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 50 条
  • [31] Cysteamine Decreases Low-Density Lipoprotein Oxidation, Causes Regression of Atherosclerosis, and Improves Liver and Muscle Function in Low-Density Lipoprotein Receptor-Deficient Mice
    Ahmad, Feroz
    Mitchell, Robert D.
    Houben, Tom
    Palo, Angela
    Yadati, Tulasi
    Parnell, Andrew J.
    Patel, Ketan
    Shiri-Sverdlov, Ronit
    Leake, David S.
    JOURNAL OF THE AMERICAN HEART ASSOCIATION, 2021, 10 (18):
  • [32] Molecular Imaging of Matrix Metalloproteinase Expression in Atherosclerotic Plaques of Mice Deficient in Apolipoprotein E or Low-Density-Lipoprotein Receptor
    Ohshima, Satoru
    Petrov, Artiom
    Fujimoto, Shinichiro
    Zhou, Jun
    Azure, Michael
    Edwards, D. Scott
    Murohara, Toyoaki
    Narula, Navneet
    Tsimikas, Sotirios
    Narula, Jagat
    JOURNAL OF NUCLEAR MEDICINE, 2009, 50 (04) : 612 - 617
  • [33] Dietary Palmitoleic Acid Attenuates Atherosclerosis Progression and Hyperlipidemia in Low-Density Lipoprotein Receptor-Deficient Mice
    Yang, Zhi-Hong
    Pryor, Milton
    Noguchi, Audrey
    Sampson, Maureen
    Johnson, Brittany
    Pryor, Matthew
    Donkor, Kwame
    Amar, Marcelo
    Remaley, Alan T.
    MOLECULAR NUTRITION & FOOD RESEARCH, 2019, 63 (12)
  • [34] Pioglitazone increases macrophage apoptosis and plaque necrosis in advanced atherosclerotic lesions of nondiabetic low-density lipoprotein receptor-null mice
    Thorp, Edward
    Kuriakose, George
    Shah, Yatrik M.
    Gonzalez, Frank J.
    Tabas, Ira
    CIRCULATION, 2007, 116 (19) : 2182 - 2190
  • [35] The lysophosphatidylcholine effector, G2A, promotes atherosclerosis in low-density lipoprotein receptor-deficient mice
    Parks, BW
    Lusis, AJ
    Kabarowski, JH
    ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2006, 26 (05) : E91 - E91
  • [36] Pharmaceutical stabilization of mast cells attenuates experimental atherogenesis in low-density lipoprotein receptor-deficient mice
    Wang, Jing
    Sjoeberg, Sara
    Tia, Viviane
    Secco, Blandine
    Chen, Han
    Yang, Min
    Sukhova, Galina K.
    Shi, Guo-Ping
    ATHEROSCLEROSIS, 2013, 229 (02) : 304 - 309
  • [37] Targeted disruption of cathepsin S reduces atherosclerosis in low-density lipoprotein receptor-deficient mice.
    Sukhova, GK
    Zhang, Y
    Pan, JH
    Libby, P
    Shi, GP
    CIRCULATION, 2001, 104 (17) : 328 - 329
  • [38] FTY720, a synthetic sphingosine 1 phosphate analogue, inhibits development of atherosclerosis in low-density lipoprotein receptor-deficient mice
    Nofer, Jerzy-Roch
    Bot, Martine
    Brodde, Martin
    Taylor, Paul J.
    Salm, Paul
    Brinkmann, Volker
    van Berkel, Theo
    Assmann, Gerd
    Biessen, Erik A. L.
    CIRCULATION, 2007, 115 (04) : 501 - 508
  • [39] Long-term stable correction of low-density lipoprotein receptor-deficient mice with a helper-dependent adenoviral vector expressing the very low-density lipoprotein receptor
    Oka, K
    Pastore, L
    Kim, IH
    Merched, A
    Nomura, S
    Lee, HJ
    Merched-Sauvage, M
    Arden-Riley, C
    Lee, B
    Finegold, M
    Beaudet, A
    Chan, L
    CIRCULATION, 2001, 103 (09) : 1274 - 1281
  • [40] Macrophage-Specific Expression of Mannose-Binding Lectin Controls Atherosclerosis in Low-Density Lipoprotein Receptor-Deficient Mice
    Matthijsen, Robert A.
    de Winther, Menno P. J.
    Kuipers, Dian
    van der Made, Ingeborg
    Weber, Christian
    Herias, M. Veronica
    Gijbels, Marion J. J.
    Buurman, Wim A.
    CIRCULATION, 2009, 119 (16) : 2188 - U101