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Brain oxytocin receptor antagonism disinhibits sodium appetite in preweanling rats
Previous studies have shown that preweanling rats do not express an endogenous sodium appetite until postnatal day 12. The present studies tested the hypothesis that prior to 12 days of age sodium appetite, induced by either central administration of angiotensin II (AngII) or adrenalectomy, is inhib...
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Published in: | Regulatory peptides 1997-01, Vol.68 (2), p.119-124 |
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creator | Chow, S.Y Sakai, R.R Fluharty, S.J Flanagan-Cato, L.M |
description | Previous studies have shown that preweanling rats do not express an endogenous sodium appetite until postnatal day 12. The present studies tested the hypothesis that prior to 12 days of age sodium appetite, induced by either central administration of angiotensin II (AngII) or adrenalectomy, is inhibited by endogenous oxytocin (OT). After 9- or 10-day old animals were given a central injection of either an OT receptor antagonist or vehicle, they were infused intraorally with 4% sodium chloride which the animals could either swallow or reject. Intake was measured as the increase from initial body weight. There was very little sodium consumption by vehicle-injected animals that received sham surgery or adrenalectomy; however, the OT receptor antagonist significantly elevated sodium consumption in adrenalectomized animals. The OT antagonist also potentiated sodium intake after AngII pretreatment. These results suggest that the neurochemical circuits necessary for the expression of sodium appetite are present and functional as early as postnatal day 9; however, until 12 days of age this behavior is suppressed by endogenous OT. |
doi_str_mv | 10.1016/S0167-0115(96)02114-3 |
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The present studies tested the hypothesis that prior to 12 days of age sodium appetite, induced by either central administration of angiotensin II (AngII) or adrenalectomy, is inhibited by endogenous oxytocin (OT). After 9- or 10-day old animals were given a central injection of either an OT receptor antagonist or vehicle, they were infused intraorally with 4% sodium chloride which the animals could either swallow or reject. Intake was measured as the increase from initial body weight. There was very little sodium consumption by vehicle-injected animals that received sham surgery or adrenalectomy; however, the OT receptor antagonist significantly elevated sodium consumption in adrenalectomized animals. The OT antagonist also potentiated sodium intake after AngII pretreatment. These results suggest that the neurochemical circuits necessary for the expression of sodium appetite are present and functional as early as postnatal day 9; however, until 12 days of age this behavior is suppressed by endogenous OT.</description><identifier>ISSN: 0167-0115</identifier><identifier>EISSN: 1873-1686</identifier><identifier>DOI: 10.1016/S0167-0115(96)02114-3</identifier><identifier>PMID: 9110383</identifier><identifier>CODEN: REPPDY</identifier><language>eng</language><publisher>Shannon: Elsevier B.V</publisher><subject>Adrenalectomy ; Angiotensin II ; Angiotensin II - pharmacology ; Animals ; Animals, Newborn ; Appetite - drug effects ; Appetite - physiology ; Biological and medical sciences ; Body Weight - drug effects ; Brain - metabolism ; Development ; Electrolyte balance ; Feeding Behavior - drug effects ; Fundamental and applied biological sciences. Psychology ; Ingestive behavior ; Metabolisms and neurohumoral controls ; Milk ; Oxytocin - pharmacology ; Rats ; Rats, Sprague-Dawley ; Receptors, Oxytocin - antagonists & inhibitors ; Sodium - administration & dosage ; Vasotocin - analogs & derivatives ; Vasotocin - pharmacology ; Vertebrates: anatomy and physiology, studies on body, several organs or systems ; Water and mineral metabolism. Osmoregulation. Acidobasic balance</subject><ispartof>Regulatory peptides, 1997-01, Vol.68 (2), p.119-124</ispartof><rights>1997 Elsevier Science B.V.