Central administration of morphine inhibits brain and liver ornithine decarboxylase activity in neonatal rats: Involvement of transcription- and non-transcription-dependent mechanisms

This study examined whether the developmental deficits usually observed in infants born to opiate addicted mothers could involve effects on ornithine decarboxylase, a growth-controlling enzyme. Intracerebroventricular (i.c.v.) injection of a single dose of morphine (2 μg) to 6-day-old rats markedly...

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Veröffentlicht in:European journal of pharmacology 1997-07, Vol.331 (2), p.145-153
Hauptverfasser: Bartolome, Jorge V, Alicke, Bruno, Bartolome, Maria B
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creator Bartolome, Jorge V
Alicke, Bruno
Bartolome, Maria B
description This study examined whether the developmental deficits usually observed in infants born to opiate addicted mothers could involve effects on ornithine decarboxylase, a growth-controlling enzyme. Intracerebroventricular (i.c.v.) injection of a single dose of morphine (2 μg) to 6-day-old rats markedly decreased basal brain and liver ornithine decarboxylase activity as well as the increases in hepatic ornithine decarboxylase activity produced by subcutaneously (s.c.) administered insulin, an important trophic hormone. Centrally applied morphine acts supraspinally to downregulate peripheral ornithine decarboxylase activity, since s.c. administration of the same dose as used i.c.v. decreased neither basal liver ornithine decarboxylase levels nor tissue responsiveness to insulin. This does not imply that the opiate is unable to affect ornithine decarboxylase when applied systemically. In fact, a robust inhibition of both basal and induced liver ornithine decarboxylase activity was obtained in rat pups given 20 μg of morphine s.c. This larger dose is able to trigger the hepatic ornithine decarboxylase effects presumably by stimulating opiate receptors located at central sites after crossing the blood–brain barrier and penetrating into the brain. Concomitant administration of naloxone plus morphine i.c.v. prevented morphine from downregulating ornithine decarboxylase activity, confirming the participation of supraspinal opioid receptors in morphine ornithine decarboxylase actions. Finally, as was the case for insulin induced stimulation of ornithine decarboxylase activity, i.c.v. injection of morphine markedly diminished insulin induced stimulation of hepatic ornithine decarboxylase mRNA accumulation. In turn, contrary to the inhibition of basal ornithine decarboxylase activity, morphine did not lower basal hepatic ornithine decarboxylase mRNA levels when given alone. Thus, CNS morphine can apparently suppress tissue ornithine decarboxylase expression through both transcriptional and posttranscriptional mechanisms. The evidence obtained suggest that postnatal exposure to opiate drugs might detrimentally affect development by altering normal tissue ornithine decarboxylase ontogeny.
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Intracerebroventricular (i.c.v.) injection of a single dose of morphine (2 μg) to 6-day-old rats markedly decreased basal brain and liver ornithine decarboxylase activity as well as the increases in hepatic ornithine decarboxylase activity produced by subcutaneously (s.c.) administered insulin, an important trophic hormone. Centrally applied morphine acts supraspinally to downregulate peripheral ornithine decarboxylase activity, since s.c. administration of the same dose as used i.c.v. decreased neither basal liver ornithine decarboxylase levels nor tissue responsiveness to insulin. This does not imply that the opiate is unable to affect ornithine decarboxylase when applied systemically. In fact, a robust inhibition of both basal and induced liver ornithine decarboxylase activity was obtained in rat pups given 20 μg of morphine s.c. This larger dose is able to trigger the hepatic ornithine decarboxylase effects presumably by stimulating opiate receptors located at central sites after crossing the blood–brain barrier and penetrating into the brain. Concomitant administration of naloxone plus morphine i.c.v. prevented morphine from downregulating ornithine decarboxylase activity, confirming the participation of supraspinal opioid receptors in morphine ornithine decarboxylase actions. Finally, as was the case for insulin induced stimulation of ornithine decarboxylase activity, i.c.v. injection of morphine markedly diminished insulin induced stimulation of hepatic ornithine decarboxylase mRNA accumulation. In turn, contrary to the inhibition of basal ornithine decarboxylase activity, morphine did not lower basal hepatic ornithine decarboxylase mRNA levels when given alone. 