Mapping Brain c-Fos Immunoreactivity after Insulin-Induced Voluntary Lard Intake: Insulin- and Lard-Associated Patterns
In addition to the inhibitory role of central insulin on food intake, insulin also acts to promote lard intake. We investigated the neural pathways involved in this facet of insulin action. Insulin or saline was infused into either the superior mesenteric or right external jugular veins of streptozo...
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description | In addition to the inhibitory role of central insulin on food intake, insulin also acts to promote lard intake. We investigated the neural pathways involved in this facet of insulin action. Insulin or saline was infused into either the superior mesenteric or right external jugular veins of streptozotocin‐diabetic rodents with elevated steady‐state circulating corticosterone concentrations. After postsurgical recovery, rats were offered the choice of chow or lard to eat. Irrespective of the site of venous infusion, insulin increased lard and decreased chow intake. After 4 days, lard was removed for 8 h. On return for 1 h, only insulin infused into the superior mesenteric vein resulted in lard intake. This facilitated distinction between the effects of circulating insulin concentrations (similar in the two insulin‐infused groups) and lard ingestion on the patterns of c‐Fos+ cells in the brain, termed insulin‐ and lard‐associated patterns, respectively. Insulin‐associated changes in c‐Fos+ cell numbers were evident in the arcuate nucleus, bed nucleus of the stria terminalis and substantia nigra pars compacta, concomitant with elevated leptin levels and reduced chow intake. Lard‐associated changes in c‐Fos+ cell numbers were observed in the nucleus of the tractus solitarius, lateral parabrachial nucleus, central nucleus of the amygdala, ventral tegmental area, nucleus accumbens shell and the prefrontal cortex, and were associated with lower levels of triglycerides and free fatty acids. The anterior paraventricular thalamic nucleus exhibited both patterns. These data collectively fit into a framework for food intake and reward and provide targets for pharmacological manipulation to influence the choice of food intake. |
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P. ; Horneman, H. F. ; Ginsberg, A. B. ; Pecoraro, N. C. ; Foster, M. T. ; Akana, S. F. ; Dallman, M. F.</creator><creatorcontrib>Warne, J. P. ; Horneman, H. F. ; Ginsberg, A. B. ; Pecoraro, N. C. ; Foster, M. T. ; Akana, S. F. ; Dallman, M. F.</creatorcontrib><description>In addition to the inhibitory role of central insulin on food intake, insulin also acts to promote lard intake. We investigated the neural pathways involved in this facet of insulin action. Insulin or saline was infused into either the superior mesenteric or right external jugular veins of streptozotocin‐diabetic rodents with elevated steady‐state circulating corticosterone concentrations. After postsurgical recovery, rats were offered the choice of chow or lard to eat. Irrespective of the site of venous infusion, insulin increased lard and decreased chow intake. After 4 days, lard was removed for 8 h. On return for 1 h, only insulin infused into the superior mesenteric vein resulted in lard intake. This facilitated distinction between the effects of circulating insulin concentrations (similar in the two insulin‐infused groups) and lard ingestion on the patterns of c‐Fos+ cells in the brain, termed insulin‐ and lard‐associated patterns, respectively. Insulin‐associated changes in c‐Fos+ cell numbers were evident in the arcuate nucleus, bed nucleus of the stria terminalis and substantia nigra pars compacta, concomitant with elevated leptin levels and reduced chow intake. Lard‐associated changes in c‐Fos+ cell numbers were observed in the nucleus of the tractus solitarius, lateral parabrachial nucleus, central nucleus of the amygdala, ventral tegmental area, nucleus accumbens shell and the prefrontal cortex, and were associated with lower levels of triglycerides and free fatty acids. The anterior paraventricular thalamic nucleus exhibited both patterns. These data collectively fit into a framework for food intake and reward and provide targets for pharmacological manipulation to influence the choice of food intake.