Literature DB >> 32161445

Inhibitory Effect of Curcumin on Artery Restenosis Following Carotid Endarterectomy and Its Associated Mechanism in vitro and in vivo.

Dapeng Zhang1, Yanhui Yang2, Yuanchao Li1, Guodong Zhang1, Zhenguo Cheng1.   

Abstract

OBJECTIVE: The present study aimed to assess the effect of curcumin (Cur) on carotid artery restenosis following carotid endarterectomy (CEA) and its associated mechanism in vivo and in vitro.
METHODS: Ang II was used to induce excessive proliferation of rabbit aortic smooth muscle cells (CCC-SMC-1) in order to establish a hemadostenosis cell model. Similarly, the animal model of carotid artery restenosis was established by carotid artery gas drying injury combined with high-fat feed prior to CEA. CCC-SMC-1 cells and animals were treated by Cur and its effects on neointimal hyperplasia, inflammation and oxidative stress were detected and observed. The proteins that were associated with the Raf/MEK/ERK pathway were detected in cells and rabbit carotid artery tissues.
RESULTS: Cur inhibited the proliferation of smooth muscle cells and neointimal formation and reduced the inflammation and oxidative stress indices. Concomitantly, Cur reduced the phosphorylation of the Raf/MEK/ERK pathway proteins.
CONCLUSION: Cur could inhibit carotid restenosis following CEA by inhibiting the activation of the Raf/MEK/ERK pathway.
© 2020 Zhang et al.

Entities:  

Keywords:  Raf/MEK/ERK; carotid endarterectomy; curcumin; restenosis; vascular smooth muscle cells

Mesh:

Substances:

Year:  2020        PMID: 32161445      PMCID: PMC7049773          DOI: 10.2147/DDDT.S229607

Source DB:  PubMed          Journal:  Drug Des Devel Ther        ISSN: 1177-8881            Impact factor:   4.162


  38 in total

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Journal:  Sci Rep       Date:  2016-09-30       Impact factor: 4.379

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  3 in total

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2.  MAGOH/MAGOHB Inhibits the Tumorigenesis of Gastric Cancer via Inactivation of b-RAF/MEK/ERK Signaling.

Authors:  Yong Zhou; Zhongqi Li; Xuan Wu; Laizhen Tou; Jingjing Zheng; Donghui Zhou
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3.  Curcumin attenuates inflammation of Macrophage-derived foam cells treated with Poly-L-lactic acid degradation via PPARγ signaling pathway.

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  3 in total

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