Cannabinoid CB1 Receptor-Dependent Long-Term Depression in Autaptic Excitatory Neurons
1 Department of Anesthesiology, University of Washington, Seattle, Washington; and 2 Department of Psychological and Brain Sciences, Gill Center for Biomolecular Science, Indiana University, Bloomington, Indiana Submitted 25 March 2009; accepted in final form 29 May 2009 Long-term depression (LTD) o...
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creator | Kellogg, Ryan Mackie, Ken Straiker, Alex |
description | 1 Department of Anesthesiology, University of Washington, Seattle, Washington; and 2 Department of Psychological and Brain Sciences, Gill Center for Biomolecular Science, Indiana University, Bloomington, Indiana
Submitted 25 March 2009;
accepted in final form 29 May 2009
Long-term depression (LTD) of synaptic signaling—lasting from tens of minutes to hours or longer—is a widespread form of synaptic plasticity in the brain. Neurons express diverse forms of LTD, including autaptic LTD (autLTD) observed in cultured hippocampal neurons, the mechanism of which remains unknown. We have recently reported that autaptic neurons express both endocannabinoid-mediated depolarization-induced suppression of excitation (DSE) and metabotropic suppression of excitation (MSE). We now report that activating cannabinoid CB 1 receptors is necessary for the induction of autLTD. Most surprisingly, CB 1 does not induce autLTD via the G i/o proteins typically activated by this receptor nor with G s . Rather, the requirements of presynaptic phospholipase C and filled calcium stores suggest G q . In autLTD, a 3- to 4-min activation of the receptor by the endocannabinoid 2-arachidonoyl glycerol leads to prolonged inhibition while leaving short-term inhibition (e.g., DSE) intact. autLTD requires activation of both metabo- and ionotropic glutamate receptors. autLTD also requires MEK/ERK activation. Under certain conditions, one or more DSE stimuli will elicit autLTD. It is becoming evident that cannabinoids mediate multiple forms of plasticity at a single synapse, stretching temporally from tens of seconds (DSE/MSE) to tens of minutes (autLTD) to hours (CB 1 desensitization). Our findings imply a remarkable flexibility for the cannabinoid signaling system whereby discrete mechanisms of CB 1 activation within a single neuron yield temporally and mechanistically distinct forms of plasticity.
Address for reprint requests and other correspondence: A. Straiker, Dept. of Psychological and Brain Sciences, Gill Center for Biomolecular Science, Indiana University, Bloomington, IN 47405 (E-mail: straiker{at}indiana.edu ) |
doi_str_mv | 10.1152/jn.00266.2009 |
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Submitted 25 March 2009;
accepted in final form 29 May 2009
Long-term depression (LTD) of synaptic signaling—lasting from tens of minutes to hours or longer—is a widespread form of synaptic plasticity in the brain. Neurons express diverse forms of LTD, including autaptic LTD (autLTD) observed in cultured hippocampal neurons, the mechanism of which remains unknown. We have recently reported that autaptic neurons express both endocannabinoid-mediated depolarization-induced suppression of excitation (DSE) and metabotropic suppression of excitation (MSE). We now report that activating cannabinoid CB 1 receptors is necessary for the induction of autLTD. Most surprisingly, CB 1 does not induce autLTD via the G i/o proteins typically activated by this receptor nor with G s . Rather, the requirements of presynaptic phospholipase C and filled calcium stores suggest G q . In autLTD, a 3- to 4-min activation of the receptor by the endocannabinoid 2-arachidonoyl glycerol leads to prolonged inhibition while leaving short-term inhibition (e.g., DSE) intact. autLTD requires activation of both metabo- and ionotropic glutamate receptors. autLTD also requires MEK/ERK activation. Under certain conditions, one or more DSE stimuli will elicit autLTD. It is becoming evident that cannabinoids mediate multiple forms of plasticity at a single synapse, stretching temporally from tens of seconds (DSE/MSE) to tens of minutes (autLTD) to hours (CB 1 desensitization). Our findings imply a remarkable flexibility for the cannabinoid signaling system whereby discrete mechanisms of CB 1 activation within a single neuron yield temporally and mechanistically distinct forms of plasticity.
