Influence of Cannabinoids on Electrically Evoked Dopamine Release and Cyclic AMP Generation in the Rat Striatum

: Using the endogenous cannabinoid receptor agonist anandamide, the synthetic agonist CP 55940 {[1α,2β(R)5α]‐(−)‐5‐(1,1‐dimethylheptyl)‐2‐[5‐hydroxy‐2‐(3‐hydroxypropyl)cyclohexyl]phenol}, and the specific antagonist SR 141716 [N‐(piperidin‐1‐yl)‐5‐(4‐chlorophenyl)‐1‐(2,4‐dichlorophenyl)‐4‐methyl‐1H‐...

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Veröffentlicht in:Journal of neurochemistry 1997-09, Vol.69 (3), p.1131-1137
Hauptverfasser: Cadogan, Anna‐Karina, Alexander, Stephen P. H., Boyd, E. Andrew, Kendall, David A.
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container_issue 3
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container_title Journal of neurochemistry
container_volume 69
creator Cadogan, Anna‐Karina
Alexander, Stephen P. H.
Boyd, E. Andrew
Kendall, David A.
description : Using the endogenous cannabinoid receptor agonist anandamide, the synthetic agonist CP 55940 {[1α,2β(R)5α]‐(−)‐5‐(1,1‐dimethylheptyl)‐2‐[5‐hydroxy‐2‐(3‐hydroxypropyl)cyclohexyl]phenol}, and the specific antagonist SR 141716 [N‐(piperidin‐1‐yl)‐5‐(4‐chlorophenyl)‐1‐(2,4‐dichlorophenyl)‐4‐methyl‐1H‐pyrazole‐3‐carboxamide hydrochloride], second messenger activation of the central cannabinoid receptor (CB1) was examined in rat striatal and cortical slices. The effects of these cannabinoid ligands on electrically evoked dopamine (DA) release from [3H]dopamine‐prelabelled striatal slices were also investigated. CP 55940 (1 µM) and anandamide (10 µM) caused significant reductions in forskolin‐stimulated cyclic AMP accumulation in rat striatal slices, which were reversed in the presence of SR 141716 (1 µM). CP 55940 (1 µM) had no effect on either KCl‐ or neurotransmitter‐stimulated 3H‐inositol phosphate accumulation in rat cortical slices. CP 55940 and anandamide caused significant reductions in the release of dopamine after electrical stimulation of [3H]dopamine‐prelabelled striatal slices, which were antagonised by SR 141716. SR 141716 alone had no effect on electrically evoked dopamine release from rat striatal slices. These data indicate that the CB1 receptors in rat striatum are negatively linked to adenylyl cyclase and dopamine release. That the CB1 receptor may influence dopamine release in the striatum suggests that cannabinoids play a modulatory role in dopaminergic neuronal pathways.
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CP 55940 (1 µM) had no effect on either KCl‐ or neurotransmitter‐stimulated 3H‐inositol phosphate accumulation in rat cortical slices. CP 55940 and anandamide caused significant reductions in the release of dopamine after electrical stimulation of [3H]dopamine‐prelabelled striatal slices, which were antagonised by SR 141716. SR 141716 alone had no effect on electrically evoked dopamine release from rat striatal slices. These data indicate that the CB1 receptors in rat striatum are negatively linked to adenylyl cyclase and dopamine release. 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H.</creatorcontrib><creatorcontrib>Boyd, E. Andrew</creatorcontrib><creatorcontrib>Kendall, David A.</creatorcontrib><title>Influence of Cannabinoids on Electrically Evoked Dopamine Release and Cyclic AMP Generation in the Rat Striatum</title><title>Journal of neurochemistry</title><addtitle>J Neurochem</addtitle><description>: Using the endogenous cannabinoid receptor agonist anandamide, the synthetic agonist CP 55940 {[1α,2β(R)5α]‐(−)‐5‐(1,1‐dimethylheptyl)‐2‐[5‐hydroxy‐2‐(3‐hydroxypropyl)cyclohexyl]phenol}, and the specific antagonist SR 141716 [N‐(piperidin‐1‐yl)‐5‐(4‐chlorophenyl)‐1‐(2,4‐dichlorophenyl)‐4‐methyl‐1H‐pyrazole‐3‐carboxamide hydrochloride], second messenger activation of the central cannabinoid receptor (CB1) was examined in rat striatal and cortical slices. The effects of these cannabinoid ligands on electrically evoked dopamine (DA) release from [3H]dopamine‐prelabelled striatal slices were also investigated. CP 55940 (1 µM) and anandamide (10 µM) caused significant reductions in forskolin‐stimulated cyclic AMP accumulation in rat striatal slices, which were reversed in the presence of SR 141716 (1 µM). CP 55940 (1 µM) had no effect on either KCl‐ or neurotransmitter‐stimulated 3H‐inositol phosphate accumulation in rat cortical slices. CP 55940 and anandamide caused significant reductions in the release of dopamine after electrical stimulation of [3H]dopamine‐prelabelled striatal slices, which were antagonised by SR 141716. SR 141716 alone had no effect on electrically evoked dopamine release from rat striatal slices. These data indicate that the CB1 receptors in rat striatum are negatively linked to adenylyl cyclase and dopamine release. That the CB1 receptor may influence dopamine release in the striatum suggests that cannabinoids play a modulatory role in dopaminergic neuronal pathways.