Olive Pomace Extract Acts as a New Potent Ferroptosis Inhibitor in Human Cells

TL;DR

Olive pomace extract shows potential as a new inhibitor of ferroptosis, a type of cell death, by reducing harmful effects in human cells.

Contribution

Olive pomace extract is identified as a novel and potent ferroptosis inhibitor in human cells.

Findings

OPE reduced ROS and lipid peroxidation induced by RSL3 in TPH-1 and HIECs cells.

OPE reversed RSL3-induced cell death by increasing GSH and the GSH/GSSG ratio.

OPE exhibited antioxidant properties confirmed through the Fenton reaction assay.

Abstract

The olive oil-production sector engages with the environment on multiple levels, and the valorization of olive pomace (OP) has emerged as a key strategy to improve the entire system’s sustainability. Numerous studies have investigated the biological effects of OP phenolic fraction for nutraceutical applications, highlighting its antioxidant properties. This study aimed to assess the effect of an OP extract (OPE) and its phenolic content on ferroptosis induced by RAS-selective lethal 3 (RSL3), an inhibitor of glutathione peroxidase 4. After characterization of OPE phenolic composition, its antioxidant properties were confirmed through the Fenton reaction assay. Subsequently, we examined the effect of OPE on ter-butyl hydroperoxide-induced ROS generation and lipid peroxidation in TPH-1 and HIECs cells and found that OPE reduced ROS and lipid peroxidation. RSL3 decreased the number of vital cells, which was associated with an elevation in ROS and lipid peroxidation, and a reduction in GSH. Interestingly, all these detrimental effects were reversed by OPE. Furthermore, OPE was also found to significantly increase GSH and the GSH/GSSG ratio per se. In conclusion, the fact that OPE decreases ROS and lipid peroxidation induced by RSL3 and augments GSH and cell viability suggests that OPE has potential as a ferroptosis inhibitor.

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