</description><identifier>ISSN: 0953-8194</identifier><identifier>EISSN: 1365-2826</identifier><identifier>DOI: 10.1111/j.1365-2826.2007.01593.x</identifier><identifier>PMID: 17850462</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Animals ; Appetite Regulation - physiology ; Arcuate Nucleus of Hypothalamus - metabolism ; Biological and medical sciences ; brain ; Brain - metabolism ; Brain Mapping ; c-Fos ; Choice Behavior ; Corticosterone - blood ; diabetes ; Diabetes Mellitus, Experimental - metabolism ; Diabetes. Impaired glucose tolerance ; Dietary Fats - metabolism ; Endocrine pancreas ; Endocrine pancreas. Apud cells (diseases) ; Endocrinopathies ; Etiopathogenesis. Screening. Investigations. Target tissue resistance ; Feeding Behavior - physiology ; Feeding. Feeding behavior ; Food Preferences - physiology ; Fundamental and applied biological sciences. Psychology ; glucocorticoids ; Hormones. Régulation ; Hypothalamus - metabolism ; Immunohistochemistry ; Injections, Intraventricular ; insulin ; Insulin - administration & dosage ; Insulin - physiology ; lard ; Male ; Medical sciences ; Neural Pathways - metabolism ; Prefrontal Cortex - metabolism ; Proto-Oncogene Proteins c-fos - metabolism ; Rats ; Rats, Sprague-Dawley ; Substantia Nigra - metabolism ; Vertebrates: anatomy and physiology, studies on body, several organs or systems ; Vertebrates: endocrinology</subject><ispartof>Journal of neuroendocrinology, 2007-10, Vol.19 (10), p.794-808</ispartof><rights>2007 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5163-fe1d2ca2b4c34d9a1b8b9c8066b885056562234e755b8d7f733a398c9379cbab3</citedby><cites>FETCH-LOGICAL-c5163-fe1d2ca2b4c34d9a1b8b9c8066b885056562234e755b8d7f733a398c9379cbab3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1365-2826.2007.01593.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1365-2826.2007.01593.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,777,781,1412,27905,27906,45555,45556</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=19064326$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17850462$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Warne, J. P.</creatorcontrib><creatorcontrib>Horneman, H. F.</creatorcontrib><creatorcontrib>Ginsberg, A. B.</creatorcontrib><creatorcontrib>Pecoraro, N. C.</creatorcontrib><creatorcontrib>Foster, M. T.</creatorcontrib><creatorcontrib>Akana, S. F.</creatorcontrib><creatorcontrib>Dallman, M. F.</creatorcontrib><title>Mapping Brain c-Fos Immunoreactivity after Insulin-Induced Voluntary Lard Intake: Insulin- and Lard-Associated Patterns</title><title>Journal of neuroendocrinology</title><addtitle>J Neuroendocrinol</addtitle><description>In addition to the inhibitory role of central insulin on food intake, insulin also acts to promote lard intake. We investigated the neural pathways involved in this facet of insulin action. Insulin or saline was infused into either the superior mesenteric or right external jugular veins of streptozotocin‐diabetic rodents with elevated steady‐state circulating corticosterone concentrations. After postsurgical recovery, rats were offered the choice of chow or lard to eat. Irrespective of the site of venous infusion, insulin increased lard and decreased chow intake. After 4 days, lard was removed for 8 h. On return for 1 h, only insulin infused into the superior mesenteric vein resulted in lard intake. This facilitated distinction between the effects of circulating insulin concentrations (similar in the two insulin‐infused groups) and lard ingestion on the patterns of c‐Fos+ cells in the brain, termed insulin‐ and lard‐associated patterns, respectively. Insulin‐associated changes in c‐Fos+ cell numbers were evident in the arcuate nucleus, bed nucleus of the stria terminalis and substantia nigra pars compacta, concomitant with elevated leptin levels and reduced chow intake. Lard‐associated changes in c‐Fos+ cell numbers were observed in the nucleus of the tractus solitarius, lateral parabrachial nucleus, central nucleus of the amygdala, ventral tegmental area, nucleus accumbens shell and the prefrontal cortex, and were associated with lower levels of triglycerides and free fatty acids. The anterior paraventricular thalamic nucleus exhibited both patterns. These data collectively fit into a framework for food intake and reward and provide targets for pharmacological manipulation to influence the choice of food intake.