6533b828fe1ef96bd1288e37

RESEARCH PRODUCT

Oxidative stress of alternariol in Caco-2 cells

Guillermina FontCelia Fernández-blancoMaría-josé Ruiz

subject

AntioxidantCell Survivalmedicine.medical_treatmentAlternariolToxicologymedicine.disease_causeSuperoxide dismutaseLactoneschemistry.chemical_compoundMalondialdehydemedicineHumansViability assaychemistry.chemical_classificationReactive oxygen speciesDose-Response Relationship DrugbiologySuperoxide DismutaseGeneral MedicineMycotoxinsCatalaseMalondialdehydeMolecular biologyOxidative StresschemistryBiochemistryCatalasebiology.proteinLipid PeroxidationCaco-2 CellsReactive Oxygen SpeciesOxidative stress

description

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.

https://doi.org/10.1016/j.toxlet.2014.07.024