α-Difluoromethylornithine Modifies FSH Secretion and Puberty Onset in the Female Rat

Abstract FSH secretion is high in immature female rats from Postnatal Day 5 to 18 and decreases thereafter. This is a relatively steroid-independent event of cerebral origin and of importance for puberty onset. Polyamines, a group of ubiquitous amines, play an essential role in tissue growth and dif...

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Veröffentlicht in:Proceedings of the Society for Experimental Biology and Medicine 1996-01, Vol.211 (1), p.76-80
Hauptverfasser: Thyssen, Sandra M., Libertun, Carlos
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Libertun, Carlos
description Abstract FSH secretion is high in immature female rats from Postnatal Day 5 to 18 and decreases thereafter. This is a relatively steroid-independent event of cerebral origin and of importance for puberty onset. Polyamines, a group of ubiquitous amines, play an essential role in tissue growth and differentiation, body weight increment, brain organization, and molecular mechanisms of hormonal action. Polyamine levels as well as the activity of ornithine decarboxylase, the limiting enzyme in polyamines biosynthesis, are highest during development. Inhibition of their synthesis during this period by α-difluoromethylornithine (DFMO), a specific and irreversible inhibitor of ornithine decarboxylase, impairs normal brain development. The present study tested the hypothesis that polyamines play a role during brain organization of reproduction. DFMO was administered following different schedules in female newborn rats, and the effect on pituitary secretion, puberty onset, and fertility was evaluated. In three groups (daily injections from Day 1 to 9, or from Day 1 to 6, or injections on alternate days from Day 1 to 9), a delay in vaginal opening and first estrous was observed. When vaginal opening was plotted against body weight, it was evident that in groups daily injected with DFMO vaginal opening occurred at a lower body weight. In the group treated on alternate days, a delay occurred but at a higher body weight than in controls. In this group, serum FSH levels on Day 10 and 20, but not on Day 30, were higher in DFMO rats. In the group treated from Day 1 to 6 daily, DFMO increased serum FSH on Postnatal Day 20. After vaginal opening, estrous cyclicity in control and DFMO injected rats was similar. There was no significant effect of treatment on fertility and litter weight or number of offspring at birth. It is concluded that DFMO, an inhibitor of ornithine decarboxylase, administered during the first week of life in female rats is followed by prolonged high FSH serum levels and delayed puberty, but once puberty occurs, fertility is normal. [P.S.E.B.M. 1996, Vol 211]
doi_str_mv 10.3181/00379727-211-43954
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This is a relatively steroid-independent event of cerebral origin and of importance for puberty onset. Polyamines, a group of ubiquitous amines, play an essential role in tissue growth and differentiation, body weight increment, brain organization, and molecular mechanisms of hormonal action. Polyamine levels as well as the activity of ornithine decarboxylase, the limiting enzyme in polyamines biosynthesis, are highest during development. Inhibition of their synthesis during this period by α-difluoromethylornithine (DFMO), a specific and irreversible inhibitor of ornithine decarboxylase, impairs normal brain development. The present study tested the hypothesis that polyamines play a role during brain organization of reproduction. DFMO was administered following different schedules in female newborn rats, and the effect on pituitary secretion, puberty onset, and fertility was evaluated. In three groups (daily injections from Day 1 to 9, or from Day 1 to 6, or injections on alternate days from Day 1 to 9), a delay in vaginal opening and first estrous was observed. When vaginal opening was plotted against body weight, it was evident that in groups daily injected with DFMO vaginal opening occurred at a lower body weight. In the group treated on alternate days, a delay occurred but at a higher body weight than in controls. In this group, serum FSH levels on Day 10 and 20, but not on Day 30, were higher in DFMO rats. In the group treated from Day 1 to 6 daily, DFMO increased serum FSH on Postnatal Day 20. After vaginal opening, estrous cyclicity in control and DFMO injected rats was similar. There was no significant effect of treatment on fertility and litter weight or number of offspring at birth. It is concluded that DFMO, an inhibitor of ornithine decarboxylase, administered during the first week of life in female rats is followed by prolonged high FSH serum levels and delayed puberty, but once puberty occurs, fertility is normal. 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This is a relatively steroid-independent event of cerebral origin and of importance for puberty onset. Polyamines, a group of ubiquitous amines, play an essential role in tissue growth and differentiation, body weight increment, brain organization, and molecular mechanisms of hormonal action. Polyamine levels as well as the activity of ornithine decarboxylase, the limiting enzyme in polyamines biosynthesis, are highest during development. Inhibition of their synthesis during this period by α-difluoromethylornithine (DFMO), a specific and irreversible inhibitor of ornithine decarboxylase, impairs normal brain development. The present study tested the hypothesis that polyamines play a role during brain organization of reproduction. DFMO was administered following different schedules in female newborn rats, and the effect on pituitary secretion, puberty onset, and fertility was evaluated. In three groups (daily injections from Day 1 to 9, or from Day 1 to 6, or injections on alternate days from Day 1 to 9), a delay in vaginal opening and first estrous was observed. When vaginal opening was plotted against body weight, it was evident that in groups daily injected with DFMO vaginal opening occurred at a lower body weight. In the group treated on alternate days, a