Medical College of Soochow University, Suzhou, China; Jiangsu Key Laboratory of Preventive and Translational Medicine for Geriatric Diseases, Soochow University, Suzhou, China.
Medical College of Soochow University, Suzhou, China.
Toxicol Appl Pharmacol. 2020 Jul 1;398:115029. doi: 10.1016/j.taap.2020.115029. Epub 2020 May 5.
Resveratrol (RSV), a natural polyphenolic compound commonly found in food, has antioxidant and aryl hydrocarbon receptor (AHR) antagonist effects. We have recently demonstrated that AHR mediated reactive oxygen species (ROS) generation contributes to the cardiac developmental toxicity of ambient fine particle matter (PM2.5). Thus, we hypothesized that RSV protects against the cardiac developmental toxicity of PM2.5 by inhibiting ROS generation and AHR activity. To test this concept, we exposed zebrafish embryos to extractable organic matter (EOM) from PM2.5 in the presence or absence of RSV. We found that RSV significantly counteracted EOM-induced cardiac malformations in zebrafish embryos. The EOM-induced ROS production, DNA damage and apoptosis in the heart of zebrafish embryos were also counteracted by RSV supplementation. Furthermore, RSV attenuated EOM-induced changes in the expression of genes involved in cardiac development (nkx2.5, sox9b, axin2), oxidative stress (nrf2a, nrf2b, gstp1, gstp2, sod1, sod2, cat) and apoptosis (p53, bax). However, RSV did not suppress EOM-induced AHR activity. In conclusion, our data indicates that RSV protects against the PM2.5-induced heart malformations by inhibiting oxidative stress rather than through AHR antagonism.
白藜芦醇(RSV)是一种常见的天然多酚化合物,存在于食物中,具有抗氧化和芳基烃受体(AHR)拮抗剂的作用。我们最近证明,AHR 介导的活性氧(ROS)生成导致环境细颗粒物(PM2.5)的心脏发育毒性。因此,我们假设 RSV 通过抑制 ROS 生成和 AHR 活性来保护 PM2.5 的心脏发育毒性。为了验证这一概念,我们在存在或不存在 RSV 的情况下,将斑马鱼胚胎暴露于 PM2.5 的可萃取有机物(EOM)中。我们发现 RSV 显著抵消了 EOM 诱导的斑马鱼胚胎心脏畸形。RSV 还可抑制 EOM 诱导的斑马鱼胚胎心脏中 ROS 产生、DNA 损伤和细胞凋亡。此外,RSV 减轻了 EOM 诱导的心脏发育相关基因(nkx2.5、sox9b、axin2)、氧化应激(nrf2a、nrf2b、gstp1、gstp2、sod1、sod2、cat)和凋亡(p53、bax)表达的变化。然而,RSV 并未抑制 EOM 诱导的 AHR 活性。总之,我们的数据表明,RSV 通过抑制氧化应激而不是通过 AHR 拮抗作用来保护 PM2.5 诱导的心脏畸形。