Increased dopaminergic and 5‐hydroxytryptaminergic activities in male rat brain following long‐term treatment with anabolic androgenic steroids
The effects of treating groups of rats with four different anabolic androgenic steroids (AAS) (testosterone, nandrolone, methandrostenolone, and oxymetholone) on 5‐hydroxytryptamine (5‐HT) and dopamine (DA) neurones in different brain regions were examined. The AAS was injected six times with 1 week...
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description | The effects of treating groups of rats with four different anabolic androgenic steroids (AAS) (testosterone, nandrolone, methandrostenolone, and oxymetholone) on 5‐hydroxytryptamine (5‐HT) and dopamine (DA) neurones in different brain regions were examined. The AAS was injected six times with 1 week's interval and the rats were sacrificed 2 days after the final injection. 5‐HT and its metabolite 5‐hydroxyindoleacetic acid (5‐HIAA), DA and its metabolites 3,4‐dihydroxyphenylacetic acid (DOPAC) and homovanillic acid (HVA) were measured. The effect on DA and 5‐HT synthesis rate was analysed as the accumulation of 3,4‐dihydroxyphenyl‐alanine (DOPA) and 5‐hydroxytryptophan (5‐HTP), respectively, after inhibition of the amino acid decarboxylase with NSD‐1015 (3‐hydroxy‐benzylhydrazine dihydrochloride). Additionally, the monoamine oxidase (MAO) activity was analysed in the hypothalamus.
The DOPAC+HVA/DA ratio was increased in the striatum in all treatment groups. However, the synthesis rate of DA was significantly increased only in the methandrostenolone treated group.
The 5‐HIAA/5‐HT ratio was increased in all treatment groups in the hippocampus, in the frontal cortex in the methandrostenolone‐treated animals and in the hypothalamus in the testosterone‐ and oxymetholone‐treated rats, while the 5‐HT synthesis rate was not affected by the AAS‐treatments.
The MAO‐A activity was increased in the oxymetholone‐treated rats while the other treatment groups were unaffected. The MAO‐B activity was not changed.
The results indicate that relatively high doses of AAS increase dopaminergic and 5‐hydroxytryptaminergic metabolism in male rat brain, probably due to enhanced turnover in these monaminergic systems.
British Journal of Pharmacology (1999) 126, 1301–1306; doi:10.1038/sj.bjp.0702412 |
doi_str_mv | 10.1038/sj.bjp.0702412 |
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The DOPAC+HVA/DA ratio was increased in the striatum in all treatment groups. However, the synthesis rate of DA was significantly increased only in the methandrostenolone treated group.
The 5‐HIAA/5‐HT ratio was increased in all treatment groups in the hippocampus, in the frontal cortex in the methandrostenolone‐treated animals and in the hypothalamus in the testosterone‐ and oxymetholone‐treated rats, while the 5‐HT synthesis rate was not affected by the AAS‐treatments.
The MAO‐A activity was increased in the oxymetholone‐treated rats while the other treatment groups were unaffected. The MAO‐B activity was not changed.
The results indicate that relatively high doses of AAS increase dopaminergic and 5‐hydroxytryptaminergic metabolism in male rat brain, probably due to enhanced turnover in these monaminergic systems.
