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Cocaine cardiotoxicity differs markedly in isolated hearts of two strains of rats exhibiting phenotypic differences in sensitivity to seizures
Isolated hearts from two strains of rats bred for sensitivity or resistance to amygdala kindling that also exhibit, in vivo, differential sensitivity to the cardiotoxicity of cocaine were studied. The goal was to determine if the differential cardiotoxic sensitivity was due, at least in part, to int...
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Published in: | Life sciences (1973) 1998, Vol.63 (8), p.625-633 |
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container_title | Life sciences (1973) |
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creator | Heavner, J.E. Shi, B. Inners-McBride, K. Asimakis, G. Wang, M.J. McIntyre, D.C. |
description | Isolated hearts from two strains of rats bred for sensitivity or resistance to amygdala kindling that also exhibit,
in vivo, differential sensitivity to the cardiotoxicity of cocaine were studied. The goal was to determine if the differential cardiotoxic sensitivity was due, at least in part, to intrinsic strain-dependent differences in the heart. The Langendorff preparation was used (n = 8 per strain). Hearts were perfused with increasing concentrations of cocaine (5 × 10
−6, 1 × 10
−5, 5 × 10
−5, 1 × 10
−4, and 5 × 10
−4 M) for 5 min with a 5 min washout between exposure to successive concentrations. Consistent with
in vivo observations, hearts from genetically slow amygdala kindling rats (Slow) required lower cocaine doses to develop cardiac arrhythmias and arrest as compared to the hearts from genetically fast amygdala kindling rats (Fast). At 5 × 10
−5M cocaine arrhythmias occurred in 38% (
3
8
) Slow and 0% Fast hearts. Five of 8 Slow hearts and none of 8 Fast hearts were arrested by 10
−4M cocaine. Arrest in Fast hearts occurred only with 5 × 10
−4M cocaine. Cocaine constricted coronary arteries (no significant difference between strains). On the other hand, coronary arteries of Slow but not Fast hearts dilated during cocaine washout after perfusion with all but the highest concentration of cocaine. We conclude that factors intrinsic to the heart and coronary artery influence the sensitivity or response of these structures to cocaine. |
doi_str_mv | 10.1016/S0024-3205(98)00314-2 |
format | article |
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in vivo, differential sensitivity to the cardiotoxicity of cocaine were studied. The goal was to determine if the differential cardiotoxic sensitivity was due, at least in part, to intrinsic strain-dependent differences in the heart. The Langendorff preparation was used (n = 8 per strain). Hearts were perfused with increasing concentrations of cocaine (5 × 10
−6, 1 × 10
−5, 5 × 10
−5, 1 × 10
−4, and 5 × 10
−4 M) for 5 min with a 5 min washout between exposure to successive concentrations. Consistent with
in vivo observations, hearts from genetically slow amygdala kindling rats (Slow) required lower cocaine doses to develop cardiac arrhythmias and arrest as compared to the hearts from genetically fast amygdala kindling rats (Fast). At 5 × 10
−5M cocaine arrhythmias occurred in 38% (
3
8
) Slow and 0% Fast hearts. Five of 8 Slow hearts and none of 8 Fast hearts were arrested by 10
−4M cocaine. Arrest in Fast hearts occurred only with 5 × 10
−4M cocaine. Cocaine constricted coronary arteries (no significant difference between strains). On the other hand, coronary arteries of Slow but not Fast hearts dilated during cocaine washout after perfusion with all but the highest concentration of cocaine. We conclude that factors intrinsic to the heart and coronary artery influence the sensitivity or response of these structures to cocaine.</description><identifier>ISSN: 0024-3205</identifier><identifier>EISSN: 1879-0631</identifier><identifier>DOI: 10.1016/S0024-3205(98)00314-2</identifier><identifier>PMID: 9718092</identifier><language>eng</language><publisher>Netherlands: Elsevier Inc</publisher><subject>Amygdala ; Animals ; Blood Pressure ; Cocaine - administration & dosage ; Cocaine - toxicity ; cocaine cardiotoxicology ; coronary artery ; Coronary Vessels - physiology ; Diastole ; differential sensitivity ; Electrocardiography ; Heart Diseases - chemically induced ; Heart Diseases - genetics ; Heart Rate ; kindling ; Kindling, Neurologic ; Langendorff preparation ; Male ; Phenotype ; Rats ; Seizures - genetics ; Time Factors ; Ventricular Function, Left</subject><ispartof>Life sciences (1973), 1998, Vol.63 (8), p.625-633</ispartof><rights>1998</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c339t-72592f29b561443938917ef6d43f5337f32b73af5d0a7b58e18fc522d26cb0d33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4024,27923,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9718092$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Heavner, J.E.