Purinergic P2X, P2Y and adenosine receptors differentially modulate hippocampal gamma oscillations

The present study was designed to investigate the role of extracellular ATP and its receptors on neuronal network activity. Gamma oscillations (30–50 Hz) were induced in the CA3 region of acute rat hippocampal slices by either acetylcholine (ACh) or kainic acid (KA). ATP reduced the power of KA-indu...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Neuropharmacology 2012-02, Vol.62 (2), p.914-924
Hauptverfasser: Schulz, Steffen B., Klaft, Zin-Juan, Rösler, Anton R., Heinemann, Uwe, Gerevich, Zoltan
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 924
container_issue 2
container_start_page 914
container_title Neuropharmacology
container_volume 62
creator Schulz, Steffen B.
Klaft, Zin-Juan
Rösler, Anton R.
Heinemann, Uwe
Gerevich, Zoltan
description The present study was designed to investigate the role of extracellular ATP and its receptors on neuronal network activity. Gamma oscillations (30–50 Hz) were induced in the CA3 region of acute rat hippocampal slices by either acetylcholine (ACh) or kainic acid (KA). ATP reduced the power of KA-induced gamma oscillations exclusively by activation of adenosine receptors after its degradation to adenosine. In contrast, ATP suppressed ACh-induced oscillations through both adenosine and ATP receptors. Activation of adenosine receptors accounts for about 55%, activation of P2 receptors for ∼45% of suppression. Monitoring the ATP degradation by ATP biosensors revealed that bath-applied ATP reaches ∼300 times lower concentrations within the slice. P2 receptors were also activated by endogenous ATP since inhibition of ATP-hydrolyzing enzymes had an inhibitory effect on ACh-induced gamma oscillations. More specific antagonists revealed that ionotropic P2X2 and/or P2X4 receptors reduced the power of ACh-induced gamma oscillations whereas metabotropic P2Y 1 receptor increased it. Intracellular recordings from CA3 pyramidal cells suggest that adenosine receptors reduce the spiking rate and the synchrony of action potentials during gamma oscillations whereas P2 receptors only modulate the firing rate of the cells. In conclusion, our results suggest that endogenously released ATP differentially modulates the power of ACh- or KA-induced gamma oscillations in the CA3 region of the hippocampus by interacting with P2X, P2Y and adenosine receptors. This article is part of a Special Issue entitled ‘Post-Traumatic Stress Disorder’. ► Activation of adenosine receptors inhibits hippocampal gamma oscillation induced by KA or ACh. ► Only the ACh-induced oscillation is influenced by P2 receptors and by endogenous ATP. ► P2X2 and/or P2X4 receptors reduce the oscillation power, P2Y 1 receptors enhance it. ► Adenosine receptors modulate spiking rate and synchrony of APs, P2Rs only the former. ► ∼300 times lower concentrations of bath-applied ATP was recorded within the slice.
doi_str_mv 10.1016/j.neuropharm.2011.09.024
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_917163188</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0028390811004485</els_id><sourcerecordid>1034820860</sourcerecordid><originalsourceid>FETCH-LOGICAL-c406t-265eee6026f70b5c55b98d3af76cd6a20d7c94bf27f5e374d32cd518a9c1ccc23</originalsourceid><addsrcrecordid>eNqFkc1O3TAQha0KVG6BV6i8g0UTxk5iO0uK-ichwaKVYGU59gR8lcTBTpB4e4wupbuymVnMd2ZG5xBCGZQMmDjblhOuMcz3Jo4lB8ZKaEvg9QeyYUpWhQRR75ENAFdF1YI6IJ9S2gJArZj6SA44B2A1lxvSXa_RTxjvvKXX_OZLLrfUTI4ah1NIeUQjWpyXEBN1vu8x4rR4MwxPdAxuHcyC9N7Pc7BmnM1A78w4GhqS9UOe-TClI7LfmyHh8Ws_JH--f_t98bO4vPrx6-L8srA1iKXgokFEAVz0ErrGNk3XKleZXgrrhOHgpG3rrueyb7CStau4dQ1TprXMWsurQ3Ky2zvH8LBiWvTok8X8xoRhTbplkomKKZXJ0_-SDKpacVACMqp2qI0hpYi9nqMfTXzKkH7JQm_1vyz0SxYaWp2zyNLPr1fWbkT3Jvxrfga-7gDMrjx6jDq7hpNF57Pni3bBv3_lGYzBoWE</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1034820860</pqid></control><display><type>article</type><title>Purinergic