</rights><rights>1997 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c436t-bf4d9da75778ab0862edb9a71d795e7e9a4fb28a5df9698d0c68e1302a8fcbe33</citedby><cites>FETCH-LOGICAL-c436t-bf4d9da75778ab0862edb9a71d795e7e9a4fb28a5df9698d0c68e1302a8fcbe33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2615214$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9110383$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chow, S.Y</creatorcontrib><creatorcontrib>Sakai, R.R</creatorcontrib><creatorcontrib>Fluharty, S.J</creatorcontrib><creatorcontrib>Flanagan-Cato, L.M</creatorcontrib><title>Brain oxytocin receptor antagonism disinhibits sodium appetite in preweanling rats</title><title>Regulatory peptides</title><addtitle>Regul Pept</addtitle><description>Previous studies have shown that preweanling rats do not express an endogenous sodium appetite until postnatal day 12. The present studies tested the hypothesis that prior to 12 days of age sodium appetite, induced by either central administration of angiotensin II (AngII) or adrenalectomy, is inhibited by endogenous oxytocin (OT). After 9- or 10-day old animals were given a central injection of either an OT receptor antagonist or vehicle, they were infused intraorally with 4% sodium chloride which the animals could either swallow or reject. Intake was measured as the increase from initial body weight. There was very little sodium consumption by vehicle-injected animals that received sham surgery or adrenalectomy; however, the OT receptor antagonist significantly elevated sodium consumption in adrenalectomized animals. The OT antagonist also potentiated sodium intake after AngII pretreatment. These results suggest that the neurochemical circuits necessary for the expression of sodium appetite are present and functional as early as postnatal day 9; however, until 12 days of age this behavior is suppressed by endogenous OT.</description><subject>Adrenalectomy</subject><subject>Angiotensin II</subject><subject>Angiotensin II - pharmacology</subject><subject>Animals</subject><subject>Animals, Newborn</subject><subject>Appetite - drug effects</subject><subject>Appetite - physiology</subject><subject>Biological and medical sciences</subject><subject>Body Weight - drug effects</subject><subject>Brain - metabolism</subject><subject>Development</subject><subject>Electrolyte balance</subject><subject>Feeding Behavior - drug effects</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Ingestive behavior</subject><subject>Metabolisms and neurohumoral controls</subject><subject>Milk</subject><subject>Oxytocin - pharmacology</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Receptors, Oxytocin - antagonists & inhibitors</subject><subject>Sodium - administration & dosage</subject><subject>Vasotocin - analogs & derivatives</subject><subject>Vasotocin - pharmacology</subject><subject>Vertebrates: anatomy and physiology, studies on body, several organs or systems</subject><subject>Water and mineral metabolism. Osmoregulation. Acidobasic balance</subject><issn>0167-0115</issn><issn>1873-1686</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><recordid>eNqFkEtv1DAQgC0EKtvCT6iUA0JwCLXjxI8TgooCUqVKPM7WxJ4Uo8QOtrfQf4-3u9prLzMjzTcPfYScM_qOUSYuvtcgW8rY8EaLt7RjrG_5E7JhSvKWCSWeks0ReU5Oc_5NKRuk5CfkRDNGueIb8u1jAh-a-O--RFuLhBbXElMDocBtDD4vjfPZh19-9CU3OTq_XRpYVyy-YFNH1oR_EcLsw22ToOQX5NkEc8aXh3xGfl59-nH5pb2--fz18sN1a3suSjtOvdMOZP1IwUiV6NCNGiRzUg8oUUM_jZ2CwU1aaOWoFQoZpx2oyY7I-Rl5vd-7pvhni7mYxWeL8wwB4zYbqfSgej5UcNiDNsWcE05mTX6BdG8YNTuX5sGl2YkyWpgHl2Z34PxwYDsu6I5TB3m1_-rQh2xhnhIE6_MR6wQbOtZX7P0ewyrjzmMy2XoMFp2vtotx0T_yyH-cKpIS</recordid><startdate>19970129</startdate><enddate>19970129</enddate><creator>Chow, S.Y</creator><creator>Sakai, R.R</creator><creator>Fluharty, S.J</creator><creator>Flanagan-Cato, L.M</creator><general>Elsevier B.V</general><general>Elsevier</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>7X8</scope></search><sort><creationdate>19970129</creationdate><title>Brain oxytocin receptor antagonism disinhibits sodium appetite in preweanling rats</title><author>Chow, S.Y ; Sakai, R.R ; Fluharty, S.J ; Flanagan-Cato, L.M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c436t-bf4d9da75778ab0862edb9a71d795e7e9a4fb28a5df9698d0c68e1302a8fcbe33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Adrenalectomy</topic><topic>Angiotensin II</topic><topic>Angiotensin II - pharmacology</topic><topic>Animals</topic><topic>Animals, Newborn</topic><topic>Appetite - drug effects</topic><topic>Appetite - physiology</topic><topic>Biological and medical sciences</topic><topic>Body Weight - drug effects</topic><topic>Brain - metabolism</topic><topic>Development</topic><topic>Electrolyte balance</topic><topic>Feeding Behavior - drug effects</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Ingestive behavior</topic><topic>Metabolisms and neurohumoral controls</topic><topic>Milk</topic><topic>Oxytocin - pharmacology</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Receptors, Oxytocin - antagonists & inhibitors</topic><topic>Sodium - administration & dosage</topic><topic>Vasotocin - analogs & derivatives</topic><topic>Vasotocin - pharmacology</topic><topic>Vertebrates: anatomy and physiology, studies on body, several organs or systems</topic><topic>Water and mineral metabolism. Osmoregulation. Acidobasic balance</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chow, S.Y</creatorcontrib><creatorcontrib>Sakai, R.R</creatorcontrib><creatorcontrib>Fluharty, S.J</creatorcontrib><creatorcontrib>Flanagan-Cato, L.M</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>MEDLINE - Academic</collection><jtitle>Regulatory peptides</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chow, S.Y</au><au>Sakai, R.R</au><au>Fluharty, S.J</au><au>Flanagan-Cato, L.M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Brain oxytocin receptor antagonism disinhibits sodium appetite in preweanling rats</atitle><jtitle>Regulatory peptides</jtitle><addtitle>Regul Pept</addtitle><date>1997-01-29</date><risdate>1997</risdate><volume>68</volume><issue>2</issue><spage>119</spage><epage>124</epage><pages>119-124</pages><issn>0167-0115</issn><eissn>1873-1686</eissn><coden>REPPDY</coden><abstract>Previous studies have shown that preweanling rats do not express an endogenous sodium appetite until postnatal day 12. The present studies tested the hypothesis that prior to 12 days of age sodium appetite, induced by either central administration of angiotensin II (AngII) or adrenalectomy, is inhibited by endogenous oxytocin (OT). After 9- or 10-day old animals were given a central injection of either an OT receptor antagonist or vehicle, they were infused intraorally with 4% sodium chloride which the animals could either swallow or reject. Intake was measured as the increase from initial body weight. There was very little sodium consumption by vehicle-injected animals that received sham surgery or adrenalectomy; however, the OT receptor antagonist significantly elevated sodium consumption in adrenalectomized animals. The OT antagonist also potentiated sodium intake after AngII pretreatment. These results suggest that the neurochemical circuits necessary for the expression of sodium appetite are present and functional as early as postnatal day 9; however, until 12 days of age this behavior is suppressed by endogenous OT.</abstract><cop>Shannon</cop><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>9110383</pmid><doi>10.1016/S0167-0115(96)02114-3</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adrenalectomy Angiotensin II Angiotensin II - pharmacology Animals Animals, Newborn Appetite - drug effects Appetite - physiology Biological and medical sciences Body Weight - drug effects Brain - metabolism Development Electrolyte balance Feeding Behavior - drug effects Fundamental and applied biological sciences. Psychology Ingestive behavior Metabolisms and neurohumoral controls Milk Oxytocin - pharmacology Rats Rats, Sprague-Dawley Receptors, Oxytocin - antagonists & inhibitors Sodium - administration & dosage Vasotocin - analogs & derivatives Vasotocin - pharmacology Vertebrates: anatomy and physiology, studies on body, several organs or systems Water and mineral metabolism. Osmoregulation. Acidobasic balance |
title | Brain oxytocin receptor antagonism disinhibits sodium appetite in preweanling rats |
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