Short-term feeding of conjugated linoleic acid does not induce hepatic steatosis in C57BL/6J mice

We investigated the effect of short-term feeding of conjugated linoleic acid (CLA) on adipose tissue weights, liver weight, hepatic lipid metabolism, and serum lipoprotein profiles in C57BL/6J mice. Mice were fed semi-synthetic diets containing either 6% high-linoleic safflower oil (HL-SAF) or 4% HL...

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Veröffentlicht in:Journal of Nutritional Science and Vitaminology 2005, Vol.51(6), pp.440-444
Hauptverfasser: Wang, Y.M.(Saga Univ. (Japan)), Nagao, K, Ujino, Y, Sakata, K, Higa, K, Inoue, N, Yanagita, T
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container_issue 6
container_start_page 440
container_title Journal of Nutritional Science and Vitaminology
container_volume 51
creator Wang, Y.M.(Saga Univ. (Japan))
Nagao, K
Ujino, Y
Sakata, K
Higa, K
Inoue, N
Yanagita, T
description We investigated the effect of short-term feeding of conjugated linoleic acid (CLA) on adipose tissue weights, liver weight, hepatic lipid metabolism, and serum lipoprotein profiles in C57BL/6J mice. Mice were fed semi-synthetic diets containing either 6% high-linoleic safflower oil (HL-SAF) or 4% HL-SAF+2% CLA for 1 wk. Short-term feeding of CLA showed an anti-obesity effect without inducing hepatomegaly in mice. In addition to the decline of hepatic triglyceride concentration, significant inhibition of delta9 desaturation of fatty acid in the total liver lipids was found in CLA-fed mice. The CLA diet significantly increased the activities of peroxisomal beta-oxidation and decreased the activities of diacylglycerol acyltransferase, a triglyceride synthesis-related enzyme, in the liver. Moreover, serum lipoprotein profiles of CLA-fed mice showed preferable changes in the atherogenic indices. However, serum leptin and adiponectin were drastically decreased by CLA feeding, suggesting that prolonged administration of CLA would induce further decrease of serum adipocytokine levels, which may be a cause of lipodystrophy in mice. These results show that short-term feeding of CLA does not induce adverse effect in C57BL/6J mice.
doi_str_mv 10.3177/jnsv.51.440
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The CLA diet significantly increased the activities of peroxisomal beta-oxidation and decreased the activities of diacylglycerol acyltransferase, a triglyceride synthesis-related enzyme, in the liver. Moreover, serum lipoprotein profiles of CLA-fed mice showed preferable changes in the atherogenic indices. However, serum leptin and adiponectin were drastically decreased by CLA feeding, suggesting that prolonged administration of CLA would induce further decrease of serum adipocytokine levels, which may be a cause of lipodystrophy in mice. These results show that short-term feeding of CLA does not induce adverse effect in C57BL/6J mice.</description><identifier>ISSN: 0301-4800</identifier><identifier>EISSN: 1881-7742</identifier><identifier>DOI: 10.3177/jnsv.51.440</identifier><identifier>PMID: 16521704</identifier><language>eng</language><publisher>Tokyo: Center for Academic Publications Japan</publisher><subject>ACIDE LINOLEIQUE ; ACIDO LINOLEICO ; Adipose Tissue - anatomy &amp; histology ; Animals ; Biological and medical sciences ; C57BL/6J mice ; conjugated linoleic acid ; diacylglycerol acyltransferase ; Diacylglycerol O-Acyltransferase - metabolism ; Diet ; ENZIMAS ; ENZYME ; ENZYMES ; Fatty Liver - chemically induced ; Gastroenterology. Liver. Pancreas. Abdomen ; GLICEROL ; GLYCEROL ; hepatic steatosis ; LINOLEIC ACID ; Linoleic Acids, Conjugated - administration &amp; dosage ; Lipid Metabolism - drug effects ; Lipoproteins - blood ; Liver - anatomy &amp; histology ; Liver - metabolism ; Liver. Biliary tract. Portal circulation. Exocrine pancreas ; Male ; Medical sciences ; MICE ; Mice, Inbred C57BL ; Obesity - prevention &amp; control ; Organ Size - drug effects ; Other diseases. 