Central Leptin Regulates Total Ceramide Content and Sterol Regulatory Element Binding Protein-1C Proteolytic Maturation in Rat White Adipose Tissue
Obesity and type 2 diabetes are associated with insulin and leptin resistance, and increased ceramide contents in target tissues. Because the adipose tissue has become a central focus in these diseases, and leptin-induced increases in insulin sensitivity may be related to effects of leptin on lipid...
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description | Obesity and type 2 diabetes are associated with insulin and leptin resistance, and increased ceramide contents in target tissues. Because the adipose tissue has become a central focus in these diseases, and leptin-induced increases in insulin sensitivity may be related to effects of leptin on lipid metabolism, we investigated herein whether central leptin was able to regulate total ceramide levels and the expression of enzymes involved in ceramide metabolism in rat white adipose tissue (WAT). After 7 d central leptin treatment, the total content of ceramides was analyzed by quantitative shotgun lipidomics mass spectrometry. The effects of leptin on the expression of several enzymes of the sphingolipid metabolism, sterol regulatory element binding protein (SREBP)-1c, and insulin-induced gene 1 (INSIG-1) in this tissue were studied. Total ceramide levels were also determined after surgical WAT denervation. Central leptin infusion significantly decreased both total ceramide content and the long-chain fatty acid ceramide species in WAT. Concomitant with these results, leptin decreased the mRNA levels of enzymes involved in de novo ceramide synthesis (SPT-1, LASS2, LASS4) and ceramide production from sphingomyelin (SMPD-1/2). The mRNA levels of enzymes of ceramide degradation (Asah1/2) and utilization (sphingomyelin synthase, ceramide kinase, glycosyl-ceramide synthase, GM3 synthase) were also down-regulated. Ceramide-lowering effects of central leptin were prevented by local autonomic nervous system denervation of WAT. Finally, central leptin treatment markedly increased INSIG-1 mRNA expression and impaired SREBP-1c activation in epididymal WAT. These observations indicate that in vivo central leptin, acting through the autonomic nervous system, regulates total ceramide levels and SREBP-1c proteolytic maturation in WAT, probably contributing to improve the overall insulin sensitivity.
Central leptin decreases total ceramide levels and prevents sterol regulatory element binding protein (SREBP-1C) proteolytic maturation in white adipose tissue, and probably, in this way, contributes to improve the overall insulin sensitivity. |
doi_str_mv | 10.1210/en.2008-0505 |
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Central leptin decreases total ceramide levels and prevents sterol regulatory element binding protein (SREBP-1C) proteolytic maturation in white adipose tissue, and probably, in this way, contributes to improve the overall insulin sensitivity.</description><identifier>ISSN: 0013-7227</identifier><identifier>EISSN: 1945-7170</identifier><identifier>DOI: 10.1210/en.2008-0505</identifier><identifier>PMID: 18801905</identifier><identifier>CODEN: ENDOAO</identifier><language>eng</language><publisher>Chevy Chase, MD: Endocrine Society</publisher><subject>Adipose tissue ; Adipose Tissue - drug effects ; Adipose Tissue - metabolism ; Animals ; Autonomic nervous system ; Biological and medical sciences ; Body fat ; Body Weight ; Ceramide kinase ; Ceramides - metabolism ; Cholesterol Esters - metabolism ; Denervation ; Diabetes mellitus (non-insulin dependent) ; Energy Intake ; Enzymes ; Fundamental and applied biological sciences. Psychology ; Gene expression ; Injections, Intraventricular ; Insulin ; Kinases ; Lactosylceramide a-2,3-sialyltransferase ; Leptin ; Leptin - administration & dosage ; Leptin - pharmacology ; Lipid metabolism ; Lipids ; Lipids - physiology ; Male ; Mass spectrometry ; Mass spectroscopy ; Maturation ; Metabolism ; Nervous system ; Phosphorylation ; Protein turnover ; Proteins ; Proteolysis ; Rats ; Rats, Wistar ; Shotguns ; Sphingomyelin ; STAT3 Transcription Factor - drug effects ; STAT3 Transcription Factor - metabolism ; Sterol Regulatory Element Binding Protein 1 - drug effects ; Sterol Regulatory Element Binding Protein 1 - metabolism ; Sterol regulatory element-binding