PPARγ activators improve glucose homeostasis by stimulating fatty acid uptake in the adipocytes

被引:113
作者
Martin, G [1 ]
Schoonjans, K [1 ]
Staels, B [1 ]
Auwerx, J [1 ]
机构
[1] Inst Pasteur, Dept Atherosclerose, INSERM, U325, F-59019 Lille, France
关键词
fatty acids; gene expression; lipid metabolism; nuclear receptors; peroxisomes; transcription factors;
D O I
10.1016/S0021-9150(97)00315-8
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
It is currently thought that the effects of PPAR gamma activation on glucose homeostasis may be due to the effect of this nuclear receptor on the production of adipocyte-derived signalling molecules, which affect muscle glucose metabolism. Potential signalling molecules derived from adipocytes and modified by PPAR gamma activation include TNF alpha and leptin, which both interfere with glucose homeostasis. In addition to its effects on these proteins, PPAR gamma also profoundly affects fatty acid metabolism. Activation of PPAR gamma will selectively induce the expression of several genes involved in fatty acid uptake, such as lipoprotein lipase, fatty acid transport protein and acyl-CoA synthetase, in adipose tissue without changing their expression in muscle tissue. This co-ordinate regulation of fatty acid partitioning by PPAR gamma results in an adipocyte 'FFA steal' causing a relative depletion of fatty acids in the muscle. Based on the well established interference of muscle fatty acid and glucose metabolism it is hypothesized that reversal of muscle fatty acid accumulation will contribute to the improvement in whole body glucose homeostasis. (C) 1998 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:S75 / S80
页数:6
相关论文
共 69 条
  • [11] TIME-DEPENDENCE OF THE INTERACTION BETWEEN LIPID AND GLUCOSE IN HUMANS
    BONADONNA, RC
    ZYCH, K
    BONI, C
    FERRANNINI, E
    DEFRONZO, RA
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1989, 257 (01): : E49 - E56
  • [12] Differential expression of peroxisome proliferator-activated receptors (PPARs): Tissue distribution of PPAR-alpha, -beta, and -gamma in the adult rat
    Braissant, O
    Foufelle, F
    Scotto, C
    Dauca, M
    Wahli, W
    [J]. ENDOCRINOLOGY, 1996, 137 (01) : 354 - 366
  • [13] The SREBP pathway: Regulation of cholesterol metabolism by proteolysis of a membrane-bound transcription factor
    Brown, MS
    Goldstein, JL
    [J]. CELL, 1997, 89 (03) : 331 - 340
  • [14] BRUNZELL JD, 1983, J LIPID RES, V24, P147
  • [15] IMPAIRED FATTY-ACID METABOLISM IN FAMILIAL COMBINED HYPERLIPIDEMIA - A MECHANISM ASSOCIATING HEPATIC APOLIPOPROTEIN-B OVERPRODUCTION AND INSULIN-RESISTANCE
    CABEZAS, MC
    DEBRUIN, TWA
    DEVALK, HW
    SHOULDERS, CC
    JANSEN, H
    ERKELENS, DW
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1993, 92 (01) : 160 - 168
  • [16] Modulation of insulin activities by leptin
    Cohen, B
    Novick, D
    Rubinstein, M
    [J]. SCIENCE, 1996, 274 (5290) : 1185 - 1188
  • [17] INSULIN RESISTANCE - A MULTIFACETED SYNDROME RESPONSIBLE FOR NIDDM, OBESITY, HYPERTENSION, DYSLIPIDEMIA, AND ATHEROSCLEROTIC CARDIOVASCULAR-DISEASE
    DEFRONZO, RA
    FERRANNINI, E
    [J]. DIABETES CARE, 1991, 14 (03) : 173 - 194
  • [18] DESILVA HV, 1994, J BIOL CHEM, V269, P2324
  • [19] The PPAR alpha-leukotriene B-4 pathway to inflammation control
    Devchand, PR
    Keller, H
    Peters, JM
    Vazquez, M
    Gonzalez, FJ
    Wahli, W
    [J]. NATURE, 1996, 384 (6604) : 39 - 43
  • [20] Thiazolidinediones repress ob gene expression in rodents via activation of peroxisome proliferator-activated receptor gamma
    DeVos, P
    Lefebvre, AM
    Miller, SG
    GuerreMillo, M
    Wong, K
    Saladin, R
    Hamann, LG
    Staels, B
    Briggs, MR
    Auwerx, J
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1996, 98 (04) : 1004 - 1009