</description><subject>Animals</subject><subject>Appetite Regulation - physiology</subject><subject>Arcuate Nucleus of Hypothalamus - metabolism</subject><subject>Biological and medical sciences</subject><subject>brain</subject><subject>Brain - metabolism</subject><subject>Brain Mapping</subject><subject>c-Fos</subject><subject>Choice Behavior</subject><subject>Corticosterone - blood</subject><subject>diabetes</subject><subject>Diabetes Mellitus, Experimental - metabolism</subject><subject>Diabetes. Impaired glucose tolerance</subject><subject>Dietary Fats - metabolism</subject><subject>Endocrine pancreas</subject><subject>Endocrine pancreas. Apud cells (diseases)</subject><subject>Endocrinopathies</subject><subject>Etiopathogenesis. Screening. Investigations. Target tissue resistance</subject><subject>Feeding Behavior - physiology</subject><subject>Feeding. Feeding behavior</subject><subject>Food Preferences - physiology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>glucocorticoids</subject><subject>Hormones. Régulation</subject><subject>Hypothalamus - metabolism</subject><subject>Immunohistochemistry</subject><subject>Injections, Intraventricular</subject><subject>insulin</subject><subject>Insulin - administration & dosage</subject><subject>Insulin - physiology</subject><subject>lard</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Neural Pathways - metabolism</subject><subject>Prefrontal Cortex - metabolism</subject><subject>Proto-Oncogene Proteins c-fos - metabolism</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Substantia Nigra - metabolism</subject><subject>Vertebrates: anatomy and physiology, studies on body, several organs or systems</subject><subject>Vertebrates: endocrinology</subject><issn>0953-8194</issn><issn>1365-2826</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkV1v0zAUhiMEYmXwF1Bu4C7BH_EXEhfbtJVCGVzAdmmdOA5ylzqdnbD23-OsVXcJvrGl87zH9nmyLMeoxGl9WJWYclYQSXhJEBIlwkzRcvssmx0Lz7MZUowWEqvqJHsV4wohLBhFL7MTLCRDFSez7OEbbDbO_87PAzifm-Kqj_livR59HyyYwf1xwy6HdrAhX_g4ds4XC9-Mxjb5Td-NfoCwy5cQmlQe4M5-PGI5-OaxUpzF2BsHQ8r8gCG18vF19qKFLto3h_00-3V1-fPic7H8Pl9cnC0LwzCnRWtxQwyQujK0ahTgWtbKSMR5LdMXGGecEFpZwVgtG9EKSoEqaRQVytRQ09Ps_b7vJvT3o42DXrtobNeBt_0YNZdEYMXYP0GC0sQQUQmUe9CEPsZgW70Jbp2moDHSkx290pMEPUnQkx39aEdvU_Tt4Y6xXtvmKXjQkYB3BwCiga4N4I2LT5xCvKKEJ-7Tnntwnd399wP0l-vL6ZTyxT7v4mC3xzyEO80FFUzfXs_17bmc0683Qs_pX3HLuhc</recordid><startdate>200710</startdate><enddate>200710</enddate><creator>Warne, J. P.</creator><creator>Horneman, H. F.</creator><creator>Ginsberg, A. B.</creator><creator>Pecoraro, N. C.</creator><creator>Foster, M. T.</creator><creator>Akana, S. F.</creator><creator>Dallman, M. F.</creator><general>Blackwell Publishing Ltd</general><general>Blackwell Science</general><scope>BSCLL</scope><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>7TK</scope><scope>7X8</scope></search><sort><creationdate>200710</creationdate><title>Mapping Brain c-Fos Immunoreactivity after Insulin-Induced Voluntary Lard Intake: Insulin- and Lard-Associated Patterns</title><author>Warne, J. P. ; Horneman, H. F. ; Ginsberg, A. B. ; Pecoraro, N. C. ; Foster, M. T. ; Akana, S. F. ; Dallman, M. 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Target tissue resistance</topic><topic>Feeding Behavior - physiology</topic><topic>Feeding. Feeding behavior</topic><topic>Food Preferences - physiology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>glucocorticoids</topic><topic>Hormones. Régulation</topic><topic>Hypothalamus - metabolism</topic><topic>Immunohistochemistry</topic><topic>Injections, Intraventricular</topic><topic>insulin</topic><topic>Insulin - administration & dosage</topic><topic>Insulin - physiology</topic><topic>lard</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Neural Pathways - metabolism</topic><topic>Prefrontal Cortex - metabolism</topic><topic>Proto-Oncogene Proteins c-fos - metabolism</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Substantia Nigra - metabolism</topic><topic>Vertebrates: anatomy and physiology, studies on body, several organs or systems</topic><topic>Vertebrates: endocrinology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Warne, J. P.