GABAergic and developmental influences on homosynaptic LTD and depotentiation in rat hippocampus
Low-frequency (1 Hz) stimulation (LFS) was used to elicit long-term depression (LTD) or depotentiation of excitatory transmission of the Schaffer collateral pathway in the CA1 region of the rat hippocampus. Both LTD and depotentiation were found to be homosynaptic and NMDA receptor (NMDAR) dependent...
Gespeichert in:
Veröffentlicht in: | The Journal of neuroscience 1995-02, Vol.15 (2), p.1577-1586 |
---|---|
Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 1586 |
---|---|
container_issue | 2 |
container_start_page | 1577 |
container_title | The Journal of neuroscience |
container_volume | 15 |
creator | Wagner, JJ Alger, BE |
description | Low-frequency (1 Hz) stimulation (LFS) was used to elicit long-term depression (LTD) or depotentiation of excitatory transmission of the Schaffer collateral pathway in the CA1 region of the rat hippocampus. Both LTD and depotentiation were found to be homosynaptic and NMDA receptor (NMDAR) dependent. As NMDAR activation can be modulated by the inhibitory GABAergic system, we tested the hypothesis that GABA plays a role in regulating these phenomena. The GABAB antagonist CGP 35348 significantly inhibited LTD, but not depotentiation, in slices from young animals (indicating that the GABAB-mediated contribution was altered following HFS). The ability to express LTD was found to be developmentally dependent, as young animals (16-22 d) consistently expressed LTD, whereas LTD was not expressed in naive slices taken from mature (5-10 weeks) animals. The GABAA antagonist bicuculline did not affect LTD in the young animals, but did enhance LTD expression in slices from mature animals. LFS was also effective in decreasing, or depotentiating, responses that had undergone long-term potentiation (LTP) by high-frequency stimulation (HFS). In contrast to LTD, depotentiation was consistently expressed in slices from both the young and mature groups. Moreover, following an HFS train, LTD (compared to initial baseline response) could be induced in mature slices previously unable to express LTD in the naive state. Thus, the role of GABA in modulating the effects of LFS varied with the prior synaptic activity in the slice as well as with the maturity of the animal. Our results suggest that the influence of both age and prior synaptic activity (i.e., HFS) on LTD induction can be explained by changes in GABAergic systems in young versus mature, and naive versus tetanized slices. |
doi_str_mv | 10.1523/jneurosci.15-02-01577.1995 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6577799</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>77158160</sourcerecordid><originalsourceid>FETCH-LOGICAL-c606t-183e1563b71730a0d13434dfb3f49a7e14e48d134bff09f65872aea700a837c93</originalsourceid><addsrcrecordid>eNqFkUFv1DAUhC1EVZbCT0CKOHBL-xwndswBaVna0mpFJWjPxus4G1eOndpJV_33OHRV6Kkn69nfjOZ5EPqI4RhXBTm5dXoKPiqTxhyKHHDF2DHmvHqFFongeVECfo0WUDDIacnKN-htjLcAwACzQ3TIasox5gv0-3z5danD1qhMuiZr9L22fui1G6XNjGvtpJ3SMfMu63zv44OTw5jg9fW3vWDwY6KNHE1ijMuCHLPODINXsh-m-A4dtNJG_X5_HqGbs9Pr1fd8fXV-sVquc0WBjjmuicYVJRuGGQEJDSYlKZt2Q9qSS6Zxqct6vty0LfCWVjUrpJYMQNaEKU6O0JdH32Ha9LpRKVOQVgzB9DI8CC-NeP7iTCe2_l7Q9HeMzwaf9gbB3006jqI3UWlrpdN-ioIxXNWYwosgpqkIzuoEfn4EVSorBt0-pcEg5iLF5Y_Tm59Xv1YXaRRQiL9FirnIJP7w_z5P0n1z_1J0ZtvtTNAi9tLaRGOx2-2SXyFmN_IHOAmrOQ</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>16995978</pqid></control><display><type>article</type><title>GABAergic and developmental influences on homosynaptic LTD and depotentiation in rat hippocampus</title><source>MEDLINE</source><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><creator>Wagner, JJ ; Alger, BE</creator><creatorcontrib>Wagner, JJ ; Alger, BE</creatorcontrib><description>Low-frequency (1 Hz) stimulation (LFS) was used to elicit long-term depression (LTD) or depotentiation