Amelioration of behavioral aberrations and oxidative markers by green tea extract in valproate induced autism in animals
Abstract Exposure to toxicants prenatally and postnatally could have deleterious consequences on the offspring. Postnatal exposure to valproate in mice pups is capable of inducing experimental autism resulting in neurobehavioral aberrations. Consumption of green tea has been associated with neuronal...
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description | Abstract Exposure to toxicants prenatally and postnatally could have deleterious consequences on the offspring. Postnatal exposure to valproate in mice pups is capable of inducing experimental autism resulting in neurobehavioral aberrations. Consumption of green tea has been associated with neuronal protection against the impact of toxicants. We investigated the role of green tea extract in reversing cardinal behavioral changes and aberrations in oxidative stress induced by valproate exposure. Young mice of both genders received a single dose of valproate (400 mg/kg subcutaneously) on postnatal day 14 followed by a daily dose of green tea extract (75 and 300 mg/kg) orally up to postnatal day 40. Mice pups were subjected to behavioral testing to assess motor co-ordination, nociceptive response, locomotion, anxiety, exploratory activity and cognition on various postnatal days up to postnatal day 40. At the end of behavioral testing, blood was withdrawn from the retro orbital plexus for the estimation of lipid peroxides. Animals were sacrificed on postnatal day 41 and whole brain was subjected to histopathological examination. Our studies revealed a significant improvement in behavioral assessments particularly with 300 mg/kg of green tea extract. Formation of markers of oxidative stress was reduced at both dose levels. Histological findings confirm the neuroprotective effect of green tea at a dose of 300 mg/kg. In conclusion it can be stated that green tea exerts neuronal cytoprotective action possibly due to anti-oxidant action and could be efficacious in the management of autism. |
doi_str_mv | 10.1016/j.brainres.2011.06.063 |
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Sikinder ; Kambam, Srilatha ; Chiluka, Vijaya Lakshmi</creator><creatorcontrib>Banji, David ; Banji, Otilia J.F ; Abbagoni, Saidulu ; Hayath, Md. Sikinder ; Kambam, Srilatha ; Chiluka, Vijaya Lakshmi</creatorcontrib><description>Abstract Exposure to toxicants prenatally and postnatally could have deleterious consequences on the offspring. Postnatal exposure to valproate in mice pups is capable of inducing experimental autism resulting in neurobehavioral aberrations. Consumption of green tea has been associated with neuronal protection against the impact of toxicants. We investigated the role of green tea extract in reversing cardinal behavioral changes and aberrations in oxidative stress induced by valproate exposure. Young mice of both genders received a single dose of valproate (400 mg/kg subcutaneously) on postnatal day 14 followed by a daily dose of green tea extract (75 and 300 mg/kg) orally up to postnatal day 40. Mice pups were subjected to behavioral testing to assess motor co-ordination, nociceptive response, locomotion, anxiety, exploratory activity and cognition on various postnatal days up to postnatal day 40. At the end of behavioral testing, blood was withdrawn from the retro orbital plexus for the estimation of lipid peroxides. Animals were sacrificed on postnatal day 41 and whole brain was subjected to histopathological examination. Our studies revealed a significant improvement in behavioral assessments particularly with 300 mg/kg of green tea extract. Formation of markers of oxidative stress was reduced at both dose levels. Histological findings confirm the neuroprotective effect of green tea at a dose of 300 mg/kg. In conclusion it can be stated that green tea exerts neuronal cytoprotective action possibly due to anti-oxidant action and could be efficacious in the management of autism.