P2X, P2Y and adenosine receptors differentially modulate hippocampal gamma oscillations</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>Schulz, Steffen B. ; Klaft, Zin-Juan ; Rösler, Anton R. ; Heinemann, Uwe ; Gerevich, Zoltan</creator><creatorcontrib>Schulz, Steffen B. ; Klaft, Zin-Juan ; Rösler, Anton R. ; Heinemann, Uwe ; Gerevich, Zoltan</creatorcontrib><description>The present study was designed to investigate the role of extracellular ATP and its receptors on neuronal network activity. Gamma oscillations (30–50 Hz) were induced in the CA3 region of acute rat hippocampal slices by either acetylcholine (ACh) or kainic acid (KA). ATP reduced the power of KA-induced gamma oscillations exclusively by activation of adenosine receptors after its degradation to adenosine. In contrast, ATP suppressed ACh-induced oscillations through both adenosine and ATP receptors. Activation of adenosine receptors accounts for about 55%, activation of P2 receptors for ∼45% of suppression. Monitoring the ATP degradation by ATP biosensors revealed that bath-applied ATP reaches ∼300 times lower concentrations within the slice. P2 receptors were also activated by endogenous ATP since inhibition of ATP-hydrolyzing enzymes had an inhibitory effect on ACh-induced gamma oscillations. More specific antagonists revealed that ionotropic P2X2 and/or P2X4 receptors reduced the power of ACh-induced gamma oscillations whereas metabotropic P2Y 1 receptor increased it. Intracellular recordings from CA3 pyramidal cells suggest that adenosine receptors reduce the spiking rate and the synchrony of action potentials during gamma oscillations whereas P2 receptors only modulate the firing rate of the cells. In conclusion, our results suggest that endogenously released ATP differentially modulates the power of ACh- or KA-induced gamma oscillations in the CA3 region of the hippocampus by interacting with P2X, P2Y and adenosine receptors. This article is part of a Special Issue entitled ‘Post-Traumatic Stress Disorder’. ► Activation of adenosine receptors inhibits hippocampal gamma oscillation induced by KA or ACh. ► Only the ACh-induced oscillation is influenced by P2 receptors and by endogenous ATP. ► P2X2 and/or P2X4 receptors reduce the oscillation power, P2Y 1 receptors enhance it. ► Adenosine receptors modulate spiking rate and synchrony of APs, P2Rs only the former. ► ∼300 times lower concentrations of bath-applied ATP was recorded within the slice.</description><identifier>ISSN: 0028-3908</identifier><identifier>EISSN: 1873-7064</identifier><identifier>DOI: 10.1016/j.neuropharm.2011.09.024</identifier><identifier>PMID: 22001427</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Acetylcholine ; Acetylcholine - pharmacology ; Action potential ; Adenosine receptors ; Adenosine Triphosphate - pharmacology ; Animals ; ATP ; Biological Clocks - drug effects ; Biological Clocks - physiology ; Biosensors ; Brain slice preparation ; Electrophysiological recording ; Enzymes ; Female ; Firing pattern ; Gamma oscillations ; Hippocampus ; Hippocampus - drug effects ; Hippocampus - metabolism ; Kainic acid ; Kainic Acid - pharmacology ; Male ; Metabotropic receptors ; Neural networks ; Neurons - drug effects ; Neurons - metabolism ; Oscillations ; P2X receptors ; P2Y receptors ; Purine P2 receptors ; Purine P2X receptors ; Purine P2Y receptors ; Pyramidal cells ; Rats ; Rats, Wistar ; Receptors, Purinergic P1 - metabolism ; Receptors, Purinergic P2X - metabolism ; Receptors, Purinergic P2Y - metabolism ; Stress</subject><ispartof>Neuropharmacology, 2012-02, Vol.62 (2), p.914-924</ispartof><rights>2011 Elsevier Ltd</rights><rights>Copyright © 2011 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c406t-265eee6026f70b5c55b98d3af76cd6a20d7c94bf27f5e374d32cd518a9c1ccc23</citedby><cites>FETCH-LOGICAL-c406t-265eee6026f70b5c55b98d3af76cd6a20d7c94bf27f5e374d32cd518a9c1ccc23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0028390811004485$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22001427$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Schulz, Steffen B.