Effects and Interactions of Natural Cannabinoids on the Isolated Heart
Abstract A Langendorff perfused rat heart preparation was designed to process dose-response effects of cardioactive drugs on rate, coronary flow, and supraaortic differential pressure (ΔP; an index of cardiac performance). In this preparation, Δ9--tetrahydrocannabinol (THC) 2 × 10-6 M to 10-5 M indu...
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Veröffentlicht in: | Experimental biology and medicine (Maywood, N.J.) N.J.), 1985-11, Vol.180 (2), p.312-316 |
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container_title | Experimental biology and medicine (Maywood, N.J.) |
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creator | Nahas, Gabriel Trouve, Renaud |
description | Abstract
A Langendorff perfused rat heart preparation was designed to process dose-response effects of cardioactive drugs on rate, coronary flow, and supraaortic differential pressure (ΔP; an index of cardiac performance). In this preparation, Δ9--tetrahydrocannabinol (THC) 2 × 10-6
M to 10-5
M induces in the isolated perfused rat heart a biphasic increase in rate (maximal at 8 × 10-6
M). Tachycardia is associated with decreases in (ΔP) and no change or decreased coronary flow. Cardiac toxicity is observed with 3 × 10-5
M. Cannabidiol (CBD) at concentrations of 9 × 10-6
M to 10-4
M has limited effect on rate while increasing ΔP and coronary flow. Cannabinol (CBN) 8 × 10-6
M to 3 × 10-4
M depresses rate and ΔP while coronary flow remains constant. Simultaneous equimolar administration of THC with CBD antagonizes or mitigates the cardiac effects of THC on rate, ΔP, and coronary flow. |
doi_str_mv | 10.3181/00379727-180-42181 |
format | Article |
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A Langendorff perfused rat heart preparation was designed to process dose-response effects of cardioactive drugs on rate, coronary flow, and supraaortic differential pressure (ΔP; an index of cardiac performance). In this preparation, Δ9--tetrahydrocannabinol (THC) 2 × 10-6
M to 10-5
M induces in the isolated perfused rat heart a biphasic increase in rate (maximal at 8 × 10-6
M). Tachycardia is associated with decreases in (ΔP) and no change or decreased coronary flow. Cardiac toxicity is observed with 3 × 10-5
M. Cannabidiol (CBD) at concentrations of 9 × 10-6
M to 10-4
M has limited effect on rate while increasing ΔP and coronary flow. Cannabinol (CBN) 8 × 10-6
M to 3 × 10-4
M depresses rate and ΔP while coronary flow remains constant. Simultaneous equimolar administration of THC with CBD antagonizes or mitigates the cardiac effects of THC on rate, ΔP, and coronary flow.</description><identifier>ISSN: 0037-9727</identifier><identifier>ISSN: 1535-3702</identifier><identifier>EISSN: 1535-3699</identifier><identifier>EISSN: 1525-1373</identifier><identifier>DOI: 10.3181/00379727-180-42181</identifier><identifier>PMID: 4048169</identifier><identifier>CODEN: PSEBAA</identifier><language>eng</language><publisher>London, England: SAGE Publications</publisher><subject>Animals ; Biological and medical sciences ; Blood Pressure - drug effects ; Cannabidiol - pharmacology ; Cannabidiol - toxicity ; Cannabinoids - pharmacology ; Cannabinoids - toxicity ; Cannabinol - pharmacology ; Cannabinol - toxicity ; Cardiac Output - drug effects ; Coronary Circulation - drug effects ; Dose-Response Relationship, Drug ; Drug addictions ; Heart - drug effects ; Heart - physiopathology ; Heart Rate - drug effects ; Hemodynamics - drug effects ; Medical sciences ; Rats ; Rats, Inbred Strains ; Tachycardia - chemically induced ; Toxicology</subject><ispartof>Experimental biology and medicine (Maywood, N.J.), 1985-11, Vol.180 (2), p.312-316</ispartof><rights>1987 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c398t-78ca2103e1d6cac97d2c21bacbd8549f0ddaac887c81cf6e38947353f016050e3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=7964216$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/4048169$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nahas, Gabriel</creatorcontrib><creatorcontrib>Trouve, Renaud</creatorcontrib><title>Effects and Interactions of Natural Cannabinoids on the Isolated Heart</title><title>Experimental biology and medicine (Maywood, N.J.)</title><addtitle>Proc Soc Exp Biol Med</addtitle><description>Abstract
A Langendorff perfused rat heart preparation was designed to process dose-response effects of cardioactive drugs on rate, coronary flow, and supraaortic differential pressure (ΔP; an index of cardiac performance). In this preparation, Δ9--tetrahydrocannabinol (THC) 2 × 10-6
M to 10-5
M induces in the isolated perfused rat heart a biphasic increase in rate (maximal at 8 × 10-6
M). Tachycardia is associated with decreases in (ΔP) and no change or decreased coronary flow. Cardiac toxicity is observed with 3 × 10-5
M. Cannabidiol (CBD) at concentrations of 9 × 10-6
M to 10-4
M has limited effect on rate while increasing ΔP and coronary flow. Cannabinol (CBN) 8 × 10-6
M to 3 × 10-4
