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Effect of tumor necrosis factor (TNF) on lipid metabolism in the diabetic rat: evidence that inhibition of adipose tissue lipoprotein lipase activity is not required for TNF-induced hyperlipidemia
Tumor necrosis factor (TNF) administration produces an increase in plasma triglycerides that may be due to inhibition of adipose lipoprotein lipase activity and/or a stimulation of hepatic lipogenesis. We now report that TNF administration to insulinopenic diabetic rats increases serum triglycerides...
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Published in: | The Journal of clinical investigation 1989-04, Vol.83 (4), p.1116-1121 |
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description | Tumor necrosis factor (TNF) administration produces an increase in plasma triglycerides that may be due to inhibition of adipose lipoprotein lipase activity and/or a stimulation of hepatic lipogenesis. We now report that TNF administration to insulinopenic diabetic rats increases serum triglycerides (2 h, 2.4-fold; 17 h, 4.3-fold). Adipose tissue lipoprotein lipase activity was markedly decreased in diabetic animals compared with controls and was not further inhibited by TNF. Incorporation of tritiated water into fatty acids in the liver was increased 45% 1-2 h after TNF and 87% at 16-17 h. These results indicate that the TNF-induced increase in circulating lipid levels can occur in the absence of a TNF-induced inhibition of adipose tissue lipoprotein lipase activity. Moreover, the clearance from the circulation of triglycerides in chylomicrons was similar in control and TNF-treated animals; these results provide further evidence that the removal of triglyceride-rich lipoproteins is not altered in the TNF-treated animals. Our data suggest that the TNF-induced stimulation of hepatic lipid synthesis may play an important role in the increase in serum triglycerides. In addition, TNF administration to diabetic animals leads to an elevation in serum glucose levels (73% at 17 h) without a change in serum insulin levels. Thus, TNF stimulation of hepatic lipogenesis is independent of changes in insulin. |
doi_str_mv | 10.1172/JCI113991 |
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R ; SOUED, M ; STAPRANS, I ; GAVIN, L. A ; DONAHUE, M. E ; BOA-JUN HUANG ; MOSER, A. H ; GULLI, R ; GRUNFELD, C</creator><creatorcontrib>FEINGOLD, K. R ; SOUED, M ; STAPRANS, I ; GAVIN, L. A ; DONAHUE, M. E ; BOA-JUN HUANG ; MOSER, A. H ; GULLI, R ; GRUNFELD, C</creatorcontrib><description>Tumor necrosis factor (TNF) administration produces an increase in plasma triglycerides that may be due to inhibition of adipose lipoprotein lipase activity and/or a stimulation of hepatic lipogenesis. We now report that TNF administration to insulinopenic diabetic rats increases serum triglycerides (2 h, 2.4-fold; 17 h, 4.3-fold). Adipose tissue lipoprotein lipase activity was markedly decreased in diabetic animals compared with controls and was not further inhibited by TNF. Incorporation of tritiated water into fatty acids in the liver was increased 45% 1-2 h after TNF and 87% at 16-17 h. These results indicate that the TNF-induced increase in circulating lipid levels can occur in the absence of a TNF-induced inhibition of adipose tissue lipoprotein lipase activity. Moreover, the clearance from the circulation of triglycerides in chylomicrons was similar in control and TNF-treated animals; these results provide further evidence that the removal of triglyceride-rich lipoproteins is not altered in the TNF-treated animals. Our data suggest that the TNF-induced stimulation of hepatic lipid synthesis may play an important role in the increase in serum triglycerides. In addition, TNF administration to diabetic animals leads to an elevation in serum glucose levels (73% at 17 h) without a change in serum insulin levels. Thus, TNF stimulation of hepatic lipogenesis is independent of changes in insulin.