of excitatory transmission of the Schaffer collateral pathway in the CA1 region of the rat hippocampus. Both LTD and depotentiation were found to be homosynaptic and NMDA receptor (NMDAR) dependent. As NMDAR activation can be modulated by the inhibitory GABAergic system, we tested the hypothesis that GABA plays a role in regulating these phenomena. The GABAB antagonist CGP 35348 significantly inhibited LTD, but not depotentiation, in slices from young animals (indicating that the GABAB-mediated contribution was altered following HFS). The ability to express LTD was found to be developmentally dependent, as young animals (16-22 d) consistently expressed LTD, whereas LTD was not expressed in naive slices taken from mature (5-10 weeks) animals. The GABAA antagonist bicuculline did not affect LTD in the young animals, but did enhance LTD expression in slices from mature animals. LFS was also effective in decreasing, or depotentiating, responses that had undergone long-term potentiation (LTP) by high-frequency stimulation (HFS). In contrast to LTD, depotentiation was consistently expressed in slices from both the young and mature groups. Moreover, following an HFS train, LTD (compared to initial baseline response) could be induced in mature slices previously unable to express LTD in the naive state. Thus, the role of GABA in modulating the effects of LFS varied with the prior synaptic activity in the slice as well as with the maturity of the animal. Our results suggest that the influence of both age and prior synaptic activity (i.e., HFS) on LTD induction can be explained by changes in GABAergic systems in young versus mature, and naive versus tetanized slices.</description><identifier>ISSN: 0270-6474</identifier><identifier>EISSN: 1529-2401</identifier><identifier>DOI: 10.1523/jneurosci.15-02-01577.1995</identifier><identifier>PMID: 7869119</identifier><language>eng</language><publisher>United States: Soc Neuroscience</publisher><subject>Aging - physiology ; Animals ; Electric Stimulation - methods ; Electrophysiology ; GABA-A Receptor Antagonists ; GABA-B Receptor Antagonists ; gamma-Aminobutyric Acid - physiology ; Hippocampus - drug effects ; Hippocampus - growth & development ; Hippocampus - physiology ; Long-Term Potentiation ; Organophosphorus Compounds - pharmacology ; Rats ; Rats, Sprague-Dawley ; Receptors, GABA-A - physiology ; Receptors, GABA-B - physiology ; Synapses - physiology</subject><ispartof>The Journal of neuroscience, 1995-02, Vol.15 (2), p.1577-1586</ispartof><rights>1995 by Society for Neuroscience 1995</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c606t-183e1563b71730a0d13434dfb3f49a7e14e48d134bff09f65872aea700a837c93</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6577799/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6577799/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27923,27924,53790,53792</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7869119$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wagner, JJ</creatorcontrib><creatorcontrib>Alger, BE</creatorcontrib><title>GABAergic and developmental influences on homosynaptic LTD and depotentiation in rat hippocampus</title><title>The Journal of neuroscience</title><addtitle>J Neurosci</addtitle><description>Low-frequency (1 Hz) stimulation (LFS) was used to elicit long-term depression (LTD) or depotentiation of excitatory transmission of the Schaffer collateral pathway in the CA1 region of the rat hippocampus. Both LTD and depotentiation were found to be homosynaptic and NMDA receptor (NMDAR) dependent. As NMDAR activation can be modulated by the inhibitory GABAergic system, we tested the hypothesis that GABA plays a role in regulating these phenomena. The GABAB antagonist CGP 35348 significantly inhibited LTD, but not depotentiation, in slices from young animals (indicating that the GABAB-mediated contribution was altered