Anti-Restenotic Roles of Dihydroaustrasulfone Alcohol Involved in Inhibiting PDGF-BB-Stimulated Proliferation and Migration of Vascular Smooth Muscle Cells

被引:23
|
作者
Li, Pei-Chuan [1 ,2 ]
Sheu, Ming-Jyh [2 ]
Ma, Wei-Fen [3 ]
Pan, Chun-Hsu [4 ]
Sheu, Jyh-Horng [5 ]
Wu, Chieh-Hsi [2 ,4 ]
机构
[1] Univ So Calif, Sch Pharm, Dept Pharmacol & Pharmaceut Sci, Los Angeles, CA 90089 USA
[2] China Med Univ, Sch Pharm, Taichung 404, Taiwan
[3] China Med Univ, Sch Nursing, Taichung 404, Taiwan
[4] Taipei Med Univ, Dept Pharm, Taipei 110, Taiwan
[5] Natl Sun Yat Sen Univ, Dept Marine Biotechnol & Resources, Kaohsiung 804, Taiwan
来源
MARINE DRUGS | 2015年 / 13卷 / 05期
关键词
dihydroaustrasulfone alcohol; anti-restenosis; neointimal hyperplasia; marine origin; GROWTH-FACTOR; SIGNALING PATHWAY; SOFT CORAL; ARTERIAL INJURY;
D O I
10.3390/md13053046
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Dihydroaustrasulfone alcohol (DA), an active compound firstly isolated from marine corals, has been reported to reveal anti-cancer and anti-inflammation activities. These reported activities of DA raised a possible application in anti-restenosis. Abnormal proliferation and migration of vascular smooth muscle cells (VSMCs) and the stimulation of platelet-derived growth factor (PDGF)-BB play major pathological processes involved in the development of restenosis. Experimental results showed that DA markedly reduced balloon injury-induced neointima formation in the rat carotid artery model and significantly inhibited PDGF-BB-stimulated proliferation and migration of VSMCs. Our data further demonstrated that translational and active levels of several critical signaling cascades involved in VSMC proliferation, such as extracellular signal-regulated kinase/mitogen-activated protein kinases (ERK/MAPK), phosphatidylinositol 3-kinase (PI3K)/AKT, and signal transducer and activator of transcription (STAT), were obviously inhibited. In addition, DA also decreased the activation and expression levels of gelatinases (matrix metalloproteinase (MMP)-2 and MMP-9) involved in cell migration. In conclusion, our findings indicate that DA can reduce balloon injury-neointimal hyperplasia, the effect of which may be modulated through suppression of VSMC proliferation and migration. These results suggest that DA has potential application as an anti-restenotic agent for the prevention of restenosis.
引用
收藏
页码:3046 / 3060
页数:15
相关论文
共 50 条
  • [1] J20619 inhibits PDGF-BB-stimulated vascular smooth muscle cell proliferation and migration
    Fang, Lian-hua
    Guo, Jing
    Li, Li
    Wu, Yu-jie
    Yan, Yu
    Xu, Xiao-na
    Wang, Shou-bao
    Yuan, Tian-yi
    Du, Guan-hua
    FASEB JOURNAL, 2014, 28 (01):
  • [2] Silencing CCL8 inhibited the proliferation and migration of PDGF-BB-stimulated human aortic smooth muscle cells
    Dai, Shipeng
    Zhang, Jiangang
    Xu, Zesheng
    BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY, 2020, 84 (08) : 1585 - 1593
  • [3] Myricitrin inhibits PDGF-BB-stimulated vascular smooth muscle cell proliferation and migration through suppressing PDGFRβ/Akt/Erk signaling
    Li, Jie
    Zhang, Mei
    Ma, Juanjuan
    INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL MEDICINE, 2015, 8 (11): : 21715 - 21723
  • [4] ROCK1 induces ERK nuclear translocation in PDGF-BB-stimulated migration of rat vascular smooth muscle cells
    Zhao, Ying
    Lv, Miao
    Lin, HaiShuang
    Hong, Yan
    Yang, FuChun
    Sun, YunLiang
    Guo, Yan
    Cui, Ying
    Li, Sheng
    Gao, Ying
    IUBMB LIFE, 2012, 64 (02) : 194 - 202
  • [5] DL-3-n-butylphthalide suppresses PDGF-BB-stimulated vascular smooth muscle cells proliferation via induction of autophagy
    Hu, Haijuan
    Liu, Bin
    Zuo, Yabei
    Liu, Demin
    Xie, Ruiqin
    Cui, Wei
    LIFE SCIENCES, 2016, 151 : 182 - 188
  • [6] Dihydroaustrasulfone Alcohol Inhibits PDGF-Induced Proliferation and Migration of Human Aortic Smooth Muscle Cells through Inhibition of the Cell Cycle
    Chen, Yao-Chang
    Wen, Zhi-Hong
    Lee, Yen-Hsien
    Chen, Chu-Lun
    Hung, Han-Chun
    Chen, Chun-Hong
    Chen, Wu-Fu
    Tsai, Min-Chien
    MARINE DRUGS, 2015, 13 (04): : 2390 - 2406
  • [7] Role and Molecular Mechanism of Cantharidin in PDGF-BB-Induced Proliferation and Migration of Vascular Smooth Muscle Cells
    Qiu, L. Q.
    Xu, C. W.
    Jiang, H.
    Xia, H.
    JOURNAL OF THE AMERICAN GERIATRICS SOCIETY, 2019, 67 : S610 - S611
  • [8] Atorvastatin inhibits PDGF-BB induced vascular smooth muscle cells proliferation and migration in cerebrovascular diseases
    Li, Cai-Yan
    Liang, Wu
    Li, Hua
    Wang, Fan
    Xie, Wan-Hong
    INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL MEDICINE, 2016, 9 (11): : 20824 - 20834
  • [9] Cullin3 (CUL3) suppresses proliferation, migration and phenotypic transformation of PDGF-BB-stimulated vascular smooth muscle cells and mitigates inflammatory response by repressing Hedgehog signaling pathway
    Xiang, Yuluan
    Li, Lihua
    Xia, Shuang
    Lv, Jinlin
    Li, Xiaoling
    BIOENGINEERED, 2021, 12 (02) : 9463 - 9472
  • [10] ANTIPROLIFERATIVE ACTIVITY OF JM92, A NEWLY SYNTHESIZED INDOLEDIONE DERIVATIVE, ON PDGF-BB-STIMULATED RAT AORTIC VASCULAR SMOOTH MUSCLE CELLS
    Yun, Y.
    Seo, J.
    Kim, T.
    Ryu, C.
    Park, E.
    Yoo, H.
    ATHEROSCLEROSIS SUPPLEMENTS, 2008, 9 (01) : 65 - 65