Cardiac postjunctional supersensitivity to β-agonists after chronic chemical sympathectomy with 6-hydroxydopamine
The sensitivity to sympathomimetic amines of isolated atria removed from sham-injected and 6-hydroxydopamine-treated (6-OHDA) guinea-pigs was examined in the presence of an extraneuronal uptake blocker and an alpha-adrenoceptor antagonist. Three weeks of pretreatment with 6-OHDA resulted in leftward...
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Veröffentlicht in: | Naunyn-Schmiedeberg's archives of pharmacology 1985-04, Vol.329 (2), p.162-166 |
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description | The sensitivity to sympathomimetic amines of isolated atria removed from sham-injected and 6-hydroxydopamine-treated (6-OHDA) guinea-pigs was examined in the presence of an extraneuronal uptake blocker and an alpha-adrenoceptor antagonist. Three weeks of pretreatment with 6-OHDA resulted in leftwards shifts of the dose-response curves for the positive chronotropic and inotropic responses of right and left atria to isoprenaline. The responses to the partial agonist salbutamol were also potentiated after 6-OHDA pretreatment, revealed as an increase in the maximum response relative to isoprenaline. The supersensitivity was post-synaptic in origin and independent of changes in disposition or metabolism, since it was observed with agonists immune to neuronal uptake and O-methylation, and in the presence of extraneuronal uptake inhibition by metanephrine. It was also specific for the beta-adrenoceptor, no supersensitivity to histamine being found. In the right atria, the supersensitivity was partially masked by an opposing depressant effect after 6-OHDA pretreatment which was observed with histamine. Dissociation constants (KA) for the left atrial inotropic responses to orciprenaline were determined by use of the antagonist Ro 03-7894. Atria from 6-OHDA-pretreated animals were supersensitive to orciprenaline, but the KA value did not differ from that after sham injection. It could therefore be concluded that the increase in sensitivity was not due to an increase in affinity for the beta-adrenoceptor. |
doi_str_mv | 10.1007/BF00501207 |
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G ; GRASSBY, P. F ; CULLING, W ; PENNY, W ; BROADLEY, K. J ; SHERIDAN, D. J</creator><creatorcontrib>CHESS-WILLIAMS, R. G ; GRASSBY, P. F ; CULLING, W ; PENNY, W ; BROADLEY, K. J ; SHERIDAN, D. J</creatorcontrib><description>The sensitivity to sympathomimetic amines of isolated atria removed from sham-injected and 6-hydroxydopamine-treated (6-OHDA) guinea-pigs was examined in the presence of an extraneuronal uptake blocker and an alpha-adrenoceptor antagonist. Three weeks of pretreatment with 6-OHDA resulted in leftwards shifts of the dose-response curves for the positive chronotropic and inotropic responses of right and left atria to isoprenaline. The responses to the partial agonist salbutamol were also potentiated after 6-OHDA pretreatment, revealed as an increase in the maximum response relative to isoprenaline. The supersensitivity was post-synaptic in origin and independent of changes in disposition or metabolism, since it was observed with agonists immune to neuronal uptake and O-methylation, and in the presence of extraneuronal uptake inhibition by metanephrine. It was also specific for the beta-adrenoceptor, no supersensitivity to histamine being found. In the right atria, the supersensitivity was partially masked by an opposing depressant effect after 6-OHDA pretreatment which was observed with histamine. Dissociation constants (KA) for the left atrial inotropic responses to orciprenaline were determined by use of the antagonist Ro 03-7894. Atria from 6-OHDA-pretreated animals were supersensitive to orciprenaline, but the KA value did not differ from that after sham injection. It could therefore be concluded that the increase in sensitivity was not due to an increase in affinity for the beta-adrenoceptor.