Sensitivity of modified Biel-maze task, compared with Y-maze task, to measure spatial learning and memory deficits of ethanol teratogenicity in the guinea pig
► Chronic prenatal ethanol exposure induces neurobehavioral deficits in offspring. ► Complex spatial working memory tasks improve sensitivity for detecting cognitive deficits. ► Speed accuracy trade-off increases frequency of errors in a spatial working memory task. Ethanol consumption during pregna...
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description | ► Chronic prenatal ethanol exposure induces neurobehavioral deficits in offspring. ► Complex spatial working memory tasks improve sensitivity for detecting cognitive deficits. ► Speed accuracy trade-off increases frequency of errors in a spatial working memory task.
Ethanol consumption during pregnancy can produce a variety of teratogenic effects in offspring, termed Fetal Alcohol Spectrum Disorders (FASD). The most debilitating and permanent consequence of chronic prenatal ethanol exposure (CPEE) is neurobehavioral teratogenicity, which often manifests as cognitive and behavioral impairments, including deficits in spatial learning and memory. This study tested the hypothesis that a modified dry-land version of the multi-choice Biel-maze task is more sensitive than the rewarded-alternation Y-maze task for the determination of spatial learning and memory deficits of ethanol teratogenicity. Pregnant guinea pigs received ethanol (4g/kg maternal body weight/day) or isocaloric-sucrose/pair-feeding (control) for 5days/week throughout gestation. CPEE resulted in ethanol neurobehavioral teratogenicity in offspring, as demonstrated by increased spontaneous locomotor activity at postnatal day (PD) 10 and decreased brain weight at euthanasia (PD 150–200). On PD 21, offspring were randomly assigned to one of two tasks to assess spatial learning and memory performance: a dry-land version of the Biel maze or a rewarded-alternation Y-maze. Animals were habituated to the environment of their assigned task and performance of each CPEE or control offspring was measured. In the modified Biel maze, CPEE and control offspring were not different for percent completed trials or time to complete a trial. However, CPEE offspring made more errors (reversals and entering dead ends) in the Biel maze, demonstrating impaired spatial learning and memory. In contrast, CPEE offspring did not have impaired performance of the rewarded-alternation Y-maze task. Therefore, the modified dry-land version of the Biel-maze task, which measures cognitive performance using a complex multi-choice design, is more sensitive in demonstrating CPEE-induced spatial learning and memory deficits compared with a simple, rewarded-alternation Y-maze task. |
doi_str_mv | 10.1016/j.bbr.2012.04.042 |
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Ethanol consumption during pregnancy can produce a variety of teratogenic effects in offspring, termed Fetal Alcohol Spectrum Disorders (FASD). The most debilitating and permanent consequence of chronic prenatal ethanol exposure (CPEE) is neurobehavioral teratogenicity, which often manifests as cognitive and behavioral impairments, including deficits in spatial learning and memory. This study tested the hypothesis that a modified dry-land version of the multi-choice Biel-maze task is more sensitive than the rewarded-alternation Y-maze task for the determination of spatial learning and memory deficits of ethanol teratogenicity. Pregnant guinea pigs received ethanol (4g/kg maternal body weight/day) or isocaloric-sucrose/pair-feeding (control) for 5days/week throughout gestation. CPEE resulted in ethanol neurobehavioral teratogenicity in offspring, as demonstrated by increased spontaneous locomotor activity at postnatal day (PD) 10 and decreased brain weight at euthanasia (PD 150–200). On PD 21, offspring were randomly assigned to one of two tasks to assess spatial learning and memory performance: a dry-land version of the Biel maze or a rewarded-alternation Y-maze. Animals were habituated to the environment of their assigned task and performance of each CPEE or control offspring was measured. In the modified Biel maze, CPEE and control offspring were not different for percent completed trials or time to complete a trial. However, CPEE offspring made more errors (reversals and entering dead ends) in the Biel maze, demonstrating impaired spatial learning and memory. In contrast, CPEE offspring did not have impaired performance of the rewarded-alternation Y-maze task. Therefore, the modified dry-land version of the Biel-maze task, which measures cognitive performance using a complex multi-choice design, is more sensitive in demonstrating CPEE-induced spatial learning and memory deficits compared with a simple, rewarded-alternation Y-maze task.