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Mol Immunol. 2017 May;85:214-221. doi: 10.1016/j.molimm.2017.02.020. Epub 2017 Mar 10.

Vitexin alleviates ox-LDL-mediated endothelial injury by inducing autophagy via AMPK signaling activation.

Author information

1
Department of Cardiology, The First Affiliated Hospital of Xinxiang Medical University, Xinxiang 453100, China.
2
Department of Cardiology, The First Affiliated Hospital of Xinxiang Medical University, Xinxiang 453100, China. Electronic address: zhigangchenxx@163.com.

Abstract

Endothelial cell injury plays a crucial role in the development and pathogenesis of cardiovascular disease. Vitexin is a natural flavonoid characterized by anti-oxidative and anti-inflammatory properties. The purpose of this study was to investigate the effects of vitexin on ox-LDL-induced endothelial dysfunction and to explore the underlying molecular mechanisms. In the present study, vitexin was found to play a protective role against ox-LDL-induced endothelial injury. Vitexin significantly promoted cell viability and inhibited apoptosis in ox-LDL-treated HUVECs. The up-regulation of cleaved Caspase-3, cleaved Caspase-9 and Bax induced by ox-LDL were inhibited by treatment with vitexin; meanwhile, the down-regulation of Bcl-2 was suppressed by vitexin. Pretreatment with vitexin was found to inhibit the ox-LDL-induced overexpression of IL-1β, IL-6, TNF-α, E-selectin, ICAM1 and VCAM1. Moreover, vitexin reduced ox-LDL-induced oxidative stress by inhibiting the production of ROS and MDA, and by promoting the expression of SOD. Furthermore, we had shown that vitexin protected against the ox-LDL induced cell injury by activating autophagy. The protective effects of vitexin in ox-LDL-treated HUVECs were all reversed following treatment with the autophagy inhibitor 3-MA. In addition, we found that vitexin increased the expression of p-AMPK and decreased the expression of p-mTOR. The combination of the AMPK inhibitor Compound C plus vitexin significantly reversed the effects of vitexin in ox-LDL-treated HUVECs, such as the inhibition of autophagy, reduction in cell viability, increase in apoptosis and ROS production. In conclusion, these data suggest that vitexin ameliorates ox-LDL-mediated endothelial injury by inducing autophagy via AMPK signaling.

KEYWORDS:

AMPK signaling; Autophagy; Endothelial dysfunction; Oxidative stress; Vitexin

PMID:
28288411
DOI:
10.1016/j.molimm.2017.02.020
[Indexed for MEDLINE]

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