Studies on memory: The cerebral spread of an engram in mice as affected by inhibitors of dopamine β-hydroxylase
Bitemporal injections of puromycin that primarily affect the hippocampal-entorhinal areas consistently cause amnesia of maze-learning in mice for 3 days after training but become consistently ineffective if given 6 or more days after training. At these later times, additional puromycin injection sit...
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Veröffentlicht in: | Pharmacology, biochemistry and behavior biochemistry and behavior, 1983-04, Vol.18 (4), p.519-523 |
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creator | Flexner, Josefa B. Flexner, Louis B. Church, Allen C. |
description | Bitemporal injections of puromycin that primarily affect the hippocampal-entorhinal areas consistently cause amnesia of maze-learning in mice for 3 days after training but become consistently ineffective if given 6 or more days after training. At these later times, additional puromycin injection sites covering widespread areas of the forebrain are necessary to induce amnesia. These observations are interpreted to indicate that the locus of the engram has become more widespread within the 6-day period. Treatment with inhibitors of dopamine β-hydroxylase for 3 days following training, retarded the spread of memory from a matter of days to a period of weeks. Repeated treatment with the inhibitors restricted engram spread for about 3 months; again spread was evident about a month after the last treatment. These observations imply that the mechanisms responsible for engram spread are capable of surviving for extraordinarily long periods of time. |
doi_str_mv | 10.1016/0091-3057(83)90274-5 |
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At these later times, additional puromycin injection sites covering widespread areas of the forebrain are necessary to induce amnesia. These observations are interpreted to indicate that the locus of the engram has become more widespread within the 6-day period. Treatment with inhibitors of dopamine β-hydroxylase for 3 days following training, retarded the spread of memory from a matter of days to a period of weeks. Repeated treatment with the inhibitors restricted engram spread for about 3 months; again spread was evident about a month after the last treatment. 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At these later times, additional puromycin injection sites covering widespread areas of the forebrain are necessary to induce amnesia. These observations are interpreted to indicate that the locus of the engram has become more widespread within the 6-day period. Treatment with inhibitors of dopamine β-hydroxylase for 3 days following training, retarded the spread of memory from a matter of days to a period of weeks. Repeated treatment with the inhibitors restricted engram spread for about 3 months; again spread was evident about a month after the last treatment. These observations imply that the mechanisms responsible for engram spread are capable of surviving for extraordinarily long periods of time.</description><subject>Animals</subject><subject>Behavior, Animal - drug effects</subject><subject>Bis(4-Methyl-1-Homopiperazinylthiocarbonyl)disulfide - pharmacology</subject><subject>Brain Chemistry - drug effects</subject><subject>Cerebral Cortex - physiology</subject><subject>Dopamine beta-Hydroxylase - antagonists & inhibitors</subject><subject>Dopamine β-hydroxylase</subject><subject>Female</subject><subject>Hippocampus</subject><subject>Injections, Subcutaneous</subject><subject>Male</subject><subject>Memory - drug effects</subject><subject>Memory spread</subject><subject>Mice</subject><subject>Phenylthiazolylthiourea - pharmacology</subject><subject>Puromycin</subject><subject>Recent memory</subject><subject>Remote memory</subject><subject>Time Factors</subject><issn>0091-3057</issn><issn>1873-5177</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1983</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc9u1DAQxq2Kqixt3wAkn1A5pPhPEscckFAFtFIlDrRna9Yes0ZJHOwsIq_VB-kz4WVXPdLTSDO_b2b0fYS85uySM96-Z0zzSrJGXXTynWZC1VVzRFa8U7JquFIvyOoJeUle5fyTMVaLVp2Qk7ZrVWmvyPR93rqAmcaRDjjEtHygdxukFhOuE_Q0TwnB0egpjBTHHwkGGgobLFLIFLxHO6Oj66W0N2Ed5pjyDndxgiGMSB8fqs3iUvyz9JDxjBx76DOeH-opuf_y-e7qurr99vXm6tNtZWXXzZV3THBXnlXOgu28ZrVkAMLX0HrgWmjBuFQonJOuBuDOIUOvrbBFpbU8JW_3e6cUf20xz2YI2WLfw4hxm03Hmlo3LXsWLFe4KPYWsN6DNsWcE3ozpTBAWgxnZpeI2dltdnabTpp_iZimyN4c9m_XA7on0SGCMv-4n2Nx43fAZLINOFp0IRVrjYvh_wf-Akw2nA0</recordid><startdate>198304</startdate><enddate>198304</enddate><creator>Flexner, Josefa B.