</description><identifier>ISSN: 0021-9738</identifier><identifier>EISSN: 1558-8238</identifier><identifier>DOI: 10.1172/JCI113991</identifier><identifier>PMID: 2703526</identifier><identifier>CODEN: JCINAO</identifier><language>eng</language><publisher>Ann Arbor, MI: American Society for Clinical Investigation</publisher><subject>Adipose Tissue - enzymology ; Animals ; Biological and medical sciences ; Blood Glucose - analysis ; Chylomicrons - metabolism ; Diabetes Mellitus, Experimental - blood ; Diabetes Mellitus, Experimental - metabolism ; Diabetes. Impaired glucose tolerance ; Endocrine pancreas. Apud cells (diseases) ; Endocrinopathies ; Etiopathogenesis. Screening. Investigations. Target tissue resistance ; Fasting ; Female ; Lipid Metabolism ; Lipids - biosynthesis ; Lipids - blood ; Lipoprotein Lipase - metabolism ; Male ; Medical sciences ; Metabolic Clearance Rate - drug effects ; Rats ; Rats, Inbred Strains ; Tumor Necrosis Factor-alpha - pharmacokinetics</subject><ispartof>The Journal of clinical investigation, 1989-04, Vol.83 (4), p.1116-1121</ispartof><rights>1991 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c399t-f8510ec4d5c46a5bd6ea76666351e37974181fac11c087cf0a8da8fa66b240603</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC303797/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC303797/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=19525779$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2703526$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>FEINGOLD, K. R</creatorcontrib><creatorcontrib>SOUED, M</creatorcontrib><creatorcontrib>STAPRANS, I</creatorcontrib><creatorcontrib>GAVIN, L. A</creatorcontrib><creatorcontrib>DONAHUE, M. E</creatorcontrib><creatorcontrib>BOA-JUN HUANG</creatorcontrib><creatorcontrib>MOSER, A. H</creatorcontrib><creatorcontrib>GULLI, R</creatorcontrib><creatorcontrib>GRUNFELD, C</creatorcontrib><title>Effect of tumor necrosis factor (TNF) on lipid metabolism in the diabetic rat: evidence that inhibition of adipose tissue lipoprotein lipase activity is not required for TNF-induced hyperlipidemia</title><title>The Journal of clinical investigation</title><addtitle>J Clin Invest</addtitle><description>Tumor necrosis factor (TNF) administration produces an increase in plasma triglycerides that may be due to inhibition of adipose lipoprotein lipase activity and/or a stimulation of hepatic lipogenesis. We now report that TNF administration to insulinopenic diabetic rats increases serum triglycerides (2 h, 2.4-fold; 17 h, 4.3-fold). Adipose tissue lipoprotein lipase activity was markedly decreased in diabetic animals compared with controls and was not further inhibited by TNF. Incorporation of tritiated water into fatty acids in the liver was increased 45% 1-2 h after TNF and 87% at 16-17 h. These results indicate that the TNF-induced increase in circulating lipid levels can occur in the absence of a TNF-induced inhibition of adipose tissue lipoprotein lipase activity. Moreover, the clearance from the circulation of triglycerides in chylomicrons was similar in control and TNF-treated animals; these results provide further evidence that the removal of triglyceride-rich lipoproteins is not altered in the TNF-treated animals. Our data suggest that the TNF-induced stimulation of hepatic lipid synthesis may play an important role in the increase in serum triglycerides. In addition, TNF administration to diabetic animals leads to an elevation in serum glucose levels (73% at 17 h) without a change in serum insulin levels. Thus, TNF stimulation of hepatic lipogenesis is independent of changes in insulin.