</description><identifier>ISSN: 0006-8993</identifier><identifier>EISSN: 1872-6240</identifier><identifier>DOI: 10.1016/j.brainres.2011.06.063</identifier><identifier>PMID: 21820650</identifier><identifier>CODEN: BRREAP</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Animals ; Anticonvulsants. Antiepileptics. Antiparkinson agents ; antioxidant activity ; anxiety ; Autism ; Autistic Disorder - chemically induced ; Autistic Disorder - drug therapy ; behavior change ; Behavior, Animal - drug effects ; Biological and medical sciences ; blood ; brain ; Brain - drug effects ; Camellia sinensis ; Child clinical studies ; cognition ; Developmental disorders ; Disease Models, Animal ; Female ; Green tea ; histopathology ; Infantile autism ; locomotion ; Male ; Maze Learning - drug effects ; Medical sciences ; Mice ; Motor Activity - drug effects ; Neurology ; Neuropharmacology ; neuroprotective effect ; oxidative stress ; Oxidative Stress - drug effects ; peroxides ; Pharmacology. Drug treatments ; Phytotherapy ; Plant Extracts - pharmacology ; Plant Extracts - therapeutic use ; plexus ; progeny ; Psychology. Psychoanalysis. Psychiatry ; Psychopathology. Psychiatry ; pups ; toxic substances ; Valproate ; Valproic Acid</subject><ispartof>Brain research, 2011-09, Vol.1410, p.141-151</ispartof><rights>Elsevier B.V.</rights><rights>2011 Elsevier B.V.</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2011 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c574t-db787543eba59e83f47b575d8776a3ab2505de6d7aa95130019214a2e18b5d4c3</citedby><cites>FETCH-LOGICAL-c574t-db787543eba59e83f47b575d8776a3ab2505de6d7aa95130019214a2e18b5d4c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.brainres.2011.06.063$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=24477045$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21820650$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Banji, David</creatorcontrib><creatorcontrib>Banji, Otilia J.F</creatorcontrib><creatorcontrib>Abbagoni, Saidulu</creatorcontrib><creatorcontrib>Hayath, Md. Sikinder</creatorcontrib><creatorcontrib>Kambam, Srilatha</creatorcontrib><creatorcontrib>Chiluka, Vijaya Lakshmi</creatorcontrib><title>Amelioration of behavioral aberrations and oxidative markers by green tea extract in valproate induced autism in animals</title><title>Brain research</title><addtitle>Brain Res</addtitle><description>Abstract Exposure to toxicants prenatally and postnatally could have deleterious consequences on the offspring. Postnatal exposure to valproate in mice pups is capable of inducing experimental autism resulting in neurobehavioral aberrations. Consumption of green tea has been associated with neuronal protection against the impact of toxicants. We investigated the role of green tea extract in reversing cardinal behavioral changes and aberrations in oxidative stress induced by valproate exposure. Young mice of both genders received a single dose of valproate (400 mg/kg subcutaneously) on postnatal day 14 followed by a daily dose of green tea extract (75 and 300 mg/kg) orally up to postnatal day 40. Mice pups were subjected to behavioral testing to assess motor co-ordination, nociceptive response, locomotion, anxiety, exploratory activity and cognition on various postnatal days up to postnatal day 40. At the end of behavioral testing, blood was withdrawn from the retro orbital plexus for the estimation of lipid peroxides. Animals were sacrificed on postnatal day 41 and whole brain was subjected to histopathological examination. Our studies revealed a significant improvement in behavioral assessments particularly with 300 mg/kg of green tea extract. Formation of markers of oxidative stress was reduced at both dose levels. Histological findings confirm the neuroprotective effect of green tea at a dose of 300 mg/kg. In conclusion it can be stated that green tea exerts neuronal cytoprotective action possibly due to anti-oxidant action and could be efficacious in the management of autism.