</description><identifier>ISSN: 0166-4328</identifier><identifier>EISSN: 1872-7549</identifier><identifier>DOI: 10.1016/j.bbr.2012.04.042</identifier><identifier>PMID: 22562040</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Age Factors ; Analysis of Variance ; Animals ; Biel maze ; Body weight ; Brain ; Brain - drug effects ; Central Nervous System Depressants - toxicity ; Cognitive ability ; Ethanol ; Ethanol - toxicity ; Ethanol neurobehavioral teratogenicity ; Female ; Fetal alcohol spectrum disorders ; Fetal alcohol syndrome ; Gestation ; Guinea pig ; Guinea Pigs ; Locomotor activity ; Male ; Maze Learning - drug effects ; Memory ; Memory Disorders - chemically induced ; Memory Disorders - pathology ; Motor Activity - drug effects ; Pregnancy ; Prenatal experience ; Prenatal Exposure Delayed Effects - physiopathology ; Progeny ; Reward ; Space Perception - drug effects ; Spatial discrimination learning ; Spatial learning and memory ; spatial memory ; Sucrose - administration & dosage ; Sweetening Agents - administration & dosage ; Teratogenicity ; Time Factors ; Y-maze</subject><ispartof>Behavioural brain research, 2012-07, Vol.233 (1), p.162-168</ispartof><rights>2012 Elsevier B.V.</rights><rights>Copyright © 2012 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c386t-226316c19c79498fcc61ae4c38be41754479c83513ebf20e7e0f540813eaeab83</citedby><cites>FETCH-LOGICAL-c386t-226316c19c79498fcc61ae4c38be41754479c83513ebf20e7e0f540813eaeab83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0166432812003038$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22562040$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dobson, Christine C.</creatorcontrib><creatorcontrib>Mongillo, Daniel L.</creatorcontrib><creatorcontrib>Poklewska-Koziell, Margo</creatorcontrib><creatorcontrib>Winterborn, Andrew</creatorcontrib><creatorcontrib>Brien, James F.</creatorcontrib><creatorcontrib>Reynolds, James N.</creatorcontrib><title>Sensitivity of modified Biel-maze task, compared with Y-maze task, to measure spatial learning and memory deficits of ethanol teratogenicity in the guinea pig</title><title>Behavioural brain research</title><addtitle>Behav Brain Res</addtitle><description>► Chronic prenatal ethanol exposure induces neurobehavioral deficits in offspring. ► Complex spatial working memory tasks improve sensitivity for detecting cognitive deficits. ► Speed accuracy trade-off increases frequency of errors in a spatial working memory task.
Ethanol consumption during pregnancy can produce a variety of teratogenic effects in offspring, termed Fetal Alcohol Spectrum Disorders (FASD). The most debilitating and permanent consequence of chronic prenatal ethanol exposure (CPEE) is neurobehavioral teratogenicity, which often manifests as cognitive and behavioral impairments, including deficits in spatial learning and memory. This study tested the hypothesis that a modified dry-land version of the multi-choice Biel-maze task is more sensitive than the rewarded-alternation Y-maze task for the determination of spatial learning and memory deficits of ethanol teratogenicity. Pregnant guinea pigs received ethanol (4g/kg maternal body weight/day) or isocaloric-sucrose/pair-feeding (control) for 5days/week throughout gestation. CPEE resulted in ethanol neurobehavioral teratogenicity in offspring, as demonstrated by increased spontaneous locomotor activity at postnatal day (PD) 10 and decreased brain weight at euthanasia (PD 150–200). On PD 21, offspring were randomly assigned to one of two tasks to assess spatial learning and memory performance: a dry-land version of the Biel maze or a rewarded-alternation Y-maze. Animals were habituated to the environment of their assigned task and performance of each CPEE or control offspring was measured. In the modified Biel maze, CPEE and control offspring were not different for percent completed trials or time to complete a trial. However, CPEE offspring made more errors (reversals and entering dead ends) in the Biel maze, demonstrating impaired spatial learning and memory. In contrast, CPEE offspring did not have impaired performance of the rewarded-alternation Y-maze task. Therefore, the modified dry-land version of the Biel-maze task, which measures cognitive performance using a complex multi-choice design, is more sensitive in demonstrating CPEE-induced spatial learning and memory deficits compared with a simple, rewarded-alternation Y-maze task.