Brain lesions and water-maze learning deficits after systemic administration of kainic acid to adult rats
The relationship between hippocampal damage and spatial learning deficiencies was studied in rats injected with kainic acid (10 mg/kg i.p.). A single injection was given either before or after the acquisition phase of the Morris water-maze task. In this acquisition phase, the animals were required t...
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Veröffentlicht in: | Brain research 1994-08, Vol.653 (1), p.92-100 |
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description | The relationship between hippocampal damage and spatial learning deficiencies was studied in rats injected with kainic acid (10 mg/kg i.p.). A single injection was given either before or after the acquisition phase of the Morris water-maze task. In this acquisition phase, the animals were required to find a hidden underwater platform starting from four different points. The task was repeated twice a day for 10 days. In the retention phase after 10 days rest, the rats repeated the same task. The damage caused by the treatment occurred in several prosencephalic areas, including the piriform and enthorhinal cortices, the thalamus and the hippocampus. In the latter, greatest damage was seen in CA1 followed by CA3 while CA2 and the gyrus dentatus appeared almost unaffected. The behavioural results indicated that kainic acid impaired but did not preclude the acquisition of the water-maze task. During the retention phase, no significant differences in latencies were found between animals that were treated before and after acquisition, thus, indicating that pretraining does not play an important role in the recovery of these spatial abilities following hippocampal lesions. |
doi_str_mv | 10.1016/0006-8993(94)90376-X |
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A single injection was given either before or after the acquisition phase of the Morris water-maze task. In this acquisition phase, the animals were required to find a hidden underwater platform starting from four different points. The task was repeated twice a day for 10 days. In the retention phase after 10 days rest, the rats repeated the same task. The damage caused by the treatment occurred in several prosencephalic areas, including the piriform and enthorhinal cortices, the thalamus and the hippocampus. In the latter, greatest damage was seen in CA1 followed by CA3 while CA2 and the gyrus dentatus appeared almost unaffected. The behavioural results indicated that kainic acid impaired but did not preclude the acquisition of the water-maze task. During the retention phase, no significant differences in latencies were found between animals that were treated before and after acquisition, thus, indicating that pretraining does not play an important role in the recovery of these spatial abilities following hippocampal lesions.</description><identifier>ISSN: 0006-8993</identifier><identifier>EISSN: 1872-6240</identifier><identifier>DOI: 10.1016/0006-8993(94)90376-X</identifier><identifier>PMID: 7982081</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Animals ; Brain - drug effects ; Brain - metabolism ; Brain - pathology ; Brain Mapping ; Glial Fibrillary Acidic Protein - metabolism ; Hippocampus ; Immunohistochemistry ; Injections, Intraperitoneal ; Kainic acid ; Kainic Acid - pharmacology ; Learning - drug effects ; Male ; Motor Activity - drug effects ; Neurotoxicity ; Rat ; Rats ; Rats, Wistar ; Reaction Time - drug effects ; Retention (Psychology) - drug effects ; Spatial learning ; Water maze</subject><ispartof>Brain research, 1994-08, Vol.653 (1), p.92-100</ispartof><rights>1994 Elsevier Science B.V. All rights reserved</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c357t-27e8bcf92d28c7b7674442fc5dc01c1015f2772cf766225b6a9216b1d603eabd3</citedby><cites>FETCH-LOGICAL-c357t-27e8bcf92d28c7b7674442fc5dc01c1015f2772cf766225b6a9216b1d603eabd3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/000689939490376X$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3536,27903,27904,65309</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7982081$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gayoso, M.J.</creatorcontrib><creatorcontrib>Primo, C.</creatorcontrib><creatorcontrib>Al-Majdalawi, A.</creatorcontrib><creatorcontrib>Fernandez, J.M.</creatorcontrib><creatorcontrib>Garrosa, M.</creatorcontrib><creatorcontrib>In˜iguez, C.</creatorcontrib><title>Brain lesions and water-maze learning deficits after systemic administration of kainic acid to adult rats</title><title>Brain research</title><addtitle>Brain Res</addtitle><description>The relationship between hippocampal damage and spatial learning deficiencies was studied in rats injected with kainic acid (10 mg/kg i.p.). A single injection was given either before or after the acquisition phase of the Morris water-maze task. In this acquisition phase, the animals were required to find a hidden underwater platform starting from four different points. The task was repeated twice a day for 10 days. In the retention phase after 10 days rest, the rats repeated the same task. The damage caused by the treatment occurred in several prosencephalic areas, including the piriform and enthorhinal cortices, the thalamus and the hippocampus. In the latter, greatest damage was seen in CA1 followed by CA3 while CA2 and the gyrus dentatus appeared almost unaffected. The behavioural results indicated that kainic acid impaired but did not preclude the acquisition of the water-maze task. During the retention phase, no significant differences in latencies were found between animals that were treated before and after acquisition, thus, indicating that pretraining does not play an important role in the recovery of these spatial abilities following hippocampal lesions.