British Journal of Pharmacology (1999) 126, 1301–1306; doi:10.1038/sj.bjp.0702412</description><identifier>ISSN: 0007-1188</identifier><identifier>EISSN: 1476-5381</identifier><identifier>DOI: 10.1038/sj.bjp.0702412</identifier><identifier>PMID: 10217522</identifier><identifier>CODEN: BJPCBM</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>3,4-Dihydroxyphenylacetic Acid - metabolism ; 5-Hydroxytryptophan - drug effects ; 5-Hydroxytryptophan - metabolism ; 5‐hydroxytryptamine ; Anabolic Agents - pharmacology ; anabolic androgenic steroids ; anabolic steroids ; Animals ; Biological and medical sciences ; Brain - drug effects ; Brain - metabolism ; Corpus Striatum - drug effects ; Corpus Striatum - metabolism ; Dihydroxyphenylalanine - drug effects ; Dihydroxyphenylalanine - metabolism ; dopamine ; Dopamine - metabolism ; Drug toxicity and drugs side effects treatment ; frontal cortex ; hippocampus ; Hippocampus - drug effects ; Hippocampus - metabolism ; Homovanillic Acid - metabolism ; Hydroxyindoleacetic Acid - metabolism ; hypothalamus ; Male ; Medical sciences ; Methandrostenolone - pharmacology ; Miscellaneous (drug allergy, mutagens, teratogens...) ; Monoamine Oxidase - drug effects ; Monoamine Oxidase - metabolism ; monoamines ; Pharmacology. Drug treatments ; Rat brain ; Rats ; Rats, Sprague-Dawley ; Serotonin - metabolism ; striatum ; Synaptosomes - drug effects ; Synaptosomes - enzymology ; Time Factors</subject><ispartof>British journal of pharmacology, 1999-03, Vol.126 (6), p.1301-1306</ispartof><rights>1999 Nature Publishing Group</rights><rights>1999 INIST-CNRS</rights><rights>Copyright 1999, Nature Publishing Group 1999 Nature Publishing Group</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5284-1bf7762185e23bb39471cc6931d365d0ac4e02c08b4b9d74abe652500255da7c3</citedby><cites>FETCH-LOGICAL-c5284-1bf7762185e23bb39471cc6931d365d0ac4e02c08b4b9d74abe652500255da7c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1565900/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1565900/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,550,723,776,780,881,1411,1427,27903,27904,45553,45554,46387,46811,53769,53771</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1721954$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10217522$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttp://kipublications.ki.se/Default.aspx?queryparsed=id:1933999$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Thiblin, Ingemar</creatorcontrib><creatorcontrib>Finn, Anja</creatorcontrib><creatorcontrib>Ross, Svante B</creatorcontrib><creatorcontrib>Stenfors, Carina</creatorcontrib><title>Increased dopaminergic and 5‐hydroxytryptaminergic activities in male rat brain following long‐term treatment with anabolic androgenic steroids</title><title>British journal of pharmacology</title><addtitle>Br J Pharmacol</addtitle><description>The effects of treating groups of rats with four different anabolic androgenic steroids (AAS) (testosterone, nandrolone, methandrostenolone, and oxymetholone) on 5‐hydroxytryptamine (5‐HT) and dopamine (DA) neurones in different brain regions were examined. The AAS was injected six times with 1 week's interval and the rats were sacrificed 2 days after the final injection. 5‐HT and its metabolite 5‐hydroxyindoleacetic acid (5‐HIAA), DA and its metabolites 3,4‐dihydroxyphenylacetic acid (DOPAC) and homovanillic acid (HVA) were measured. The effect on DA and 5‐HT synthesis rate was analysed as the accumulation of 3,4‐dihydroxyphenyl‐alanine (DOPA) and 5‐hydroxytryptophan (5‐HTP), respectively, after inhibition of the amino acid decarboxylase with NSD‐1015 (3‐hydroxy‐benzylhydrazine dihydrochloride). Additionally, the monoamine oxidase (MAO) activity was analysed in the hypothalamus.
The DOPAC+HVA/DA ratio was increased in the striatum in all treatment groups. However, the synthesis rate of DA was significantly increased only in the methandrostenolone treated group.
The 5‐HIAA/5‐HT ratio was increased in all treatment groups in the hippocampus, in the frontal cortex in the methandrostenolone‐treated animals and in the hypothalamus in the testosterone‐ and oxymetholone‐treated rats, while the 5‐HT synthesis rate was not affected by the AAS‐treatments.
The MAO‐A activity was increased in the oxymetholone‐treated rats while the other treatment groups were unaffected. The MAO‐B activity was not changed.
The results indicate that relatively high doses of AAS increase dopaminergic and 5‐hydroxytryptaminergic metabolism in male rat brain, probably due to enhanced turnover in these monaminergic systems.
