorcontrib>Kalaivani, Periyathambi</creatorcontrib><creatorcontrib>Ranju, Vijayan</creatorcontrib><creatorcontrib>Janani, Srinivasan</creatorcontrib><creatorcontrib>Pramila, Bakthavachalam</creatorcontrib><creatorcontrib>Saravana Babu, Chidambaram</creatorcontrib><title>Prenatal Exposure to Lamotrigine: Effects on Postnatal Development and Behaviour in Rat Offspring</title><title>ISRN neuroscience</title><addtitle>ISRN Neurosci</addtitle><description>Use of antiepileptic drugs (AEDs) in pregnancy warrants various side effects and also deleterious effects on fetal development. The present study was carried out to assess the effects of prenatal exposure to lamotrigine (LTG) on postnatal development and behavioural alterations of offspring. Adult male and female Sprague Dawley rats weighing 150–180 g b. wt. were allowed to copulate and pregnancy was confirmed by vaginal cytology. Pregnant rats were treated with LTG (11.5, 23, and 46 mg/kg, p.o) from gestational day 3 (GND 3) and this treatment continued till postnatal day 11 (PND 11). Offspring were separated from their dam on day 21 following parturition. LTG, at 46 mg/kg, p.o, produced severe clinical signs of toxicity leading to death of dam between GND 15 and 17. LTG, at 11.5 and 23 mg/kg, p.o, showed significant alterations in offspring’s incisors eruption and vaginal opening when compared to age matched controls. LTG (23 mg/kg, p.o) exposed female offspring expressed hyperactive behaviour and decreased GABA-A receptor expression when compared to control rats. These results reveal that prenatal exposure to LTG may impart differential postnatal behavioural alterations between male and female rats which paves way for further investigations.</description><issn>2314-4661</issn><issn>2314-4661</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>RHX</sourceid><recordid>eNp9kN9LwzAQx4MoTuaefJc8K3VJmrSND4LO-QMGG6LP5dYmW6RNRtJN_e_tqI754j3cHdznvnd8ETqj5IpSIYaMUD6kScyFPEAnLKY84klCD_f6HhqE8E7akJwyLo9Rr81JGtP4BMHMKwsNVHj8uXJh7RVuHJ5A7RpvFsaqazzWWhVNwM7imQtNR9-rjarcqla2wWBLfKeWsDFu7bGx-AUaPNU6rLyxi1N0pKEKavBT--jtYfw6eoom08fn0e0kKlhCZQRZTBSkIArOIS3LIqVCZkXJS6q0YnFCGIkJ05RLXRLI5iJjdK4ky0AKoCTuo5tOd7We16os2s88VHn7Qw3-K3dg8r8Ta5b5wm1yTrgQIm0FLjuBwrsQvNK7XUryrdn51uy8M7ulz_fP7dhfa1vgogOWxpbwYf5V-wbNbIfk</recordid><startdate>20140414</startdate><enddate>20140414</enddate><creator>Sathiya, Sekar</creator><creator>Ganesh, Murugan</creator><creator>Kalaivani, Periyathambi</creator><creator>Ranju, Vijayan</creator><creator>Janani, Srinivasan</creator><creator>Pramila, Bakthavachalam</creator><creator>Saravana Babu, Chidambaram</creator><general>Hindawi Publishing Corporation</general><scope>RHU</scope><scope>RHW</scope><scope>RHX</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>5PM</scope></search><sort><creationdate>20140414</creationdate><title>Prenatal Exposure to Lamotrigine: Effects on Postnatal Development and Behaviour in Rat Offspring</title><author>Sathiya, Sekar ; Ganesh, Murugan ; Kalaivani, Periyathambi ; Ranju, Vijayan ; Janani, Srinivasan ; Pramila, Bakthavachalam ; Saravana Babu, Chidambaram</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2619-a830ea7a5c44a7ddc71598cd4d1efe236020302f149fd0a8b5821be928a95a103</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sathiya, Sekar</creatorcontrib><creatorcontrib>Ganesh, Murugan</creatorcontrib><creatorcontrib>Kalaivani, Periyathambi</creatorcontrib><creatorcontrib>Ranju, Vijayan</creatorcontrib><creatorcontrib>Janani, Srinivasan</creatorcontrib><creatorcontrib>Pramila, Bakthavachalam</creatorcontrib><creatorcontrib>Saravana Babu, Chidambaram</creatorcontrib><collection>Hindawi Publishing Complete</collection><collection>Hindawi Publishing Subscription Journals</collection><collection>Hindawi Publishing Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>ISRN neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sathiya, Sekar</au><au>Ganesh, Murugan</au><au>Kalaivani, Periyathambi</au><au>Ranju, Vijayan</au><au>Janani, Srinivasan</au><au>Pramila, Bakthavachalam</au><au>Saravana Babu, Chidambaram</au><au>Depino, A. M.</au><au>Berger, I.</au><au>Kulesza, R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Prenatal Exposure to Lamotrigine: Effects on Postnatal Development and Behaviour in Rat Offspring</atitle><jtitle>ISRN neuroscience</jtitle><addtitle>ISRN Neurosci</addtitle><date>2014-04-14</date><risdate>2014</risdate><volume>2014</volume><spage>163459</spage><epage>8</epage><pages>163459-8</pages><issn>2314-4661</issn><eissn>2314-4661</eissn><abstract>Use of antiepileptic drugs (AEDs) in pregnancy warrants various side effects and also deleterious effects on fetal development. The present study was carried out to assess the effects of prenatal exposure to lamotrigine (LTG) on postnatal development and behavioural alterations of offspring. Adult male and female Sprague Dawley rats weighing 150–180 g b. wt. were allowed to copulate and pregnancy was confirmed by vaginal cytology. Pregnant rats were treated with LTG (11.5, 23, and 46 mg/kg, p.o) from gestational day 3 (GND 3) and this treatment continued till postnatal day 11 (PND 11). Offspring were separated from their dam on day 21 following parturition. LTG, at 46 mg/kg, p.o, produced severe clinical signs of toxicity leading to death of dam between GND 15 and 17. LTG, at 11.5 and 23 mg/kg, p.o, showed significant alterations in offspring’s incisors eruption and vaginal opening when compared to age matched controls. LTG (23 mg/kg, p.o) exposed female offspring expressed hyperactive behaviour and decreased GABA-A receptor expression when compared to control rats. These results reveal that prenatal exposure to LTG may impart differential postnatal behavioural alterations between male and female rats which paves way for further investigations.</abstract><cop>United States</cop><pub>Hindawi Publishing Corporation</pub><pmid>24967313</pmid><doi>10.1155/2014/163459</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2314-4661 |
ispartof | ISRN neuroscience, 2014-04, Vol.2014, p.163459-8 |
issn | 2314-4661 2314-4661 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4045557 |
source | Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; PubMed Central Open Access |
title | Prenatal Exposure to Lamotrigine: Effects on Postnatal Development and Behaviour in Rat Offspring |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-21T20%3A56%3A45IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-pubmed_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Prenatal%20Exposure%20to%20Lamotrigine:%20Effects%20on%20Postnatal%20Development%20and%20Behaviour%20in%20Rat%20Offspring&rft.jtitle=ISRN%20neuroscience&rft.au=Sathiya,%20Sekar&rft.date=2014-04-14&rft.volume=2014&rft.spage=163459&rft.epage=8&rft.pages=163459-8&rft.issn=2314-4661&rft.eissn=2314-4661&rft_id=info:doi/10.1155/2014/163459&rft_dat=%3Cpubmed_cross%3E24967313%3C/pubmed_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/24967313&rfr_iscdi=true |