College of Life and Environmental Sciences, Hangzhou Normal University, Xuelin Road 16#, Xiasha Gaojiao Dongqu, Hangzhou, Zhejiang Province, 310036, China.
College of Life and Environmental Sciences, Hangzhou Normal University, Xuelin Road 16#, Xiasha Gaojiao Dongqu, Hangzhou, Zhejiang Province, 310036, China; Key Laboratory of Hangzhou City for Ecosystem Protection and Restoration, Hangzhou Normal University, Hangzhou, 310036, China.
Environ Pollut. 2018 Jul;238:1035-1043. doi: 10.1016/j.envpol.2018.02.037. Epub 2018 Feb 17.
Perfluorooctanoic acid (PFOA) is widely distributed in various environmental media and is toxic to organisms. This study demonstrated that PFOA induces hepatotoxicity in the frog and evaluated the role of CYP3A and the Nrf2-ARE signaling pathway in regulating responses to PFOA-induced hepatotoxicity. Rana nigromaculata were exposed to 0, 0.01, 0.1, 0.5, or 1 mg/L PFOA solutions in a static-renewal system for 14 days. Liver tissue samples were collected 24 h after the last treatment. Hepatic histology was observed by HE staining and transmission electron microscopy. The oxidative stress levels in the liver were measured. The expression levels of CYP3A, Nrf2, NQO1, and HO-1 mRNA were measured by quantitative reverse transcription-polymerase chain reaction. PFOA-treated frog liver tissue exhibited diffuse cell borders, cytoplasmic vacuolization, broken nuclei, nuclear chromatin margination, and swollen mitochondria. In addition, the livers of PFOA-treated frogs showed a significantly elevated content of reactive oxygen species, malondialdehyde, glutathione and glutathione S-transferase activity compared to the livers of control frogs. However, the glutathione peroxidase activities concomitantly decreased in PFOA-treated frogs compared to those in the control group. Furthermore, compared with control frogs, the expression levels of CYP3A, Nrf2, and NQO1 mRNA significantly increased in PFOA-treated frogs. HO-1 mRNA expression remarkably increased only in groups treated with 0.5 or 1 mg/L PFOA. Our results indicate that PFOA induces hepatotoxicity in a dose-dependent manner. Furthermore, the results of the comparison analysis between different gender groups illustrated that PFOA is more toxic to female frogs than male frogs. Our results demonstrated that PFOA causes liver damage and that CYP3A enhances PFOA-induced female frogs hepatotoxicity are more virulent than male through biotransformation, and the activation of the Nrf2-ARE pathway is induced to protect against hepatotoxicity in Rana nigromaculata, all of which provide the scientific basis for the protection of amphibians against environmental contaminants.
全氟辛酸(PFOA)广泛分布于各种环境介质中,对生物体具有毒性。本研究表明,PFOA 可诱导蛙类产生肝毒性,并评估 CYP3A 和 Nrf2-ARE 信号通路在调节 PFOA 诱导的肝毒性反应中的作用。采用静态更新系统将黑斑蛙暴露于 0、0.01、0.1、0.5 或 1mg/L 的 PFOA 溶液中 14 天,末次染毒 24h 后采集肝脏组织样本。通过 HE 染色和透射电镜观察肝组织学变化,检测肝组织氧化应激水平,采用实时荧光定量 PCR 检测 CYP3A、Nrf2、NQO1 和 HO-1mRNA 的表达水平。结果显示,PFOA 处理后的蛙肝组织细胞边界弥漫性模糊、细胞质空泡化、细胞核破碎、核染色质边缘化、线粒体肿胀。此外,与对照组相比,PFOA 处理组的蛙肝组织中活性氧、丙二醛、谷胱甘肽和谷胱甘肽 S-转移酶的活性显著升高,而谷胱甘肽过氧化物酶的活性则显著降低。与对照组相比,PFOA 处理组的 CYP3A、Nrf2 和 NQO1mRNA 的表达水平显著升高,HO-1mRNA 的表达水平仅在 0.5 或 1mg/L PFOA 处理组中显著升高。结果表明,PFOA 呈剂量依赖性诱导肝毒性,并且雌雄两性间比较分析结果显示,PFOA 对雌性蛙的毒性强于雄性。本研究结果表明,PFOA 可导致黑斑蛙肝损伤,CYP3A 通过生物转化增强 PFOA 诱导的雌性蛙肝毒性,激活 Nrf2-ARE 通路以抵抗肝毒性,为保护两栖动物免受环境污染物的侵害提供了科学依据。