Address for reprint requests and other correspondence: A. Straiker, Dept. of Psychological and Brain Sciences, Gill Center for Biomolecular Science, Indiana University, Bloomington, IN 47405 (E-mail: straiker{at}indiana.edu )</description><identifier>ISSN: 0022-3077</identifier><identifier>EISSN: 1522-1598</identifier><identifier>DOI: 10.1152/jn.00266.2009</identifier><identifier>PMID: 19494194</identifier><language>eng</language><publisher>United States: Am Phys Soc</publisher><subject>Analysis of Variance ; Animals ; Cells, Cultured ; Electric Stimulation ; Excitatory Postsynaptic Potentials - physiology ; Extracellular Signal-Regulated MAP Kinases - metabolism ; Hippocampus - physiology ; Long-Term Synaptic Depression - physiology ; MAP Kinase Kinase Kinases - metabolism ; Mice ; Mice, Knockout ; Neurons - physiology ; Patch-Clamp Techniques ; Receptor, Cannabinoid, CB1 - antagonists & inhibitors ; Receptor, Cannabinoid, CB1 - genetics ; Receptor, Cannabinoid, CB1 - metabolism ; Receptors, Glutamate - metabolism ; Synapses - physiology ; Time Factors</subject><ispartof>Journal of neurophysiology, 2009-08, Vol.102 (2), p.1160-1171</ispartof><rights>Copyright © 2009, American Physiological Society 2009</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19494194$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kellogg, Ryan</creatorcontrib><creatorcontrib>Mackie, Ken</creatorcontrib><creatorcontrib>Straiker, Alex</creatorcontrib><title>Cannabinoid CB1 Receptor-Dependent Long-Term Depression in Autaptic Excitatory Neurons</title><title>Journal of neurophysiology</title><addtitle>J Neurophysiol</addtitle><description>1 Department of Anesthesiology, University of Washington, Seattle, Washington; and 2 Department of Psychological and Brain Sciences, Gill Center for Biomolecular Science, Indiana University, Bloomington, Indiana
Submitted 25 March 2009;
accepted in final form 29 May 2009
Long-term depression (LTD) of synaptic signaling—lasting from tens of minutes to hours or longer—is a widespread form of synaptic plasticity in the brain. Neurons express diverse forms of LTD, including autaptic LTD (autLTD) observed in cultured hippocampal neurons, the mechanism of which remains unknown. We have recently reported that autaptic neurons express both endocannabinoid-mediated depolarization-induced suppression of excitation (DSE) and metabotropic suppression of excitation (MSE). We now report that activating cannabinoid CB 1 receptors is necessary for the induction of autLTD. Most surprisingly, CB 1 does not induce autLTD via the G i/o proteins typically activated by this receptor nor with G s . Rather, the requirements of presynaptic phospholipase C and filled calcium stores suggest G q . In autLTD, a 3- to 4-min activation of the receptor by the endocannabinoid 2-arachidonoyl glycerol leads to prolonged inhibition while leaving short-term inhibition (e.g., DSE) intact. autLTD requires activation of both metabo- and ionotropic glutamate receptors. autLTD also requires MEK/ERK activation. Under certain conditions, one or more DSE stimuli will elicit autLTD. It is becoming evident that cannabinoids mediate multiple forms of plasticity at a single synapse, stretching temporally from tens of seconds (DSE/MSE) to tens of minutes (autLTD) to hours (CB 1 desensitization). Our findings imply a remarkable flexibility for the cannabinoid signaling system whereby discrete mechanisms of CB 1 activation within a single neuron yield temporally and mechanistically distinct forms of plasticity.
Address for reprint requests and other correspondence: A. Straiker, Dept. of Psychological and Brain Sciences, Gill Center for Biomolecular Science, Indiana University, Bloomington, IN 47405 (E-mail: straiker{at}indiana.edu )</description><subject>Analysis of Variance</subject><subject>Animals</subject><subject>Cells, Cultured</subject><subject>Electric Stimulation</subject><subject>Excitatory Postsynaptic Potentials - physiology</subject><subject>Extracellular Signal-Regulated MAP Kinases - metabolism</subject><subject>Hippocampus - physiology</subject><subject>Long-Term Synaptic Depression - physiology</subject><subject>MAP Kinase Kinase Kinases - metabolism</subject><subject>Mice</subject><subject>Mice, Knockout</subject><subject>Neurons - physiology</subject><subject>Patch-Clamp Techniques</subject><subject>Receptor, Cannabinoid, CB1 - antagonists & inhibitors</subject><subject>Receptor, Cannabinoid, CB1 - genetics</subject><subject>Receptor, Cannabinoid, CB1 - metabolism</subject><subject>Receptors, Glutamate - metabolism</subject><subject>Synapses - physiology</subject><subject>Time Factors</subject><issn>0022-3077</issn><issn>1522-1598</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVUMtOwzAQtBAIyuPIFeWEuKSsXwm5IEF5ShVICLharmM3rlI72AnQv8eIh-CyK83MzuwuQvsYxhhzcrxwYwBSFGMCUK2hUcJIjnl1so5GiSA5hbLcQtsxLgCg5EA20RauWMVSGaHniXROzqzzts4m5zh70Ep3vQ_5he60q7Xrs6l38_xRh2WWsKBjtN5l1mVnQy-73qrs8l3ZXqahVXanh-Bd3EUbRrZR7333HfR0dfk4ucmn99e3k7Np3jAgfc6oMabSdckxlpiWwCpTc8ZNWSmjiNKcQkE4A1UYaaihVFVQm3QRmQEYoDvo9Mu3G2ZLXau0bpCt6IJdyrASXlrxn3G2EXP_KkhJGGUsGRx-GwT_MujYi6WNSretdNoPURQlZwWFz6SDv0m_ET-vTIKjL0Fj582bDVp0zSq9qvXzlVg4gYEIIjAugH4AEvmE0g</recordid><startdate>20090801</startdate><enddate>20090801</enddate><creator>Kellogg, Ryan</creator><creator>Mackie, Ken</creator><creator>Straiker, Alex</creator><general>Am