The effects of putative 5-hydroxytryptamine receptor active agents on D-amphetamine self-administration in controls and rats with 5,7-dihydroxytryptamine median forebrain bundle lesions

Animals in which 5,7-dihydroxytryptamine (5,7-DHT) was bilaterally injected into the median forebrain bundle (MFB) and sham lesioned animals were allowed access to an apparatus which delivered, upon lever pressing, intravenous D-amphetamine injections. MFB lesioned rats achieved stable self-injectio...

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Veröffentlicht in:Brain research 1984-06, Vol.303 (1), p.153-162
Hauptverfasser: LECCESE, A. P, LYNESS, W. H
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description Animals in which 5,7-dihydroxytryptamine (5,7-DHT) was bilaterally injected into the median forebrain bundle (MFB) and sham lesioned animals were allowed access to an apparatus which delivered, upon lever pressing, intravenous D-amphetamine injections. MFB lesioned rats achieved stable self-injections patterns and self-administered more drug per test session than controls. A number of agents known to either directly or indirectly affect 5-hydroxytryptamine (5-HT) receptor function were administered prior to D-amphetamine access. The responses to these pretreatments in lesioned vs non-lesioned rats were markedly different. Pretreatment with L-tryptophan reduced the number of D-amphetamine self-injections in sham lesioned rats but had no effect in MFB lesioned animals. Fluoxetine pretreatment, likewise, reduced responding in non-lesioned rats and had no observable effect in lesioned animals. Quipazine markedly reduced self-injection in control rats but was not evaluated in the lesioned group. The putative 5-HT antagonists utilized, cyproheptadine and methysergide, unpredictably reduced self-injection frequency of non-lesioned animals in a dose related manner. When MFB lesioned animals were pretreated with cyproheptadine, rapid bursts of lever pressing were observed and 3 of 6 animals thus treated died as a result (presumably amphetamine overdose). In the remaining animals, methysergide produced a similar marked increase in self-injection rate. While these data may suggest that, in some instances, non-serotonergic mechanisms are involved, for the most part it would appear that 5-HT containing neurons are of major import in some aspect of D-amphetamine self-administration.
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Fluoxetine pretreatment, likewise, reduced responding in non-lesioned rats and had no observable effect in lesioned animals. Quipazine markedly reduced self-injection in control rats but was not evaluated in the lesioned group. The putative 5-HT antagonists utilized, cyproheptadine and methysergide, unpredictably reduced self-injection frequency of non-lesioned animals in a dose related manner. When MFB lesioned animals were pretreated with cyproheptadine, rapid bursts of lever pressing were observed and 3 of 6 animals thus treated died as a result (presumably amphetamine overdose). In the remaining animals, methysergide produced a similar marked increase in self-injection rate. 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H</creatorcontrib><title>The effects of putative 5-hydroxytryptamine receptor active agents on D-amphetamine self-administration in controls and rats with 5,7-dihydroxytryptamine median forebrain bundle lesions</title><title>Brain research</title><addtitle>Brain Res</addtitle><description>Animals in which 5,7-dihydroxytryptamine (5,7-DHT) was bilaterally injected into the median forebrain bundle (MFB) and sham lesioned animals were allowed access to an apparatus which delivered, upon lever pressing, intravenous D-amphetamine injections. MFB lesioned rats achieved stable self-injections patterns and self-administered more drug per test session than controls. A number of agents known to either directly or indirectly affect 5-hydroxytryptamine (5-HT) receptor function were administered prior to D-amphetamine access. The responses to these pretreatments in lesioned vs non-lesioned rats were markedly different. 