Developmental and cardiac toxicity assessment of Ethyl 3-(N-butylacetamido) propanoate (EBAAP) in zebrafish embryos

斑马鱼 发育毒性 氧化应激 过氧化氢酶 丙二醛 超氧化物歧化酶 毒性 活性氧 男科 生物 心脏发育 药理学 心脏毒性 化学 细胞生物学 内分泌学 内科学 生物化学 遗传学 医学 基因 妊娠期 胚胎干细胞 怀孕
作者
Qiang Luo,Li Ai,Shuqiong Tang,Hua Zhang,Jinze Ma,Xiaoping Xiao,Keyuan Zhong,GY Tian,Bo Cheng,Cong Xiong,Xiaobei Chen,Huiqiang Lu
出处
期刊:Aquatic Toxicology [Elsevier]
卷期号:261: 106572-106572
标识
DOI:10.1016/j.aquatox.2023.106572
摘要

Ethyl 3-(N-butylacetamido) propanoate (EBAAP) is one of the most widely used mosquito repellents worldwide, and is also commonly used to produce cosmetics. Residues have recently been detected in surface and groundwater in many countries, and their potential to harm the environment is unknown. Therefore, more studies are needed to fully assess the toxicity of EBAAP. This is the first investigation into the developmental toxicity and cardiotoxicity of EBAAP on zebrafish embryos. EBAAP was toxic to zebrafish, with a lethal concentration 50 (LC50) of 140 mg/L at 72 hours post fertilization (hpf). EBAAP exposure also reduced body length, slowed the yolk absorption rate, induced spinal curvature and pericardial edema, decreased heart rate, promoted linear lengthening of the heart, and diminished cardiac pumping ability. The expression of heart developmental-related genes (nkx2.5, myh6, tbx5a, vmhc, gata4, tbx2b) was dysregulated, intracellular oxidative stress increased significantly, the activities of catalase (CAT) and superoxide dismutase (SOD) decreased, and malondialdehyde (MDA) content increased significantly. The expression of apoptosis-related genes (bax/bcl2, p53, caspase9, caspase3) was significantly upregulated. In conclusion, EBAAP induced abnormal morphology and heart defects during the early stages of zebrafish embryo development by potentially inducing the generation and accumulation of reactive oxygen species (ROS) in vivo and activating the oxidative stress response. These events dysregulate the expression of several genes and activate endogenous apoptosis pathways, eventually leading to developmental disorders and heart defects.
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