Phys Soc</general><general>American Physiological Society</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20090801</creationdate><title>Cannabinoid CB1 Receptor-Dependent Long-Term Depression in Autaptic Excitatory Neurons</title><author>Kellogg, Ryan ; Mackie, Ken ; Straiker, Alex</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-h402t-43fff9ed7511a137049fd545f79cfc2ce53062540c6faf3f33c90df0772b00f03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Analysis of Variance</topic><topic>Animals</topic><topic>Cells, Cultured</topic><topic>Electric Stimulation</topic><topic>Excitatory Postsynaptic Potentials - physiology</topic><topic>Extracellular Signal-Regulated MAP Kinases - metabolism</topic><topic>Hippocampus - physiology</topic><topic>Long-Term Synaptic Depression - physiology</topic><topic>MAP Kinase Kinase Kinases - metabolism</topic><topic>Mice</topic><topic>Mice, Knockout</topic><topic>Neurons - physiology</topic><topic>Patch-Clamp Techniques</topic><topic>Receptor, Cannabinoid, CB1 - antagonists & inhibitors</topic><topic>Receptor, Cannabinoid, CB1 - genetics</topic><topic>Receptor, Cannabinoid, CB1 - metabolism</topic><topic>Receptors, Glutamate - metabolism</topic><topic>Synapses - physiology</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kellogg, Ryan</creatorcontrib><creatorcontrib>Mackie, Ken</creatorcontrib><creatorcontrib>Straiker, Alex</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of neurophysiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kellogg, Ryan</au><au>Mackie, Ken</au><au>Straiker, Alex</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cannabinoid CB1 Receptor-Dependent Long-Term Depression in Autaptic Excitatory Neurons</atitle><jtitle>Journal of neurophysiology</jtitle><addtitle>J Neurophysiol</addtitle><date>2009-08-01</date><risdate>2009</risdate><volume>102</volume><issue>2</issue><spage>1160</spage><epage>1171</epage><pages>1160-1171</pages><issn>0022-3077</issn><eissn>1522-1598</eissn><abstract>1 Department of Anesthesiology, University of Washington, Seattle, Washington; and 2 Department of Psychological and Brain Sciences, Gill Center for Biomolecular Science, Indiana University, Bloomington, Indiana
Submitted 25 March 2009;
accepted in final form 29 May 2009
Long-term depression (LTD) of synaptic signaling—lasting from tens of minutes to hours or longer—is a widespread form of synaptic plasticity in the brain. Neurons express diverse forms of LTD, including autaptic LTD (autLTD) observed in cultured hippocampal neurons, the mechanism of which remains unknown. We have recently reported that autaptic neurons express both endocannabinoid-mediated depolarization-induced suppression of excitation (DSE) and metabotropic suppression of excitation (MSE). We now report that activating cannabinoid CB 1 receptors is necessary for the induction of autLTD. Most surprisingly, CB 1 does not induce autLTD via the G i/o proteins typically activated by this receptor nor with G s . Rather, the requirements of presynaptic phospholipase C and filled calcium stores suggest G q . In autLTD, a 3- to 4-min activation of the receptor by the endocannabinoid 2-arachidonoyl glycerol leads to prolonged inhibition while leaving short-term inhibition (e.g., DSE) intact. autLTD requires activation of both metabo- and ionotropic glutamate receptors. autLTD also requires MEK/ERK activation. Under certain conditions, one or more DSE stimuli will elicit autLTD. It is becoming evident that cannabinoids mediate multiple forms of plasticity at a single synapse, stretching temporally from tens of seconds (DSE/MSE) to tens of minutes (autLTD) to hours (CB 1 desensitization). Our findings imply a remarkable flexibility for the cannabinoid signaling system whereby discrete mechanisms of CB 1 activation within a single neuron yield temporally and mechanistically distinct forms of plasticity.
Address for reprint requests and other correspondence: A. Straiker, Dept. of Psychological and Brain Sciences, Gill Center for Biomolecular Science, Indiana University, Bloomington, IN 47405 (E-mail: straiker{at}indiana.edu )</abstract><cop>United States</cop><pub>Am Phys Soc</pub><pmid>19494194</pmid><doi>10.1152/jn.00266.2009</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Analysis of Variance Animals Cells, Cultured Electric Stimulation Excitatory Postsynaptic Potentials - physiology Extracellular Signal-Regulated MAP Kinases - metabolism Hippocampus - physiology Long-Term Synaptic Depression - physiology MAP Kinase Kinase Kinases - metabolism Mice Mice, Knockout Neurons - physiology Patch-Clamp Techniques Receptor, Cannabinoid, CB1 - antagonists & inhibitors Receptor, Cannabinoid, CB1 - genetics Receptor, Cannabinoid, CB1 - metabolism Receptors, Glutamate - metabolism Synapses - physiology Time Factors |
title | Cannabinoid CB1 Receptor-Dependent Long-Term Depression in Autaptic Excitatory Neurons |
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