</description><subject>Adipose Tissue - enzymology</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Blood Glucose - analysis</subject><subject>Chylomicrons - metabolism</subject><subject>Diabetes Mellitus, Experimental - blood</subject><subject>Diabetes Mellitus, Experimental - metabolism</subject><subject>Diabetes. Impaired glucose tolerance</subject><subject>Endocrine pancreas. Apud cells (diseases)</subject><subject>Endocrinopathies</subject><subject>Etiopathogenesis. Screening. Investigations. Target tissue resistance</subject><subject>Fasting</subject><subject>Female</subject><subject>Lipid Metabolism</subject><subject>Lipids - biosynthesis</subject><subject>Lipids - blood</subject><subject>Lipoprotein Lipase - metabolism</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Metabolic Clearance Rate - drug effects</subject><subject>Rats</subject><subject>Rats, Inbred Strains</subject><subject>Tumor Necrosis Factor-alpha - pharmacokinetics</subject><issn>0021-9738</issn><issn>1558-8238</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1989</creationdate><recordtype>article</recordtype><recordid>eNpVUcFu1DAUjBCoLIUDH4DkCxU9pNhJHDtIHKpVC60quJRz9OI8sw8lcWo7K-3_8WF429UCvlhPM29m7Mmyt4JfCKGKj7frGyHKphHPspWQUue6KPXzbMV5IfJGlfpl9iqEX5yLqpLVSXZSKF7Kol5lv6-sRROZsywuo_NsQuNdoMAsmJjmD_ffrs-Zm9hAM_VsxAidGyiMjCYWN8h6gg4jGeYhfmK4pR4ngwmCmCgb6ihSWk8G0NPsQoIohAX3gm72LiI9ikNCkiVtKe5Y8p9cZB4fFvLYM5uSpCA5Tf1i0rzZzegfE-FI8Dp7YWEI-OZwn2Y_rq_u11_zu-9fbtaXd7lJfxNzq6XgaKpemqoG2fU1gqrTKaXAUjWqElqkZwthuFbGctA9aAt13RUVr3l5mn1-0p2XbsTe4BQ9DO3saQS_ax1Q-z8y0ab96bZtyffyaf_ssO_dw4IhtiMFg8MAE7oltErrRipRJ-L5E3HfRfBojx6Ct_vG22Pjifvu31BH5qHihL8_4BAMDNbDZCj8FWxkIZVqyj_2rLhf</recordid><startdate>19890401</startdate><enddate>19890401</enddate><creator>FEINGOLD, K. R</creator><creator>SOUED, M</creator><creator>STAPRANS, I</creator><creator>GAVIN, L. A</creator><creator>DONAHUE, M. E</creator><creator>BOA-JUN HUANG</creator><creator>MOSER, A. H</creator><creator>GULLI, R</creator><creator>GRUNFELD, C</creator><general>American Society for Clinical Investigation</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>5PM</scope></search><sort><creationdate>19890401</creationdate><title>Effect of tumor necrosis factor (TNF) on lipid metabolism in the diabetic rat: evidence that inhibition of adipose tissue lipoprotein lipase activity is not required for TNF-induced hyperlipidemia</title><author>FEINGOLD, K. R ; SOUED, M ; STAPRANS, I ; GAVIN, L. A ; DONAHUE, M. E ; BOA-JUN HUANG ; MOSER, A. H ; GULLI, R ; GRUNFELD, C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c399t-f8510ec4d5c46a5bd6ea76666351e37974181fac11c087cf0a8da8fa66b240603</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1989</creationdate><topic>Adipose Tissue - enzymology</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Blood Glucose - analysis</topic><topic>Chylomicrons - metabolism</topic><topic>Diabetes Mellitus, Experimental - blood</topic><topic>Diabetes Mellitus, Experimental - metabolism</topic><topic>Diabetes. Impaired glucose tolerance</topic><topic>Endocrine pancreas. Apud cells (diseases)</topic><topic>Endocrinopathies</topic><topic>Etiopathogenesis. Screening. Investigations. Target tissue resistance</topic><topic>Fasting</topic><topic>Female</topic><topic>Lipid Metabolism</topic><topic>Lipids - biosynthesis</topic><topic>Lipids - blood</topic><topic>Lipoprotein Lipase - metabolism</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Metabolic Clearance Rate - drug effects</topic><topic>Rats</topic><topic>Rats, Inbred Strains</topic><topic>Tumor Necrosis Factor-alpha - pharmacokinetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>FEINGOLD, K. R</creatorcontrib><creatorcontrib>SOUED, M</creatorcontrib><creatorcontrib>STAPRANS, I</creatorcontrib><creatorcontrib>GAVIN, L. A</creatorcontrib><creatorcontrib>DONAHUE, M. E</creatorcontrib><creatorcontrib>BOA-JUN HUANG</creatorcontrib><creatorcontrib>MOSER, A. H</creatorcontrib><creatorcontrib>GULLI, R</creatorcontrib><creatorcontrib>GRUNFELD, C</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>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of clinical investigation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>FEINGOLD, K. R</au><au>SOUED, M</au><au>STAPRANS, I</au><au>GAVIN, L. A</au><au>DONAHUE, M. E</au><au>BOA-JUN HUANG</au><au>MOSER, A. H</au><au>GULLI, R</au><au>GRUNFELD, C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of tumor necrosis factor (TNF) on lipid metabolism in the diabetic rat: evidence that inhibition of adipose tissue lipoprotein lipase activity is not required for TNF-induced hyperlipidemia</atitle><jtitle>The Journal of clinical investigation</jtitle><addtitle>J Clin Invest</addtitle><date>1989-04-01</date><risdate>1989</risdate><volume>83</volume><issue>4</issue><spage>1116</spage><epage>1121</epage><pages>1116-1121</pages><issn>0021-9738</issn><eissn>1558-8238</eissn><coden>JCINAO</coden><abstract>Tumor necrosis factor (TNF) administration produces an increase in plasma triglycerides that may be due to inhibition of adipose lipoprotein lipase activity and/or a stimulation of hepatic lipogenesis. We now report that TNF administration to insulinopenic diabetic rats increases serum triglycerides (2 h, 2.4-fold; 17 h, 4.3-fold). Adipose tissue lipoprotein lipase activity was markedly decreased in diabetic animals compared with controls and was not further inhibited by TNF. Incorporation of tritiated water into fatty acids in the liver was increased 45% 1-2 h after TNF and 87% at 16-17 h. These results indicate that the TNF-induced increase in circulating lipid levels can occur in the absence of a TNF-induced inhibition of adipose tissue lipoprotein lipase activity. Moreover, the clearance from the circulation of triglycerides in chylomicrons was similar in control and TNF-treated animals; these results provide further evidence that the removal of triglyceride-rich lipoproteins is not altered in the TNF-treated animals. Our data suggest that the TNF-induced stimulation of hepatic lipid synthesis may play an important role in the increase in serum triglycerides. In addition, TNF administration to diabetic animals leads to an elevation in serum glucose levels (73% at 17 h) without a change in serum insulin levels. Thus, TNF stimulation of hepatic lipogenesis is independent of changes in insulin.</abstract><cop>Ann Arbor, MI</cop><pub>American Society for Clinical Investigation</pub><pmid>2703526</pmid><doi>10.1172/JCI113991</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adipose Tissue - enzymology Animals Biological and medical sciences Blood Glucose - analysis Chylomicrons - metabolism Diabetes Mellitus, Experimental - blood Diabetes Mellitus, Experimental - metabolism Diabetes. Impaired glucose tolerance Endocrine pancreas. Apud cells (diseases) Endocrinopathies Etiopathogenesis. Screening. Investigations. Target tissue resistance Fasting Female Lipid Metabolism Lipids - biosynthesis Lipids - blood Lipoprotein Lipase - metabolism Male Medical sciences Metabolic Clearance Rate - drug effects Rats Rats, Inbred Strains Tumor Necrosis Factor-alpha - pharmacokinetics |
title | Effect of tumor necrosis factor (TNF) on lipid metabolism in the diabetic rat: evidence that inhibition of adipose tissue lipoprotein lipase activity is not required for TNF-induced hyperlipidemia |
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