Cannabinoid signalling

After their discovery, the two known cannabinoid receptors, CB 1 and CB 2, have been the focus of research into the cellular signalling mechanisms of cannabinoids. The initial assessment, mainly derived from expression studies, was that cannabinoids, via G i/o proteins, negatively modulate cyclic AM...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Life sciences (1973) 2006-01, Vol.78 (6), p.549-563
Hauptverfasser: Demuth, Dirk G., Molleman, Areles
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 563
container_issue 6
container_start_page 549
container_title Life sciences (1973)
container_volume 78
creator Demuth, Dirk G.
Molleman, Areles
description After their discovery, the two known cannabinoid receptors, CB 1 and CB 2, have been the focus of research into the cellular signalling mechanisms of cannabinoids. The initial assessment, mainly derived from expression studies, was that cannabinoids, via G i/o proteins, negatively modulate cyclic AMP levels, and activate inward rectifying K + channels. Recent findings have complicated this assessment on different levels: (1) cannabinoids include a wide range of compounds with varying profiles of affinity and efficacy at the known CB receptors, and these profiles do not necessarily match their biological activity; (2) CB receptors appear to be intrinsically active and possibly coupled to more than one type of G protein; (3) CB receptor signalling mechanisms are diverse and dependent on the system studied; (4) cannabinoids have other targets than CB receptors. The aim of this mini review is to discuss the current literature regarding CB receptor signalling pathways. These include regulation of adenylyl cyclase, MAP kinase, intracellular Ca 2+, and ion channels. In addition, actions of cannabinoids that are not mediated by CB 1 or CB 2 receptors are discussed.
doi_str_mv 10.1016/j.lfs.2005.05.055
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_67573893</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0024320505006727</els_id><sourcerecordid>67573893</sourcerecordid><originalsourceid>FETCH-LOGICAL-c351t-1a88a27ea99df1b2aa22cecdb29766a9cc9012c8c3105b60cef6d96c37a1450e3</originalsourceid><addsrcrecordid>eNp9kM1LAzEQxYMotlavghfx5G3XmaTJbvAkxS8oeNFzyCazJWWb1U0r-N-bfoA34cFcfu8x7zF2hVAioLpbll2bSg4gy53kERtjXekClMBjNgbg00JwkCN2ltISMigrccpGqBD0VMCYXc5sjLYJsQ_-JoVFtF0X4uKcnbS2S3RxuBP28fT4Pnsp5m_Pr7OHeeGExHWBtq4tr8hq7VtsuLWcO3K-4bpSymrnNCB3tRMIslHgqFVeKycqi1MJJCbsdp_7OfRfG0prswrJUdfZSP0mGVXlh2stMoh70A19SgO15nMIKzv8GASzHcMsTR7DbMcwO8nsuT6Eb5oV-T_HoX0G7vcA5YrfgQaTXKDoyIeB3Nr4PvwT_wv_623x</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>67573893</pqid></control><display><type>article</type><title>Cannabinoid signalling</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals Complete</source><creator>Demuth, Dirk G. ; Molleman, Areles</creator><creatorcontrib>Demuth, Dirk G. ; Molleman, Areles</creatorcontrib><description>After their discovery, the two known cannabinoid receptors, CB 1 and CB 2, have been the focus of research into the cellular signalling mechanisms of cannabinoids. The initial assessment, mainly derived from expression studies, was that cannabinoids, via G i/o proteins, negatively modulate cyclic AMP levels, and activate inward rectifying K + channels. Recent findings have complicated this assessment on different levels: (1) cannabinoids include a wide range of compounds with varying profiles of affinity and efficacy at the known CB receptors, and these profiles do not necessarily match their biological activity; (2) CB receptors appear to be intrinsically active and possibly coupled to more than one type of G protein; (3) CB receptor signalling mechanisms are diverse and dependent on the system studied; (4) cannabinoids have other targets than CB receptors. The aim of this mini review is to discuss the current literature regarding CB receptor signalling pathways. These include regulation of adenylyl cyclase, MAP kinase, intracellular Ca 2+, and ion channels. In addition, actions of cannabinoids that are not mediated by CB 1 or CB 2 receptors are discussed.