British Journal of Pharmacology (1999) 126, 1301–1306; doi:10.1038/sj.bjp.0702412</description><subject>3,4-Dihydroxyphenylacetic Acid - metabolism</subject><subject>5-Hydroxytryptophan - drug effects</subject><subject>5-Hydroxytryptophan - metabolism</subject><subject>5‐hydroxytryptamine</subject><subject>Anabolic Agents - pharmacology</subject><subject>anabolic androgenic steroids</subject><subject>anabolic steroids</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Brain - drug effects</subject><subject>Brain - metabolism</subject><subject>Corpus Striatum - drug effects</subject><subject>Corpus Striatum - metabolism</subject><subject>Dihydroxyphenylalanine - drug effects</subject><subject>Dihydroxyphenylalanine - metabolism</subject><subject>dopamine</subject><subject>Dopamine - metabolism</subject><subject>Drug toxicity and drugs side effects treatment</subject><subject>frontal cortex</subject><subject>hippocampus</subject><subject>Hippocampus - drug effects</subject><subject>Hippocampus - metabolism</subject><subject>Homovanillic Acid - metabolism</subject><subject>Hydroxyindoleacetic Acid - metabolism</subject><subject>hypothalamus</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Methandrostenolone - pharmacology</subject><subject>Miscellaneous (drug allergy, mutagens, teratogens...)</subject><subject>Monoamine Oxidase - drug effects</subject><subject>Monoamine Oxidase - metabolism</subject><subject>monoamines</subject><subject>Pharmacology. Drug treatments</subject><subject>Rat brain</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Serotonin - metabolism</subject><subject>striatum</subject><subject>Synaptosomes - drug effects</subject><subject>Synaptosomes - enzymology</subject><subject>Time Factors</subject><issn>0007-1188</issn><issn>1476-5381</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>D8T</sourceid><recordid>eNqFksGO1SAUhhujca6jW5eGhXHXK1Ao7cbEmagzySS60DWhQHu5UqjAnWt3PoKJb-iTiGmjd1az4sD_nf9wkr8oniO4RbBqXsf9tttPW8ggJgg_KDaIsLqkVYMeFhsIISsRapqz4kmMewizyOjj4gxBjBjFeFP8unYyaBG1AspPYjROh8FIIJwC9PePn7tZBf99TmGe0okqk7k1yegIjAOjsBoEkUAXRL723lp_NG4A1rsheyQdRpDylDRql8DRpF32F523y6DgB-1yGTPojYpPi0e9sFE_W8_z4sv7d58vr8qbjx-uL9_elJLihpSo6xmrMWqoxlXXVS1hSMq6rZCqaqqgkERDLGHTka5VjIhO1xRTCDGlSjBZnRfl4huPejp0fApmFGHmXhi-Pn3NleY1pIyyzL9Z-KyMWsm8TBD2TttdxZkdH_wtR7SmLYTZ4NVqEPy3g46JjyZKba1w2h8ir1uGCKH3g4hVtGlrlMHtAsrgYwy6__cbBPnfgPC45zkgfA1IbnhxusMJviQiAy9XQEQpbB-Ekyb-5xhGLSUZqxbsaKye75nKLz5dIUhI9Qetb9uc</recordid><startdate>199903</startdate><enddate>199903</enddate><creator>Thiblin, Ingemar</creator><creator>Finn, Anja</creator><creator>Ross, Svante B</creator><creator>Stenfors, Carina</creator><general>Blackwell Publishing Ltd</general><general>Nature Publishing</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>7TK</scope><scope>7X8</scope><scope>5PM</scope><scope>ADTPV</scope><scope>AOWAS</scope><scope>D8T</scope><scope>ZZAVC</scope></search><sort><creationdate>199903</creationdate><title>Increased dopaminergic and 5‐hydroxytryptaminergic activities in male rat brain following long‐term treatment with anabolic androgenic steroids</title><author>Thiblin, Ingemar ; Finn, Anja ; Ross, Svante B ; Stenfors, Carina</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5284-1bf7762185e23bb39471cc6931d365d0ac4e02c08b4b9d74abe652500255da7c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>3,4-Dihydroxyphenylacetic Acid - metabolism</topic><topic>5-Hydroxytryptophan - drug effects</topic><topic>5-Hydroxytryptophan - metabolism</topic><topic>5‐hydroxytryptamine</topic><topic>Anabolic Agents - pharmacology</topic><topic>anabolic androgenic steroids</topic><topic>anabolic steroids</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Brain - drug effects</topic><topic>Brain - metabolism</topic><topic>Corpus Striatum - drug effects</topic><topic>Corpus Striatum - metabolism</topic><topic>Dihydroxyphenylalanine - drug effects</topic><topic>Dihydroxyphenylalanine - metabolism</topic><topic>dopamine</topic><topic>Dopamine - metabolism</topic><topic>Drug toxicity and drugs side effects treatment</topic><topic>frontal cortex</topic><topic>hippocampus</topic><topic>Hippocampus - drug effects</topic><topic>Hippocampus - metabolism</topic><topic>Homovanillic Acid - metabolism</topic><topic>Hydroxyindoleacetic Acid - metabolism</topic><topic>hypothalamus</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Methandrostenolone - pharmacology</topic><topic>Miscellaneous (drug allergy, mutagens, teratogens...)