</description><subject>Acetylcholine - metabolism</subject><subject>Adenylyl Cyclases - metabolism</subject><subject>Animals</subject><subject>Arachidonic Acids - pharmacology</subject><subject>Biological and medical sciences</subject><subject>Cannabinoid receptor</subject><subject>Cannabinoids - antagonists &amp; inhibitors</subject><subject>Cannabinoids - pharmacology</subject><subject>Cerebral Cortex - drug effects</subject><subject>Cerebral Cortex - physiology</subject><subject>Corpus Striatum - drug effects</subject><subject>Corpus Striatum - physiology</subject><subject>Cyclic AMP</subject><subject>Cyclic AMP - metabolism</subject><subject>Cyclohexanols - pharmacology</subject><subject>Dopamine</subject><subject>Dopamine - metabolism</subject><subject>Drug addictions</subject><subject>Electric Stimulation</subject><subject>Endocannabinoids</subject><subject>In Vitro Techniques</subject><subject>Kinetics</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Phosphatidylinositols - metabolism</subject><subject>Piperidines - pharmacology</subject><subject>Polyunsaturated Alkamides</subject><subject>Potassium Chloride - pharmacology</subject><subject>Pyrazoles - pharmacology</subject><subject>Rat</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Receptors, Cannabinoid</subject><subject>Receptors, Drug - agonists</subject><subject>Receptors, Drug - physiology</subject><subject>Rimonabant</subject><subject>Second Messenger Systems - drug effects</subject><subject>Second Messenger Systems - physiology</subject><subject>Striatum</subject><subject>Toxicology</subject><issn>0022-3042</issn><issn>1471-4159</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVkE9v1DAQxS0EKkvLR0CyBOKW4H-JY3Gq0qUtKlC1cLYcZyK8OPY2TqD77Ztot3vnNBq992aefgi9pySnRJSfNjkVkmaCFiqnSsm8VIRTymn--AKtjtpLtCKEsYwTwV6jNyltCKGlKOkJOlGsYooXKxSvQ-cnCBZw7HBtQjCNC9G1CceA1x7sODhrvN_h9d_4B1p8EbemdwHwHXgwCbAJLa531juLz7_d4ksIMJjRzXEX8Ph7NpoR389nzDj1Z-hVZ3yCt4d5in59Wf-sr7KbH5fX9flNZoVkNGOcMUEJg6JtiqoC1nKrCsOrkgtblY1sSyIoLbhkIKtKCFCK88J2DTOcm5afoo_7u9shPkyQRt27ZMF7EyBOSUvFClbIajZ-3hvtEFMaoNPbwfVm2GlK9IJbb_SCVC9I9YJbP-PWj3P63eHN1PTQHrMHvrP-4aCbNFPsBhOsS0cbk3P5ailxsbf9cx52_9NAf_1eP2_8CZZ3m3k</recordid><startdate>199709</startdate><enddate>199709</enddate><creator>Cadogan, Anna‐Karina</creator><creator>Alexander, Stephen P. H.</creator><creator>Boyd, E. Andrew</creator><creator>Kendall, David A.</creator><general>Blackwell Science Ltd</general><general>Blackwell</general><scope>IQODW</scope><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>7X8</scope></search><sort><creationdate>199709</creationdate><title>Influence of Cannabinoids on Electrically Evoked Dopamine Release and Cyclic AMP Generation in the Rat Striatum</title><author>Cadogan, Anna‐Karina ; Alexander, Stephen P. H. ; Boyd, E. Andrew ; Kendall, David A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4721-23224102e5db588e2d3c95a38634c86b7d604115372e78844e99335cfb2a33ad3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Acetylcholine - metabolism</topic><topic>Adenylyl Cyclases - metabolism</topic><topic>Animals</topic><topic>Arachidonic Acids - pharmacology</topic><topic>Biological and medical sciences</topic><topic>Cannabinoid receptor</topic><topic>Cannabinoids - antagonists &amp; inhibitors</topic><topic>Cannabinoids - pharmacology</topic><topic>Cerebral Cortex - drug effects</topic><topic>Cerebral Cortex - physiology</topic><topic>Corpus Striatum - drug effects</topic><topic>Corpus Striatum - physiology</topic><topic>Cyclic AMP</topic><topic>Cyclic AMP - metabolism</topic><topic>Cyclohexanols - pharmacology</topic><topic>Dopamine</topic><topic>Dopamine - metabolism</topic><topic>Drug addictions</topic><topic>Electric Stimulation</topic><topic>Endocannabinoids</topic><topic>In Vitro Techniques</topic><topic>Kinetics</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Phosphatidylinositols - metabolism</topic><topic>Piperidines - pharmacology</topic><topic>Polyunsaturated Alkamides</topic><topic>Potassium Chloride - pharmacology</topic><topic>Pyrazoles - pharmacology</topic><topic>Rat</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Receptors, Cannabinoid</topic><topic>Receptors, Drug - agonists</topic><topic>Receptors, Drug - physiology</topic><topic>Rimonabant</topic><topic>Second Messenger Systems - drug effects</topic><topic>Second Messenger Systems - physiology</topic><topic>Striatum</topic><topic>Toxicology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cadogan, Anna‐Karina</creatorcontrib><creatorcontrib>Alexander, Stephen P. H.