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In addition to the decline of hepatic triglyceride concentration, significant inhibition of delta9 desaturation of fatty acid in the total liver lipids was found in CLA-fed mice. The CLA diet significantly increased the activities of peroxisomal beta-oxidation and decreased the activities of diacylglycerol acyltransferase, a triglyceride synthesis-related enzyme, in the liver. Moreover, serum lipoprotein profiles of CLA-fed mice showed preferable changes in the atherogenic indices. However, serum leptin and adiponectin were drastically decreased by CLA feeding, suggesting that prolonged administration of CLA would induce further decrease of serum adipocytokine levels, which may be a cause of lipodystrophy in mice. 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Abdomen</subject><subject>GLICEROL</subject><subject>GLYCEROL</subject><subject>hepatic steatosis</subject><subject>LINOLEIC ACID</subject><subject>Linoleic Acids, Conjugated - administration &amp; dosage</subject><subject>Lipid Metabolism - drug effects</subject><subject>Lipoproteins - blood</subject><subject>Liver - anatomy &amp; histology</subject><subject>Liver - metabolism</subject><subject>Liver. Biliary tract. Portal circulation. Exocrine pancreas</subject><subject>Male</subject><subject>Medical sciences</subject><subject>MICE</subject><subject>Mice, Inbred C57BL</subject><subject>Obesity - prevention &amp; control</subject><subject>Organ Size - drug effects</subject><subject>Other diseases. Semiology</subject><subject>Oxidation-Reduction</subject><subject>Peroxisomes - metabolism</subject><subject>RATON</subject><subject>Safflower Oil - administration &amp; dosage</subject><subject>SOURIS</subject><issn>0301-4800</issn><issn>1881-7742</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkc-PEyEYhonRuN3Vk2cNF0-b6cIAA3N0689NE03U8-QrfLQ006EBauJ_L3Wa3Qsc3ifvmzwfIW84Wwqu9d1-yn-Wii-lZM_IghvDG61l-5wsmGC8kYaxK3Kd854x2RtpXpIr3qmWayYXBH7uYipNwXSgHtGFaUujpzZO-9MWCjo6himOGCwFGxx1ETOdYqFhcieLdIdHKDXMBaHEHHIN6Erp-_Vd90APweIr8sLDmPH15b8hvz9_-rX62qy_f_m2-rBurGp1aRwTrVa23yBI09veMdVpEHJje-sdR-mEVb10nGtvlJcCHHrpDbPA0YIRN-R27rUp5pzQD8cUDpD-DpwNZ1HDWdSg-FBFVfrdTB9PmwO6J_ZipgLvLwBkC6NPMNmQnzgtNW87UbmPM7fPBbb4CECqWkb8P8p7Lc7D3fzU_cfY7iANONWat3ONhzjANtWphx8tY935aLIX_wA4YpLI</recordid><startdate>20051201</startdate><enddate>20051201</enddate><creator>Wang, Y.M.(Saga Univ. 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Abdomen</topic><topic>GLICEROL</topic><topic>GLYCEROL</topic><topic>hepatic steatosis</topic><topic>LINOLEIC ACID</topic><topic>Linoleic Acids, Conjugated - administration &amp; dosage</topic><topic>Lipid Metabolism - drug effects</topic><topic>Lipoproteins - blood</topic><topic>Liver - anatomy &amp; histology</topic><topic>Liver - metabolism</topic><topic>Liver. Biliary tract. Portal circulation. Exocrine pancreas</topic><topic>Male</topic><topic>Medical sciences</topic><topic>MICE</topic><topic>Mice, Inbred C57BL</topic><topic>Obesity - prevention &amp; control</topic><topic>Organ Size - drug effects</topic><topic>Other diseases. Semiology</topic><topic>Oxidation-Reduction</topic><topic>Peroxisomes - metabolism</topic><topic>RATON</topic><topic>Safflower Oil - administration &amp; dosage</topic><topic>SOURIS</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Y.M.(Saga Univ. 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subjects ACIDE LINOLEIQUE
ACIDO LINOLEICO
Adipose Tissue - anatomy & histology
Animals
Biological and medical sciences
C57BL/6J mice
conjugated linoleic acid
diacylglycerol acyltransferase
Diacylglycerol O-Acyltransferase - metabolism
Diet
ENZIMAS
ENZYME
ENZYMES
Fatty Liver - chemically induced
Gastroenterology. Liver. Pancreas. Abdomen
GLICEROL
GLYCEROL
hepatic steatosis
LINOLEIC ACID
Linoleic Acids, Conjugated - administration & dosage
Lipid Metabolism - drug effects
Lipoproteins - blood
Liver - anatomy & histology
Liver - metabolism
Liver. Biliary tract. Portal circulation. Exocrine pancreas
Male
Medical sciences
MICE
Mice, Inbred C57BL
Obesity - prevention & control
Organ Size - drug effects
Other diseases. Semiology
Oxidation-Reduction
Peroxisomes - metabolism
RATON
Safflower Oil - administration & dosage
SOURIS
title Short-term feeding of conjugated linoleic acid does not induce hepatic steatosis in C57BL/6J mice
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