Antagonism of Oxytocin Prevents Suckling- and Estradiol-Induced, But Not Progesterone-Induced, Secretion of Prolactin
In female rats, estradiol (E2) and suckling induce prolactin (PRL) secretion. This involves inhibition of hypothalamic dopaminergic tone and stimulation by a PRL-releasing hormone, possibly oxytocin (OT). Infusing an OT antagonist (OTA) iv, we evaluated the role of OT on suckling- and E2-induced PRL...
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description | In female rats, estradiol (E2) and suckling induce prolactin (PRL) secretion. This involves inhibition of hypothalamic dopaminergic tone and stimulation by a PRL-releasing hormone, possibly oxytocin (OT). Infusing an OT antagonist (OTA) iv, we evaluated the role of OT on suckling- and E2-induced PRL secretion. Three days after parturition at 0900 h, lactating dams were fitted with 24-h osmotic minipumps filled with saline or OTA. On d 5 of lactation, pups were separated from their dams for 6 h. Immediately or 20 min after the resumption of suckling, dam trunk blood was collected. Also, ovariectomized (OVX) rats were treated with E2 (OVE) and OTA at 1000 h on d 1. Blood samples were obtained from 1300 to 2100 h on d 2 for PRL measurements. Additionally, OVX rats were evaluated on d 2 after receiving progesterone (P4). OTA blocked suckling and E2-induced release of PRL but not that induced by E2+P4. Pups from treated dams failed to gain weight when allowed to nurse for 20 min on d 5 but gained more than 7 g when nursed on d 7 of lactation, indicating that the OTA was active 48 h later. Western blot analysis showed that E2 treatment increased OT receptors in the anterior pituitary when compared with OVX animals. No further increase was observed in response to the P4, suggesting that the enhancing effect of P4 on E2-induced PRL release may act through mechanisms independent of OT. These data demonstrate the role of OT in the control of suckling and steroid-induced PRL secretion.
Oxytocin controls the steroid-induced and suckling-induced release of prolactin. |
doi_str_mv | 10.1210/en.2008-1611 |
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Oxytocin controls the steroid-induced and suckling-induced release of prolactin.</description><identifier>ISSN: 0013-7227</identifier><identifier>EISSN: 1945-7170</identifier><identifier>DOI: 10.1210/en.2008-1611</identifier><identifier>PMID: 19106214</identifier><identifier>CODEN: ENDOAO</identifier><language>eng</language><publisher>Chevy Chase, MD: Endocrine Society</publisher><subject>17β-Estradiol ; Animals ; Animals, Newborn ; Animals, Suckling ; Biological and medical sciences ; Blood ; Breastfeeding & lactation ; Dopamine receptors ; Estradiol - pharmacology ; Female ; Fundamental and applied biological sciences. Psychology ; Hormones ; Hypothalamus ; Infusion Pumps ; Juveniles ; Lactation ; Lactation - drug effects ; Ornipressin - administration & dosage ; Ornipressin - analogs & derivatives ; Ornipressin - pharmacology ; Ovariectomy ; Ovariectomy - veterinary ; Oxytocin ; Oxytocin - antagonists & inhibitors ; Oxytocin - physiology ; Parturition ; Pituitary (anterior) ; Progesterone ; Progesterone - pharmacology ; Prolactin ; Prolactin - secretion ; Rats ; Rats, Sprague-Dawley ; Secretion ; Sex hormones ; Sucking Behavior - drug effects ; Suckling behavior ; Vertebrates: endocrinology</subject><ispartof>Endocrinology (Philadelphia), 2009-05, Vol.150 (5), p.2292-2299</ispartof><rights>Copyright © 2009 by The Endocrine Society 2009</rights><rights>2009 INIST-CNRS</rights><rights>Copyright © 2009 by The Endocrine Society</rights><rights>Copyright © 2009 by The Endocrine Society 2009</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c516t-f495b9324cb5a613d92ecc001e76be3e2c7334e6e9483e1c631d5d44e9d073303</citedby><cites>FETCH-LOGICAL-c516t-f495b9324cb5a613d92ecc001e76be3e2c7334e6e9483e1c631d5d44e9d073303</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=21453251$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19106214$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kennett, Jessica E</creatorcontrib><creatorcontrib>Poletini, Maristela O</creatorcontrib><creatorcontrib>Fitch, Cheryl A</creatorcontrib><creatorcontrib>Freeman, Marc E</creatorcontrib><title>Antagonism of Oxytocin Prevents Suckling- and Estradiol-Induced, But Not Progesterone-Induced, Secretion of Prolactin</title><title>Endocrinology (Philadelphia)</title><addtitle>Endocrinology</addtitle><description>In female rats, estradiol (E2) and suckling induce prolactin (PRL) secretion. This involves inhibition of hypothalamic dopaminergic tone and stimulation by a PRL-releasing hormone, possibly oxytocin (OT). Infusing an OT antagonist (OTA) iv, we evaluated the role of OT on suckling- and E2-induced PRL secretion. Three days after parturition at 0900 h, lactating dams were fitted with 24-h osmotic minipumps filled with saline or OTA. On d 5 of lactation, pups were separated from their dams for 6 h. Immediately or 20 min after the resumption of suckling, dam trunk blood was collected. Also, ovariectomized (OVX) rats were treated with E2 (OVE) and OTA at 1000 h on d 1. Blood samples were obtained from 1300 to 2100 h on d 2 for PRL measurements. Additionally, OVX rats were evaluated on d 2 after receiving progesterone (P4). OTA blocked suckling and E2-induced release of PRL but not that induced by E2+P4. Pups from treated dams failed to gain weight when allowed to nurse for 20 min on d 5 but gained more than 7 g when nursed on d 7 of lactation, indicating that the OTA was active 48 h later. Western blot analysis showed that E2 treatment increased OT receptors in the anterior pituitary when compared with OVX animals. No further increase was observed in response to the P4, suggesting that the enhancing effect of P4 on E2-induced PRL release may act through mechanisms independent of OT. These data demonstrate the role of OT in the control of suckling and steroid-induced PRL secretion.
