“…Multiple studies have shown that AFB 1 and its metabolites have high oxidative activity and genotoxicity, which might cause gene mutations, oxidative stress damage, apoptosis, and mitochondrial dysfunction in the metabolic systems such as the liver and kidney, reproductive system, nervous system, immune system, and digestive system of human and animals. , AFB 1 can also cross the blood–brain barrier and cause neurotoxicity in the central nervous system. Moreover, AFB 1 inhibits antioxidant protein expression, induces cell cycle arrest and DNA damage, leading to the mitochondria-dependent apoptosis of various nerve cells . The reproductive toxic effects of AFB 1 were observed in different animal studies through in vitro maturation (IVM), in vitro fertilization (IVF), measurement of physiological indicators including ROS and GSH, detection of DNA damage markers, and multiple omics analyses. − In addition to inducing increased oxidative stress and DNA damage, AFB 1 reduces the expression of cell cycle-related genes in porcine and mouse oocytes, resulting in cell cycle abnormalities. , AFB 1 has toxic effects on the germ cells and accessory cells of livestock such as bovines, sheep, and goats, thus seriously endangering the development of gametes and fertilized eggs and causing great economic losses. ,,, Furthermore, previous study reported the presence of AFB 1 in fetal cord blood following maternal exposure to AFB 1 , which might significantly affect fetal development …”