</creator><creator>Flexner, Louis B.</creator><creator>Church, Allen C.</creator><general>Elsevier Inc</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><scope>7X8</scope></search><sort><creationdate>198304</creationdate><title>Studies on memory: The cerebral spread of an engram in mice as affected by inhibitors of dopamine β-hydroxylase</title><author>Flexner, Josefa B. ; Flexner, Louis B. ; Church, Allen C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c388t-fd021d2677dcac8f90430aa2f4a6fa192920137e2dd3d4aa1dde0ef9c2cd26993</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1983</creationdate><topic>Animals</topic><topic>Behavior, Animal - drug effects</topic><topic>Bis(4-Methyl-1-Homopiperazinylthiocarbonyl)disulfide - pharmacology</topic><topic>Brain Chemistry - drug effects</topic><topic>Cerebral Cortex - physiology</topic><topic>Dopamine beta-Hydroxylase - antagonists & inhibitors</topic><topic>Dopamine β-hydroxylase</topic><topic>Female</topic><topic>Hippocampus</topic><topic>Injections, Subcutaneous</topic><topic>Male</topic><topic>Memory - drug effects</topic><topic>Memory spread</topic><topic>Mice</topic><topic>Phenylthiazolylthiourea - pharmacology</topic><topic>Puromycin</topic><topic>Recent memory</topic><topic>Remote memory</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Flexner, Josefa B.</creatorcontrib><creatorcontrib>Flexner, Louis B.</creatorcontrib><creatorcontrib>Church, Allen 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>Animal Behavior Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Pharmacology, biochemistry and behavior</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Flexner, Josefa B.</au><au>Flexner, Louis B.</au><au>Church, Allen C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Studies on memory: The cerebral spread of an engram in mice as affected by inhibitors of dopamine β-hydroxylase</atitle><jtitle>Pharmacology, biochemistry and behavior</jtitle><addtitle>Pharmacol Biochem Behav</addtitle><date>1983-04</date><risdate>1983</risdate><volume>18</volume><issue>4</issue><spage>519</spage><epage>523</epage><pages>519-523</pages><issn>0091-3057</issn><eissn>1873-5177</eissn><abstract>Bitemporal injections of puromycin that primarily affect the hippocampal-entorhinal areas consistently cause amnesia of maze-learning in mice for 3 days after training but become consistently ineffective if given 6 or more days after training. At these later times, additional puromycin injection sites covering widespread areas of the forebrain are necessary to induce amnesia. These observations are interpreted to indicate that the locus of the engram has become more widespread within the 6-day period. Treatment with inhibitors of dopamine β-hydroxylase for 3 days following training, retarded the spread of memory from a matter of days to a period of weeks. Repeated treatment with the inhibitors restricted engram spread for about 3 months; again spread was evident about a month after the last treatment. These observations imply that the mechanisms responsible for engram spread are capable of surviving for extraordinarily long periods of time.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>6867057</pmid><doi>10.1016/0091-3057(83)90274-5</doi><tpages>5</tpages></addata></record> |
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subjects | Animals Behavior, Animal - drug effects Bis(4-Methyl-1-Homopiperazinylthiocarbonyl)disulfide - pharmacology Brain Chemistry - drug effects Cerebral Cortex - physiology Dopamine beta-Hydroxylase - antagonists & inhibitors Dopamine β-hydroxylase Female Hippocampus Injections, Subcutaneous Male Memory - drug effects Memory spread Mice Phenylthiazolylthiourea - pharmacology Puromycin Recent memory Remote memory Time Factors |
title | Studies on memory: The cerebral spread of an engram in mice as affected by inhibitors of dopamine β-hydroxylase |
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