College of Life Science, Henan Normal University, Xinxiang, 453007, PR China.
College of Life Science, Henan Normal University, Xinxiang, 453007, PR China.
Chemosphere. 2023 Sep;335:139029. doi: 10.1016/j.chemosphere.2023.139029. Epub 2023 May 25.
Nanomaterials have attracted much attention in the biomedical field. Black phosphorus quantum dots (BPQDs) have shown great potential in biomedical applications, but their potential risks to biosafety and environmental stability have not been fully evaluated. In the present study, zebrafish (Danio rerio) embryos were exposed to 0, 2.5, 5 and 10 mg/L BPQDs from 2 to 144 h post-fertilization (hpf) to explore developmental toxicity. The results showed that exposure to BPQDs for 96 h induced developmental malformations (tail deformation, yolk sac edema, pericardial edema, and spinal curvature) in zebrafish embryos. ROS and antioxidant enzyme activities (CAT, SOD, MDA and T-AOC) were substantially altered and the acetylcholinesterase (AChE) enzyme activity was significantly decreased in the BPQDs exposed groups. Locomotor behavior was inhibited after BPQDs exposure for 144 h in zebrafish larvae. A significant increase in 8-OHdG content indicates DNA oxidative damage in embryos. In addition, obvious apoptotic fluorescence signals were detected in the brain, spine, yolk sac and heart. At the molecular level, the mRNA transcript levels of key genes related to skeletal development (igf1, gh, MyoD and LOX), neurodevelopment (gfap, pomca, bdnf and Mbpa), cardiovascular development (Myh6, Nkx2.5, Myl7, Tbx2b, Tbx5 and Gata4) and apoptosis (p53, Bax, Bcl-2, apaf1, caspase-3 and caspase-9) were abnormal after BPQDs exposure. In conclusion, BPQDs induced morphological malformations, oxidative stress, locomotor behavior disorders, DNA oxidative damage and apoptosis in zebrafish embryos. This study provides a basis for further study on the toxic effects of BPQDs.
纳米材料在生物医学领域引起了广泛关注。黑磷量子点(BPQDs)在生物医学应用中显示出巨大的潜力,但它们对生物安全性和环境稳定性的潜在风险尚未得到充分评估。在本研究中,使用斑马鱼(Danio rerio)胚胎从受精后 2 至 144 小时(hpf)暴露于 0、2.5、5 和 10 mg/L 的 BPQDs 中,以探究其发育毒性。结果表明,BPQDs 暴露 96 小时可诱导斑马鱼胚胎发生发育畸形(尾巴变形、卵黄囊水肿、心包水肿和脊柱弯曲)。暴露于 BPQDs 会显著改变活性氧(ROS)和抗氧化酶活性(CAT、SOD、MDA 和 T-AOC),并显著降低乙酰胆碱酯酶(AChE)酶活性。BPQDs 暴露 144 小时后,斑马鱼幼虫的运动行为受到抑制。胚胎中 8-OHdG 含量的显著增加表明 DNA 氧化损伤。此外,在大脑、脊柱、卵黄囊和心脏中检测到明显的凋亡荧光信号。在分子水平上,与骨骼发育(igf1、gh、MyoD 和 LOX)、神经发育(gfap、pomca、bdnf 和 Mbpa)、心血管发育(Myh6、Nkx2.5、Myl7、Tbx2b、Tbx5 和 Gata4)和凋亡(p53、Bax、Bcl-2、apaf1、caspase-3 和 caspase-9)相关的关键基因的 mRNA 转录水平异常。综上所述,BPQDs 可诱导斑马鱼胚胎出现形态畸形、氧化应激、运动行为障碍、DNA 氧化损伤和凋亡。本研究为进一步研究 BPQDs 的毒性作用提供了依据。