Pioglitazone inhibits connective tissue growth factor expression in advanced atherosclerotic plaques in low-density lipoprotein receptor-deficient mice

被引:30
作者
Game, Bryan A.
He, Lin
Jarido, Veronica
Nareika, Alena
Jaffa, Ayad A.
Lopes-Virella, Maria F.
Huang, Yan
机构
[1] Med Univ S Carolina, Dept Med, Div Endocrinol Diabet & Med Genet, Ralph H Johnson Vet Affairs Med Ctr, Charleston, SC 29403 USA
[2] Med Univ S Carolina, Dept Med, Div Endocrinol Diabet & Med Genet, Charleston, SC 29425 USA
关键词
diabetes mellitus; peroxisome proliferator-activated receptor; thiazolidinediones; connective tissue growth factor; arteriosclerosis;
D O I
10.1016/j.atherosclerosis.2006.06.025
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Connective tissue growth factor (CTGF) is expressed in atherosclerotic plaques. It is generally recognized that CTGF contributes to atherosclerosis by stimulating vascular smooth muscle cell (VSMC) proliferation and extracellular matrix production during the development of atherosclerosis. Recent studies indicate that CTGF may also contribute to plaque destabilization as it induces apoptosis and stimulates MMP-2 expression in VSMCs. Thiazolidinediones (TZDs), a new class of insulin sensitizing drugs for type 2 diabetes, inhibit atherosclerosis. However, their effect on CTGF expression in atherosclerotic plaques remains unknown. In this study, male LDL receptor-deficient mice were fed high-fat diet for 4 months to induce the formation of atherosclerotic plaques and then given the high-fat diet with or without pioglitazone for the next 3 months. At the end of the 7-month study, CTGF expression in aortic atherosclerotic lesions was examined. Results showed that CTGF expression was increased in mice fed the high-fat diet by seven-fold as compared to that in mice fed normal chow, but the treatment with pioglitazone significantly inhibited the high-fat diet-induced CTGF expression. To verify these in vivo observations, in vitro studies using human aortic SMC were conducted. Quantitative real-time PCR and Western blot showed that pioglitazone inhibited TGF-beta-stimulated CTGF expression. In conclusion, the present study has demonstrated that pioglitazone inhibits CTGF expression in mouse advanced atherosclerotic plaques and in cultured human SMCs, and hence unveiled a possible mechanism potentially involved in the inhibition of atherosclerosis by TZD. (c) 2006 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:85 / 91
页数:7
相关论文
共 27 条
  • [21] PYORALA K, 1987, Diabetes Metabolism Reviews, V3, P463
  • [22] Mechanisms of disease - Atherosclerosis - An inflammatory disease
    Ross, R
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1999, 340 (02) : 115 - 126
  • [23] Pioglitazone, a peroxisome proliferator-activated receptor-γ agonist, attenuates left ventricular remodeling and failure after experimental myocardial infarction
    Shiomi, T
    Tsutsui, H
    Hayashidani, S
    Suematsu, N
    Ikeuchi, M
    Wen, J
    Ishibashi, M
    Kubota, T
    Egashira, K
    Takeshita, A
    [J]. CIRCULATION, 2002, 106 (24) : 3126 - 3132
  • [24] Mechanisms of low-density lipoprotein-induced expression of connective tissue growth factor in human aortic endothelial cells
    Sohn, M
    Tan, Y
    Wang, B
    Klein, RL
    Trojanowska, M
    Jaffa, AA
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2006, 290 (04): : H1624 - H1634
  • [25] Pioglitazone, a PPAR-γ ligand, provides protection from dextran sulfate sodium-induced colitis in mice in association with inhibition of the NF-κB-cytokine cascade
    Takagi, T
    Naito, Y
    Tomatsuri, N
    Handa, O
    Ichikawa, H
    Yoshida, N
    Yoshikawa, T
    [J]. REDOX REPORT, 2002, 7 (05) : 283 - 289
  • [26] Vascular inflammation is negatively autoregulated by interaction between CCAAT/enhancer-binding protein-δ and peroxisome proliferator-activated receptor-γ
    Takata, Y
    Kitami, Y
    Yang, ZH
    Nakamura, M
    Okura, T
    Hiwada, K
    [J]. CIRCULATION RESEARCH, 2002, 91 (05) : 427 - 433
  • [27] Effect of pioglitazone on the early stage of type 2 diabetic nephropathy in KK/Ta mice
    Tanimoto, M
    Fan, QL
    Gohda, T
    Shike, T
    Makita, Y
    Tomino, Y
    [J]. METABOLISM-CLINICAL AND EXPERIMENTAL, 2004, 53 (11): : 1473 - 1479