delay occurred but at a higher body weight than in controls. In this group, serum FSH levels on Day 10 and 20, but not on Day 30, were higher in DFMO rats. In the group treated from Day 1 to 6 daily, DFMO increased serum FSH on Postnatal Day 20. After vaginal opening, estrous cyclicity in control and DFMO injected rats was similar. There was no significant effect of treatment on fertility and litter weight or number of offspring at birth. It is concluded that DFMO, an inhibitor of ornithine decarboxylase, administered during the first week of life in female rats is followed by prolonged high FSH serum levels and delayed puberty, but once puberty occurs, fertility is normal. [P.S.E.B.M. 1996, Vol 211]</description><subject>Animals</subject><subject>Body Weight - drug effects</subject><subject>Eflornithine - pharmacology</subject><subject>Enzyme Inhibitors - pharmacology</subject><subject>Female</subject><subject>Follicle Stimulating Hormone - metabolism</subject><subject>Ornithine Decarboxylase Inhibitors</subject><subject>Prolactin - blood</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Sexual Maturation - drug effects</subject><issn>0037-9727</issn><issn>1535-3699</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUtOwzAURS0EKqWwASQkj5iF-hPb8RAVSpGKiigdW07yQl3lU2Jn0GWxEdZESsuY0RvcoyvddxC6puSO04SOCeFKK6YiRmkUcy3iEzSkgouIS61P0XAPRHviHF14vyGECsXkAA0SoWPJ2BCtvr-iB1eUXdM2FYT1rmza2oW1qwG_NLkrHHg8Xc7wErIWgmtqbOscv3YptGGHF7WHgF2NwxrwFCpbAn6z4RKdFbb0cHW8I7SaPr5PZtF88fQ8uZ9HW6ZUiDgHGcccNKiMS8Jipq3OM6KzJLVSJooRLYpMckkTkecyVzInltIk1YKm_bgRuj30btvmswMfTOV8BmVpa2g6b5TSUgil_gWpSKSQMe3BmyPYpRXkZtu6yrY7c3xYn48PubcfYDZN19b9QEOJ2Rsxf0ZMb8T8GuE_jT56lg</recordid><startdate>199601</startdate><enddate>199601</enddate><creator>Thyssen, Sandra M.</creator><creator>Libertun, Carlos</creator><general>SAGE Publications</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7TK</scope><scope>7X8</scope></search><sort><creationdate>199601</creationdate><title>α-Difluoromethylornithine Modifies FSH Secretion and Puberty Onset in the Female Rat</title><author>Thyssen, Sandra M. ; Libertun, Carlos</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p277t-33e6443e9e7c3602429a9dc09c8ba66872095fc636185dd6d76d0a118b951b003</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>Animals</topic><topic>Body Weight - drug effects</topic><topic>Eflornithine - pharmacology</topic><topic>Enzyme Inhibitors - pharmacology</topic><topic>Female</topic><topic>Follicle Stimulating Hormone - metabolism</topic><topic>Ornithine Decarboxylase Inhibitors</topic><topic>Prolactin - blood</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Sexual Maturation - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Thyssen, Sandra M.</creatorcontrib><creatorcontrib>Libertun, Carlos</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Proceedings of the Society for Experimental Biology and Medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Thyssen, Sandra M.</au><au>Libertun, Carlos</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>α-Difluoromethylornithine Modifies FSH Secretion and Puberty Onset in the Female Rat</atitle><jtitle>Proceedings of the Society for Experimental Biology and Medicine</jtitle><addtitle>Proc Soc Exp Biol Med</addtitle><date>1996-01</date><risdate>1996</risdate><volume>211</volume><issue>1</issue><spage>76</spage><epage>80</epage><pages>76-80</pages><issn>0037-9727</issn><eissn>1535-3699</eissn><abstract>Abstract FSH secretion is high in immature female rats from Postnatal Day 5 to 18 and decreases thereafter. This is a relatively steroid-independent event of cerebral origin and of importance for puberty onset. Polyamines, a group of ubiquitous amines, play an essential role in tissue growth and differentiation, body weight increment, brain organization, and molecular mechanisms of hormonal action. Polyamine levels as well as the activity of ornithine decarboxylase, the limiting enzyme in polyamines biosynthesis, are highest during development. Inhibition of their synthesis during this period by α-difluoromethylornithine (DFMO), a specific and irreversible inhibitor of ornithine decarboxylase, impairs normal brain development. The present study tested the hypothesis that polyamines play a role during brain organization of reproduction. DFMO was administered following different schedules in female newborn rats, and the effect on pituitary secretion, puberty onset, and fertility was evaluated. In three groups (daily injections from Day 1 to 9, or from Day 1 to 6, or injections on alternate days from Day 1 to 9), a delay in vaginal opening and first estrous was observed. When vaginal opening was plotted against body weight, it was evident that in groups daily injected with DFMO vaginal opening occurred at a lower body weight. In the group treated on alternate days, a delay occurred but at a higher body weight than in controls. In this group, serum FSH levels on Day 10 and 20, but not on Day 30, were higher in DFMO rats. In the group treated from Day 1 to 6 daily, DFMO increased serum FSH on Postnatal Day 20. After vaginal opening, estrous cyclicity in control and DFMO injected rats was similar. There was no significant effect of treatment on fertility and litter weight or number of offspring at birth. It is concluded that DFMO, an inhibitor of ornithine decarboxylase, administered during the first week of life in female rats is followed by prolonged high FSH serum levels and delayed puberty, but once puberty occurs, fertility is normal. [P.S.E.B.M. 1996, Vol 211]</abstract><cop>London, England</cop><pub>SAGE Publications</pub><pmid>8594622</pmid><doi>10.3181/00379727-211-43954</doi><tpages>5</tpages></addata></record>
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subjects Animals
Body Weight - drug effects
Eflornithine - pharmacology
Enzyme Inhibitors - pharmacology
Female
Follicle Stimulating Hormone - metabolism
Ornithine Decarboxylase Inhibitors
Prolactin - blood
Rats
Rats, Sprague-Dawley
Sexual Maturation - drug effects
title α-Difluoromethylornithine Modifies FSH Secretion and Puberty Onset in the Female Rat
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