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Oxidative stress of alternariol in Caco-2 cells
Celia Fernández-Blanco1, Guillermina Font1, Maria-Jose Ruiz1
1Laboratory of Toxicology, Faculty of Pharmacy, University of Valencia, Av. Vicent Andrés Estellés s/n, 46100 Burjassot, Valencia, Spain.
Abstract:
Alternariol (AOH) is a mycotoxin produced by fungus Alternaria. It is found in a wide variety of fruits and cereals products. AOH is able to damage human health. The aim of this study was to evaluate the cytotoxicity of AOH in human colon adenocarcinoma (Caco-2) cells. Moreover, some events related to oxidative stress were evaluated: reactive oxygen species (ROS) generated by oxidation of 2',7'-dichlorodihydrofluorescein diacetate; peroxidation of lipid (LPO) by malondialdehyde (MDA) production; and antioxidant enzymatic capability of catalase (CAT) and superoxide dismutase (SOD). Cytotoxicity of AOH (from 3.125 to 100 μM) was determined during 24, 48 and 72 h of exposure by different endpoints. AOH decreased cell viability by MTT, NR and PC assays. However, no IC50 values were obtained by any of the assays tested. AOH induced a strong oxidative stress in Caco-2 cells by generation of ROS production and LPO associated with a rise in the SOD activity at all concentration tested. ROS increased 1.2-fold with respect to the control and MDA production ranged from 130% to 250% compared to control. Our results demonstrated that in spite of AOH showing cytotoxic effect on Caco-2 cells at the highest concentration tested, oxidative stress by LPO and ROS was observed at all concentrations assayed. This could cause an injury and be hazardous to health.
Insights
Alternariol (AOH), a mycotoxin from Alternaria, causes oxidative stress in human colon cells (Caco-2). While not reaching lethal doses, AOH increased reactive oxygen species (ROS) and lipid peroxidation, posing health risks.
Area of Science:
- Toxicology
- Cell Biology
- Mycotoxicology
Background:
- Alternariol (AOH) is a mycotoxin produced by Alternaria fungi, commonly found in food products.
- AOH exposure poses potential risks to human health due to its toxic properties.
Purpose of the Study:
- To investigate the cytotoxic effects of AOH on human colon adenocarcinoma (Caco-2) cells.
- To evaluate AOH-induced oxidative stress markers, including reactive oxygen species (ROS), lipid peroxidation (LPO), and antioxidant enzyme activity (catalase and superoxide dismutase).
Main Methods:
- Caco-2 cells were exposed to varying concentrations of AOH (3.125–100 μM) for 24, 48, and 72 hours.
- Cytotoxicity was assessed using MTT, NR, and PC assays.
- Oxidative stress was measured by quantifying ROS production, malondialdehyde (MDA) levels (for LPO), and the activity of superoxide dismutase (SOD) and catalase (CAT).
Main Results:
- AOH reduced cell viability in Caco-2 cells, though no IC50 values were determined.
- Significant oxidative stress was induced by AOH, evidenced by increased ROS production (1.2-fold) and elevated MDA levels (130%–250% increase).
- Superoxide dismutase (SOD) activity increased at all tested concentrations of AOH.
Conclusions:
- AOH exhibits cytotoxic effects on Caco-2 cells, particularly at higher concentrations.
- AOH induces significant oxidative stress, characterized by ROS generation and lipid peroxidation, even at lower concentrations.
- The observed oxidative stress and cytotoxicity suggest potential health hazards associated with AOH exposure.
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