Oxytocin controls the steroid-induced and suckling-induced release of prolactin.</description><subject>17β-Estradiol</subject><subject>Animals</subject><subject>Animals, Newborn</subject><subject>Animals, Suckling</subject><subject>Biological and medical sciences</subject><subject>Blood</subject><subject>Breastfeeding & lactation</subject><subject>Dopamine receptors</subject><subject>Estradiol - pharmacology</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Hormones</subject><subject>Hypothalamus</subject><subject>Infusion Pumps</subject><subject>Juveniles</subject><subject>Lactation</subject><subject>Lactation - drug effects</subject><subject>Ornipressin - administration & dosage</subject><subject>Ornipressin - analogs & derivatives</subject><subject>Ornipressin - pharmacology</subject><subject>Ovariectomy</subject><subject>Ovariectomy - veterinary</subject><subject>Oxytocin</subject><subject>Oxytocin - antagonists & inhibitors</subject><subject>Oxytocin - physiology</subject><subject>Parturition</subject><subject>Pituitary (anterior)</subject><subject>Progesterone</subject><subject>Progesterone - pharmacology</subject><subject>Prolactin</subject><subject>Prolactin - secretion</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Secretion</subject><subject>Sex hormones</subject><subject>Sucking Behavior - drug effects</subject><subject>Suckling behavior</subject><subject>Vertebrates: endocrinology</subject><issn>0013-7227</issn><issn>1945-7170</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kVFrFDEUhYModlt981kGRPrSqblJJrPzItRStVCsUH0O2eTOmjqbbJNMsf_eDDt0FfQphPvdc8_hEPIK6CkwoO_QnzJKlzVIgCdkAZ1o6hZa-pQsKAVet4y1B-QwpdvyFULw5-QAOqCSgViQ8cxnvQ7epU0V-ur610MOxvnqa8R79DlVN6P5OTi_rivtbXWRctTWhaG-9HY0aE-qD2OuvoRcNsIaU8YYPO6nN2giZhf8pF6QQZvs_AvyrNdDwpfze0S-f7z4dv65vrr-dHl-dlWbBmSue9E1q44zYVaNlsBtx9CYEgNbuUKOzLScC5TYiSVHMJKDbawQ2FlaJpQfkfc73e242qA1JVHUg9pGt9HxQQXt1N8T736odbhXTLbQUV4E3swCMdyNJZ66DWP0xbPiwGnTySWVhTrZUSaGlCL2jxeAqqkkhV5NJamppIK__tPVHp5bKcDbGdDJ6KGP2huXHrmCNJw1k9Dxjgvj9n8n6_kk35HobTDRedxGTGmf5p9GfwN9CLfy</recordid><startdate>20090501</startdate><enddate>20090501</enddate><creator>Kennett, Jessica E</creator><creator>Poletini, Maristela O</creator><creator>Fitch, Cheryl A</creator><creator>Freeman, Marc E</creator><general>Endocrine Society</general><general>Oxford University Press</general><general>The Endocrine Society</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>7QG</scope><scope>7QP</scope><scope>7QR</scope><scope>7T5</scope><scope>7TM</scope><scope>7TO</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>P64</scope><scope>5PM</scope></search><sort><creationdate>20090501</creationdate><title>Antagonism of Oxytocin Prevents Suckling- and Estradiol-Induced, But Not Progesterone-Induced, Secretion of Prolactin</title><author>Kennett, Jessica E ; Poletini, Maristela O ; Fitch, Cheryl A ; Freeman, Marc E</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c516t-f495b9324cb5a613d92ecc001e76be3e2c7334e6e9483e1c631d5d44e9d073303</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>17β-Estradiol</topic><topic>Animals</topic><topic>Animals, Newborn</topic><topic>Animals, Suckling</topic><topic>Biological and medical sciences</topic><topic>Blood</topic><topic>Breastfeeding & lactation</topic><topic>Dopamine receptors</topic><topic>Estradiol - pharmacology</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Hormones</topic><topic>Hypothalamus</topic><topic>Infusion Pumps</topic><topic>Juveniles</topic><topic>Lactation</topic><topic>Lactation - drug effects</topic><topic>Ornipressin - administration & dosage</topic><topic>Ornipressin - analogs & derivatives</topic><topic>Ornipressin - pharmacology</topic><topic>Ovariectomy</topic><topic>Ovariectomy - veterinary</topic><topic>Oxytocin</topic><topic>Oxytocin - antagonists & inhibitors</topic><topic>Oxytocin - physiology</topic><topic>Parturition</topic><topic>Pituitary (anterior)</topic><topic>Progesterone</topic><topic>Progesterone - pharmacology</topic><topic>Prolactin</topic><topic>Prolactin - secretion</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Secretion</topic><topic>Sex