Leptin Responsiveness in Chronically Decerebrate Rats
Peripheral infusions of physiological doses of leptin decrease body fat mass, but it is not known whether this results from direct effects on peripheral tissue or activation of central leptin receptors. In this study, we infused chronically decerebrate (CD) rats, in which the forebrain was surgicall...
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description | Peripheral infusions of physiological doses of leptin decrease body fat mass, but it is not known whether this results from direct effects on peripheral tissue or activation of central leptin receptors. In this study, we infused chronically decerebrate (CD) rats, in which the forebrain was surgically isolated from the caudal brainstem, with 60 μg leptin/d or PBS for 14 d from ip mini-osmotic pumps. The CD rats were tube fed an amount of food equivalent to the intake of ad libitum-fed intact controls or 75% of this amount to account for their reduced energy expenditure. Control rats fed ad libitum or tube fed 75, 100, or 125% of their ad libitum intake also were peripherally infused with leptin or PBS. CD rats had a lower serum testosterone, energy expenditure, and lean body mass compared with controls but had increased levels of adiponectin and leptin and were obese. Leptin increased body fat and decreased energy expenditure during the light period in 100%-fed CD rats, but not 75%-fed CD rats. Leptin decreased body fat of ad libitum- and 100%-fed but not 75%-fed or 125%-fed intact controls. Energy expenditure did not change in any control group. These results show that leptin can change body fat independent of a change in food intake or energy expenditure, that the forebrain normally prevents leptin from inhibiting energy expenditure through mechanisms initiated in the caudal brainstem or peripheral tissues, and that the leptin response in both intact and CD rats is determined by the energy status of the animal. |
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S ; Bartness, Timothy J ; Grill, Harvey J</creator><creatorcontrib>Harris, Ruth B. S ; Bartness, Timothy J ; Grill, Harvey J</creatorcontrib><description>Peripheral infusions of physiological doses of leptin decrease body fat mass, but it is not known whether this results from direct effects on peripheral tissue or activation of central leptin receptors. In this study, we infused chronically decerebrate (CD) rats, in which the forebrain was surgically isolated from the caudal brainstem, with 60 μg leptin/d or PBS for 14 d from ip mini-osmotic pumps. The CD rats were tube fed an amount of food equivalent to the intake of ad libitum-fed intact controls or 75% of this amount to account for their reduced energy expenditure. Control rats fed ad libitum or tube fed 75, 100, or 125% of their ad libitum intake also were peripherally infused with leptin or PBS. CD rats had a lower serum testosterone, energy expenditure, and lean body mass compared with controls but had increased levels of adiponectin and leptin and were obese. Leptin increased body fat and decreased energy expenditure during the light period in 100%-fed CD rats, but not 75%-fed CD rats. Leptin decreased body fat of ad libitum- and 100%-fed but not 75%-fed or 125%-fed intact controls. Energy expenditure did not change in any control group. These results show that leptin can change body fat independent of a change in food intake or energy expenditure, that the forebrain normally prevents leptin from inhibiting energy expenditure through mechanisms initiated in the caudal brainstem or peripheral tissues, and that the leptin response in both intact and CD rats is determined by the energy status of the animal.</description><identifier>ISSN: 0013-7227</identifier><identifier>EISSN: 1945-7170</identifier><identifier>DOI: 10.1210/en.2006-1565</identifier><identifier>PMID: 17615147</identifier><identifier>CODEN: ENDOAO</identifier><language>eng</language><publisher>Bethesda, MD: Endocrine Society</publisher><subject>Adiponectin ; Adipose Tissue - drug effects ; Adipose Tissue - pathology ; Animals ; Biological and medical sciences ; Body Composition - drug effects ; Body fat ; Body mass ; Brain stem ; Chronic Disease ; Decerebrate State - complications ; Decerebrate State - metabolism ; Decerebrate State - pathology ; Decerebrate State - physiopathology ; Eating ; Energy ; Energy balance ; Energy expenditure ; Energy Metabolism ; Food intake ; Forebrain ; Fundamental and applied biological sciences. Psychology ; Infusion Pumps ; Lean body mass ; Leptin - administration & dosage ; Leptin - pharmacology ; Leptin receptors ; Male ; Obesity - etiology ; Oxygen Consumption ; Physiological effects ; Prosencephalon - physiology ; Rats ; Rats, Sprague-Dawley ; Testosterone ; Testosterone - blood ; Vertebrates: endocrinology</subject><ispartof>Endocrinology (Philadelphia), 2007-10, Vol.148 (10), p.4623-4633</ispartof><rights>Copyright © 2007 by the Endocrine Society 2007</rights><rights>2007 INIST-CNRS</rights><rights>Copyright © 2007 by the Endocrine Society</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c527t-bf75455c7a1145844c63094fff5fce22d168e4311f4ac37bcf878dd26351f8403</citedby><cites>FETCH-LOGICAL-c527t-bf75455c7a1145844c63094fff5fce22d168e4311f4ac37bcf878dd26351f8403</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=19101049$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17615147$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Harris, Ruth B. S</creatorcontrib><creatorcontrib>Bartness, Timothy J</creatorcontrib><creatorcontrib>Grill, Harvey J</creatorcontrib><title>Leptin Responsiveness in Chronically Decerebrate Rats</title><title>Endocrinology (Philadelphia)</title><addtitle>Endocrinology</addtitle><description>Peripheral infusions of physiological doses of leptin decrease body fat mass, but it is not known whether this results from direct effects on peripheral tissue or activation of central leptin receptors. In this study, we infused chronically decerebrate (CD) rats, in which the forebrain was surgically isolated from the caudal brainstem, with 60 μg leptin/d or PBS for 14 d from ip mini-osmotic pumps. The CD rats were tube fed an amount of food equivalent to the intake of ad libitum-fed intact controls or 75% of this amount to account for their reduced energy expenditure. Control rats fed ad libitum or tube fed 75, 100, or 125% of their ad libitum intake also were peripherally infused with leptin or PBS. CD rats had a lower serum testosterone, energy expenditure, and lean body mass compared with controls but had increased levels of adiponectin and leptin and were obese. Leptin increased body fat and decreased energy expenditure during the light period in 100%-fed CD rats, but not 75%-fed CD rats. Leptin decreased body fat of ad libitum- and 100%-fed but not 75%-fed or 125%-fed intact controls. Energy expenditure did not change in any control group. These results show that leptin can change body fat independent of a change in food intake or energy expenditure, that the forebrain normally prevents leptin from inhibiting energy expenditure through mechanisms initiated in the caudal brainstem or peripheral tissues, and that the leptin response in both intact and CD rats is determined by the energy status of the animal.</description><subject>Adiponectin</subject><subject>Adipose Tissue - drug effects</subject><subject>Adipose Tissue - pathology</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Body Composition - drug effects</subject><subject>Body fat</subject><subject>Body mass</subject><subject>Brain stem</subject><subject>Chronic Disease</subject><subject>Decerebrate State - complications</subject><subject>Decerebrate State - metabolism</subject><subject>Decerebrate State - pathology</subject><subject>Decerebrate State - physiopathology</subject><subject>Eating</subject><subject>Energy</subject><subject>Energy balance</subject><subject>Energy expenditure</subject><subject>Energy Metabolism</subject><subject>Food intake</subject><subject>Forebrain</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Infusion Pumps</subject><subject>Lean body mass</subject><subject>Leptin - administration & dosage</subject><subject>Leptin - pharmacology</subject><subject>Leptin receptors</subject><subject>Male</subject><subject>Obesity - etiology</subject><subject>Oxygen Consumption</subject><subject>Physiological effects</subject><subject>Prosencephalon - physiology</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Testosterone</subject><subject>Testosterone - blood</subject><subject>Vertebrates: endocrinology</subject><issn>0013-7227</issn><issn>1945-7170</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp10c1LHDEYB-BQKnW1vfUsC1K9OJo333MsW7XCgiD1HLKZNzgym5kmMwX_-2bZgYViTyHh4f34hZCvQK-BAb3BeM0oVRVIJT-QBdRCVho0_UgWlAKvNGP6mJzk_FquQgj-iRyDViBB6AWRaxzGNi6fMA99zO0fjJjzsrysXlIfW--67m35Az0m3CQ34vLJjfkzOQquy_hlPk_J893tr9XPav14_7D6vq68ZHqsNkFLIaXXDkBII4RXnNYihCCDR8YaUAYFBwjCea43PhhtmoYpLiEYQfkpudjXHVL_e8I82m2bPXadi9hP2SrDDFO1KfD8H_jaTymW2SwHTqWpFRNFXe2VT33OCYMdUrt16c0CtbswLUa7C9Puwiz8bC46bbbYHPCcXgHfZuByCSokF32bD64GClTUxV3uXT8N_2tZzS35XmJsep_aiEMq_3HY5t1B_wL6T5ch</recordid><startdate>20071001</startdate><enddate>20071001</enddate><creator>Harris, Ruth B. S</creator><creator>Bartness, Timothy J</creator><creator>Grill, Harvey J</creator><general>Endocrine Society</general><general>Oxford University Press</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>7X8</scope></search><sort><creationdate>20071001</creationdate><title>Leptin Responsiveness in Chronically Decerebrate Rats</title><author>Harris, Ruth B. S ; Bartness, Timothy J ; Grill, Harvey