</creatorcontrib><creatorcontrib>Klaft, Zin-Juan</creatorcontrib><creatorcontrib>Rösler, Anton R.</creatorcontrib><creatorcontrib>Heinemann, Uwe</creatorcontrib><creatorcontrib>Gerevich, Zoltan</creatorcontrib><title>Purinergic P2X, P2Y and adenosine receptors differentially modulate hippocampal gamma oscillations</title><title>Neuropharmacology</title><addtitle>Neuropharmacology</addtitle><description>The present study was designed to investigate the role of extracellular ATP and its receptors on neuronal network activity. Gamma oscillations (30–50 Hz) were induced in the CA3 region of acute rat hippocampal slices by either acetylcholine (ACh) or kainic acid (KA). ATP reduced the power of KA-induced gamma oscillations exclusively by activation of adenosine receptors after its degradation to adenosine. In contrast, ATP suppressed ACh-induced oscillations through both adenosine and ATP receptors. Activation of adenosine receptors accounts for about 55%, activation of P2 receptors for ∼45% of suppression. Monitoring the ATP degradation by ATP biosensors revealed that bath-applied ATP reaches ∼300 times lower concentrations within the slice. P2 receptors were also activated by endogenous ATP since inhibition of ATP-hydrolyzing enzymes had an inhibitory effect on ACh-induced gamma oscillations. More specific antagonists revealed that ionotropic P2X2 and/or P2X4 receptors reduced the power of ACh-induced gamma oscillations whereas metabotropic P2Y 1 receptor increased it. Intracellular recordings from CA3 pyramidal cells suggest that adenosine receptors reduce the spiking rate and the synchrony of action potentials during gamma oscillations whereas P2 receptors only modulate the firing rate of the cells. In conclusion, our results suggest that endogenously released ATP differentially modulates the power of ACh- or KA-induced gamma oscillations in the CA3 region of the hippocampus by interacting with P2X, P2Y and adenosine receptors. This article is part of a Special Issue entitled ‘Post-Traumatic Stress Disorder’. ► Activation of adenosine receptors inhibits hippocampal gamma oscillation induced by KA or ACh. ► Only the ACh-induced oscillation is influenced by P2 receptors and by endogenous ATP. ► P2X2 and/or P2X4 receptors reduce the oscillation power, P2Y 1 receptors enhance it. ► Adenosine receptors modulate spiking rate and synchrony of APs, P2Rs only the former. ► ∼300 times lower concentrations of bath-applied ATP was recorded within the slice.</description><subject>Acetylcholine</subject><subject>Acetylcholine - pharmacology</subject><subject>Action potential</subject><subject>Adenosine receptors</subject><subject>Adenosine Triphosphate - pharmacology</subject><subject>Animals</subject><subject>ATP</subject><subject>Biological Clocks - drug effects</subject><subject>Biological Clocks - physiology</subject><subject>Biosensors</subject><subject>Brain slice preparation</subject><subject>Electrophysiological recording</subject><subject>Enzymes</subject><subject>Female</subject><subject>Firing pattern</subject><subject>Gamma oscillations</subject><subject>Hippocampus</subject><subject>Hippocampus - drug effects</subject><subject>Hippocampus - metabolism</subject><subject>Kainic acid</subject><subject>Kainic Acid - pharmacology</subject><subject>Male</subject><subject>Metabotropic receptors</subject><subject>Neural networks</subject><subject>Neurons - drug effects</subject><subject>Neurons - metabolism</subject><subject>Oscillations</subject><subject>P2X receptors</subject><subject>P2Y receptors</subject><subject>Purine P2 receptors</subject><subject>Purine P2X receptors</subject><subject>Purine P2Y