Different effects of conjugated linoleic acid isomers on lipoprotein lipase activity in 3T3-L1 adipocytes

被引:70
作者
Lin, YG [1 ]
Kreeft, A [1 ]
Schuurbiers, JAE [1 ]
Draijer, R [1 ]
机构
[1] Unilever Res Labs Vlaardingen, NL-3130 AC Vlaardingen, Netherlands
关键词
3T3; L1; adipocytes; conjugated linoleic acid; lipoprotein lipase; fatty acids;
D O I
10.1016/S0955-2863(00)00155-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Conjugated linoleic acids (CLAs) are the positional and geometric isomers of Linoleic acid. In the present study the effects of cis-9, trans-11 CLA (c9,t11 CLA) and trans-10, cis-12 CLA (t10,c12 CLA) on intracellular and heparin-releasable (HR-) lipoprotein lipase(LPL) activity in 3T3-L1 adipocytes were investigated. Cells were exposed to the two CLA isomers and linoleic acid, which were bound to bovine serum albumin (BSA). In the adipocytes insulin up-regulated and tumor necrosis factor alpha (TNF alpha) down-regulated HR-LPL activity, which corresponds with the findings in vivo. The experimental fatty acids at low concentrations (<30 <mu>mol/L) moderately increased intracellular and HR-LPL activity; At a concentration of 100 mu mol/L, c9,t11 CLA and t10,c12 CLA suppressed HR-LPL activity to 20 and 24% below the BSA control level, respectively, while linoleic acid had no effect unless its concentration was as-high as 1000 mu mol/L. Insulin abolished the inhibitory effect of c9,t11 CLA, but not of t10,c12 CLA. In the presence of insulin, t10,c12 CLA inhibited HR-LPL activity by 41% compared to BSA control. In contrast to TNF alpha, which suppressed both intracellular LPL and HR-LPL activity, CLAs suppressed HR-LPL activity without decreasing intracellular LPL activity. Additionally, t10,c12 CLA (100 mu mol/L) partially prevented TNF alpha -induced decrease of intracellular LPL activity. These results indicate that CLAs differ from linoleic acid in regulating HR-LPL activity, and t10,c12 CLA appeared to be more effective than c9,t11 CLA. (C) 2001 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:183 / 189
页数:7
相关论文
共 34 条
[1]   Macrophage lipoprotein lipase promotes foam cell formation and atherosclerosis in vivo [J].
Babaev, VR ;
Fazio, S ;
Gleaves, LA ;
Carter, KJ ;
Semenkovich, CF ;
Linton, MF .
JOURNAL OF CLINICAL INVESTIGATION, 1999, 103 (12) :1697-1705
[2]   Conjugated linoleic acids alter milk fatty acid composition and inhibit milk fat secretion in dairy cows [J].
Chouinard, PY ;
Corneau, L ;
Barbano, DM ;
Metzger, LE ;
Bauman, DE .
JOURNAL OF NUTRITION, 1999, 129 (08) :1579-1584
[3]   Effects of conjugated linoleic acid (CLA) isomers on lipid levels and peroxisome proliferation in the hamster [J].
de Deckere, EAM ;
van Amelsvoort, JMM ;
McNeill, GP ;
Jones, P .
BRITISH JOURNAL OF NUTRITION, 1999, 82 (04) :309-317
[4]   Conjugated linoleic acid rapidly reduces body fat content in mice without affecting energy intake [J].
Delany, JP ;
Blohm, F ;
Truett, AA ;
Scimeca, JA ;
West, DB .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 1999, 276 (04) :R1172-R1179
[5]   Lipoprotein lipase and the disposition of dietary fatty acids [J].
Fielding, BA ;
Frayn, KN .
BRITISH JOURNAL OF NUTRITION, 1998, 80 (06) :495-502
[6]   MECHANISMS OF INCREASED LIPOPROTEIN-LIPASE IN FAT-CELLS OF OBESE ZUCKER RATS [J].
FRIED, SK ;
TURKENKOPF, IJ ;
GOLDBERG, IJ ;
DOOLITTLE, MH ;
KIRCHGESSNER, TG ;
SCHOTZ, MC ;
JOHNSON, PR ;
GREENWOOD, MRC .
AMERICAN JOURNAL OF PHYSIOLOGY, 1991, 261 (05) :E653-E660
[7]   NUTRITION-INDUCED VARIATIONS IN RESPONSIVENESS TO INSULIN EFFECTS ON LIPOPROTEIN-LIPASE ACTIVITY IN ISOLATED RAT FAT-CELLS [J].
FRIED, SK ;
VELAZQUEZ, N ;
NOBEL, J .
JOURNAL OF NUTRITION, 1990, 120 (09) :1087-1095
[8]   RELATIONSHIPS BETWEEN PLASMA-FREE FATTY-ACID CONCENTRATION, ENDOGENOUS GLUCOSE-PRODUCTION, AND FASTING HYPERGLYCEMIA IN NORMAL AND NON-INSULIN-DEPENDENT DIABETIC INDIVIDUALS [J].
GOLAY, A ;
SWISLOCKI, ALM ;
CHEN, YDI ;
REAVEN, GM .
METABOLISM-CLINICAL AND EXPERIMENTAL, 1987, 36 (07) :692-696
[9]  
Goldberg IJ, 1996, J LIPID RES, V37, P693
[10]  
Henderson HE, 1999, J LIPID RES, V40, P735