</description><subject>Age Factors</subject><subject>Analysis of Variance</subject><subject>Animals</subject><subject>Biel maze</subject><subject>Body weight</subject><subject>Brain</subject><subject>Brain - drug effects</subject><subject>Central Nervous System Depressants - toxicity</subject><subject>Cognitive ability</subject><subject>Ethanol</subject><subject>Ethanol - toxicity</subject><subject>Ethanol neurobehavioral teratogenicity</subject><subject>Female</subject><subject>Fetal alcohol spectrum disorders</subject><subject>Fetal alcohol syndrome</subject><subject>Gestation</subject><subject>Guinea pig</subject><subject>Guinea Pigs</subject><subject>Locomotor activity</subject><subject>Male</subject><subject>Maze Learning - drug effects</subject><subject>Memory</subject><subject>Memory Disorders - chemically induced</subject><subject>Memory Disorders - pathology</subject><subject>Motor Activity - drug effects</subject><subject>Pregnancy</subject><subject>Prenatal experience</subject><subject>Prenatal Exposure Delayed Effects - physiopathology</subject><subject>Progeny</subject><subject>Reward</subject><subject>Space Perception - drug effects</subject><subject>Spatial discrimination learning</subject><subject>Spatial learning and memory</subject><subject>spatial memory</subject><subject>Sucrose - administration & dosage</subject><subject>Sweetening Agents - administration & dosage</subject><subject>Teratogenicity</subject><subject>Time Factors</subject><subject>Y-maze</subject><issn>0166-4328</issn><issn>1872-7549</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kU2LFDEQhoMo7rj6A7xIjh7sMUmnv_DkLn7Bggf14ClUp6tnauxO2iS9Mv4Yf6sZZhVPQkFRvE-9IfUy9lSKrRSyfnnY9n3YKiHVVuhc6h7byLZRRVPp7j7bZKYudKnaC_YoxoMQQotKPmQXSlW1ysOG_fqELlKiW0pH7kc--4FGwoFfEU7FDD-RJ4jfXnDr5wVCFn5Q2vOv_0rJ8xkhrgF5XCARTHxCCI7cjoMbsjj7cOQDjmQpxdMzmPbg_MQTBkh-h-6kHDk5nvbIdys5BL7Q7jF7MMIU8cldv2Rf3r75fP2-uPn47sP165vClm2dCqXqUtZWdrbpdNeO1tYSUGexRy3zNXTT2basZIn9qAQ2KMZKizbPgNC35SV7fvZdgv--YkxmpmhxmsChX6ORQrWiFJ3SGZVn1AYfY8DRLIFmCMcMmVMs5mByLOYUixE6l8o7z-7s137G4e_Gnxwy8OoMYP7kLWEw0RI6iwMFtMkMnv5j_xsMjZ-Q</recordid><startdate>20120715</startdate><enddate>20120715</enddate><creator>Dobson, Christine C.</creator><creator>Mongillo, Daniel L.</creator><creator>Poklewska-Koziell, Margo</creator><creator>Winterborn, Andrew</creator><creator>Brien, James F.</creator><creator>Reynolds, James N.</creator><general>Elsevier B.V</general><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>20120715</creationdate><title>Sensitivity of modified Biel-maze task, compared with Y-maze task, to measure spatial learning and memory deficits of ethanol teratogenicity in the guinea pig</title><author>Dobson, Christine C. ; Mongillo, Daniel L. ; Poklewska-Koziell, Margo ; Winterborn, Andrew ; Brien, James F. ; Reynolds, James N.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c386t-226316c19c79498fcc61ae4c38be41754479c83513ebf20e7e0f540813eaeab83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Age Factors</topic><topic>Analysis of Variance</topic><topic>Animals</topic><topic>Biel maze</topic><topic>Body weight</topic><topic>Brain</topic><topic>Brain - drug effects</topic><topic>Central Nervous System Depressants - toxicity</topic><topic>Cognitive ability</topic><topic>Ethanol</topic><topic>Ethanol - toxicity</topic><topic>Ethanol neurobehavioral teratogenicity</topic><topic>Female</topic><topic>Fetal alcohol spectrum disorders</topic><topic>Fetal alcohol syndrome</topic><topic>Gestation</topic><topic>Guinea pig</topic><topic>Guinea Pigs</topic><topic>Locomotor activity</topic><topic>Male</topic><topic>Maze Learning - drug effects</topic><topic>Memory</topic><topic>Memory Disorders - chemically induced</topic><topic>Memory Disorders - pathology</topic><topic>Motor Activity - drug effects</topic><topic>Pregnancy</topic><topic>Prenatal experience</topic><topic>Prenatal Exposure Delayed Effects - physiopathology</topic><topic>Progeny</topic><topic>Reward</topic><topic>Space Perception - drug effects</topic><topic>Spatial discrimination learning</topic><topic>Spatial learning and memory</topic><topic>spatial memory</topic><topic>Sucrose - administration & dosage</topic><topic>Sweetening Agents - administration & dosage</topic><topic>Teratogenicity</topic><topic>Time Factors</topic><topic>Y-maze</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dobson, Christine C.