Prevention of Aflatoxin B1-Induced DNA Breaks by β-D-Glucan
Eduardo Madrigal-Bujaidar,
José Antonio Morales-González,
Manuel Sánchez-Gutiérrez,
Jeannett A. Izquierdo-Vega,
Alicia Reyes-Arellano,
Isela Álvarez-González,
Ricardo Pérez-Pasten,
Eduardo Madrigal-Santillán
Affiliations
Eduardo Madrigal-Bujaidar
Genetics Laboratory, National School of Biological Sciences, IPN. "Unidad A. López Mateos". Av. Wilfrido Massieu. Zacatenco, México, DF 07738, Mexico
José Antonio Morales-González
Conservation Medicine Laboratory, Superior School of Medicine, IPN. "Unidad Casco de Santo Tomas". Plan de San Luis y Díaz Mirón. México, DF 11340, Mexico
Manuel Sánchez-Gutiérrez
Institute of Health Sciences, Autonomous University of Hidalgo State, Ex-Hacienda de la Concepción, Tilcuautla, Hidalgo 42160, Mexico
Jeannett A. Izquierdo-Vega
Institute of Health Sciences, Autonomous University of Hidalgo State, Ex-Hacienda de la Concepción, Tilcuautla, Hidalgo 42160, Mexico
Alicia Reyes-Arellano
Organic Chemistry Department, National School of Biological Sciences, IPN. "Unidad Casco de Santo Tomas". Carpio y Plan de Ayala. México, DF 11340, Mexico
Isela Álvarez-González
Genetics Laboratory, National School of Biological Sciences, IPN. "Unidad A. López Mateos". Av. Wilfrido Massieu. Zacatenco, México, DF 07738, Mexico
Ricardo Pérez-Pasten
Preclinical Toxicology Laboratory, National School of Biological Sciences, IPN. "Unidad A. López Mateos". Av. Wilfrido Massieu. Zacatenco, México, DF 07738, Mexico
Eduardo Madrigal-Santillán
Conservation Medicine Laboratory, Superior School of Medicine, IPN. "Unidad Casco de Santo Tomas". Plan de San Luis y Díaz Mirón. México, DF 11340, Mexico
Aflatoxins are a group of naturally-occurring carcinogens that are known to contaminate different human and animal foodstuffs. Aflatoxin B1 (AFB1) is the most genotoxic hepatocarcinogenic compound of all of the aflatoxins. In this report, we explore the capacity of β-D-glucan (Glu) to reduce the DNA damage induced by AFB1 in mouse hepatocytes. For this purpose, we applied the comet assay to groups of animals that were first administered Glu in three doses (100, 400 and 700 mg/kg bw, respectively) and, 20 min later, 1.0 mg/kg of AFB1. Liver cells were obtained at 4, 10 and 16 h after the chemical administration and examined. The results showed no protection of the damage induced by AFB1 with the low dose of the polysaccharide, but they did reveal antigenotoxic activity exerted by the two high doses. In addition, we induced a co-crystallization between both compounds, determined their fusion points and analyzed the molecules by UV spectroscopy. The data suggested the formation of a supramolecular complex between AFB1 and β-D-glucan.