</description><subject>Animals</subject><subject>Brain - drug effects</subject><subject>Brain - metabolism</subject><subject>Brain - pathology</subject><subject>Brain Mapping</subject><subject>Glial Fibrillary Acidic Protein - metabolism</subject><subject>Hippocampus</subject><subject>Immunohistochemistry</subject><subject>Injections, Intraperitoneal</subject><subject>Kainic acid</subject><subject>Kainic Acid - pharmacology</subject><subject>Learning - drug effects</subject><subject>Male</subject><subject>Motor Activity - drug effects</subject><subject>Neurotoxicity</subject><subject>Rat</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Reaction Time - drug effects</subject><subject>Retention (Psychology) - drug effects</subject><subject>Spatial learning</subject><subject>Water maze</subject><issn>0006-8993</issn><issn>1872-6240</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kEtLBDEQhIMouj7-gUJOoofRJDOTTC6CLr5A8KKwt5BJOhKdhyZZZf31Zt3Fo6cm_VVV6ELokJIzSig_J4TwopGyPJHVqSSl4MVsA01oI1jBWUU20eRPsoN2Y3zNz7KUZBttC9kw0tAJ8ldB-wF3EP04RKwHi790glD0-hvyWofBDy_YgvPGpyxwGeK4iAl6b7C2vR98TEGn7Mejw285bgmMtziNWTDvEs447qMtp7sIB-u5h55vrp-md8XD4-399PKhMGUtUsEENK1xklnWGNEKLqqqYs7U1hBq8uG1Y0Iw4wTnjNUt15JR3lLLSQm6teUeOl7lvofxYw4xqd5HA12nBxjnUQne1FLULAurldCEMcYATr0H3-uwUJSoZcNqWZ9a1qdkpX4bVrNsO1rnz9se7J9pXWnmFysO-chPD0FF42EwYH0Ak5Qd_f8f_ABOzIwI</recordid><startdate>19940808</startdate><enddate>19940808</enddate><creator>Gayoso, M.J.</creator><creator>Primo, C.</creator><creator>Al-Majdalawi, A.</creator><creator>Fernandez, J.M.</creator><creator>Garrosa, M.</creator><creator>In˜iguez, C.</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>7X8</scope></search><sort><creationdate>19940808</creationdate><title>Brain lesions and water-maze learning deficits after systemic administration of kainic acid to adult rats</title><author>Gayoso, M.J. ; Primo, C. ; Al-Majdalawi, A. ; Fernandez, J.M. ; Garrosa, M. ; In˜iguez, C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c357t-27e8bcf92d28c7b7674442fc5dc01c1015f2772cf766225b6a9216b1d603eabd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1994</creationdate><topic>Animals</topic><topic>Brain - drug effects</topic><topic>Brain - metabolism</topic><topic>Brain - pathology</topic><topic>Brain Mapping</topic><topic>Glial Fibrillary Acidic Protein - metabolism</topic><topic>Hippocampus</topic><topic>Immunohistochemistry</topic><topic>Injections, Intraperitoneal</topic><topic>Kainic acid</topic><topic>Kainic Acid - pharmacology</topic><topic>Learning - drug effects</topic><topic>Male</topic><topic>Motor Activity - drug effects</topic><topic>Neurotoxicity</topic><topic>Rat</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Reaction Time - drug effects</topic><topic>Retention (Psychology) - drug effects</topic><topic>Spatial learning</topic><topic>Water maze</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gayoso, M.J.</creatorcontrib><creatorcontrib>Primo, C.</creatorcontrib><creatorcontrib>Al-Majdalawi, A.</creatorcontrib><creatorcontrib>Fernandez, J.M.</creatorcontrib><creatorcontrib>Garrosa, M.</creatorcontrib><creatorcontrib>In˜iguez, C.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Brain research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gayoso, M.J.</au><au>Primo, C.</au><au>Al-Majdalawi, A.</au><au>Fernandez, J.M.</au><au>Garrosa, M.</au><au>In˜iguez, C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Brain lesions and water-maze learning deficits after systemic administration of kainic acid to adult rats</atitle><jtitle>Brain research</jtitle><addtitle>Brain Res</addtitle><date>1994-08-08</date><risdate>1994</risdate><volume>653</volume><issue>1</issue><spage>92</spage><epage>100</epage><pages>92-100</pages><issn>0006-8993</issn><eissn>1872-6240</eissn><abstract>The relationship between hippocampal damage and spatial learning deficiencies was studied in rats injected with kainic acid (10 mg/kg i.p.). A single injection was given either before or after the acquisition phase of the Morris water-maze task. In this acquisition phase, the animals were required to find a hidden underwater platform starting from four different points. The task was repeated twice a day for 10 days. In the retention phase after 10 days rest, the rats repeated the same task. The damage caused by the treatment occurred in several prosencephalic areas, including the piriform and enthorhinal cortices, the thalamus and the hippocampus. In the latter, greatest damage was seen in CA1 followed by CA3 while CA2 and the gyrus dentatus appeared almost unaffected. The behavioural results indicated that kainic acid impaired but did not preclude the acquisition of the water-maze task. During the retention phase, no significant differences in latencies were found between animals that were treated before and after acquisition, thus, indicating that pretraining does not play an important role in the recovery of these spatial abilities following hippocampal lesions.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>7982081</pmid><doi>10.1016/0006-8993(94)90376-X</doi><tpages>9</tpages></addata></record> |
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subjects | Animals Brain - drug effects Brain - metabolism Brain - pathology Brain Mapping Glial Fibrillary Acidic Protein - metabolism Hippocampus Immunohistochemistry Injections, Intraperitoneal Kainic acid Kainic Acid - pharmacology Learning - drug effects Male Motor Activity - drug effects Neurotoxicity Rat Rats Rats, Wistar Reaction Time - drug effects Retention (Psychology) - drug effects Spatial learning Water maze |
title | Brain lesions and water-maze learning deficits after systemic administration of kainic acid to adult rats |
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