</creatorcontrib><creatorcontrib>Mongillo, Daniel L.</creatorcontrib><creatorcontrib>Poklewska-Koziell, Margo</creatorcontrib><creatorcontrib>Winterborn, Andrew</creatorcontrib><creatorcontrib>Brien, James F.</creatorcontrib><creatorcontrib>Reynolds, James N.</creatorcontrib><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>Behavioural brain research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dobson, Christine C.</au><au>Mongillo, Daniel L.</au><au>Poklewska-Koziell, Margo</au><au>Winterborn, Andrew</au><au>Brien, James F.</au><au>Reynolds, James N.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Sensitivity of modified Biel-maze task, compared with Y-maze task, to measure spatial learning and memory deficits of ethanol teratogenicity in the guinea pig</atitle><jtitle>Behavioural brain research</jtitle><addtitle>Behav Brain Res</addtitle><date>2012-07-15</date><risdate>2012</risdate><volume>233</volume><issue>1</issue><spage>162</spage><epage>168</epage><pages>162-168</pages><issn>0166-4328</issn><eissn>1872-7549</eissn><abstract>► Chronic prenatal ethanol exposure induces neurobehavioral deficits in offspring. ► Complex spatial working memory tasks improve sensitivity for detecting cognitive deficits. ► Speed accuracy trade-off increases frequency of errors in a spatial working memory task.
Ethanol consumption during pregnancy can produce a variety of teratogenic effects in offspring, termed Fetal Alcohol Spectrum Disorders (FASD). The most debilitating and permanent consequence of chronic prenatal ethanol exposure (CPEE) is neurobehavioral teratogenicity, which often manifests as cognitive and behavioral impairments, including deficits in spatial learning and memory. This study tested the hypothesis that a modified dry-land version of the multi-choice Biel-maze task is more sensitive than the rewarded-alternation Y-maze task for the determination of spatial learning and memory deficits of ethanol teratogenicity. Pregnant guinea pigs received ethanol (4g/kg maternal body weight/day) or isocaloric-sucrose/pair-feeding (control) for 5days/week throughout gestation. CPEE resulted in ethanol neurobehavioral teratogenicity in offspring, as demonstrated by increased spontaneous locomotor activity at postnatal day (PD) 10 and decreased brain weight at euthanasia (PD 150–200). On PD 21, offspring were randomly assigned to one of two tasks to assess spatial learning and memory performance: a dry-land version of the Biel maze or a rewarded-alternation Y-maze. Animals were habituated to the environment of their assigned task and performance of each CPEE or control offspring was measured. In the modified Biel maze, CPEE and control offspring were not different for percent completed trials or time to complete a trial. However, CPEE offspring made more errors (reversals and entering dead ends) in the Biel maze, demonstrating impaired spatial learning and memory. In contrast, CPEE offspring did not have impaired performance of the rewarded-alternation Y-maze task. Therefore, the modified dry-land version of the Biel-maze task, which measures cognitive performance using a complex multi-choice design, is more sensitive in demonstrating CPEE-induced spatial learning and memory deficits compared with a simple, rewarded-alternation Y-maze task.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>22562040</pmid><doi>10.1016/j.bbr.2012.04.042</doi><tpages>7</tpages></addata></record> |
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subjects | Age Factors Analysis of Variance Animals Biel maze Body weight Brain Brain - drug effects Central Nervous System Depressants - toxicity Cognitive ability Ethanol Ethanol - toxicity Ethanol neurobehavioral teratogenicity Female Fetal alcohol spectrum disorders Fetal alcohol syndrome Gestation Guinea pig Guinea Pigs Locomotor activity Male Maze Learning - drug effects Memory Memory Disorders - chemically induced Memory Disorders - pathology Motor Activity - drug effects Pregnancy Prenatal experience Prenatal Exposure Delayed Effects - physiopathology Progeny Reward Space Perception - drug effects Spatial discrimination learning Spatial learning and memory spatial memory Sucrose - administration & dosage Sweetening Agents - administration & dosage Teratogenicity Time Factors Y-maze |
title | Sensitivity of modified Biel-maze task, compared with Y-maze task, to measure spatial learning and memory deficits of ethanol teratogenicity in the guinea pig |
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