Molecular Neuroscience and Vascular Biology Laboratory, Department of Neurosurgery, University of Kentucky, Lexington, KY 40536.
Environ Toxicol Pharmacol. 2008 Mar;25(2):251-9. doi: 10.1016/j.etap.2007.10.020.
Exposure to specific congeners of polychlorinated biphenyls (PCBs) can induce proinflammatory alterations, which may contribute to the formation of blood-borne tumor metastasis. The main aim of the present study was to establish an experimental model of PCB exposure in which PCBs are administered by oral gavage, which resembles the human exposure through the food chain. To determine structure-function relationship, we studied induction of inflammatory responses in the livers, lungs and brains of mice treated with PCB77 (a major coplanar PCB), PCB104 (a non-coplanar PCB with multiple ortho-chlorine substituents), and PCB153 (a major non-coplanar PCB) after a single gavage dose (150 µmol/kg body weight). The strongest expression of proinflammatory proteins occurred 24 h following the PCB administration independent of the class of PCB congeners. These data indicate that food-chain exposure to PCBs can induce proinflammatory mediators in organs that are potential targets for PCB-induced toxicity.
接触特定的多氯联苯(PCBs)同系物会引起促炎改变,这可能有助于血液传播肿瘤转移的形成。本研究的主要目的是建立一种通过口服灌胃给予 PCBs 的实验模型,这类似于人类通过食物链暴露于 PCBs。为了确定结构-功能关系,我们研究了经单次灌胃剂量(150µmol/kg 体重)后,PCB77(一种主要的共平面 PCB)、PCB104(一种具有多个邻位氯取代基的非共平面 PCB)和 PCB153(一种主要的非共平面 PCB)处理的小鼠肝脏、肺和脑中炎症反应的诱导。在给予 PCBs 后 24 小时,无论 PCB 同系物的类别如何,促炎蛋白的表达最强。这些数据表明,通过食物链接触 PCBs 会在可能成为 PCB 诱导毒性的靶器官中诱导促炎介质。