</description><identifier>ISSN: 0028-1298</identifier><identifier>EISSN: 1432-1912</identifier><identifier>DOI: 10.1007/BF00501207</identifier><identifier>PMID: 2861571</identifier><identifier>CODEN: NSAPCC</identifier><language>eng</language><publisher>Heidelberg: Springer</publisher><subject>Adrenergic beta-Agonists - pharmacology ; Adrenergic beta-Antagonists - pharmacology ; Animals ; Applied sciences ; Benzofurans - pharmacology ; Biological and medical sciences ; Catecholaminergic system ; Dose-Response Relationship, Drug ; Exact sciences and technology ; Guinea Pigs ; Heart - drug effects ; Heart Rate - drug effects ; Histamine - pharmacology ; Hydroxydopamines ; In Vitro Techniques ; Male ; Medical sciences ; Metaproterenol - antagonists & inhibitors ; Metaproterenol - pharmacology ; Myocardial Contraction - drug effects ; Neuropharmacology ; Neurotransmitters. Neurotransmission. Receptors ; Other techniques and industries ; Oxidopamine ; Pharmacology. Drug treatments ; Sympathectomy, Chemical</subject><ispartof>Naunyn-Schmiedeberg's archives of pharmacology, 1985-04, Vol.329 (2), p.162-166</ispartof><rights>1986 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></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=8544786$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=8838646$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2861571$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>CHESS-WILLIAMS, R. G</creatorcontrib><creatorcontrib>GRASSBY, P. F</creatorcontrib><creatorcontrib>CULLING, W</creatorcontrib><creatorcontrib>PENNY, W</creatorcontrib><creatorcontrib>BROADLEY, K. J</creatorcontrib><creatorcontrib>SHERIDAN, D. J</creatorcontrib><title>Cardiac postjunctional supersensitivity to β-agonists after chronic chemical sympathectomy with 6-hydroxydopamine</title><title>Naunyn-Schmiedeberg's archives of pharmacology</title><addtitle>Naunyn Schmiedebergs Arch Pharmacol</addtitle><description>The sensitivity to sympathomimetic amines of isolated atria removed from sham-injected and 6-hydroxydopamine-treated (6-OHDA) guinea-pigs was examined in the presence of an extraneuronal uptake blocker and an alpha-adrenoceptor antagonist. Three weeks of pretreatment with 6-OHDA resulted in leftwards shifts of the dose-response curves for the positive chronotropic and inotropic responses of right and left atria to isoprenaline. The responses to the partial agonist salbutamol were also potentiated after 6-OHDA pretreatment, revealed as an increase in the maximum response relative to isoprenaline. The supersensitivity was post-synaptic in origin and independent of changes in disposition or metabolism, since it was observed with agonists immune to neuronal uptake and O-methylation, and in the presence of extraneuronal uptake inhibition by metanephrine. It was also specific for the beta-adrenoceptor, no supersensitivity to histamine being found. In the right atria, the supersensitivity was partially masked by an opposing depressant effect after 6-OHDA pretreatment which was observed with histamine. Dissociation constants (KA) for the left atrial inotropic responses to orciprenaline were determined by use of the antagonist Ro 03-7894. Atria from 6-OHDA-pretreated animals were supersensitive to orciprenaline, but the KA value did not differ from that after sham injection. It could therefore be concluded that the increase in sensitivity was not due to an increase in affinity for the beta-adrenoceptor.</description><subject>Adrenergic beta-Agonists - pharmacology</subject><subject>Adrenergic beta-Antagonists - pharmacology</subject><subject>Animals</subject><subject>Applied sciences</subject><subject>Benzofurans - pharmacology</subject><subject>Biological and medical sciences</subject><subject>Catecholaminergic system</subject><subject>Dose-Response Relationship, Drug</subject><subject>Exact sciences and technology</subject><subject>Guinea Pigs</subject><subject>Heart - drug effects</subject><subject>Heart Rate - drug effects</subject><subject>Histamine - pharmacology</subject><subject>Hydroxydopamines</subject><subject>In Vitro Techniques</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Metaproterenol - antagonists & inhibitors</subject><subject>Metaproterenol - pharmacology</subject><subject>Myocardial Contraction - drug effects</subject><subject>Neuropharmacology</subject><subject>Neurotransmitters. Neurotransmission. Receptors</subject><subject>Other techniques and