Laboratory of Environment-immunological and neurological Diseases, Research Center of Basic Medical Sciences, Hubei University of Science and Technology, Xianning, 437100, China.
Laboratory of Environment Biomedicine, Central China Normal University, Wuhan, 430079, China.
Food Chem Toxicol. 2019 Apr;126:152-161. doi: 10.1016/j.fct.2019.02.024. Epub 2019 Feb 19.
Diisodecyl phthalate (DIDP) is a new type of phthalate used in the coating of pharmaceutical pills and in plastic food wrappers. This research was conducted to investigate whether DIDP could cause learning and memory impairment in mice, using formaldehyde (FA) to construct a positive control. Behavioral analysis showed that oral administration of 15 mg kg·d DIDP combined with inhalation of 1 mg m FA led to learning and memory impairment in mice. Histopathological observations of the brain showed that the pathological alterations in the hippocampi. Detection of testosterone (T) and estradiol (E2) levels in the brain and serum showed that E2 levels were associated with learning and memory disorders. Reactive oxygen species (ROS), reduced glutathione (GSH), malondialdehyde (MDA), and 8-hydroxy-2-deoxyguanosine (8-OH-dG) revealed the increased oxidative stress levels. Detection of caspase-3, NF-κB, the phosphorylated cAMP response-element binding protein (p-CREB) and the brain derived neurotrophic factor (BDNF) showed that the protective effect mediated by BDNF, is reduced. However, some of these effects were blocked by the administration of Vitmin E (VitE, 100 mg kg·d) or 17β-estradiol (17β-E2, 100 μg kg). These data suggest that DIDP may aggravate the FA-exposure-induced learning and memory impairment in mice, and that 17β-E2 could be utilized to avoid these adverse effects.
邻苯二甲酸二异癸酯(DIDP)是一种用于药物丸涂层和塑料食品包装的新型邻苯二甲酸酯。本研究旨在探讨 DIDP 是否会导致小鼠学习和记忆障碍,并使用甲醛(FA)构建阳性对照。行为分析表明,口服 15mg/kg·d DIDP 联合吸入 1mg/m FA 导致小鼠学习和记忆障碍。大脑的组织病理学观察显示海马区的病理改变。大脑和血清中睾丸酮(T)和雌二醇(E2)水平的检测表明,E2 水平与学习和记忆障碍有关。活性氧(ROS)、还原型谷胱甘肽(GSH)、丙二醛(MDA)和 8-羟基-2-脱氧鸟苷(8-OH-dG)显示氧化应激水平升高。检测 caspase-3、NF-κB、磷酸化 cAMP 反应元件结合蛋白(p-CREB)和脑源性神经营养因子(BDNF)表明,BDNF 介导的保护作用减弱。然而,这些作用中的一些被 Vitmin E(VitE,100mg/kg·d)或 17β-雌二醇(17β-E2,100μg/kg)的给药所阻断。这些数据表明,DIDP 可能会加重 FA 暴露引起的小鼠学习和记忆障碍,并且 17β-E2 可用于避免这些不良反应。