</description><subject>Animals</subject><subject>Anticonvulsants. Antiepileptics. Antiparkinson agents</subject><subject>antioxidant activity</subject><subject>anxiety</subject><subject>Autism</subject><subject>Autistic Disorder - chemically induced</subject><subject>Autistic Disorder - drug therapy</subject><subject>behavior change</subject><subject>Behavior, Animal - drug effects</subject><subject>Biological and medical sciences</subject><subject>blood</subject><subject>brain</subject><subject>Brain - drug effects</subject><subject>Camellia sinensis</subject><subject>Child clinical studies</subject><subject>cognition</subject><subject>Developmental disorders</subject><subject>Disease Models, Animal</subject><subject>Female</subject><subject>Green tea</subject><subject>histopathology</subject><subject>Infantile autism</subject><subject>locomotion</subject><subject>Male</subject><subject>Maze Learning - drug effects</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Motor Activity - drug effects</subject><subject>Neurology</subject><subject>Neuropharmacology</subject><subject>neuroprotective effect</subject><subject>oxidative stress</subject><subject>Oxidative Stress - drug effects</subject><subject>peroxides</subject><subject>Pharmacology. Drug treatments</subject><subject>Phytotherapy</subject><subject>Plant Extracts - pharmacology</subject><subject>Plant Extracts - therapeutic use</subject><subject>plexus</subject><subject>progeny</subject><subject>Psychology. Psychoanalysis. Psychiatry</subject><subject>Psychopathology. Psychiatry</subject><subject>pups</subject><subject>toxic substances</subject><subject>Valproate</subject><subject>Valproic Acid</subject><issn>0006-8993</issn><issn>1872-6240</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkk1r3DAQhk1pabZp_0KqS8nJW31a9qU0hH5BoIc0ZzGWxqk2tpxK9rL77yvjTQu9FAaG0TyaGd6ZorhgdMsoq97vtm0EHyKmLaeMbWmVTTwrNqzWvKy4pM-LDaW0KuumEWfFq5R2ORSioS-LM85qTitFN8XhasDejxEmPwYydqTFn7BfHnoCLcY1kQgER8aDdzncIxkgPmBMpD2S-4gYyIRA8DBFsBPxgeyhf4wjTJgDN1t0BObJp2HJQfAD9Ol18aLLDt-c_Hlx9_nTj-uv5c33L9-ur25Kq7ScStfqWispsAXVYC06qVullau1rkBAyxVVDiunARrFBKWs4UwCR1a3ykkrzovLtW4e6NeMaTKDTxb7HgKOczIN1UzzmleZrFbSxjGliJ15jHnUeDSMmkV0szNPoptFdEOrbCJ_vDi1mNsB3Z9vTypn4N0JgGSh7yIE69NfTkqtqVSZe7tyHYwG7mNm7m5zJ5U31whdy0x8XAnMku09RpOsx5AV9hHtZNzo_z_th39K2N4Hn-d6wCOm3TjHkBdimEncUHO7HNFyQywX5UJS8RsTAcMG</recordid><startdate>20110902</startdate><enddate>20110902</enddate><creator>Banji, David</creator><creator>Banji, Otilia J.F</creator><creator>Abbagoni, Saidulu</creator><creator>Hayath, Md. Sikinder</creator><creator>Kambam, Srilatha</creator><creator>Chiluka, Vijaya Lakshmi</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>FBQ</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QG</scope><scope>7TK</scope></search><sort><creationdate>20110902</creationdate><title>Amelioration of behavioral aberrations and oxidative markers by green tea extract in valproate induced autism in animals</title><author>Banji, David ; Banji, Otilia J.F ; Abbagoni, Saidulu ; Hayath, Md. Sikinder ; Kambam, Srilatha ; Chiluka, Vijaya Lakshmi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c574t-db787543eba59e83f47b575d8776a3ab2505de6d7aa95130019214a2e18b5d4c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Animals</topic><topic>Anticonvulsants. Antiepileptics. Antiparkinson agents</topic><topic>antioxidant activity</topic><topic>anxiety</topic><topic>Autism</topic><topic>Autistic Disorder - chemically induced</topic><topic>Autistic Disorder - drug therapy</topic><topic>behavior change</topic><topic>Behavior, Animal - drug effects</topic><topic>Biological and medical sciences</topic><topic>blood</topic><topic>brain</topic><topic>Brain - drug effects</topic><topic>Camellia sinensis</topic><topic>Child clinical studies</topic><topic>cognition</topic><topic>Developmental disorders</topic><topic>Disease Models, Animal</topic><topic>Female</topic><topic>Green tea</topic><topic>histopathology</topic><topic>Infantile autism</topic><topic>locomotion</topic><topic>Male</topic><topic>Maze Learning - drug effects</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Motor Activity - drug effects</topic><topic>Neurology</topic><topic>Neuropharmacology</topic><topic>neuroprotective effect</topic><topic>oxidative stress</topic><topic>Oxidative Stress - drug effects</topic><topic>peroxides</topic><topic>Pharmacology. Drug treatments</topic><topic>Phytotherapy</topic><topic>Plant Extracts - pharmacology</topic><topic>Plant Extracts - therapeutic