receptors</subject><subject>Pyramidal cells</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Receptors, Purinergic P1 - metabolism</subject><subject>Receptors, Purinergic P2X - metabolism</subject><subject>Receptors, Purinergic P2Y - metabolism</subject><subject>Stress</subject><issn>0028-3908</issn><issn>1873-7064</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc1O3TAQha0KVG6BV6i8g0UTxk5iO0uK-ichwaKVYGU59gR8lcTBTpB4e4wupbuymVnMd2ZG5xBCGZQMmDjblhOuMcz3Jo4lB8ZKaEvg9QeyYUpWhQRR75ENAFdF1YI6IJ9S2gJArZj6SA44B2A1lxvSXa_RTxjvvKXX_OZLLrfUTI4ah1NIeUQjWpyXEBN1vu8x4rR4MwxPdAxuHcyC9N7Pc7BmnM1A78w4GhqS9UOe-TClI7LfmyHh8Ws_JH--f_t98bO4vPrx6-L8srA1iKXgokFEAVz0ErrGNk3XKleZXgrrhOHgpG3rrueyb7CStau4dQ1TprXMWsurQ3Ky2zvH8LBiWvTok8X8xoRhTbplkomKKZXJ0_-SDKpacVACMqp2qI0hpYi9nqMfTXzKkH7JQm_1vyz0SxYaWp2zyNLPr1fWbkT3Jvxrfga-7gDMrjx6jDq7hpNF57Pni3bBv3_lGYzBoWE</recordid><startdate>20120201</startdate><enddate>20120201</enddate><creator>Schulz, Steffen B.</creator><creator>Klaft, Zin-Juan</creator><creator>Rösler, Anton R.</creator><creator>Heinemann, Uwe</creator><creator>Gerevich, Zoltan</creator><general>Elsevier Ltd</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></search><sort><creationdate>20120201</creationdate><title>Purinergic P2X, P2Y and adenosine receptors differentially modulate hippocampal gamma oscillations</title><author>Schulz, Steffen B. ; Klaft, Zin-Juan ; Rösler, Anton R. ; Heinemann, Uwe ; Gerevich, Zoltan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c406t-265eee6026f70b5c55b98d3af76cd6a20d7c94bf27f5e374d32cd518a9c1ccc23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Acetylcholine</topic><topic>Acetylcholine - pharmacology</topic><topic>Action potential</topic><topic>Adenosine receptors</topic><topic>Adenosine Triphosphate - pharmacology</topic><topic>Animals</topic><topic>ATP</topic><topic>Biological Clocks - drug effects</topic><topic>Biological Clocks - physiology</topic><topic>Biosensors</topic><topic>Brain slice preparation</topic><topic>Electrophysiological recording</topic><topic>Enzymes</topic><topic>Female</topic><topic>Firing pattern</topic><topic>Gamma oscillations</topic><topic>Hippocampus</topic><topic>Hippocampus - drug effects</topic><topic>Hippocampus - metabolism</topic><topic>Kainic acid</topic><topic>Kainic Acid - pharmacology</topic><topic>Male</topic><topic>Metabotropic receptors</topic><topic>Neural networks</topic><topic>Neurons - drug effects</topic><topic>Neurons - metabolism</topic><topic>Oscillations</topic><topic>P2X receptors</topic><topic>P2Y receptors</topic><topic>Purine P2 receptors</topic><topic>Purine P2X receptors</topic><topic>Purine P2Y receptors</topic><topic>Pyramidal cells</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Receptors, Purinergic P1 - metabolism</topic><topic>Receptors, Purinergic P2X - metabolism</topic><topic>Receptors, Purinergic P2Y - metabolism</topic><topic>Stress</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Schulz, Steffen B.</creatorcontrib><creatorcontrib>Klaft, Zin-Juan</creatorcontrib><creatorcontrib>Rösler, Anton R.</creatorcontrib><creatorcontrib>Heinemann, Uwe</creatorcontrib><creatorcontrib>Gerevich, Zoltan</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><jtitle>Neuropharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Schulz, Steffen B.</au><au>Klaft, Zin-Juan</au><au>Rösler, Anton R.