Anthocyans-rich Aronia melanocarpa extract possesses ability to protect endothelial progenitor cells against angiotensin II induced dysfunction.

Phytomedicine

Department of Pharmacognosy and Molecular Basis of Phytotherapy, Faculty of Pharmacy, Medical University of Warsaw, Banacha 1, 02-097 Warsaw, Poland. Electronic address:

Published: December 2015

AI Article Synopsis

  • Endothelial progenitor cells (EPCs) can help combat atherosclerosis, but their function may be hindered by angiotensin II, which induces oxidative stress and accelerates aging in these cells.
  • Chokeberry fruit extract, rich in anthocyanins with strong antioxidant properties, was tested to see if it could mitigate the harmful effects of angiotensin II on EPCs.
  • The study found that chokeberry extract improved EPC growth, reduced cell aging, and enhanced their migration and ability to form new blood vessels, suggesting it could be beneficial in preventing coronary artery disease.

Article Abstract

Background: Endothelial progenitor cells (EPC) may provide protection against atherosclerosis and plaque rupture by their innate ability to replace dysfunctional or damaged endothelial cells in plaque microvessels. There is evidence that angiotensin II may impair the angiogenic functions of EPCs in the atherosclerotic plaque by accelerating senescence and inhibiting their proliferation through oxidative stress induction.

Purpose: In this study, we examined whether chokeberry (Aronia melanocarpa) fruit extract, containing mainly anthocyanins with potent antioxidative properties, could protect EPCs against angiotensin-induced oxidative stress.

Methods: EPCs were isolated from peripheral blood of young healthy volunteers and cultivated on fibronectin-coated plates in the presence or absence of angiotensin II (1 µM) and chokeberry extract (1-25 µg/ml).

Results: EPCs exposed to chokeberry extract prior to angiotensin II showed a significant increase of proliferation and telomerase activity, and a decrease in the percentage of senescent cells and intracellular ROS formation in comparison to angiotensin II treated cells. Furthermore, extract increased migration ability, adhesion to fibronectin and the angiogenic potential of EPC in vitro diminished by angiotensin II in a concentration-dependent manner. That effect was related to the activation of the Nrf2 transcription factor and the increase of HO-1 expression.

Conclusions: Our results suggested that chokeberry extract may protect EPCs against angiotensin II-induced dysfunction and could play a potential role in the prevention of coronary artery disease.

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Source
http://dx.doi.org/10.1016/j.phymed.2015.10.009DOI Listing

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