Functional relationship between oxytocin and appetite for carbohydrates versus saccharin
Centrally acting oxytocin (OT) inhibits feeding. Recent evidence suggests a link between OT and control of carbohydrate and saccharin intake, but it is unclear whether OT affects appetite for only carbohydrates, especially sweet ones, or sweet tastants irrespective of their carbohydrate content. The...
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Veröffentlicht in: | Neuroreport 2014-08, Vol.25 (12), p.909-914 |
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description | Centrally acting oxytocin (OT) inhibits feeding. Recent evidence suggests a link between OT and control of carbohydrate and saccharin intake, but it is unclear whether OT affects appetite for only carbohydrates, especially sweet ones, or sweet tastants irrespective of their carbohydrate content. Therefore, a blood–brain barrier penetrant OT receptor antagonist, L-368,899, was administered in mice and intake of liquid diets containing carbohydrates sucrose, glucose, fructose, polycose, or cornstarch (CS) or the noncarbohydrate, noncaloric sweetener saccharin was studied in episodic intake paradigmsone in which only one tastant was available and the other in which a choice between a carbohydrate (sucrose, glucose, or fructose) and saccharin was provided. We also used real-time PCR to examine hypothalamic Ot mRNA levels in mice provided short-term access to sucrose, CS, or saccharin. In the no-choice paradigm, L-368,899 increased the intake of all carbohydrates, whereas its effect on saccharin consumption showed only a trend. A 10 times lower dose (0.3 mg/kg) stimulated intake of sucrose than other carbohydrates. In the choice test, a very low 0.1 mg/kg dose of L-368,899 doubled the proportion of sucrose consumption relative to saccharin, but did not affect fructose or glucose preference. Ot gene expression increased after sucrose and CS, but not saccharin exposure compared with the controls; however, a higher level of significance was detected in the sucrose group. We conclude that OT inhibits appetite for carbohydrates. Sucrose consumption considerably enhances Ot gene expression and is particularly sensitive to OT receptor blockade, suggesting a special functional relationship between OT and sugar intake. |
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Recent evidence suggests a link between OT and control of carbohydrate and saccharin intake, but it is unclear whether OT affects appetite for only carbohydrates, especially sweet ones, or sweet tastants irrespective of their carbohydrate content. Therefore, a blood–brain barrier penetrant OT receptor antagonist, L-368,899, was administered in mice and intake of liquid diets containing carbohydrates sucrose, glucose, fructose, polycose, or cornstarch (CS) or the noncarbohydrate, noncaloric sweetener saccharin was studied in episodic intake paradigmsone in which only one tastant was available and the other in which a choice between a carbohydrate (sucrose, glucose, or fructose) and saccharin was provided. We also used real-time PCR to examine hypothalamic Ot mRNA levels in mice provided short-term access to sucrose, CS, or saccharin. In the no-choice paradigm, L-368,899 increased the intake of all carbohydrates, whereas its effect on saccharin consumption showed only a trend. A 10 times lower dose (0.3 mg/kg) stimulated intake of sucrose than other carbohydrates. In the choice test, a very low 0.1 mg/kg dose of L-368,899 doubled the proportion of sucrose consumption relative to saccharin, but did not affect fructose or glucose preference. Ot gene expression increased after sucrose and CS, but not saccharin exposure compared with the controls; however, a higher level of significance was detected in the sucrose group. We conclude that OT inhibits appetite for carbohydrates. Sucrose consumption considerably enhances Ot gene expression and is particularly sensitive to OT receptor blockade, suggesting a special functional relationship between OT and sugar intake.</description><identifier>ISSN: 0959-4965</identifier><identifier>EISSN: 1473-558X</identifier><identifier>DOI: 10.1097/WNR.0000000000000201</identifier><identifier>PMID: 24893201</identifier><language>eng</language><publisher>Hagerstown, MD: Wolters Kluwer Health | Lippincott Williams & Wilkins</publisher><subject>Animals ; Appetite - drug effects ; Appetite - physiology ; Biological and medical sciences ; Bornanes - pharmacology ; Central Nervous System Agents - pharmacology ; Choice Behavior - drug effects ; Choice Behavior - physiology ; Dietary Carbohydrates - administration & dosage ; Dose-Response Relationship, Drug ; Food Preferences - drug effects ; Food Preferences - physiology ; Fundamental and applied biological sciences. Psychology ; Hypothalamus - drug effects ; Hypothalamus - physiology ; Male ; Mice, Inbred C57BL ; Oxytocin - metabolism ; Piperazines - pharmacology ; Receptors, Oxytocin - antagonists & inhibitors ; Receptors, Oxytocin - metabolism ; RNA, Messenger - metabolism ; Saccharin - administration & dosage ; Vertebrates: nervous system and sense organs</subject><ispartof>Neuroreport, 2014-08, Vol.25 (12), p.909-914</ispartof><rights>2014 Wolters Kluwer Health | Lippincott Williams & Wilkins</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5181-a4fe1fca0bf35a0a7092d67d210591cdd42dcb860ad081f12d5507fcba3bc3713</citedby><cites>FETCH-LOGICAL-c5181-a4fe1fca0bf35a0a7092d67d210591cdd42dcb860ad081f12d5507fcba3bc3713</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,27929,27930</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=28613165$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24893201$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Herisson, Florence M</creatorcontrib><creatorcontrib>Brooks, Lydia L</creatorcontrib><creatorcontrib>Waas, Joseph R</creatorcontrib><creatorcontrib>Levine, Allen S</creatorcontrib><creatorcontrib>Olszewski, Pawel K</creatorcontrib><title>Functional relationship between oxytocin and appetite for carbohydrates versus saccharin</title><title>Neuroreport</title><addtitle>Neuroreport</addtitle><description>Centrally acting oxytocin (OT) inhibits feeding. Recent evidence suggests a link between OT and control of carbohydrate and saccharin intake, but it is unclear whether OT affects appetite for only carbohydrates, especially sweet ones, or sweet tastants irrespective of their carbohydrate content. Therefore, a blood–brain barrier penetrant OT receptor antagonist, L-368,899, was administered in mice and intake of liquid diets containing carbohydrates sucrose, glucose, fructose, polycose, or cornstarch (CS) or the noncarbohydrate, noncaloric sweetener saccharin was studied in episodic intake paradigmsone in which only one tastant was available and the other in which a choice between a carbohydrate (sucrose, glucose, or fructose) and saccharin was provided. We also used real-time PCR to examine hypothalamic Ot mRNA levels in mice provided short-term access to sucrose, CS, or saccharin. In the no-choice paradigm, L-368,899 increased the intake of all carbohydrates, whereas its effect on saccharin consumption showed only a trend. A 10 times lower dose (0.3 mg/kg) stimulated intake of sucrose than other carbohydrates. In the choice test, a very low 0.1 mg/kg dose of L-368,899 doubled the proportion of sucrose consumption relative to saccharin, but did not affect fructose or glucose preference. Ot gene expression increased after sucrose and CS, but not saccharin exposure compared with the controls; however, a higher level of significance was detected in the sucrose group. We conclude that OT inhibits appetite for carbohydrates. Sucrose consumption considerably enhances Ot gene expression and is particularly sensitive to OT receptor blockade, suggesting a special functional relationship between OT and sugar intake.</description><subject>Animals</subject><subject>Appetite - drug effects</subject><subject>Appetite - physiology</subject><subject>Biological and medical sciences</subject><subject>Bornanes - pharmacology</subject><subject>Central Nervous System Agents - pharmacology</subject><subject>Choice Behavior - drug effects</subject><subject>Choice Behavior - physiology</subject><subject>Dietary Carbohydrates - administration & dosage</subject><subject>Dose-Response Relationship, Drug</subject><subject>Food Preferences - drug effects</subject><subject>Food Preferences - physiology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Hypothalamus - drug effects</subject><subject>Hypothalamus - physiology</subject><subject>Male</subject><subject>Mice, Inbred C57BL</subject><subject>Oxytocin - metabolism</subject><subject>Piperazines - pharmacology</subject><subject>Receptors, Oxytocin - antagonists & inhibitors</subject><subject>Receptors, Oxytocin - metabolism</subject><subject>RNA, Messenger - metabolism</subject><subject>Saccharin - administration & dosage</subject><subject>Vertebrates: nervous system and sense organs</subject><issn>0959-4965</issn><issn>1473-558X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0Mtu1DAUgGELgejQ8gao8gaJTVqf2E7iJaooIFWthFq1u-jEFyXgiYPtMJ23J9VMoeoCvLEX37Gtn5B3wE6Aqfr09vLbCXu6SgYvyApEzQspm7uXZMWUVIVQlTwgb1L6vhjFoHlNDkrRKL74Fbk7n0edhzCip9F6fDimfphoZ_PG2pGG-20OehgpjobiNNk8ZEtdiFRj7EK_NRGzTfSXjWlONKHWPcZhPCKvHPpk3-73Q3Jz_un67EtxcfX569nHi0JLaKBA4Sw4jaxzXCLDmqnSVLUpgUkF2hhRGt01FUPDGnBQGilZ7XSHvNO8Bn5IPuzunWL4OduU2_WQtPUeRxvm1ELFJRMMlPg_lULwslRVvVCxozqGlKJ17RSHNcZtC6x9yN8u-dvn-Zex4_0Lc7e25s_QY-8FvN8DTBq9izjqIf11TQUcKrm4Zuc2weel7A8_b2xse4s-9__-w2_Xb593</recordid><startdate>20140820</startdate><enddate>20140820</enddate><creator>Herisson, Florence M</creator><creator>Brooks, Lydia L</creator><creator>Waas, Joseph R</creator><creator>Levine, Allen S</creator><creator>Olszewski, Pawel K</creator><general>Wolters Kluwer Health | Lippincott Williams & Wilkins</general><general>Lippincott Williams & Wilkins</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><scope>7TK</scope></search><sort><creationdate>20140820</creationdate><title>Functional relationship between oxytocin and appetite for carbohydrates versus saccharin</title><author>Herisson, Florence M ; Brooks, Lydia