Resveratrol inhibits high glucose induced collagen upregulation in cardiac fibroblasts through regulating TGF-β1-Smad3 signaling pathway

被引:25
作者
Liu, Junhui [1 ,2 ]
Zhuo, Xiaozhen [1 ]
Liu, Weimin [1 ]
Wan, Zhaofei [1 ]
Liang, Xiao [1 ]
Gao, Shanshan [1 ]
Yuan, Zuyi [1 ]
Wu, Yue [1 ]
机构
[1] Xi An Jiao Tong Univ, Hlth Sci Ctr, Affiliated Hosp 1, Dept Cardiol, Xian 710061, Shaanxi, Peoples R China
[2] Xi An Jiao Tong Univ, Hlth Sci Ctr, Affiliated Hosp 1, Dept Clin Lab, Xian 710061, Shaanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
Resveratrol (Res); Cardiac fibrosis; Angiotensin II (Ang II); Cardiac fibroblasts (CFs); Collagens; ANGIOTENSIN-II; TGF-BETA; FIBROSIS; ACTIVATION; RECEPTOR; HEART; CARDIOMYOPATHY; HYPERTROPHY; DISEASE; IMPACT;
D O I
10.1016/j.cbi.2014.12.031
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
Cardiac fibrosis is a common pathological process presented in a variety of diseases, including hypertension and diabetes. Cardiac fibroblasts (CFs) have been identified as the most important participants in the development of cardiac fibrosis. Exposure of cultured CFs to high glucose (HG) or angiotensin II (Ang II) resulted in increased collagen synthesis. Resveratrol (Res) is a natural polyphenol exhibiting anti-fibrosis effects in a number of different organs fibrosis process, whether Res can prevent HG and Ang II induced fibrosis response in CFs remains unclear. The aim of this work was to evaluate the effects of Res in HG and Ang II induced fibrosis response in CFs. We cultured rat CFs in either normal glucose (5.6 mM) or HG (25 mM) media in the presence of Res or not and the changes in collagens synthesis and TGF-beta 1 production were assessed by Real-time PCR, Western blotting, and enzyme linked immunosorbent assay (ELISA). Furthermore, normal and diabetic mice (induced by single dose of streptozotocin (100 mg/kg) via tail vein) receiving Res (10 mg/kg) were used to explore the effects of Res on cardiac fibrosis in vivo. Masson staining and immunohistochemistry were performed to visualize cardiac collagen deposition. Results indicate that CFs exposed to HG condition shows enhanced proliferation rate. Furthermore, in the presence of HG or Ang II, CFs exhibited increased collagens synthesis and TGF-beta 1 production. And these effects were abolished by Res intervention. In vivo results show that diabetic mice exhibit increased collagen deposition in the cardiac compared with the normal mice. And this change was prevented by the treatment of Res. These results suggest that Res possesses a potential antifibrogenic effect in hypertension and diabetes-related cardiac fibrosis. Moreover, the action mechanism is probably associated with its ability to reduce TGF-beta 1 content in CFs. (C) 2014 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:45 / 52
页数:8
相关论文
共 50 条
  • [21] NLRC5 silencing improves cardiac fibrosis by regulation of TGF-β1/Smad3 signaling pathway
    Huang, Mingjian
    Pan, Chaoxin
    He, Xinbing
    Wang, Qinggao
    Wu, Wanli
    Yang, Qinghua
    Zhang, Zhenqian
    Wen, Zhihao
    Liang, Yiqiang
    Luo, Jinwei
    INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL MEDICINE, 2018, 11 (11): : 12059 - +
  • [22] Muscone inhibits angiotensin II-induced cardiac hypertrophy through the STAT3, MAPK and TGF-β/SMAD signaling pathways
    Liu, Yi-jiang
    Xu, Jia-jia
    Yang, Cui
    Li, Yan-lin
    Chen, Min-wei
    Liu, Shi-xiao
    Zheng, Xiang-hui
    Luo, Ping
    Li, Rui
    Xiao, Di
    Shan, Zhong-gui
    MOLECULAR BIOLOGY REPORTS, 2024, 51 (01)
  • [23] TSG-6 Inhibits the Growth of Keloid Fibroblasts Via Mediating the TGF-β1/Smad Signaling Pathway
    Li, Xin-Yi
    Weng, Xiao-Juan
    Li, Xiao-Jing
    Tian, Xiao-Yu
    JOURNAL OF INVESTIGATIVE SURGERY, 2021, 34 (09) : 947 - 956
  • [24] Daidzein suppresses TGF-β1-induced cardiac fibroblast activation via the TGF-β1/SMAD2/3 signaling pathway
    Shu, Jiangcheng
    Hu, Lizhi
    Wu, Yichen
    Chen, Long
    Huang, Kai
    Wang, Zhaohui
    Liang, Minglu
    EUROPEAN JOURNAL OF PHARMACOLOGY, 2022, 919
  • [25] Resveratrol inhibits TGF-β1-induced fibrotic effects in human fibroblasts
    Fan, Jianwu
    Wei, Shuang
    Zhang, Xiaoyan
    Chen, Li
    Zhang, Xin
    Jiang, Yaping
    Sheng, Minjie
    Chen, Yihui
    ENVIRONMENTAL HEALTH AND PREVENTIVE MEDICINE, 2023, 28
  • [26] Notch signaling inhibits cardiac fibroblast to myofibroblast transformation by antagonizing TGF-β1/Smad3 signaling
    Zhou, Xue-liang
    Fang, Yi-hu
    Wan, Li
    Xu, Qi-rong
    Huang, Huang
    Zhu, Rong-rong
    Wu, Qi-cai
    Liu, Ji-chun
    JOURNAL OF CELLULAR PHYSIOLOGY, 2019, 234 (06) : 8834 - 8845
  • [27] Silencing FHL2 inhibits bleomycin-induced pulmonary fibrosis through the TGF-β1/Smad signaling pathway
    Shi, Mengkun
    Cui, Huixia
    Shi, Jialun
    Mei, Yunqing
    EXPERIMENTAL CELL RESEARCH, 2023, 423 (02)
  • [28] Telmisartan inhibited angiotensin II-induced collagen metabolic imbalance without directly targeting TGF-β 1/Smad signaling pathway in cardiac fibroblasts
    Zhang, Y.
    Zhao, N. A.
    Wang, J-K.
    Zhu, S-M.
    Zhu, H-L.
    Liu, B.
    Cui, Q-W.
    Guan, G-C.
    Tian, G.
    MINERVA CARDIOANGIOLOGICA, 2015, 63 (06): : 507 - 514
  • [29] PTEN inhibitor attenuates cardiac fibrosis by regulating the M2 macrophage phenotype via the PI3K/AKT/TGF-β/Smad 2/3 signaling pathway
    Zhuang, Chenchen
    Guo, Ziyi
    Zhu, Jumo
    Wang, Wenjuan
    Sun, Runmin
    Qi, Miaomiao
    Wang, Qiongying
    Fan, Xin
    Ma, Runxin
    Yu, Jing
    INTERNATIONAL JOURNAL OF CARDIOLOGY, 2022, 356 : 88 - 96
  • [30] The role of TGFβ receptor 1-smad3 signaling in regulating the osteoclastic mode affected by fluoride
    Yu, Haolan
    Jiang, Ningning
    Yu, XiuHua
    Zhao, Zhitao
    Zhang, Xiuyun
    Xu, Hui
    TOXICOLOGY, 2018, 393 : 73 - 82