</creatorcontrib><creatorcontrib>Horneman, H. F.</creatorcontrib><creatorcontrib>Ginsberg, A. B.</creatorcontrib><creatorcontrib>Pecoraro, N. C.</creatorcontrib><creatorcontrib>Foster, M. 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F.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mapping Brain c-Fos Immunoreactivity after Insulin-Induced Voluntary Lard Intake: Insulin- and Lard-Associated Patterns</atitle><jtitle>Journal of neuroendocrinology</jtitle><addtitle>J Neuroendocrinol</addtitle><date>2007-10</date><risdate>2007</risdate><volume>19</volume><issue>10</issue><spage>794</spage><epage>808</epage><pages>794-808</pages><issn>0953-8194</issn><eissn>1365-2826</eissn><abstract>In addition to the inhibitory role of central insulin on food intake, insulin also acts to promote lard intake. We investigated the neural pathways involved in this facet of insulin action. Insulin or saline was infused into either the superior mesenteric or right external jugular veins of streptozotocin‐diabetic rodents with elevated steady‐state circulating corticosterone concentrations. After postsurgical recovery, rats were offered the choice of chow or lard to eat. Irrespective of the site of venous infusion, insulin increased lard and decreased chow intake. After 4 days, lard was removed for 8 h. On return for 1 h, only insulin infused into the superior mesenteric vein resulted in lard intake. This facilitated distinction between the effects of circulating insulin concentrations (similar in the two insulin‐infused groups) and lard ingestion on the patterns of c‐Fos+ cells in the brain, termed insulin‐ and lard‐associated patterns, respectively. Insulin‐associated changes in c‐Fos+ cell numbers were evident in the arcuate nucleus, bed nucleus of the stria terminalis and substantia nigra pars compacta, concomitant with elevated leptin levels and reduced chow intake. Lard‐associated changes in c‐Fos+ cell numbers were observed in the nucleus of the tractus solitarius, lateral parabrachial nucleus, central nucleus of the amygdala, ventral tegmental area, nucleus accumbens shell and the prefrontal cortex, and were associated with lower levels of triglycerides and free fatty acids. The anterior paraventricular thalamic nucleus exhibited both patterns. These data collectively fit into a framework for food intake and reward and provide targets for pharmacological manipulation to influence the choice of food intake.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>17850462</pmid><doi>10.1111/j.1365-2826.2007.01593.x</doi><tpages>15</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Appetite Regulation - physiology Arcuate Nucleus of Hypothalamus - metabolism Biological and medical sciences brain Brain - metabolism Brain Mapping c-Fos Choice Behavior Corticosterone - blood diabetes Diabetes Mellitus, Experimental - metabolism Diabetes. Impaired glucose tolerance Dietary Fats - metabolism Endocrine pancreas Endocrine pancreas. Apud cells (diseases) Endocrinopathies Etiopathogenesis. Screening. Investigations. Target tissue resistance Feeding Behavior - physiology Feeding. Feeding behavior Food Preferences - physiology Fundamental and applied biological sciences. Psychology glucocorticoids Hormones. Régulation Hypothalamus - metabolism Immunohistochemistry Injections, Intraventricular insulin Insulin - administration & dosage Insulin - physiology lard Male Medical sciences Neural Pathways - metabolism Prefrontal Cortex - metabolism Proto-Oncogene Proteins c-fos - metabolism Rats Rats, Sprague-Dawley Substantia Nigra - metabolism Vertebrates: anatomy and physiology, studies on body, several organs or systems Vertebrates: endocrinology |
title | Mapping Brain c-Fos Immunoreactivity after Insulin-Induced Voluntary Lard Intake: Insulin- and Lard-Associated Patterns |
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