Key Laboratory of Drinking Water Science and Technology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085, China; State Key Laboratory of Environmental Aquatic Chemistry, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085, China; University of Chinese Academy of Sciences, Beijing, 100049, China.
Key Laboratory of Drinking Water Science and Technology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085, China.
Environ Pollut. 2018 Dec;243(Pt A):480-491. doi: 10.1016/j.envpol.2018.09.009. Epub 2018 Sep 5.
To assess hepatotoxicity and to determine the underlying mechanisms of carbamazepine (CBZ) toxicity in fish, histopathology and the liver proteome were examined after Chinese rare minnow (Gobiocypris rarus) were exposed to 1, 10, and 100 μg/L CBZ for 28 days. Histopathological changes included disruption of spatial structure, pyknotic nuclei, cellular vacuolization and deformation of cell nuclei, in addition to marked swelling of hepatocytes in all treatment groups. Protein analysis revealed that there were gender-specific responses in rare minnow following exposure, and there were 47 proteins in females and 22 proteins in males identified as differentially abundant following CBZ treatments. Pathway analysis revealed that cellular processes affected by CBZ included apoptosis, cell differentiation, cell proliferation, and the respiratory chain, indicating impaired energy homeostasis. Noteworthy was that 15 proteins identified as different in abundance were associated with carcinogenicity. Relative mRNA levels for select transcripts were consistent with the changes of proteins N-myc downstream regulated gene (NDRG), Tropomyosin 2-Beta (TPM2) and annexin A4 (ANXA4). Protein pyruvate kinase, liver and RBC (PKLR) were increased at 1 and 100 μg/L CBZ without significant difference in transcript levels. These findings characterize molecular responses and histological changes in the liver that generate new insights into CBZ hepatotoxicity in Chinese rare minnow.
为了评估卡马西平(CBZ)的肝毒性并确定其毒性的潜在机制,我们在中华鳑鲏(Gobiocypris rarus)暴露于 1、10 和 100μg/L CBZ 28 天后,对其进行了组织病理学和肝脏蛋白质组学检查。组织病理学变化包括空间结构破坏、核固缩、细胞空泡化和细胞核变形,以及所有处理组中肝细胞明显肿胀。蛋白质分析显示,暴露后稀有鲫鱼存在性别特异性反应,在雌性中有 47 种蛋白质和雄性中有 22 种蛋白质被鉴定为 CBZ 处理后的差异丰富。途径分析表明,受 CBZ 影响的细胞过程包括细胞凋亡、细胞分化、细胞增殖和呼吸链,表明能量稳态受损。值得注意的是,鉴定出的 15 种差异丰富的蛋白质与致癌性有关。一些选择的转录本的相对 mRNA 水平与蛋白质 N-myc 下游调节基因(NDRG)、原肌球蛋白 2-Beta(TPM2)和膜联蛋白 A4(ANXA4)的变化一致。在 1 和 100μg/L CBZ 时,蛋白质丙酮酸激酶、肝脏和 RBC(PKLR)增加,但转录水平没有显著差异。这些发现描述了肝脏中的分子反应和组织学变化,为中华鳑鲏的 CBZ 肝毒性提供了新的见解。