Alternariol induce toxicity via cell death and mitochondrial damage on Caco-2 cells. (February 2016)

• Record Type: Journal Article
• Authors: Fernández-Blanco, Celia; Juan-García, Ana; Juan, Cristina; Font, Guillermina; Ruiz, Maria-Jose
• Is Part Of: Food and chemical toxicology. Volume 88(2016)
• Page Start: 32
• Page End: 39
• Publication Date: 2016-02
• Subjects: Alternariol -- Cell cycle -- Membrane potential -- Necrosis-apoptosis -- Degradation products -- LC–MS/MS -- Caco-2 cells; Toxicology -- Periodicals; Food poisoning -- Periodicals; Food Poisoning -- Periodicals; Toxicology -- Periodicals; Toxicologie -- Périodiques; Intoxications alimentaires -- Périodiques; Food poisoning; Toxicology; Periodicals; Electronic journals; 615.9
• DOI: 10.1016/j.fct.2015.11.022
• Languages: English
• ISSNs: 0278-6915

Abstract

Abstract: Alternariol (AOH), a mycotoxin produced by Alternaria sp, appears as food contaminant in fruit, vegetables and cereal products. Its toxicity has been demonstrated, but the mechanisms involved have not been elucidated yet. In this study, the pathways triggered by AOH and degradation products generated on Caco-2 cells were evaluated. Cells were exposed to AOH sub-cytotoxic concentrations of 15, 30 and 60 μM. Cell cycle disruption, the induction of apoptosis/necrosis and changes in mitochondrial membrane potential (Δψm) after 24 and 48 h was asses by flow cytometry. Also, AOH and its degradation products were evaluated after 24 and 48 h by high-performance liquid chromatography with tandem mass spectrometric (LC-MS/MS) to detect and quantify its levels. Cell cycle was significantly decreased at G1 phase and increased at S and G2/M phase at the time of exposure. AOH induced necrosis, apoptosis/necrosis and loss of Δψm in a dose and time-dependent manner. The concentrations of AOH quantified in the culture media exposed to AOH decreased as the exposure time was increased. In conclusion, AOH caused cytotoxic effects supported by blocking cell cycle, decreasing cell proliferation and increasing apoptosis/necrosis cells. Highlights: AOH induced apoptosis/necrosis and mitochondrial disruption in Caco-2 cells. AOH caused toxic effects supported by blocking cell cycle in Caco-2 cells. The concentrations of AOH in the culture media decreased as the exposure time was increased.