</description><identifier>ISSN: 0024-3205</identifier><identifier>EISSN: 1879-0631</identifier><identifier>DOI: 10.1016/j.lfs.2005.05.055</identifier><identifier>PMID: 16109430</identifier><language>eng</language><publisher>Netherlands: Elsevier Inc</publisher><subject>Adenylyl Cyclases - metabolism ; Animals ; Calcium - metabolism ; Cannabinoid receptor ; Cannabinoids ; Cannabinoids - pharmacology ; G proteins ; GTP-Binding Proteins - physiology ; Humans ; Ion channels ; Ion Channels - physiology ; Mitogen-Activated Protein Kinases - metabolism ; Receptor, Cannabinoid, CB1 - physiology ; Receptor, Cannabinoid, CB2 - physiology ; Receptors, N-Methyl-D-Aspartate - drug effects ; Receptors, Opioid - drug effects ; Receptors, Serotonin, 5-HT3 - drug effects ; Second messengers ; Signal transduction ; Signal Transduction - physiology ; TRPV Cation Channels - drug effects</subject><ispartof>Life sciences (1973), 2006-01, Vol.78 (6), p.549-563</ispartof><rights>2005 Elsevier Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c351t-1a88a27ea99df1b2aa22cecdb29766a9cc9012c8c3105b60cef6d96c37a1450e3</citedby><cites>FETCH-LOGICAL-c351t-1a88a27ea99df1b2aa22cecdb29766a9cc9012c8c3105b60cef6d96c37a1450e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.lfs.2005.05.055$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16109430$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Demuth, Dirk G.</creatorcontrib><creatorcontrib>Molleman, Areles</creatorcontrib><title>Cannabinoid signalling</title><title>Life sciences (1973)</title><addtitle>Life Sci</addtitle><description>After their discovery, the two known cannabinoid receptors, CB 1 and CB 2, have been the focus of research into the cellular signalling mechanisms of cannabinoids. The initial assessment, mainly derived from expression studies, was that cannabinoids, via G i/o proteins, negatively modulate cyclic AMP levels, and activate inward rectifying K + channels. Recent findings have complicated this assessment on different levels: (1) cannabinoids include a wide range of compounds with varying profiles of affinity and efficacy at the known CB receptors, and these profiles do not necessarily match their biological activity; (2) CB receptors appear to be intrinsically active and possibly coupled to more than one type of G protein; (3) CB receptor signalling mechanisms are diverse and dependent on the system studied; (4) cannabinoids have other targets than CB receptors. The aim of this mini review is to discuss the current literature regarding CB receptor signalling pathways. These include regulation of adenylyl cyclase, MAP kinase, intracellular Ca 2+, and ion channels. In addition, actions of cannabinoids that are not mediated by CB 1 or CB 2 receptors are discussed.</description><subject>Adenylyl Cyclases - metabolism</subject><subject>Animals</subject><subject>Calcium - metabolism</subject><subject>Cannabinoid receptor</subject><subject>Cannabinoids</subject><subject>Cannabinoids - pharmacology</subject><subject>G proteins</subject><subject>GTP-Binding Proteins - physiology</subject><subject>Humans</subject><subject>Ion channels</subject><subject>Ion Channels - physiology</subject><subject>Mitogen-Activated Protein Kinases - metabolism</subject><subject>Receptor, Cannabinoid, CB1 - physiology</subject><subject>Receptor, Cannabinoid, CB2 - physiology</subject><subject>Receptors, N-Methyl-D-Aspartate - drug effects</subject><subject>Receptors, Opioid - drug effects</subject><subject>Receptors, Serotonin, 5-HT3 - drug effects</subject><subject>Second messengers</subject><subject>Signal transduction</subject><subject>Signal Transduction - physiology</subject><subject>TRPV Cation Channels - drug effects</subject><issn>0024-3205</issn><issn>1879-0631</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kM1LAzEQxYMotlavghfx5G3XmaTJbvAkxS8oeNFzyCazJWWb1U0r-N-bfoA34cFcfu8x7zF2hVAioLpbll2bSg4gy53kERtjXekClMBjNgbg00JwkCN2ltISMigrccpGqBD0VMCYXc5sjLYJsQ_-JoVFtF0X4uKcnbS2S3RxuBP28fT4Pnsp5m_Pr7OHeeGExHWBtq4tr8hq7VtsuLWcO3K-4bpSymrnNCB3tRMIslHgqFVeKycqi1MJJCbsdp_7OfRfG0prswrJUdfZSP0mGVXlh2stMoh70A19SgO15nMIKzv8GASzHcMsTR7DbMcwO8nsuT6Eb5oV-T_HoX0G7vcA5YrfgQaTXKDoyIeB3Nr4PvwT_wv_623x</recordid><startdate>20060102</startdate><enddate>20060102</enddate><creator>Demuth, Dirk G.