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...
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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 |
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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> |
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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 |
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