industries</subject><subject>Oxidopamine</subject><subject>Pharmacology. Drug treatments</subject><subject>Sympathectomy, Chemical</subject><issn>0028-1298</issn><issn>1432-1912</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1985</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkL1OwzAURi0EKqWwsCNlQGwBXzv-G6GigFSJBebISRzqqomD7QB5LR6EZyKIirVM3736zr3DQegU8CVgLK5uFhgzDASLPTSFjJIUFJB9NMWYyBSIkofoKIQ1xpgDYxM0IXIcBEyRn2tfWV0mnQtx3bdltK7VmyT0nfHBtMFG-2bjkESXfH2m-sW1NsSQ6Doan5QrP-7lmKax5c_Z0HQ6rkwZXTMk7zauEp6uhsq7j6FynW5sa47RQa03wZxsc4aeF7dP8_t0-Xj3ML9eph0lPKZC1aCLrKh1DVBpYgpOGOayZqYuCBVUF0WGgUulSCUVVIQZKBSnpBKMgKQzdPH7t_PutTch5o0NpdlsdGtcH3LBQRIBbCc4GqWMKfIPEBTjTI3g2Rbsi8ZUeedto_2Qb7WP_fm212HUVnvdljb8YVJSyTO-E2NZJiSn33Tpn3Q</recordid><startdate>198504</startdate><enddate>198504</enddate><creator>CHESS-WILLIAMS, R. G</creator><creator>GRASSBY, P. 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Neurotransmission. Receptors</topic><topic>Other techniques and industries</topic><topic>Oxidopamine</topic><topic>Pharmacology. Drug treatments</topic><topic>Sympathectomy, Chemical</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>CHESS-WILLIAMS, R. G</creatorcontrib><creatorcontrib>GRASSBY, P. F</creatorcontrib><creatorcontrib>CULLING, W</creatorcontrib><creatorcontrib>PENNY, W</creatorcontrib><creatorcontrib>BROADLEY, K. J</creatorcontrib><creatorcontrib>SHERIDAN, D. 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J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cardiac postjunctional supersensitivity to β-agonists after chronic chemical sympathectomy with 6-hydroxydopamine</atitle><jtitle>Naunyn-Schmiedeberg's archives of pharmacology</jtitle><addtitle>Naunyn Schmiedebergs Arch Pharmacol</addtitle><date>1985-04</date><risdate>1985</risdate><volume>329</volume><issue>2</issue><spage>162</spage><epage>166</epage><pages>162-166</pages><issn>0028-1298</issn><eissn>1432-1912</eissn><coden>NSAPCC</coden><abstract>The sensitivity to sympathomimetic amines of isolated atria removed from sham-injected and 6-hydroxydopamine-treated (6-OHDA) guinea-pigs was examined in the presence of an extraneuronal uptake blocker and an alpha-adrenoceptor antagonist. Three weeks of pretreatment with 6-OHDA resulted in leftwards shifts of the dose-response curves for the positive chronotropic and inotropic responses of right and left atria to isoprenaline. The responses to the partial agonist salbutamol were also potentiated after 6-OHDA pretreatment, revealed as an increase in the maximum response relative to isoprenaline. The supersensitivity was post-synaptic in origin and independent of changes in disposition or metabolism, since it was observed with agonists immune to neuronal uptake and O-methylation, and in the presence of extraneuronal uptake inhibition by metanephrine. It was also specific for the beta-adrenoceptor, no supersensitivity to histamine being found. In the right atria, the supersensitivity was partially masked by an opposing depressant effect after 6-OHDA pretreatment which was observed with histamine. Dissociation constants (KA) for the left atrial inotropic responses to orciprenaline were determined by use of the antagonist Ro 03-7894. Atria from 6-OHDA-pretreated animals were supersensitive to orciprenaline, but the KA value did not differ from that after sham injection. 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subjects | Adrenergic beta-Agonists - pharmacology Adrenergic beta-Antagonists - pharmacology Animals Applied sciences Benzofurans - pharmacology Biological and medical sciences Catecholaminergic system Dose-Response Relationship, Drug Exact sciences and technology Guinea Pigs Heart - drug effects Heart Rate - drug effects Histamine - pharmacology Hydroxydopamines In Vitro Techniques Male Medical sciences Metaproterenol - antagonists & inhibitors Metaproterenol - pharmacology Myocardial Contraction - drug effects Neuropharmacology Neurotransmitters. Neurotransmission. Receptors Other techniques and industries Oxidopamine Pharmacology. Drug treatments Sympathectomy, Chemical |
title | Cardiac postjunctional supersensitivity to β-agonists after chronic chemical sympathectomy with 6-hydroxydopamine |
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