</creatorcontrib><creatorcontrib>Shi, B.</creatorcontrib><creatorcontrib>Inners-McBride, K.</creatorcontrib><creatorcontrib>Asimakis, G.</creatorcontrib><creatorcontrib>Wang, M.J.</creatorcontrib><creatorcontrib>McIntyre, D.C.</creatorcontrib><title>Cocaine cardiotoxicity differs markedly in isolated hearts of two strains of rats exhibiting phenotypic differences in sensitivity to seizures</title><title>Life sciences (1973)</title><addtitle>Life Sci</addtitle><description>Isolated hearts from two strains of rats bred for sensitivity or resistance to amygdala kindling that also exhibit,
in vivo, differential sensitivity to the cardiotoxicity of cocaine were studied. The goal was to determine if the differential cardiotoxic sensitivity was due, at least in part, to intrinsic strain-dependent differences in the heart. The Langendorff preparation was used (n = 8 per strain). Hearts were perfused with increasing concentrations of cocaine (5 × 10
−6, 1 × 10
−5, 5 × 10
−5, 1 × 10
−4, and 5 × 10
−4 M) for 5 min with a 5 min washout between exposure to successive concentrations. Consistent with
in vivo observations, hearts from genetically slow amygdala kindling rats (Slow) required lower cocaine doses to develop cardiac arrhythmias and arrest as compared to the hearts from genetically fast amygdala kindling rats (Fast). At 5 × 10
−5M cocaine arrhythmias occurred in 38% (
3
8
) Slow and 0% Fast hearts. Five of 8 Slow hearts and none of 8 Fast hearts were arrested by 10
−4M cocaine. Arrest in Fast hearts occurred only with 5 × 10
−4M cocaine. Cocaine constricted coronary arteries (no significant difference between strains). On the other hand, coronary arteries of Slow but not Fast hearts dilated during cocaine washout after perfusion with all but the highest concentration of cocaine. We conclude that factors intrinsic to the heart and coronary artery influence the sensitivity or response of these structures to cocaine.</description><subject>Amygdala</subject><subject>Animals</subject><subject>Blood Pressure</subject><subject>Cocaine - administration & dosage</subject><subject>Cocaine - toxicity</subject><subject>cocaine cardiotoxicology</subject><subject>coronary artery</subject><subject>Coronary Vessels - physiology</subject><subject>Diastole</subject><subject>differential sensitivity</subject><subject>Electrocardiography</subject><subject>Heart Diseases - chemically induced</subject><subject>Heart Diseases - genetics</subject><subject>Heart Rate</subject><subject>kindling</subject><subject>Kindling, Neurologic</subject><subject>Langendorff preparation</subject><subject>Male</subject><subject>Phenotype</subject><subject>Rats</subject><subject>Seizures - genetics</subject><subject>Time Factors</subject><subject>Ventricular Function, Left</subject><issn>0024-3205</issn><issn>1879-0631</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><recordid>eNqFkc1uEzEUhS0EKmnhESp5hWAx4J_xzHiFUAQFqRILYG157GtyYTIOtlMaHoJnxpNE3bKy7Hvud-RzCLnm7DVnvHvzhTHRNlIw9VIPrxiTvG3EI7LiQ68b1kn-mKweJE_JZc4_GGNK9fKCXOieD0yLFfm7js7iDNTZ5DGWeI8Oy4F6DAFSplubfoKfDhRnijlOtoCnG7CpZBoDLb8jzSVVwvGabH2G-w2OWHD-TncbmGM57NCdgTA7yAsrw5yr5m7xKpUB-GefID8jT4KdMjw_n1fk24f3X9cfm9vPN5_W724bJ6UuTS-UFkHoUXW8baWWg-Y9hM63Migp-yDF2EsblGe2H9UAfAhOCeFF50bmpbwiL07cXYq_9pCL2WJ2ME12hrjPhnftoGXfVaE6CV2KOScIZpewhnIwnJmlB3PswSwhGz2YYw9G1L3rs8F-3IJ_2DoHX-dvT3Oov7xDSCY7XNLxmMAV4yP-x-EfubWa5Q</recordid><startdate>1998</startdate><enddate>1998</enddate><creator>Heavner, J.E.</creator><creator>Shi, B.</creator><creator>Inners-McBride, K.</creator><creator>Asimakis, G.</creator><creator>Wang, M.J.</creator><creator>McIntyre, D.C.