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Psychiatry</subject><subject>Psychopharmacology</subject><subject>Quipazine - pharmacology</subject><subject>Rats</subject><subject>Rats, Inbred Strains</subject><subject>Serotonin - physiology</subject><subject>Substance-Related Disorders - physiopathology</subject><subject>Tryptophan - pharmacology</subject><issn>0006-8993</issn><issn>1872-6240</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1984</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNplkcFuGyEQhlGVyHXSvEEqccihkUIKyy7LHiO3SStZysU9W7Mw1ERrdgU4qR8tb1fSWr7kNAz_N_-gH0IuBb8VXKivnHPFdNfJL7q-7nhVSSY_kLnQbcVUVfMTMj8iH8lZSk-llbLjMzJTSvBaiTl5XW2QonNocqKjo9MuQ_bPSBu22ds4_tnnuJ8ybH1AGtHglMdIwfxj4DeGt7FAvzHYThs8cAkHx8CWs085Fr9C-EDNGHIch0QhWFquE33xeUObm5ZZ_37bFq2HQN0YsY9Q5vtdsAPSAVMxTJ_IqYMh4cWhnpNf999Xix9s-fjwc3G3ZJNQbWa1lQ1X0lYa0DaNMMJ1jXOtcboCobuqhCJMb2rUJRrhTMd76XpX19iC1lqek8__faddX560nqLfQtyvDxEW_eqgQzIwuAjB-HTESvrlE5T8C8Hnhi0</recordid><startdate>19840611</startdate><enddate>19840611</enddate><creator>LECCESE, A. 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H</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p167t-4d35063d28aed551c1f95ff7cf82a18920001cbc4e83901fc90b3fbf44e7a8883</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1984</creationdate><topic>5,7-Dihydroxytryptamine - pharmacology</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Cyproheptadine - pharmacology</topic><topic>Dextroamphetamine</topic><topic>Fluoxetine - pharmacology</topic><topic>Humans</topic><topic>Male</topic><topic>Medial Forebrain Bundle - physiopathology</topic><topic>Medical sciences</topic><topic>Methysergide - pharmacology</topic><topic>Neural Pathways - physiopathology</topic><topic>Neuropharmacology</topic><topic>Pharmacology. Drug treatments</topic><topic>Psychoanaleptics: cns stimulant, antidepressant agent, nootropic agent, mood stabilizer..., (alzheimer disease)</topic><topic>Psychology. Psychoanalysis. Psychiatry</topic><topic>Psychopharmacology</topic><topic>Quipazine - pharmacology</topic><topic>Rats</topic><topic>Rats, Inbred Strains</topic><topic>Serotonin - physiology</topic><topic>Substance-Related Disorders - physiopathology</topic><topic>Tryptophan - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>LECCESE, A. P</creatorcontrib><creatorcontrib>LYNESS, W. H</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><jtitle>Brain research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>LECCESE, A. P</au><au>LYNESS, W. H</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The effects of putative 5-hydroxytryptamine receptor active agents on D-amphetamine self-administration in controls and rats with 5,7-dihydroxytryptamine median forebrain bundle lesions</atitle><jtitle>Brain research</jtitle><addtitle>Brain Res</addtitle><date>1984-06-11</date><risdate>1984</risdate><volume>303</volume><issue>1</issue><spage>153</spage><epage>162</epage><pages>153-162</pages><issn>0006-8993</issn><eissn>1872-6240</eissn><coden>BRREAP</coden><abstract>Animals in which 5,7-dihydroxytryptamine (5,7-DHT) was bilaterally injected into the median forebrain bundle (MFB) and sham lesioned animals were allowed access to an apparatus which delivered, upon lever pressing, intravenous D-amphetamine injections. MFB lesioned rats achieved stable self-injections patterns and self-administered more drug per test session than controls. 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subjects 5,7-Dihydroxytryptamine - pharmacology
Animals
Biological and medical sciences
Cyproheptadine - pharmacology
Dextroamphetamine
Fluoxetine - pharmacology
Humans
Male
Medial Forebrain Bundle - physiopathology
Medical sciences
Methysergide - pharmacology
Neural Pathways - physiopathology
Neuropharmacology
Pharmacology. Drug treatments
Psychoanaleptics: cns stimulant, antidepressant agent, nootropic agent, mood stabilizer..., (alzheimer disease)
Psychology. Psychoanalysis. Psychiatry
Psychopharmacology
Quipazine - pharmacology
Rats
Rats, Inbred Strains
Serotonin - physiology
Substance-Related Disorders - physiopathology
Tryptophan - pharmacology
title The effects of putative 5-hydroxytryptamine receptor active agents on D-amphetamine self-administration in controls and rats with 5,7-dihydroxytryptamine median forebrain bundle lesions
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