J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c527t-bf75455c7a1145844c63094fff5fce22d168e4311f4ac37bcf878dd26351f8403</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Adiponectin</topic><topic>Adipose Tissue - drug effects</topic><topic>Adipose Tissue - pathology</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Body Composition - drug effects</topic><topic>Body fat</topic><topic>Body mass</topic><topic>Brain stem</topic><topic>Chronic Disease</topic><topic>Decerebrate State - complications</topic><topic>Decerebrate State - metabolism</topic><topic>Decerebrate State - pathology</topic><topic>Decerebrate State - physiopathology</topic><topic>Eating</topic><topic>Energy</topic><topic>Energy balance</topic><topic>Energy expenditure</topic><topic>Energy Metabolism</topic><topic>Food intake</topic><topic>Forebrain</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Infusion Pumps</topic><topic>Lean body mass</topic><topic>Leptin - administration & dosage</topic><topic>Leptin - pharmacology</topic><topic>Leptin receptors</topic><topic>Male</topic><topic>Obesity - etiology</topic><topic>Oxygen Consumption</topic><topic>Physiological effects</topic><topic>Prosencephalon - physiology</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Testosterone</topic><topic>Testosterone - blood</topic><topic>Vertebrates: endocrinology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Harris, Ruth B. S</creatorcontrib><creatorcontrib>Bartness, Timothy J</creatorcontrib><creatorcontrib>Grill, Harvey J</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>MEDLINE - Academic</collection><jtitle>Endocrinology (Philadelphia)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Harris, Ruth B. S</au><au>Bartness, Timothy J</au><au>Grill, Harvey J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Leptin Responsiveness in Chronically Decerebrate Rats</atitle><jtitle>Endocrinology (Philadelphia)</jtitle><addtitle>Endocrinology</addtitle><date>2007-10-01</date><risdate>2007</risdate><volume>148</volume><issue>10</issue><spage>4623</spage><epage>4633</epage><pages>4623-4633</pages><issn>0013-7227</issn><eissn>1945-7170</eissn><coden>ENDOAO</coden><abstract>Peripheral infusions of physiological doses of leptin decrease body fat mass, but it is not known whether this results from direct effects on peripheral tissue or activation of central leptin receptors. In this study, we infused chronically decerebrate (CD) rats, in which the forebrain was surgically isolated from the caudal brainstem, with 60 μg leptin/d or PBS for 14 d from ip mini-osmotic pumps. The CD rats were tube fed an amount of food equivalent to the intake of ad libitum-fed intact controls or 75% of this amount to account for their reduced energy expenditure. Control rats fed ad libitum or tube fed 75, 100, or 125% of their ad libitum intake also were peripherally infused with leptin or PBS. CD rats had a lower serum testosterone, energy expenditure, and lean body mass compared with controls but had increased levels of adiponectin and leptin and were obese. Leptin increased body fat and decreased energy expenditure during the light period in 100%-fed CD rats, but not 75%-fed CD rats. Leptin decreased body fat of ad libitum- and 100%-fed but not 75%-fed or 125%-fed intact controls. Energy expenditure did not change in any control group. These results show that leptin can change body fat independent of a change in food intake or energy expenditure, that the forebrain normally prevents leptin from inhibiting energy expenditure through mechanisms initiated in the caudal brainstem or peripheral tissues, and that the leptin response in both intact and CD rats is determined by the energy status of the animal.</abstract><cop>Bethesda, MD</cop><pub>Endocrine Society</pub><pmid>17615147</pmid><doi>10.1210/en.2006-1565</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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source | Oxford University Press Journals All Titles (1996-Current); MEDLINE; EZB-FREE-00999 freely available EZB journals |
subjects | Adiponectin Adipose Tissue - drug effects Adipose Tissue - pathology Animals Biological and medical sciences Body Composition - drug effects Body fat Body mass Brain stem Chronic Disease Decerebrate State - complications Decerebrate State - metabolism Decerebrate State - pathology Decerebrate State - physiopathology Eating Energy Energy balance Energy expenditure Energy Metabolism Food intake Forebrain Fundamental and applied biological sciences. Psychology Infusion Pumps Lean body mass Leptin - administration & dosage Leptin - pharmacology Leptin receptors Male Obesity - etiology Oxygen Consumption Physiological effects Prosencephalon - physiology Rats Rats, Sprague-Dawley Testosterone Testosterone - blood Vertebrates: endocrinology |
title | Leptin Responsiveness in Chronically Decerebrate Rats |
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