hormones</topic><topic>Sucking Behavior - drug effects</topic><topic>Suckling behavior</topic><topic>Vertebrates: endocrinology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kennett, Jessica E</creatorcontrib><creatorcontrib>Poletini, Maristela O</creatorcontrib><creatorcontrib>Fitch, Cheryl A</creatorcontrib><creatorcontrib>Freeman, Marc E</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>Animal Behavior Abstracts</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Immunology Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Endocrinology (Philadelphia)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kennett, Jessica E</au><au>Poletini, Maristela O</au><au>Fitch, Cheryl A</au><au>Freeman, Marc E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Antagonism of Oxytocin Prevents Suckling- and Estradiol-Induced, But Not Progesterone-Induced, Secretion of Prolactin</atitle><jtitle>Endocrinology (Philadelphia)</jtitle><addtitle>Endocrinology</addtitle><date>2009-05-01</date><risdate>2009</risdate><volume>150</volume><issue>5</issue><spage>2292</spage><epage>2299</epage><pages>2292-2299</pages><issn>0013-7227</issn><eissn>1945-7170</eissn><coden>ENDOAO</coden><abstract>In female rats, estradiol (E2) and suckling induce prolactin (PRL) secretion. This involves inhibition of hypothalamic dopaminergic tone and stimulation by a PRL-releasing hormone, possibly oxytocin (OT). Infusing an OT antagonist (OTA) iv, we evaluated the role of OT on suckling- and E2-induced PRL secretion. Three days after parturition at 0900 h, lactating dams were fitted with 24-h osmotic minipumps filled with saline or OTA. On d 5 of lactation, pups were separated from their dams for 6 h. Immediately or 20 min after the resumption of suckling, dam trunk blood was collected. Also, ovariectomized (OVX) rats were treated with E2 (OVE) and OTA at 1000 h on d 1. Blood samples were obtained from 1300 to 2100 h on d 2 for PRL measurements. Additionally, OVX rats were evaluated on d 2 after receiving progesterone (P4). OTA blocked suckling and E2-induced release of PRL but not that induced by E2+P4. Pups from treated dams failed to gain weight when allowed to nurse for 20 min on d 5 but gained more than 7 g when nursed on d 7 of lactation, indicating that the OTA was active 48 h later. Western blot analysis showed that E2 treatment increased OT receptors in the anterior pituitary when compared with OVX animals. No further increase was observed in response to the P4, suggesting that the enhancing effect of P4 on E2-induced PRL release may act through mechanisms independent of OT. These data demonstrate the role of OT in the control of suckling and steroid-induced PRL secretion.
Oxytocin controls the steroid-induced and suckling-induced release of prolactin.</abstract><cop>Chevy Chase, MD</cop><pub>Endocrine Society</pub><pmid>19106214</pmid><doi>10.1210/en.2008-1611</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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source | Oxford University Press Journals All Titles (1996-Current); MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection |
subjects | 17β-Estradiol Animals Animals, Newborn Animals, Suckling Biological and medical sciences Blood Breastfeeding & lactation Dopamine receptors Estradiol - pharmacology Female Fundamental and applied biological sciences. Psychology Hormones Hypothalamus Infusion Pumps Juveniles Lactation Lactation - drug effects Ornipressin - administration & dosage Ornipressin - analogs & derivatives Ornipressin - pharmacology Ovariectomy Ovariectomy - veterinary Oxytocin Oxytocin - antagonists & inhibitors Oxytocin - physiology Parturition Pituitary (anterior) Progesterone Progesterone - pharmacology Prolactin Prolactin - secretion Rats Rats, Sprague-Dawley Secretion Sex hormones Sucking Behavior - drug effects Suckling behavior Vertebrates: endocrinology |
title | Antagonism of Oxytocin Prevents Suckling- and Estradiol-Induced, But Not Progesterone-Induced, Secretion of Prolactin |
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