Xiangya School of Public Health, Central South University, Changsha 410078, Hunan Province, PR China.
Xiangya School of Public Health, Central South University, Changsha 410078, Hunan Province, PR China; Hunan Food and Drug Vocational College, Changsha 410078, Hunan Province, PR China.
Fish Shellfish Immunol. 2023 Aug;139:108906. doi: 10.1016/j.fsi.2023.108906. Epub 2023 Jun 20.
Synthetic phenolic antioxidants (SPAs) are an environmental concern due to their persistence nature and bioaccumulation. However, the hepatoxicity and mechanisms of SPAs in aquatic organisms remain poorly understood. In this study, grass carp were exposed to two representative SPAs (BHA and BHT) at environmentally relevant levels (0.1 μM) for 30 days. We observed that BHA and BHT exposure significantly increased the levels of serum aminotransferase (ALT) and aspartate aminotransferase (AST) in grass carp, accompanied by mild inflammatory cell infiltration and irregularity in the shape of hepatocytes. Dihydro ethylenediamine staining showed that BHA and BHT exposure resulted in elevated levels of superoxide levels, accompanied by increased antioxidant enzyme activities (T-AOC, SOD, CAT, GSH-PX) and MDA levels, which is suggestive of oxidative stress responses in the liver of grass carp. Besides, BHA and BHT could dock into the pocket of phosphatidylinositol 3-kinases (PI3K) and thereby inhibiting PI3K/mammalian target of rapamycin (mTOR)/protein kinase B (AKT) signaling cascades. Meanwhile, our results clarified that BHA and BHT could promote autophagosome production and increase the expression of key autophagy proteins, likely due to inhibition of PI3K/mTOR/AKT signaling pathway. Moreover, BHA and BHT could induce apoptotic process by upregulating the expression of Bax, Caspase3 and Caspase8 and downregulating Bcl2 expression. Notably, BHT exhibited more hepatoxicity on the indicators of the apoptosis and oxidative stress than BHA. In summary, our findings demonstrated that BHA and BHT exposure could induce liver damage induced via regulating ROS/PI3K-mediated autophagic hyperactivation, which is a crucial step in triggering hepatocyte death. This study provides novel insight into the potential mechanisms underlying liver damage caused by BHA and BHT in aquatic organisms, and offers a new theoretical basis for ecological risk assessment of SPAs.
合成酚类抗氧化剂(SPAs)由于其持久性和生物累积性而成为环境关注的焦点。然而,水生生物中 SPA 的肝毒性及其机制仍知之甚少。在这项研究中,草鱼暴露于两种代表性 SPA(BHA 和 BHT)在环境相关水平(0.1 μM)下 30 天。我们观察到 BHA 和 BHT 暴露显著增加了草鱼血清转氨酶(ALT)和天冬氨酸转氨酶(AST)的水平,伴随着轻度炎症细胞浸润和肝细胞形状不规则。二氢乙二胺染色显示,BHA 和 BHT 暴露导致超氧化物水平升高,同时抗氧化酶活性(总抗氧化能力、SOD、CAT、GSH-PX)和 MDA 水平升高,提示草鱼肝脏发生氧化应激反应。此外,BHA 和 BHT 可以与磷脂酰肌醇 3-激酶(PI3K)结合口袋结合,从而抑制 PI3K/哺乳动物雷帕霉素靶蛋白(mTOR)/蛋白激酶 B(AKT)信号级联。同时,我们的结果阐明,BHA 和 BHT 可以通过促进自噬体的产生并增加关键自噬蛋白的表达来促进自噬,这可能是由于抑制了 PI3K/mTOR/AKT 信号通路。此外,BHA 和 BHT 可以通过上调 Bax、Caspase3 和 Caspase8 的表达和下调 Bcl2 的表达来诱导凋亡过程。值得注意的是,BHT 对凋亡和氧化应激指标的肝毒性比 BHA 更强。总之,我们的研究结果表明,BHA 和 BHT 暴露可通过调节 ROS/PI3K 介导的自噬过度激活诱导肝损伤,这是触发肝细胞死亡的关键步骤。本研究为水生生物中 BHA 和 BHT 引起的肝损伤潜在机制提供了新的见解,并为 SPA 的生态风险评估提供了新的理论依据。