Witzmann F A, Parker D N
Department of Biology, Indiana University Purdue-University at Indianapolis, Columbus 47203.
Toxicol Lett. 1991 Jun;57(1):29-36. doi: 10.1016/0378-4274(91)90116-n.
The effect after 8 days of 20 and 50 mg/kg in vivo exposure to perfluoro-n-decanoic acid (PFDA) on the protein pattern of rat liver whole homogenates was studied using high-resolution, large-scale two-dimensional polyacrylamide gel electrophoresis. PFDA exposure altered 13 proteins reproducibly in each of 5 samples tested. While most of the altered proteins remained unidentified, several known mitochondrial proteins were induced by PFDA as were others in a dose-related manner. Conversely, PFDA caused the reduction of albumin as well as several unknown proteins, also in a dose-related manner. Cytoskeletal proteins were unaffected by PFDA. The present results suggest that PFDA's toxic mechanism may involve more than membrane integration and lipid accumulation. Changes in the two-dimensional protein pattern indicate that selective protein synthetic or catabolic processes may undergo qualitative alterations after PFDA treatment as well.
采用高分辨率、大规模二维聚丙烯酰胺凝胶电泳,研究了大鼠肝脏全匀浆在体内暴露于20和50mg/kg全氟正癸酸(PFDA)8天后对蛋白质图谱的影响。在测试的5个样本中,每个样本中PFDA暴露可重复地改变了13种蛋白质。虽然大多数改变的蛋白质仍未鉴定,但几种已知的线粒体蛋白质被PFDA诱导,其他蛋白质也呈剂量相关方式被诱导。相反,PFDA也以剂量相关方式导致白蛋白以及几种未知蛋白质减少。细胞骨架蛋白不受PFDA影响。目前的结果表明,PFDA的毒性机制可能不仅仅涉及膜整合和脂质积累。二维蛋白质图谱的变化表明,PFDA处理后,选择性蛋白质合成或分解代谢过程也可能发生定性改变。