following HFS). The ability to express LTD was found to be developmentally dependent, as young animals (16-22 d) consistently expressed LTD, whereas LTD was not expressed in naive slices taken from mature (5-10 weeks) animals. The GABAA antagonist bicuculline did not affect LTD in the young animals, but did enhance LTD expression in slices from mature animals. LFS was also effective in decreasing, or depotentiating, responses that had undergone long-term potentiation (LTP) by high-frequency stimulation (HFS). In contrast to LTD, depotentiation was consistently expressed in slices from both the young and mature groups. Moreover, following an HFS train, LTD (compared to initial baseline response) could be induced in mature slices previously unable to express LTD in the naive state. Thus, the role of GABA in modulating the effects of LFS varied with the prior synaptic activity in the slice as well as with the maturity of the animal. Our results suggest that the influence of both age and prior synaptic activity (i.e., HFS) on LTD induction can be explained by changes in GABAergic systems in young versus mature, and naive versus tetanized slices.</description><subject>Aging - physiology</subject><subject>Animals</subject><subject>Electric Stimulation - methods</subject><subject>Electrophysiology</subject><subject>GABA-A Receptor Antagonists</subject><subject>GABA-B Receptor Antagonists</subject><subject>gamma-Aminobutyric Acid - physiology</subject><subject>Hippocampus - drug effects</subject><subject>Hippocampus - growth & development</subject><subject>Hippocampus - physiology</subject><subject>Long-Term Potentiation</subject><subject>Organophosphorus Compounds - pharmacology</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Receptors, GABA-A - physiology</subject><subject>Receptors, GABA-B - physiology</subject><subject>Synapses - physiology</subject><issn>0270-6474</issn><issn>1529-2401</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUFv1DAUhC1EVZbCT0CKOHBL-xwndswBaVna0mpFJWjPxus4G1eOndpJV_33OHRV6Kkn69nfjOZ5EPqI4RhXBTm5dXoKPiqTxhyKHHDF2DHmvHqFFongeVECfo0WUDDIacnKN-htjLcAwACzQ3TIasox5gv0-3z5danD1qhMuiZr9L22fui1G6XNjGvtpJ3SMfMu63zv44OTw5jg9fW3vWDwY6KNHE1ijMuCHLPODINXsh-m-A4dtNJG_X5_HqGbs9Pr1fd8fXV-sVquc0WBjjmuicYVJRuGGQEJDSYlKZt2Q9qSS6Zxqct6vty0LfCWVjUrpJYMQNaEKU6O0JdH32Ha9LpRKVOQVgzB9DI8CC-NeP7iTCe2_l7Q9HeMzwaf9gbB3006jqI3UWlrpdN-ioIxXNWYwosgpqkIzuoEfn4EVSorBt0-pcEg5iLF5Y_Tm59Xv1YXaRRQiL9FirnIJP7w_z5P0n1z_1J0ZtvtTNAi9tLaRGOx2-2SXyFmN_IHOAmrOQ</recordid><startdate>19950201</startdate><enddate>19950201</enddate><creator>Wagner, JJ</creator><creator>Alger, BE</creator><general>Soc Neuroscience</general><general>Society for Neuroscience</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>7TK</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19950201</creationdate><title>GABAergic and developmental influences on homosynaptic LTD and depotentiation in rat hippocampus</title><author>Wagner, JJ ; Alger, BE</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c606t-183e1563b71730a0d13434dfb3f49a7e14e48d134bff09f65872aea700a837c93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>Aging - physiology</topic><topic>Animals</topic><topic>Electric Stimulation - methods</topic><topic>Electrophysiology</topic><topic>GABA-A Receptor Antagonists</topic><topic>GABA-B Receptor Antagonists</topic><topic>gamma-Aminobutyric Acid - physiology</topic><topic>Hippocampus - drug effects</topic><topic>Hippocampus - growth & development</topic><topic>Hippocampus - physiology</topic><topic>Long-Term Potentiation</topic><topic>Organophosphorus Compounds - pharmacology</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Receptors, GABA-A - physiology</topic><topic>Receptors, GABA-B - physiology</topic><topic>Synapses - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wagner, JJ</creatorcontrib><creatorcontrib>Alger, BE</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wagner, JJ</au><au>Alger, BE</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>GABAergic