protein ; Sterols ; Transcription ; Vertebrates: endocrinology</subject><ispartof>Endocrinology (Philadelphia), 2009-01, Vol.150 (1), p.169-178</ispartof><rights>Copyright © 2009 by the Endocrine Society 2009</rights><rights>2009 INIST-CNRS</rights><rights>Copyright © 2009 by the Endocrine Society</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c461t-99bd31bc1bc944d7931a8c102d7cc9848c258f8f68943b542402db9ff11e076e3</citedby><cites>FETCH-LOGICAL-c461t-99bd31bc1bc944d7931a8c102d7cc9848c258f8f68943b542402db9ff11e076e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4024,27923,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=21002390$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18801905$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bonzón-Kulichenko, Elena</creatorcontrib><creatorcontrib>Schwudke, Dominik</creatorcontrib><creatorcontrib>Gallardo, Nilda</creatorcontrib><creatorcontrib>Moltó, Eduardo</creatorcontrib><creatorcontrib>Fernández-Agulló, Teresa</creatorcontrib><creatorcontrib>Shevchenko, Andrej</creatorcontrib><creatorcontrib>Andrés, Antonio</creatorcontrib><title>Central Leptin Regulates Total Ceramide Content and Sterol Regulatory Element Binding Protein-1C Proteolytic Maturation in Rat White Adipose Tissue</title><title>Endocrinology (Philadelphia)</title><addtitle>Endocrinology</addtitle><description>Obesity and type 2 diabetes are associated with insulin and leptin resistance, and increased ceramide contents in target tissues. Because the adipose tissue has become a central focus in these diseases, and leptin-induced increases in insulin sensitivity may be related to effects of leptin on lipid metabolism, we investigated herein whether central leptin was able to regulate total ceramide levels and the expression of enzymes involved in ceramide metabolism in rat white adipose tissue (WAT). After 7 d central leptin treatment, the total content of ceramides was analyzed by quantitative shotgun lipidomics mass spectrometry. The effects of leptin on the expression of several enzymes of the sphingolipid metabolism, sterol regulatory element binding protein (SREBP)-1c, and insulin-induced gene 1 (INSIG-1) in this tissue were studied. Total ceramide levels were also determined after surgical WAT denervation. Central leptin infusion significantly decreased both total ceramide content and the long-chain fatty acid ceramide species in WAT. Concomitant with these results, leptin decreased the mRNA levels of enzymes involved in de novo ceramide synthesis (SPT-1, LASS2, LASS4) and ceramide production from sphingomyelin (SMPD-1/2). The mRNA levels of enzymes of ceramide degradation (Asah1/2) and utilization (sphingomyelin synthase, ceramide kinase, glycosyl-ceramide synthase, GM3 synthase) were also down-regulated. Ceramide-lowering effects of central leptin were prevented by local autonomic nervous system denervation of WAT. Finally, central leptin treatment markedly increased INSIG-1 mRNA expression and impaired SREBP-1c activation in epididymal WAT. These observations indicate that in vivo central leptin, acting through the autonomic nervous system, regulates total ceramide levels and SREBP-1c proteolytic maturation in WAT, probably contributing to improve the overall insulin sensitivity.
Central leptin decreases total ceramide levels and prevents sterol regulatory element binding protein (SREBP-1C) proteolytic maturation in white adipose tissue, and probably, in this way, contributes to improve the overall insulin sensitivity.</description><subject>Adipose tissue</subject><subject>Adipose Tissue - drug effects</subject><subject>Adipose Tissue - metabolism</subject><subject>Animals</subject><subject>Autonomic nervous system</subject><subject>Biological and medical sciences</subject><subject>Body fat</subject><subject>Body Weight</subject><subject>Ceramide kinase</subject><subject>Ceramides - metabolism</subject><subject>Cholesterol Esters - metabolism</subject><subject>Denervation</subject><subject>Diabetes mellitus (non-insulin dependent)</subject><subject>Energy Intake</subject><subject>Enzymes</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gene expression</subject><subject>Injections, Intraventricular</subject><subject>Insulin</subject><subject>Kinases</subject><subject>Lactosylceramide a-2,3-sialyltransferase</subject><subject>Leptin</subject><subject>Leptin - administration & dosage</subject><subject>Leptin - pharmacology</subject><subject>Lipid metabolism</subject><subject>Lipids</subject><subject>Lipids - physiology</subject><subject>Male</subject><subject>Mass spectrometry</subject><subject>Mass spectroscopy</subject><subject>Maturation</subject><subject>Metabolism</subject><subject>Nervous system</subject><subject>Phosphorylation</subject><subject>Protein turnover</subject><subject>Proteins</subject><subject>Proteolysis</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Shotguns</subject><subject>Sphingomyelin</subject><subject>STAT3 Transcription Factor - drug effects</subject><subject>STAT3 Transcription Factor - metabolism</subject><subject>Sterol Regulatory Element Binding Protein 1 - drug effects</subject><subject>Sterol Regulatory Element Binding Protein 1 - metabolism</subject><subject>Sterol regulatory element-binding protein</subject><subject>Sterols</subject><subject>Transcription</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>eNp10UuL1TAUAOAginMd3bmWgKgbO-bVNlmOZXzAFUWvuCxpejpm6E1qki7u7_APm9LqgCgE8jgf55xwEHpMyQVllLwCd8EIkQUpSXkH7agSZVHTmtxFO0IoL2rG6jP0IMabfBVC8PvojEpJqCLlDv1swKWgR7yHKVmHP8P1POoEER98ys8NBH20PeDGu5Qp1q7HXxIEP_62Ppzw1QjHJfraut66a_wp-ATWFbRZj348JWvwB53moJP1Di-1dMLfvtsE-LK3k4-ADzbGGR6ie4MeIzza9nP09c3VoXlX7D--fd9c7gsjKpoKpbqe087kpYToa8WploYS1tfGKCmkYaUc5FBJJXhXCiZyqFPDQCmQugJ-jp6veafgf8wQU3u00cA4agd-jm1V1ZIJoTJ8-he88XNwubeWU05KVXNWZfVyVSb4GAMM7RTsUYdTS0m7jKoF1y6japdRZf5kSzp3R-hv8TabDJ5tQEejxyFoZ2z843JCwrgi2b1YnZ-n_5UstpJ8leB6b4J1MAWI8fY3_2z0F4zLuS8</recordid><startdate>200901</startdate><enddate>200901</enddate><creator>Bonzón-Kulichenko, Elena</creator><creator>Schwudke, Dominik</creator><creator>Gallardo, Nilda</creator><creator>Moltó, Eduardo</creator><creator>Fernández-Agulló, Teresa</creator><creator>Shevchenko, Andrej</creator><creator>Andrés, Antonio</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>200901</creationdate><title>Central Leptin Regulates Total Ceramide Content and Sterol Regulatory Element Binding Protein-1C Proteolytic Maturation in Rat White Adipose Tissue</title><author>Bonzón-Kulichenko, Elena ; Schwudke, Dominik ; Gallardo, Nilda ; Moltó, Eduardo ; Fernández-Agulló, Teresa ; Shevchenko, Andrej ; Andrés, Antonio</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c461t-99bd31bc1bc944d7931a8c102d7cc9848c258f8f68943b542402db9ff11e076e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Adipose tissue</topic><topic>Adipose Tissue - drug effects</topic><topic>Adipose Tissue - metabolism</topic><topic>Animals</topic><topic>Autonomic nervous system</topic><topic>Biological and medical sciences</topic><topic>Body fat</topic><topic>Body Weight</topic><topic>Ceramide kinase</topic><topic>Ceramides - metabolism</topic><topic>Cholesterol Esters - metabolism</topic><topic>Denervation</topic><topic>Diabetes mellitus (non-insulin dependent)</topic><topic>Energy Intake</topic><topic>Enzymes</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gene expression</topic><topic>Injections, Intraventricular</topic><topic>Insulin</topic><topic>Kinases</topic><topic>Lactosylceramide a-2,3-sialyltransferase</topic><topic>Leptin</topic><topic>Leptin - administration & dosage</topic><topic>Leptin - pharmacology</topic><topic>Lipid metabolism</topic><topic>Lipids</topic><topic>Lipids - physiology</topic><topic>Male</topic><topic>Mass spectrometry</topic><topic>Mass spectroscopy</topic><topic>Maturation</topic><topic>Metabolism</topic><topic>Nervous system</topic><topic>Phosphorylation</topic><topic>Protein turnover</topic><topic>Proteins</topic><topic>Proteolysis</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Shotguns</topic><topic>Sphingomyelin</topic><topic>STAT3 Transcription Factor - drug effects</topic><topic>STAT3 Transcription Factor - metabolism</topic><topic>Sterol Regulatory Element Binding Protein 1 - drug effects</topic><topic>Sterol Regulatory Element Binding Protein 1 - metabolism</topic><topic>Sterol regulatory element-binding protein</topic><topic>Sterols</topic><topic>Transcription</topic><topic>Vertebrates: endocrinology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bonzón-Kulichenko, Elena</creatorcontrib><creatorcontrib>Schwudke, Dominik</creatorcontrib><creatorcontrib>Gallardo, Nilda</creatorcontrib><creatorcontrib>Moltó, Eduardo</creatorcontrib><creatorcontrib>Fernández-Agulló, Teresa</creatorcontrib><creatorcontrib>Shevchenko, Andrej</creatorcontrib><creatorcontrib>Andrés, Antonio</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>Bonzón-Kulichenko, Elena</au><au>Schwudke, Dominik</au><au>Gallardo, Nilda</au><au>Moltó, Eduardo</au><au>Fernández-Agulló, Teresa</au><au>Shevchenko, Andrej</au><au>Andrés, Antonio</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Central Leptin Regulates Total Ceramide Content and Sterol Regulatory Element Binding Protein-1C Proteolytic Maturation in Rat White Adipose Tissue</atitle><jtitle>Endocrinology (Philadelphia)</jtitle><addtitle>Endocrinology</addtitle><date>2009-01</date><risdate>2009</risdate><volume>150</volume><issue>1</issue><spage>169</spage><epage>178</epage><pages>169-178</pages><issn>0013-7227</issn><eissn>1945-7170</eissn><coden>ENDOAO</coden><abstract>Obesity and type 2 diabetes are associated with insulin and leptin resistance, and increased ceramide contents in target tissues. Because the adipose tissue has become a central focus in these diseases, and leptin-induced increases in insulin sensitivity may be related to effects of leptin on lipid metabolism, we investigated herein whether central leptin was able to regulate total ceramide levels and the expression of enzymes involved in ceramide metabolism in rat white adipose tissue (WAT). After 7 d central leptin treatment, the total content of ceramides was analyzed by quantitative shotgun lipidomics mass spectrometry. The effects of leptin on the expression of several enzymes of the sphingolipid metabolism, sterol regulatory element binding protein (SREBP)-1c, and insulin-induced gene 1 (INSIG-1) in this tissue were studied. Total ceramide levels were also determined after surgical WAT denervation. Central leptin infusion significantly decreased both total ceramide content and the long-chain fatty acid ceramide species in WAT. Concomitant with these results, leptin decreased the mRNA levels of enzymes involved in de novo ceramide synthesis (SPT-1, LASS2, LASS4) and ceramide production from sphingomyelin (SMPD-1/2). The mRNA levels of enzymes of ceramide degradation (Asah1/2) and utilization (sphingomyelin synthase, ceramide kinase, glycosyl-ceramide synthase, GM3 synthase) were also down-regulated. Ceramide-lowering effects of central leptin were prevented by local autonomic nervous system denervation of WAT. Finally, central leptin treatment markedly increased INSIG-1 mRNA expression and impaired SREBP-1c activation in epididymal WAT. These observations indicate that in vivo central leptin, acting through the autonomic nervous system, regulates total ceramide levels and SREBP-1c proteolytic maturation in WAT, probably contributing to improve the overall insulin sensitivity.
Central leptin decreases total ceramide levels and prevents sterol regulatory element binding protein (SREBP-1C) proteolytic maturation in white adipose tissue, and probably, in this way, contributes to improve the overall insulin sensitivity.</abstract><cop>Chevy Chase, MD</cop><pub>Endocrine Society</pub><pmid>18801905</pmid><doi>10.1210/en.2008-0505</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adipose tissue Adipose Tissue - drug effects Adipose Tissue - metabolism Animals Autonomic nervous system Biological and medical sciences Body fat Body Weight Ceramide kinase Ceramides - metabolism Cholesterol Esters - metabolism Denervation Diabetes mellitus (non-insulin dependent) Energy Intake Enzymes Fundamental and applied biological sciences. Psychology Gene expression Injections, Intraventricular Insulin Kinases Lactosylceramide a-2,3-sialyltransferase Leptin Leptin - administration & dosage Leptin - pharmacology Lipid metabolism Lipids Lipids - physiology Male Mass spectrometry Mass spectroscopy Maturation Metabolism Nervous system Phosphorylation Protein turnover Proteins Proteolysis Rats Rats, Wistar Shotguns Sphingomyelin STAT3 Transcription Factor - drug effects STAT3 Transcription Factor - metabolism Sterol Regulatory Element Binding Protein 1 - drug effects Sterol Regulatory Element Binding Protein 1 - metabolism Sterol regulatory element-binding protein Sterols Transcription Vertebrates: endocrinology |
title | Central Leptin Regulates Total Ceramide Content and Sterol Regulatory Element Binding Protein-1C Proteolytic Maturation in Rat White Adipose Tissue |
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