use</topic><topic>plexus</topic><topic>progeny</topic><topic>Psychology. Psychoanalysis. Psychiatry</topic><topic>Psychopathology. Psychiatry</topic><topic>pups</topic><topic>toxic substances</topic><topic>Valproate</topic><topic>Valproic Acid</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Banji, David</creatorcontrib><creatorcontrib>Banji, Otilia J.F</creatorcontrib><creatorcontrib>Abbagoni, Saidulu</creatorcontrib><creatorcontrib>Hayath, Md. Sikinder</creatorcontrib><creatorcontrib>Kambam, Srilatha</creatorcontrib><creatorcontrib>Chiluka, Vijaya Lakshmi</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Neurosciences Abstracts</collection><jtitle>Brain research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Banji, David</au><au>Banji, Otilia J.F</au><au>Abbagoni, Saidulu</au><au>Hayath, Md. Sikinder</au><au>Kambam, Srilatha</au><au>Chiluka, Vijaya Lakshmi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Amelioration of behavioral aberrations and oxidative markers by green tea extract in valproate induced autism in animals</atitle><jtitle>Brain research</jtitle><addtitle>Brain Res</addtitle><date>2011-09-02</date><risdate>2011</risdate><volume>1410</volume><spage>141</spage><epage>151</epage><pages>141-151</pages><issn>0006-8993</issn><eissn>1872-6240</eissn><coden>BRREAP</coden><abstract>Abstract Exposure to toxicants prenatally and postnatally could have deleterious consequences on the offspring. Postnatal exposure to valproate in mice pups is capable of inducing experimental autism resulting in neurobehavioral aberrations. Consumption of green tea has been associated with neuronal protection against the impact of toxicants. We investigated the role of green tea extract in reversing cardinal behavioral changes and aberrations in oxidative stress induced by valproate exposure. Young mice of both genders received a single dose of valproate (400 mg/kg subcutaneously) on postnatal day 14 followed by a daily dose of green tea extract (75 and 300 mg/kg) orally up to postnatal day 40. Mice pups were subjected to behavioral testing to assess motor co-ordination, nociceptive response, locomotion, anxiety, exploratory activity and cognition on various postnatal days up to postnatal day 40. At the end of behavioral testing, blood was withdrawn from the retro orbital plexus for the estimation of lipid peroxides. Animals were sacrificed on postnatal day 41 and whole brain was subjected to histopathological examination. Our studies revealed a significant improvement in behavioral assessments particularly with 300 mg/kg of green tea extract. Formation of markers of oxidative stress was reduced at both dose levels. Histological findings confirm the neuroprotective effect of green tea at a dose of 300 mg/kg. In conclusion it can be stated that green tea exerts neuronal cytoprotective action possibly due to anti-oxidant action and could be efficacious in the management of autism.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>21820650</pmid><doi>10.1016/j.brainres.2011.06.063</doi><tpages>11</tpages></addata></record> |
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subjects | Animals Anticonvulsants. Antiepileptics. Antiparkinson agents antioxidant activity anxiety Autism Autistic Disorder - chemically induced Autistic Disorder - drug therapy behavior change Behavior, Animal - drug effects Biological and medical sciences blood brain Brain - drug effects Camellia sinensis Child clinical studies cognition Developmental disorders Disease Models, Animal Female Green tea histopathology Infantile autism locomotion Male Maze Learning - drug effects Medical sciences Mice Motor Activity - drug effects Neurology Neuropharmacology neuroprotective effect oxidative stress Oxidative Stress - drug effects peroxides Pharmacology. Drug treatments Phytotherapy Plant Extracts - pharmacology Plant Extracts - therapeutic use plexus progeny Psychology. Psychoanalysis. Psychiatry Psychopathology. Psychiatry pups toxic substances Valproate Valproic Acid |
title | Amelioration of behavioral aberrations and oxidative markers by green tea extract in valproate induced autism in animals |
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