</creator><creator>Molleman, Areles</creator><general>Elsevier Inc</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>7X8</scope></search><sort><creationdate>20060102</creationdate><title>Cannabinoid signalling</title><author>Demuth, Dirk G. ; Molleman, Areles</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c351t-1a88a27ea99df1b2aa22cecdb29766a9cc9012c8c3105b60cef6d96c37a1450e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Adenylyl Cyclases - metabolism</topic><topic>Animals</topic><topic>Calcium - metabolism</topic><topic>Cannabinoid receptor</topic><topic>Cannabinoids</topic><topic>Cannabinoids - pharmacology</topic><topic>G proteins</topic><topic>GTP-Binding Proteins - physiology</topic><topic>Humans</topic><topic>Ion channels</topic><topic>Ion Channels - physiology</topic><topic>Mitogen-Activated Protein Kinases - metabolism</topic><topic>Receptor, Cannabinoid, CB1 - physiology</topic><topic>Receptor, Cannabinoid, CB2 - physiology</topic><topic>Receptors, N-Methyl-D-Aspartate - drug effects</topic><topic>Receptors, Opioid - drug effects</topic><topic>Receptors, Serotonin, 5-HT3 - drug effects</topic><topic>Second messengers</topic><topic>Signal transduction</topic><topic>Signal Transduction - physiology</topic><topic>TRPV Cation Channels - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Demuth, Dirk G.</creatorcontrib><creatorcontrib>Molleman, Areles</creatorcontrib><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>Life sciences (1973)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Demuth, Dirk G.</au><au>Molleman, Areles</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cannabinoid signalling</atitle><jtitle>Life sciences (1973)</jtitle><addtitle>Life Sci</addtitle><date>2006-01-02</date><risdate>2006</risdate><volume>78</volume><issue>6</issue><spage>549</spage><epage>563</epage><pages>549-563</pages><issn>0024-3205</issn><eissn>1879-0631</eissn><abstract>After their discovery, the two known cannabinoid receptors, CB 1 and CB 2, have been the focus of research into the cellular signalling mechanisms of cannabinoids. The initial assessment, mainly derived from expression studies, was that cannabinoids, via G i/o proteins, negatively modulate cyclic AMP levels, and activate inward rectifying K + channels. Recent findings have complicated this assessment on different levels: (1) cannabinoids include a wide range of compounds with varying profiles of affinity and efficacy at the known CB receptors, and these profiles do not necessarily match their biological activity; (2) CB receptors appear to be intrinsically active and possibly coupled to more than one type of G protein; (3) CB receptor signalling mechanisms are diverse and dependent on the system studied; (4) cannabinoids have other targets than CB receptors. The aim of this mini review is to discuss the current literature regarding CB receptor signalling pathways. These include regulation of adenylyl cyclase, MAP kinase, intracellular Ca 2+, and ion channels. In addition, actions of cannabinoids that are not mediated by CB 1 or CB 2 receptors are discussed.</abstract><cop>Netherlands</cop><pub>Elsevier Inc</pub><pmid>16109430</pmid><doi>10.1016/j.lfs.2005.05.055</doi><tpages>15</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0024-3205
ispartof Life sciences (1973), 2006-01, Vol.78 (6), p.549-563
issn 0024-3205
1879-0631
language eng
recordid cdi_proquest_miscellaneous_67573893
source MEDLINE; Elsevier ScienceDirect Journals Complete
subjects Adenylyl Cyclases - metabolism
Animals
Calcium - metabolism
Cannabinoid receptor
Cannabinoids
Cannabinoids - pharmacology
G proteins
GTP-Binding Proteins - physiology
Humans
Ion channels
Ion Channels - physiology
Mitogen-Activated Protein Kinases - metabolism
Receptor, Cannabinoid, CB1 - physiology
Receptor, Cannabinoid, CB2 - physiology
Receptors, N-Methyl-D-Aspartate - drug effects
Receptors, Opioid - drug effects
Receptors, Serotonin, 5-HT3 - drug effects
Second messengers
Signal transduction
Signal Transduction - physiology
TRPV Cation Channels - drug effects
title Cannabinoid signalling
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-05T03%3A32%3A52IST&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=Cannabinoid%20signalling&rft.jtitle=Life%20sciences%20(1973)&rft.au=Demuth,%20Dirk%20G.&rft.date=2006-01-02&rft.volume=78&rft.issue=6&rft.spage=549&rft.epage=563&rft.pages=549-563&rft.issn=0024-3205&rft.eissn=1879-0631&rft_id=info:doi/10.1016/j.lfs.2005.05.055&rft_dat=%3Cproquest_cross%3E67573893%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=67573893&rft_id=info:pmid/16109430&rft_els_id=S0024320505006727&rfr_iscdi=true