L ; Waas, Joseph R ; Levine, Allen S ; Olszewski, Pawel K</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5181-a4fe1fca0bf35a0a7092d67d210591cdd42dcb860ad081f12d5507fcba3bc3713</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Animals</topic><topic>Appetite - drug effects</topic><topic>Appetite - physiology</topic><topic>Biological and medical sciences</topic><topic>Bornanes - pharmacology</topic><topic>Central Nervous System Agents - pharmacology</topic><topic>Choice Behavior - drug effects</topic><topic>Choice Behavior - physiology</topic><topic>Dietary Carbohydrates - administration & dosage</topic><topic>Dose-Response Relationship, Drug</topic><topic>Food Preferences - drug effects</topic><topic>Food Preferences - physiology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Hypothalamus - drug effects</topic><topic>Hypothalamus - physiology</topic><topic>Male</topic><topic>Mice, Inbred C57BL</topic><topic>Oxytocin - metabolism</topic><topic>Piperazines - pharmacology</topic><topic>Receptors, Oxytocin - antagonists & inhibitors</topic><topic>Receptors, Oxytocin - metabolism</topic><topic>RNA, Messenger - metabolism</topic><topic>Saccharin - administration & dosage</topic><topic>Vertebrates: nervous system and sense organs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Herisson, Florence M</creatorcontrib><creatorcontrib>Brooks, Lydia L</creatorcontrib><creatorcontrib>Waas, Joseph R</creatorcontrib><creatorcontrib>Levine, Allen S</creatorcontrib><creatorcontrib>Olszewski, Pawel K</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><collection>Neurosciences Abstracts</collection><jtitle>Neuroreport</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Herisson, Florence M</au><au>Brooks, Lydia L</au><au>Waas, Joseph R</au><au>Levine, Allen S</au><au>Olszewski, Pawel K</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Functional relationship between oxytocin and appetite for carbohydrates versus saccharin</atitle><jtitle>Neuroreport</jtitle><addtitle>Neuroreport</addtitle><date>2014-08-20</date><risdate>2014</risdate><volume>25</volume><issue>12</issue><spage>909</spage><epage>914</epage><pages>909-914</pages><issn>0959-4965</issn><eissn>1473-558X</eissn><abstract>Centrally acting oxytocin (OT) inhibits feeding. Recent evidence suggests a link between OT and control of carbohydrate and saccharin intake, but it is unclear whether OT affects appetite for only carbohydrates, especially sweet ones, or sweet tastants irrespective of their carbohydrate content. Therefore, a blood–brain barrier penetrant OT receptor antagonist, L-368,899, was administered in mice and intake of liquid diets containing carbohydrates sucrose, glucose, fructose, polycose, or cornstarch (CS) or the noncarbohydrate, noncaloric sweetener saccharin was studied in episodic intake paradigmsone in which only one tastant was available and the other in which a choice between a carbohydrate (sucrose, glucose, or fructose) and saccharin was provided. We also used real-time PCR to examine hypothalamic Ot mRNA levels in mice provided short-term access to sucrose, CS, or saccharin. In the no-choice paradigm, L-368,899 increased the intake of all carbohydrates, whereas its effect on saccharin consumption showed only a trend. A 10 times lower dose (0.3 mg/kg) stimulated intake of sucrose than other carbohydrates. In the choice test, a very low 0.1 mg/kg dose of L-368,899 doubled the proportion of sucrose consumption relative to saccharin, but did not affect fructose or glucose preference. Ot gene expression increased after sucrose and CS, but not saccharin exposure compared with the controls; however, a higher level of significance was detected in the sucrose group. We conclude that OT inhibits appetite for carbohydrates. Sucrose consumption considerably enhances Ot gene expression and is particularly sensitive to OT receptor blockade, suggesting a special functional relationship between OT and sugar intake.</abstract><cop>Hagerstown, MD</cop><pub>Wolters Kluwer Health | Lippincott Williams & Wilkins</pub><pmid>24893201</pmid><doi>10.1097/WNR.0000000000000201</doi><tpages>6</tpages></addata></record> |
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subjects | Animals Appetite - drug effects Appetite - physiology Biological and medical sciences Bornanes - pharmacology Central Nervous System Agents - pharmacology Choice Behavior - drug effects Choice Behavior - physiology Dietary Carbohydrates - administration & dosage Dose-Response Relationship, Drug Food Preferences - drug effects Food Preferences - physiology Fundamental and applied biological sciences. Psychology Hypothalamus - drug effects Hypothalamus - physiology Male Mice, Inbred C57BL Oxytocin - metabolism Piperazines - pharmacology Receptors, Oxytocin - antagonists & inhibitors Receptors, Oxytocin - metabolism RNA, Messenger - metabolism Saccharin - administration & dosage Vertebrates: nervous system and sense organs |
title | Functional relationship between oxytocin and appetite for carbohydrates versus saccharin |
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