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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Veröffentlicht in:Endocrinology (Philadelphia) 2009-01, Vol.150 (1), p.169-178
Hauptverfasser: Bonzón-Kulichenko, Elena, Schwudke, Dominik, Gallardo, Nilda, Moltó, Eduardo, Fernández-Agulló, Teresa, Shevchenko, Andrej, Andrés, Antonio
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container_issue 1
container_start_page 169
container_title Endocrinology (Philadelphia)
container_volume 150
creator Bonzón-Kulichenko, Elena
Schwudke, Dominik
Gallardo, Nilda
Moltó, Eduardo
Fernández-Agulló, Teresa
Shevchenko, Andrej
Andrés, Antonio
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.
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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. 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Psychology ; Gene expression ; Injections, Intraventricular ; Insulin ; Kinases ; Lactosylceramide a-2,3-sialyltransferase ; Leptin ; Leptin - administration &amp; 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&amp;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. 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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. 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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 &amp; 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 &amp; 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 &amp; 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. 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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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