Liang Feng, Yan Biao
School of Laboratory Medicine, Hubei University of Chinese Medicine, Wuhan, PR China.
Research Center of Basic Medical Sciences, Hubei University of Science and Technology, Xianning, PR China.
Toxicol Ind Health. 2020 Jan;36(1):30-40. doi: 10.1177/0748233719900861.
As a general alternative, diisononyl phthalate (DINP) has gradually replaced di(2-ethylhexyl) phthalate (DEHP) as the main plasticizer used in polyvinyl chloride. Like DEHP, DINP can also be released into the environment, resulting in humans being exposed through skin contact. This study aims to explore whether oxidative damage to hepatic and renal tissues can be induced by dermal exposure to DINP in mice. Forty-two male Balb/c mice were divided into six groups. The five DINP dermal exposure groups were exposed to different doses of DINP (0.02, 0.2, 2, 20, and 200 mg/kg) for 28 consecutive days. The pathological alterations to the skin, liver, and kidney in the mice were examined. Levels of reactive oxygen species (ROS), reduced glutathione (GSH), malondialdehyde (MDA), and DNA-protein cross-links (DPC) in the liver and kidney were also determined to investigate oxidative damage. The experimental results showed that the levels of ROS, MDA, and DPC coefficients increased gradually in a dose-dependent manner, whereas the level of GSH decreased accordingly. When the exposure dose was ≥20 mg/kg, ROS, GSH, MDA content, and the DPC coefficient were significantly different compared to the control group ( < 0.05). These results suggest that a high dose of DINP can induce oxidative stress and histopathological alterations in the liver and kidney via dermal exposure.
作为一种普遍的替代品,邻苯二甲酸二异壬酯(DINP)已逐渐取代邻苯二甲酸二(2-乙基己基)酯(DEHP),成为聚氯乙烯中使用的主要增塑剂。与DEHP一样,DINP也会释放到环境中,导致人类通过皮肤接触而暴露。本研究旨在探讨小鼠经皮肤接触DINP是否会诱导肝组织和肾组织的氧化损伤。42只雄性Balb/c小鼠被分为6组。5个DINP皮肤暴露组连续28天暴露于不同剂量的DINP(0.02、0.2、2、20和200mg/kg)。检查小鼠皮肤、肝脏和肾脏的病理变化。还测定了肝脏和肾脏中活性氧(ROS)、还原型谷胱甘肽(GSH)、丙二醛(MDA)和DNA-蛋白质交联(DPC)的水平,以研究氧化损伤。实验结果表明,ROS、MDA和DPC系数水平呈剂量依赖性逐渐升高,而GSH水平相应降低。当暴露剂量≥20mg/kg时,与对照组相比,ROS、GSH、MDA含量和DPC系数有显著差异(<0.05)。这些结果表明,高剂量的DINP可通过皮肤接触诱导肝脏和肾脏的氧化应激和组织病理学改变。