</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>7U7</scope><scope>C1K</scope></search><sort><creationdate>1998</creationdate><title>Cocaine cardiotoxicity differs markedly in isolated hearts of two strains of rats exhibiting phenotypic differences in sensitivity to seizures</title><author>Heavner, J.E. ; Shi, B. ; Inners-McBride, K. ; Asimakis, G. ; Wang, M.J. ; McIntyre, D.C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c339t-72592f29b561443938917ef6d43f5337f32b73af5d0a7b58e18fc522d26cb0d33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Amygdala</topic><topic>Animals</topic><topic>Blood Pressure</topic><topic>Cocaine - administration & dosage</topic><topic>Cocaine - toxicity</topic><topic>cocaine cardiotoxicology</topic><topic>coronary artery</topic><topic>Coronary Vessels - physiology</topic><topic>Diastole</topic><topic>differential sensitivity</topic><topic>Electrocardiography</topic><topic>Heart Diseases - chemically induced</topic><topic>Heart Diseases - genetics</topic><topic>Heart Rate</topic><topic>kindling</topic><topic>Kindling, Neurologic</topic><topic>Langendorff preparation</topic><topic>Male</topic><topic>Phenotype</topic><topic>Rats</topic><topic>Seizures - genetics</topic><topic>Time Factors</topic><topic>Ventricular Function, Left</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Heavner, J.E.</creatorcontrib><creatorcontrib>Shi, B.</creatorcontrib><creatorcontrib>Inners-McBride, K.</creatorcontrib><creatorcontrib>Asimakis, G.</creatorcontrib><creatorcontrib>Wang, M.J.</creatorcontrib><creatorcontrib>McIntyre, D.C.</creatorcontrib><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>Life sciences (1973)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Heavner, J.E.</au><au>Shi, B.</au><au>Inners-McBride, K.</au><au>Asimakis, G.</au><au>Wang, M.J.</au><au>McIntyre, D.C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cocaine cardiotoxicity differs markedly in isolated hearts of two strains of rats exhibiting phenotypic differences in sensitivity to seizures</atitle><jtitle>Life sciences (1973)</jtitle><addtitle>Life Sci</addtitle><date>1998</date><risdate>1998</risdate><volume>63</volume><issue>8</issue><spage>625</spage><epage>633</epage><pages>625-633</pages><issn>0024-3205</issn><eissn>1879-0631</eissn><abstract>Isolated hearts from two strains of rats bred for sensitivity or resistance to amygdala kindling that also exhibit,
in vivo, differential sensitivity to the cardiotoxicity of cocaine were studied. The goal was to determine if the differential cardiotoxic sensitivity was due, at least in part, to intrinsic strain-dependent differences in the heart. The Langendorff preparation was used (n = 8 per strain). Hearts were perfused with increasing concentrations of cocaine (5 × 10
−6, 1 × 10
−5, 5 × 10
−5, 1 × 10
−4, and 5 × 10
−4 M) for 5 min with a 5 min washout between exposure to successive concentrations. Consistent with
in vivo observations, hearts from genetically slow amygdala kindling rats (Slow) required lower cocaine doses to develop cardiac arrhythmias and arrest as compared to the hearts from genetically fast amygdala kindling rats (Fast). At 5 × 10
−5M cocaine arrhythmias occurred in 38% (
3
8
) Slow and 0% Fast hearts. Five of 8 Slow hearts and none of 8 Fast hearts were arrested by 10
−4M cocaine. Arrest in Fast hearts occurred only with 5 × 10
−4M cocaine. Cocaine constricted coronary arteries (no significant difference between strains). On the other hand, coronary arteries of Slow but not Fast hearts dilated during cocaine washout after perfusion with all but the highest concentration of cocaine. We conclude that factors intrinsic to the heart and coronary artery influence the sensitivity or response of these structures to cocaine.</abstract><cop>Netherlands</cop><pub>Elsevier Inc</pub><pmid>9718092</pmid><doi>10.1016/S0024-3205(98)00314-2</doi><tpages>9</tpages></addata></record> |
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subjects | Amygdala Animals Blood Pressure Cocaine - administration & dosage Cocaine - toxicity cocaine cardiotoxicology coronary artery Coronary Vessels - physiology Diastole differential sensitivity Electrocardiography Heart Diseases - chemically induced Heart Diseases - genetics Heart Rate kindling Kindling, Neurologic Langendorff preparation Male Phenotype Rats Seizures - genetics Time Factors Ventricular Function, Left |
title | Cocaine cardiotoxicity differs markedly in isolated hearts of two strains of rats exhibiting phenotypic differences in sensitivity to seizures |
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