</au><au>Heinemann, Uwe</au><au>Gerevich, Zoltan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Purinergic P2X, P2Y and adenosine receptors differentially modulate hippocampal gamma oscillations</atitle><jtitle>Neuropharmacology</jtitle><addtitle>Neuropharmacology</addtitle><date>2012-02-01</date><risdate>2012</risdate><volume>62</volume><issue>2</issue><spage>914</spage><epage>924</epage><pages>914-924</pages><issn>0028-3908</issn><eissn>1873-7064</eissn><abstract>The present study was designed to investigate the role of extracellular ATP and its receptors on neuronal network activity. Gamma oscillations (30–50 Hz) were induced in the CA3 region of acute rat hippocampal slices by either acetylcholine (ACh) or kainic acid (KA). ATP reduced the power of KA-induced gamma oscillations exclusively by activation of adenosine receptors after its degradation to adenosine. In contrast, ATP suppressed ACh-induced oscillations through both adenosine and ATP receptors. Activation of adenosine receptors accounts for about 55%, activation of P2 receptors for ∼45% of suppression. Monitoring the ATP degradation by ATP biosensors revealed that bath-applied ATP reaches ∼300 times lower concentrations within the slice. P2 receptors were also activated by endogenous ATP since inhibition of ATP-hydrolyzing enzymes had an inhibitory effect on ACh-induced gamma oscillations. More specific antagonists revealed that ionotropic P2X2 and/or P2X4 receptors reduced the power of ACh-induced gamma oscillations whereas metabotropic P2Y 1 receptor increased it. Intracellular recordings from CA3 pyramidal cells suggest that adenosine receptors reduce the spiking rate and the synchrony of action potentials during gamma oscillations whereas P2 receptors only modulate the firing rate of the cells. In conclusion, our results suggest that endogenously released ATP differentially modulates the power of ACh- or KA-induced gamma oscillations in the CA3 region of the hippocampus by interacting with P2X, P2Y and adenosine receptors. This article is part of a Special Issue entitled ‘Post-Traumatic Stress Disorder’. ► Activation of adenosine receptors inhibits hippocampal gamma oscillation induced by KA or ACh. ► Only the ACh-induced oscillation is influenced by P2 receptors and by endogenous ATP. ► P2X2 and/or P2X4 receptors reduce the oscillation power, P2Y 1 receptors enhance it. ► Adenosine receptors modulate spiking rate and synchrony of APs, P2Rs only the former. ► ∼300 times lower concentrations of bath-applied ATP was recorded within the slice.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>22001427</pmid><doi>10.1016/j.neuropharm.2011.09.024</doi><tpages>11</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0028-3908
ispartof Neuropharmacology, 2012-02, Vol.62 (2), p.914-924
issn 0028-3908
1873-7064
language eng
recordid cdi_proquest_miscellaneous_917163188
source MEDLINE; Elsevier ScienceDirect Journals
subjects Acetylcholine
Acetylcholine - pharmacology
Action potential
Adenosine receptors
Adenosine Triphosphate - pharmacology
Animals
ATP
Biological Clocks - drug effects
Biological Clocks - physiology
Biosensors
Brain slice preparation
Electrophysiological recording
Enzymes
Female
Firing pattern
Gamma oscillations
Hippocampus
Hippocampus - drug effects
Hippocampus - metabolism
Kainic acid
Kainic Acid - pharmacology
Male
Metabotropic receptors
Neural networks
Neurons - drug effects
Neurons - metabolism
Oscillations
P2X receptors
P2Y receptors
Purine P2 receptors
Purine P2X receptors
Purine P2Y receptors
Pyramidal cells
Rats
Rats, Wistar
Receptors, Purinergic P1 - metabolism
Receptors, Purinergic P2X - metabolism
Receptors, Purinergic P2Y - metabolism
Stress
title Purinergic P2X, P2Y and adenosine receptors differentially modulate hippocampal gamma oscillations
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-28T13%3A39%3A39IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Purinergic%20P2X,%20P2Y%20and%20adenosine%20receptors%20differentially%20modulate%20hippocampal%20gamma%20oscillations&rft.jtitle=Neuropharmacology&rft.au=Schulz,%20Steffen%20B.&rft.date=2012-02-01&rft.volume=62&rft.issue=2&rft.spage=914&rft.epage=924&rft.pages=914-924&rft.issn=0028-3908&rft.eissn=1873-7064&rft_id=info:doi/10.1016/j.neuropharm.2011.09.024&rft_dat=%3Cproquest_cross%3E1034820860%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1034820860&rft_id=info:pmid/22001427&rft_els_id=S0028390811004485&rfr_iscdi=true