and developmental influences on homosynaptic LTD and depotentiation in rat hippocampus</atitle><jtitle>The Journal of neuroscience</jtitle><addtitle>J Neurosci</addtitle><date>1995-02-01</date><risdate>1995</risdate><volume>15</volume><issue>2</issue><spage>1577</spage><epage>1586</epage><pages>1577-1586</pages><issn>0270-6474</issn><eissn>1529-2401</eissn><abstract>Low-frequency (1 Hz) stimulation (LFS) was used to elicit long-term depression (LTD) or depotentiation of excitatory transmission of the Schaffer collateral pathway in the CA1 region of the rat hippocampus. Both LTD and depotentiation were found to be homosynaptic and NMDA receptor (NMDAR) dependent. As NMDAR activation can be modulated by the inhibitory GABAergic system, we tested the hypothesis that GABA plays a role in regulating these phenomena. The GABAB antagonist CGP 35348 significantly inhibited LTD, but not depotentiation, in slices from young animals (indicating that the GABAB-mediated contribution was altered following HFS). The ability to express LTD was found to be developmentally dependent, as young animals (16-22 d) consistently expressed LTD, whereas LTD was not expressed in naive slices taken from mature (5-10 weeks) animals. The GABAA antagonist bicuculline did not affect LTD in the young animals, but did enhance LTD expression in slices from mature animals. LFS was also effective in decreasing, or depotentiating, responses that had undergone long-term potentiation (LTP) by high-frequency stimulation (HFS). In contrast to LTD, depotentiation was consistently expressed in slices from both the young and mature groups. Moreover, following an HFS train, LTD (compared to initial baseline response) could be induced in mature slices previously unable to express LTD in the naive state. Thus, the role of GABA in modulating the effects of LFS varied with the prior synaptic activity in the slice as well as with the maturity of the animal. Our results suggest that the influence of both age and prior synaptic activity (i.e., HFS) on LTD induction can be explained by changes in GABAergic systems in young versus mature, and naive versus tetanized slices.</abstract><cop>United States</cop><pub>Soc Neuroscience</pub><pmid>7869119</pmid><doi>10.1523/jneurosci.15-02-01577.1995</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0270-6474 |
ispartof | The Journal of neuroscience, 1995-02, Vol.15 (2), p.1577-1586 |
issn | 0270-6474 1529-2401 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6577799 |
source | MEDLINE; EZB-FREE-00999 freely available EZB journals; PubMed Central |
subjects | Aging - physiology Animals Electric Stimulation - methods Electrophysiology GABA-A Receptor Antagonists GABA-B Receptor Antagonists gamma-Aminobutyric Acid - physiology Hippocampus - drug effects Hippocampus - growth & development Hippocampus - physiology Long-Term Potentiation Organophosphorus Compounds - pharmacology Rats Rats, Sprague-Dawley Receptors, GABA-A - physiology Receptors, GABA-B - physiology Synapses - physiology |
title | GABAergic and developmental influences on homosynaptic LTD and depotentiation in rat hippocampus |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-09T09%3A34%3A05IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=GABAergic%20and%20developmental%20influences%20on%20homosynaptic%20LTD%20and%20depotentiation%20in%20rat%20hippocampus&rft.jtitle=The%20Journal%20of%20neuroscience&rft.au=Wagner,%20JJ&rft.date=1995-02-01&rft.volume=15&rft.issue=2&rft.spage=1577&rft.epage=1586&rft.pages=1577-1586&rft.issn=0270-6474&rft.eissn=1529-2401&rft_id=info:doi/10.1523/jneurosci.15-02-01577.1995&rft_dat=%3Cproquest_pubme%3E77158160%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=16995978&rft_id=info:pmid/7869119&rfr_iscdi=true |