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Intracerebroventricular (i.c.v.) injection of a single dose of morphine (2 μg) to 6-day-old rats markedly decreased basal brain and liver ornithine decarboxylase activity as well as the increases in hepatic ornithine decarboxylase activity produced by subcutaneously (s.c.) administered insulin, an important trophic hormone. Centrally applied morphine acts supraspinally to downregulate peripheral ornithine decarboxylase activity, since s.c. administration of the same dose as used i.c.v. decreased neither basal liver ornithine decarboxylase levels nor tissue responsiveness to insulin. This does not imply that the opiate is unable to affect ornithine decarboxylase when applied systemically. In fact, a robust inhibition of both basal and induced liver ornithine decarboxylase activity was obtained in rat pups given 20 μg of morphine s.c. This larger dose is able to trigger the hepatic ornithine decarboxylase effects presumably by stimulating opiate receptors located at central sites after crossing the blood–brain barrier and penetrating into the brain. Concomitant administration of naloxone plus morphine i.c.v. prevented morphine from downregulating ornithine decarboxylase activity, confirming the participation of supraspinal opioid receptors in morphine ornithine decarboxylase actions. Finally, as was the case for insulin induced stimulation of ornithine decarboxylase activity, i.c.v. injection of morphine markedly diminished insulin induced stimulation of hepatic ornithine decarboxylase mRNA accumulation. In turn, contrary to the inhibition of basal ornithine decarboxylase activity, morphine did not lower basal hepatic ornithine decarboxylase mRNA levels when given alone. Thus, CNS morphine can apparently suppress tissue ornithine decarboxylase expression through both transcriptional and posttranscriptional mechanisms. The evidence obtained suggest that postnatal exposure to opiate drugs might detrimentally affect development by altering normal tissue ornithine decarboxylase ontogeny.</description><subject>Analgesics, Opioid - administration &amp; dosage</subject><subject>Analgesics, Opioid - pharmacology</subject><subject>Animals</subject><subject>Animals, Newborn - metabolism</subject><subject>Blotting, Northern</subject><subject>Brain - drug effects</subject><subject>Brain - enzymology</subject><subject>Development</subject><subject>Dose-Response Relationship, Drug</subject><subject>Female</subject><subject>Growth</subject><subject>Hypoglycemic Agents - pharmacology</subject><subject>Injections, Intraventricular</subject><subject>Insulin</subject><subject>Insulin - pharmacology</subject><subject>Intracerebroventricular</subject><subject>Liver - drug effects</subject><subject>Liver - enzymology</subject><subject>Morphine - administration &amp; dosage</subject><subject>Morphine - pharmacology</subject><subject>Opiate</subject><subject>Ornithine Decarboxylase - metabolism</subject><subject>Ornithine Decarboxylase Inhibitors</subject><subject>Ornithine decarboxylase mRNA</subject><subject>Poly A - metabolism</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>RNA - biosynthesis</subject><subject>RNA - isolation &amp; purification</subject><subject>Transcription, Genetic - physiology</subject><subject>β-Endorphin</subject><issn>0014-2999</issn><issn>1879-0712</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc2OFCEUhYnRjO3oI0zCyuiilJ-iaNyYScefSSZxoa4JBZc0pgpKqK7YT-brSXV3JnE1K26459zvwkHohpJ3lNDu_XdCaNswpdQbJd8SSlrRiCdoQ7dSNURS9hRtHiTP0YtSfhFChGLiCl0pJlsl-Qb93UGcsxmwcWOIodR6Dini5PGY8rQPEXCI-9CHueA-mxCxiQ4PYYGMU45hPkkcWJP79Oc4mALY2DksYT5WJ46QopkroA4uH_BdXNKwwFipK6PiYrE5TCu0OY2Otfj_2sEE0a2OEeze1C3H8hI982Yo8OpyXqOfnz_92H1t7r99udvd3jeWKzo3nSVWcOh8x6Sn1HrZeu8EY6ozylplpFKG97Z2PPWt7AmzrXScc--23bbn1-j1ee6U0-8DlFmPoVgYBlMfdihaKsaFJNtHhbRrRdsyXoXiLLQ5lZLB6ymH0eSjpkSvyepTsnqNTSupT8lqUX03F8ChH8E9uC5R1v7Hcx_qdywBsi42QLTgQgY7a5fCI4R_tlG5vg</recordid><startdate>19970723</startdate><enddate>19970723</enddate><creator>Bartolome, Jorge V</creator><creator>Alicke, Bruno</creator><creator>Bartolome, Maria B</creator><general>Elsevier B.V</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>7TK</scope><scope>7X8</scope></search><sort><creationdate>19970723</creationdate><title>Central administration of morphine inhibits brain and liver ornithine decarboxylase activity in neonatal rats: Involvement of transcription- and non-transcription-dependent mechanisms</title><author>Bartolome, Jorge V ; Alicke, Bruno ; Bartolome, Maria B</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c391t-6c0c53e6f627f11cf74ffd52296a9cc9a799a3bc1cff1f47b02c47d333fd868b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Analgesics, Opioid - administration &amp; dosage</topic><topic>Analgesics, Opioid - pharmacology</topic><topic>Animals</topic><topic>Animals, Newborn - metabolism</topic><topic>Blotting, Northern</topic><topic>Brain - drug effects</topic><topic>Brain - enzymology</topic><topic>Development</topic><topic>Dose-Response Relationship, Drug</topic><topic>Female</topic><topic>Growth</topic><topic>Hypoglycemic Agents - pharmacology</topic><topic>Injections, Intraventricular</topic><topic>Insulin</topic><topic>Insulin - pharmacology</topic><topic>Intracerebroventricular</topic><topic>Liver - drug effects</topic><topic>Liver - enzymology</topic><topic>Morphine - administration &amp; dosage</topic><topic>Morphine - pharmacology</topic><topic>Opiate</topic><topic>Ornithine Decarboxylase - metabolism</topic><topic>Ornithine Decarboxylase Inhibitors</topic><topic>Ornithine decarboxylase mRNA</topic><topic>Poly A - metabolism</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>RNA - biosynthesis</topic><topic>RNA - isolation &amp; purification</topic><topic>Transcription, Genetic - physiology</topic><topic>β-Endorphin</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bartolome, Jorge V</creatorcontrib><creatorcontrib>Alicke, Bruno</creatorcontrib><creatorcontrib>Bartolome, Maria B</creatorcontrib><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><jtitle>European journal of pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bartolome, Jorge V</au><au>Alicke, Bruno</au><au>Bartolome, Maria B</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Central administration of morphine inhibits brain and liver ornithine decarboxylase activity in neonatal rats: Involvement of transcription- and non-transcription-dependent mechanisms</atitle><jtitle>European journal of pharmacology</jtitle><addtitle>Eur J Pharmacol</addtitle><date>1997-07-23</date><risdate>1997</risdate><volume>331</volume><issue>2</issue><spage>145</spage><epage>153</epage><pages>145-153</pages><issn>0014-2999</issn><eissn>1879-0712</eissn><abstract>This study examined whether the developmental deficits usually observed in infants born to opiate addicted mothers could involve effects on ornithine decarboxylase, a growth-controlling enzyme. Intracerebroventricular (i.c.v.) injection of a single dose of morphine (2 μg) to 6-day-old rats markedly decreased basal brain and liver ornithine decarboxylase activity as well as the increases in hepatic ornithine decarboxylase activity produced by subcutaneously (s.c.) administered insulin, an important trophic hormone. Centrally applied morphine acts supraspinally to downregulate peripheral ornithine decarboxylase activity, since s.c. administration of the same dose as used i.c.v. decreased neither basal liver ornithine decarboxylase levels nor tissue responsiveness to insulin. This does not imply that the opiate is unable to affect ornithine decarboxylase when applied systemically. In fact, a robust inhibition of both basal and induced liver ornithine decarboxylase activity was obtained in rat pups given 20 μg of morphine s.c. This larger dose is able to trigger the hepatic ornithine decarboxylase effects presumably by stimulating opiate receptors located at central sites after crossing the blood–brain barrier and penetrating into the brain. Concomitant administration of naloxone plus morphine i.c.v. prevented morphine from downregulating ornithine decarboxylase activity, confirming the participation of supraspinal opioid receptors in morphine ornithine decarboxylase actions. Finally, as was the case for insulin induced stimulation of ornithine decarboxylase activity, i.c.v. injection of morphine markedly diminished insulin induced stimulation of hepatic ornithine decarboxylase mRNA accumulation. In turn, contrary to the inhibition of basal ornithine decarboxylase activity, morphine did not lower basal hepatic ornithine decarboxylase mRNA levels when given alone. Thus, CNS morphine can apparently suppress tissue ornithine decarboxylase expression through both transcriptional and posttranscriptional mechanisms. The evidence obtained suggest that postnatal exposure to opiate drugs might detrimentally affect development by altering normal tissue ornithine decarboxylase ontogeny.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>9274973</pmid><doi>10.1016/S0014-2999(97)01045-5</doi><tpages>9</tpages></addata></record>
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subjects Analgesics, Opioid - administration & dosage
Analgesics, Opioid - pharmacology
Animals
Animals, Newborn - metabolism
Blotting, Northern
Brain - drug effects
Brain - enzymology
Development
Dose-Response Relationship, Drug
Female
Growth
Hypoglycemic Agents - pharmacology
Injections, Intraventricular
Insulin
Insulin - pharmacology
Intracerebroventricular
Liver - drug effects
Liver - enzymology
Morphine - administration & dosage
Morphine - pharmacology
Opiate
Ornithine Decarboxylase - metabolism
Ornithine Decarboxylase Inhibitors
Ornithine decarboxylase mRNA
Poly A - metabolism
Rats
Rats, Sprague-Dawley
RNA - biosynthesis
RNA - isolation & purification
Transcription, Genetic - physiology
β-Endorphin
title Central administration of morphine inhibits brain and liver ornithine decarboxylase activity in neonatal rats: Involvement of transcription- and non-transcription-dependent mechanisms
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