</creatorcontrib><creatorcontrib>Boyd, E. Andrew</creatorcontrib><creatorcontrib>Kendall, David A.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of neurochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cadogan, Anna‐Karina</au><au>Alexander, Stephen P. H.</au><au>Boyd, E. Andrew</au><au>Kendall, David A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Influence of Cannabinoids on Electrically Evoked Dopamine Release and Cyclic AMP Generation in the Rat Striatum</atitle><jtitle>Journal of neurochemistry</jtitle><addtitle>J Neurochem</addtitle><date>1997-09</date><risdate>1997</risdate><volume>69</volume><issue>3</issue><spage>1131</spage><epage>1137</epage><pages>1131-1137</pages><issn>0022-3042</issn><eissn>1471-4159</eissn><coden>JONRA9</coden><abstract>: Using the endogenous cannabinoid receptor agonist anandamide, the synthetic agonist CP 55940 {[1α,2β(R)5α]‐(−)‐5‐(1,1‐dimethylheptyl)‐2‐[5‐hydroxy‐2‐(3‐hydroxypropyl)cyclohexyl]phenol}, and the specific antagonist SR 141716 [N‐(piperidin‐1‐yl)‐5‐(4‐chlorophenyl)‐1‐(2,4‐dichlorophenyl)‐4‐methyl‐1H‐pyrazole‐3‐carboxamide hydrochloride], second messenger activation of the central cannabinoid receptor (CB1) was examined in rat striatal and cortical slices. The effects of these cannabinoid ligands on electrically evoked dopamine (DA) release from [3H]dopamine‐prelabelled striatal slices were also investigated. CP 55940 (1 µM) and anandamide (10 µM) caused significant reductions in forskolin‐stimulated cyclic AMP accumulation in rat striatal slices, which were reversed in the presence of SR 141716 (1 µM). CP 55940 (1 µM) had no effect on either KCl‐ or neurotransmitter‐stimulated 3H‐inositol phosphate accumulation in rat cortical slices. CP 55940 and anandamide caused significant reductions in the release of dopamine after electrical stimulation of [3H]dopamine‐prelabelled striatal slices, which were antagonised by SR 141716. SR 141716 alone had no effect on electrically evoked dopamine release from rat striatal slices. These data indicate that the CB1 receptors in rat striatum are negatively linked to adenylyl cyclase and dopamine release. That the CB1 receptor may influence dopamine release in the striatum suggests that cannabinoids play a modulatory role in dopaminergic neuronal pathways.</abstract><cop>Oxford, UK</cop><pub>Blackwell Science Ltd</pub><pmid>9282935</pmid><doi>10.1046/j.1471-4159.1997.69031131.x</doi><tpages>7</tpages></addata></record>
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source Wiley Free Content; MEDLINE; Wiley Online Library Journals Frontfile Complete; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Free Full-Text Journals in Chemistry
subjects Acetylcholine - metabolism
Adenylyl Cyclases - metabolism
Animals
Arachidonic Acids - pharmacology
Biological and medical sciences
Cannabinoid receptor
Cannabinoids - antagonists & inhibitors
Cannabinoids - pharmacology
Cerebral Cortex - drug effects
Cerebral Cortex - physiology
Corpus Striatum - drug effects
Corpus Striatum - physiology
Cyclic AMP
Cyclic AMP - metabolism
Cyclohexanols - pharmacology
Dopamine
Dopamine - metabolism
Drug addictions
Electric Stimulation
Endocannabinoids
In Vitro Techniques
Kinetics
Male
Medical sciences
Phosphatidylinositols - metabolism
Piperidines - pharmacology
Polyunsaturated Alkamides
Potassium Chloride - pharmacology
Pyrazoles - pharmacology
Rat
Rats
Rats, Wistar
Receptors, Cannabinoid
Receptors, Drug - agonists
Receptors, Drug - physiology
Rimonabant
Second Messenger Systems - drug effects
Second Messenger Systems - physiology
Striatum
Toxicology
title Influence of Cannabinoids on Electrically Evoked Dopamine Release and Cyclic AMP Generation in the Rat Striatum
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