M depresses rate and ΔP while coronary flow remains constant. Simultaneous equimolar administration of THC with CBD antagonizes or mitigates the cardiac effects of THC on rate, ΔP, and coronary flow.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Blood Pressure - drug effects</subject><subject>Cannabidiol - pharmacology</subject><subject>Cannabidiol - toxicity</subject><subject>Cannabinoids - pharmacology</subject><subject>Cannabinoids - toxicity</subject><subject>Cannabinol - pharmacology</subject><subject>Cannabinol - toxicity</subject><subject>Cardiac Output - drug effects</subject><subject>Coronary Circulation - drug effects</subject><subject>Dose-Response Relationship, Drug</subject><subject>Drug addictions</subject><subject>Heart - drug effects</subject><subject>Heart - physiopathology</subject><subject>Heart Rate - drug effects</subject><subject>Hemodynamics - drug effects</subject><subject>Medical sciences</subject><subject>Rats</subject><subject>Rats, Inbred Strains</subject><subject>Tachycardia - chemically induced</subject><subject>Toxicology</subject><issn>0037-9727</issn><issn>1535-3702</issn><issn>1535-3699</issn><issn>1525-1373</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1985</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kD1PwzAQhi0EKqXwB5CQMiC2UDtOYntEVUsrVbDAbF38AalSp9jOwL_HpaUj00l3z_ue9CB0S_AjJZxMMaZMsILlhOO8LNLqDI1JRauc1kKco_EeyPfEJboKYYMxqVhRj9CoxCUntRijxdxao2LIwOls5aLxoGLbu5D1NnuBOHjoshk4B03r-lanvcvip8lWoe8gGp0tDfh4jS4sdMHcHOcEvS_mb7Nlvn59Xs2e1rmigseccQUFwdQQXStQgulCFaQB1WhelcJirQEU50xxomxtKBcloxW1mNS4woZO0MOhd-f7r8GEKLdtUKbrwJl-CJKUFHPBywQWB1D5PgRvrNz5dgv-WxIs9_LknzyZ5MlfeSl0d2wfmq3Rp8jRVrrfH-8QFHTWg1NtOGFM1KmnTtj0gAX4MHLTD94lJ_89_gFrPYOq</recordid><startdate>198511</startdate><enddate>198511</enddate><creator>Nahas, Gabriel</creator><creator>Trouve, Renaud</creator><general>SAGE Publications</general><general>Blackwell Science</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>7U7</scope><scope>C1K</scope></search><sort><creationdate>198511</creationdate><title>Effects and Interactions of Natural Cannabinoids on the Isolated Heart</title><author>Nahas, Gabriel ; Trouve, Renaud</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c398t-78ca2103e1d6cac97d2c21bacbd8549f0ddaac887c81cf6e38947353f016050e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1985</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Blood Pressure - drug effects</topic><topic>Cannabidiol - pharmacology</topic><topic>Cannabidiol - toxicity</topic><topic>Cannabinoids - pharmacology</topic><topic>Cannabinoids - toxicity</topic><topic>Cannabinol - pharmacology</topic><topic>Cannabinol - toxicity</topic><topic>Cardiac Output - drug effects</topic><topic>Coronary Circulation - drug effects</topic><topic>Dose-Response Relationship, Drug</topic><topic>Drug addictions</topic><topic>Heart - drug effects</topic><topic>Heart - physiopathology</topic><topic>Heart Rate - drug effects</topic><topic>Hemodynamics - drug effects</topic><topic>Medical sciences</topic><topic>Rats</topic><topic>Rats, Inbred Strains</topic><topic>Tachycardia - chemically induced</topic><topic>Toxicology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nahas, Gabriel</creatorcontrib><creatorcontrib>Trouve, Renaud</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>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Experimental biology and medicine (Maywood, N.J.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nahas, Gabriel</au><au>Trouve, Renaud</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects and Interactions of Natural Cannabinoids on the Isolated Heart</atitle><jtitle>Experimental biology and medicine (Maywood, N.J.)</jtitle><addtitle>Proc Soc Exp Biol Med</addtitle><date>1985-11</date><risdate>1985</risdate><volume>180</volume><issue>2</issue><spage>312</spage><epage>316</epage><pages>312-316</pages><issn>0037-9727</issn><issn>1535-3702</issn><eissn>1535-3699</eissn><eissn>1525-1373</eissn><coden>PSEBAA</coden><abstract>Abstract
A Langendorff perfused rat heart preparation was designed to process dose-response effects of cardioactive drugs on rate, coronary flow, and supraaortic differential pressure (ΔP; an index of cardiac performance). In this preparation, Δ9--tetrahydrocannabinol (THC) 2 × 10-6
M to 10-5
M induces in the isolated perfused rat heart a biphasic increase in rate (maximal at 8 × 10-6
M). Tachycardia is associated with decreases in (ΔP) and no change or decreased coronary flow. Cardiac toxicity is observed with 3 × 10-5
M. Cannabidiol (CBD) at concentrations of 9 × 10-6
M to 10-4
M has limited effect on rate while increasing ΔP and coronary flow. Cannabinol (CBN) 8 × 10-6
M to 3 × 10-4
M depresses rate and ΔP while coronary flow remains constant. Simultaneous equimolar administration of THC with CBD antagonizes or mitigates the cardiac effects of THC on rate, ΔP, and coronary flow.</abstract><cop>London, England</cop><pub>SAGE Publications</pub><pmid>4048169</pmid><doi>10.3181/00379727-180-42181</doi><tpages>5</tpages></addata></record> |
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source | MEDLINE; Alma/SFX Local Collection |
subjects | Animals Biological and medical sciences Blood Pressure - drug effects Cannabidiol - pharmacology Cannabidiol - toxicity Cannabinoids - pharmacology Cannabinoids - toxicity Cannabinol - pharmacology Cannabinol - toxicity Cardiac Output - drug effects Coronary Circulation - drug effects Dose-Response Relationship, Drug Drug addictions Heart - drug effects Heart - physiopathology Heart Rate - drug effects Hemodynamics - drug effects Medical sciences Rats Rats, Inbred Strains Tachycardia - chemically induced Toxicology |
title | Effects and Interactions of Natural Cannabinoids on the Isolated Heart |
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