</topic><topic>Monoamine Oxidase - drug effects</topic><topic>Monoamine Oxidase - metabolism</topic><topic>monoamines</topic><topic>Pharmacology. Drug treatments</topic><topic>Rat brain</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Serotonin - metabolism</topic><topic>striatum</topic><topic>Synaptosomes - drug effects</topic><topic>Synaptosomes - enzymology</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Thiblin, Ingemar</creatorcontrib><creatorcontrib>Finn, Anja</creatorcontrib><creatorcontrib>Ross, Svante B</creatorcontrib><creatorcontrib>Stenfors, Carina</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>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>SwePub</collection><collection>SwePub Articles</collection><collection>SWEPUB Freely available online</collection><collection>SwePub Articles full text</collection><jtitle>British journal of pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Thiblin, Ingemar</au><au>Finn, Anja</au><au>Ross, Svante B</au><au>Stenfors, Carina</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Increased dopaminergic and 5‐hydroxytryptaminergic activities in male rat brain following long‐term treatment with anabolic androgenic steroids</atitle><jtitle>British journal of pharmacology</jtitle><addtitle>Br J Pharmacol</addtitle><date>1999-03</date><risdate>1999</risdate><volume>126</volume><issue>6</issue><spage>1301</spage><epage>1306</epage><pages>1301-1306</pages><issn>0007-1188</issn><eissn>1476-5381</eissn><coden>BJPCBM</coden><abstract>The effects of treating groups of rats with four different anabolic androgenic steroids (AAS) (testosterone, nandrolone, methandrostenolone, and oxymetholone) on 5‐hydroxytryptamine (5‐HT) and dopamine (DA) neurones in different brain regions were examined. The AAS was injected six times with 1 week's interval and the rats were sacrificed 2 days after the final injection. 5‐HT and its metabolite 5‐hydroxyindoleacetic acid (5‐HIAA), DA and its metabolites 3,4‐dihydroxyphenylacetic acid (DOPAC) and homovanillic acid (HVA) were measured. The effect on DA and 5‐HT synthesis rate was analysed as the accumulation of 3,4‐dihydroxyphenyl‐alanine (DOPA) and 5‐hydroxytryptophan (5‐HTP), respectively, after inhibition of the amino acid decarboxylase with NSD‐1015 (3‐hydroxy‐benzylhydrazine dihydrochloride). Additionally, the monoamine oxidase (MAO) activity was analysed in the hypothalamus.
The DOPAC+HVA/DA ratio was increased in the striatum in all treatment groups. However, the synthesis rate of DA was significantly increased only in the methandrostenolone treated group.
The 5‐HIAA/5‐HT ratio was increased in all treatment groups in the hippocampus, in the frontal cortex in the methandrostenolone‐treated animals and in the hypothalamus in the testosterone‐ and oxymetholone‐treated rats, while the 5‐HT synthesis rate was not affected by the AAS‐treatments.
The MAO‐A activity was increased in the oxymetholone‐treated rats while the other treatment groups were unaffected. The MAO‐B activity was not changed.
The results indicate that relatively high doses of AAS increase dopaminergic and 5‐hydroxytryptaminergic metabolism in male rat brain, probably due to enhanced turnover in these monaminergic systems.
British Journal of Pharmacology (1999) 126, 1301–1306; doi:10.1038/sj.bjp.0702412</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>10217522</pmid><doi>10.1038/sj.bjp.0702412</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 3,4-Dihydroxyphenylacetic Acid - metabolism 5-Hydroxytryptophan - drug effects 5-Hydroxytryptophan - metabolism 5‐hydroxytryptamine Anabolic Agents - pharmacology anabolic androgenic steroids anabolic steroids Animals Biological and medical sciences Brain - drug effects Brain - metabolism Corpus Striatum - drug effects Corpus Striatum - metabolism Dihydroxyphenylalanine - drug effects Dihydroxyphenylalanine - metabolism dopamine Dopamine - metabolism Drug toxicity and drugs side effects treatment frontal cortex hippocampus Hippocampus - drug effects Hippocampus - metabolism Homovanillic Acid - metabolism Hydroxyindoleacetic Acid - metabolism hypothalamus Male Medical sciences Methandrostenolone - pharmacology Miscellaneous (drug allergy, mutagens, teratogens...) Monoamine Oxidase - drug effects Monoamine Oxidase - metabolism monoamines Pharmacology. Drug treatments Rat brain Rats Rats, Sprague-Dawley Serotonin - metabolism striatum Synaptosomes - drug effects Synaptosomes - enzymology Time Factors |
title | Increased dopaminergic and 5‐hydroxytryptaminergic activities in male rat brain following long‐term treatment with anabolic androgenic steroids |
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