Characterization of selective resistance to insulin signaling in the vasculature of obese Zucker (fa/fa) rats

被引:486
作者
Jiang, ZY [1 ]
Lin, YW [1 ]
Clemont, A [1 ]
Feener, EP [1 ]
Hein, KD [1 ]
Igarashi, M [1 ]
Yamauchi, T [1 ]
White, MF [1 ]
King, GL [1 ]
机构
[1] Harvard Univ, Sch Med, Joslin Diabet Ctr, Div Res, Boston, MA 02215 USA
关键词
D O I
10.1172/JCI5971
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Both insulin resistance and hyperinsulinemia have been reported to be independent risk factors for cardiovascular diseases. However, little is known regarding insulin signaling in the vascular tissues in insulin-resistant states. In this report, insulin signaling on the phosphatidylinositol 3-kinase (PI 3-kinase) and mitogen-activated protein (MAP) kinase pathways were compared in vascular tissues of lean and obese Zucker (fa/fa) rats in both ex vivo and in vivo studies. Ex vivo, insulin-stimulated tyrosine phosphorylation of insulin receptor beta subunits (IR beta) in the aorta and microvessels of obese rats was significantly decreased compared with lean rats, although the protein levels of IR beta in the 2 groups were not different. Insulin-induced tyrosine phosphorylation of insulin receptor substrates 1 and 2 (IRS-1 and IRS-2) and their protein levels were decreased in the aorta of obese rats compared with lean rats. The association of p85 subunit to the IRS proteins and the IRS-associated PI 3-kinase activities stimulated by insulin in the aorta of obese rats were significantly decreased compared with the lean rats. In addition, insulin-stimulated serine phosphorylation of Akt, a downstream kinase of PI 3-kinase pathway, was also reduced significantly in isolated microvessels from obese rats compared with the lean rats. In euglycemic clamp studies, insulin infusion greatly increased tyrosine phosphorylation of IR beta- and IRS-2-associated PI 3-kinase activity in the aorta of lean rats, but only slight increases were observed in obese rats. In contrast, insulin stimulated tyrosine phosphorylation of MAP kinase (ERK-1/2) equally in isolated microvessels of lean and obese rats, although basal tyrosine phosphorylation of ERK-1/2 was higher in the obese rats. To our knowledge, these data provided the first direct measurements of insulin signaling in the vascular tissues, and documented a selective resistance to PI 3-kinase (but not to MAP kinase pathway) in the vascular tissues of obese Zucker rats.
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页码:447 / 457
页数:11
相关论文
共 56 条
  • [1] Alterations in skeletal muscle protein-tyrosine phosphatase activity and expression in insulin-resistant human obesity and diabetes
    Ahmad, F
    Azevedo, JL
    Cortright, R
    Dohm, GL
    Goldstein, BJ
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1997, 100 (02) : 449 - 458
  • [2] Altered expression levels and impaired steps in the pathway to phosphatidylinositol 3-kinase activation via insulin receptor substrates 1 and 2 in Zucker fatty rats
    Anai, M
    Funaki, M
    Ogihara, T
    Terasaki, J
    Inukai, K
    Katagiri, H
    Fukushima, Y
    Yazaki, Y
    Kikuchi, M
    Oka, Y
    Asano, T
    [J]. DIABETES, 1998, 47 (01) : 13 - 23
  • [3] HYPERINSULINEMIA PRODUCES BOTH SYMPATHETIC NEURAL ACTIVATION AND VASODILATION IN NORMAL HUMANS
    ANDERSON, EA
    HOFFMAN, RP
    BALON, TW
    SINKEY, CA
    MARK, AL
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1991, 87 (06) : 2246 - 2252
  • [4] Insulin and angiotensin II are additive in stimulating TGF-beta 1 and matrix mRNAs in mesangial cells
    Anderson, PW
    Zhang, XY
    Tian, J
    Correale, JD
    Xi, PX
    Yang, D
    Graf, K
    Law, RE
    Hsueh, WA
    [J]. KIDNEY INTERNATIONAL, 1996, 50 (03) : 745 - 753
  • [5] Chronic activation of protein kinase C in soleus muscles and other tissues of insulin-resistant type II diabetic Goto-Kakizaki (GK), obese/aged, and obese/Zucker rats - A mechanism for inhibiting glycogen synthesis
    Avignon, A
    Yamada, K
    Zhou, XP
    Spencer, B
    Cardona, O
    SabaSiddique, S
    Galloway, L
    Standaert, ML
    Farese, RV
    [J]. DIABETES, 1996, 45 (10) : 1396 - 1404
  • [6] INSULIN, INSULIN-LIKE GROWTH FACTOR-I AND PLATELET-DERIVED GROWTH-FACTOR INTERACT ADDITIVELY IN THE INDUCTION OF THE PROTOONCOGENE C-MYC AND CELLULAR PROLIFERATION IN CULTURED BOVINE AORTIC SMOOTH-MUSCLE CELLS
    BANSKOTA, NK
    TAUB, R
    ZELLNER, K
    KING, GL
    [J]. MOLECULAR ENDOCRINOLOGY, 1989, 3 (08) : 1183 - 1190
  • [7] MECHANISMS OF FATTY ACID-INDUCED INHIBITION OF GLUCOSE-UPTAKE
    BODEN, G
    CHEN, XH
    RUIZ, J
    WHITE, JV
    ROSSETTI, L
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1994, 93 (06) : 2438 - 2446
  • [8] BRAY GA, 1977, FED PROC, V36, P148
  • [9] Insulin, but not contraction, activates Akt/PKB in isolated rat skeletal muscle
    Brozinick, JT
    Birnbaum, MJ
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (24) : 14679 - 14682
  • [10] INSULIN-RECEPTOR KINASE IN HUMAN SKELETAL-MUSCLE FROM OBESE SUBJECTS WITH AND WITHOUT NONINSULIN DEPENDENT DIABETES
    CARO, JF
    SINHA, MK
    RAJU, SM
    ITTOOP, O
    PORIES, WJ
    FLICKINGER, EG
    MEELHEIM, D
    DOHM, GL
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1987, 79 (05) : 1330 - 1337