Koskela A, Finnilä M A, Korkalainen M, Spulber S, Koponen J, Håkansson H, Tuukkanen J, Viluksela M
Institute of Cancer Research and Translational Medicine, MRC Oulu and Department of Anatomy and Cell Biology, Faculty of Medicine, University of Oulu, Oulu, Finland.
Research Unit of Medical Imaging, Physics and Technology, University of Oulu, Oulu, Finland.
Toxicol Appl Pharmacol. 2016 Jun 15;301:14-21. doi: 10.1016/j.taap.2016.04.002. Epub 2016 Apr 9.
Perfluorooctanoic acid (PFOA) is a ubiquitous and persistent environmental chemical, which has been used extensively due to its stability and surface tension-lowering properties. Toxicological effects include induction of neonatal mortality and reproductive toxicity. In this study, pregnant C57BL/6 mice were exposed orally to 0.3mg PFOA/kg/day throughout pregnancy, and female offspring were studied at the age of 13 or 17months. Morphometrical and biomechanical properties of femurs and tibias were analyzed with micro-computed tomography and 3-point bending, and bone PFOA concentrations were determined by mass spectrometry. The effects of PFOA on bone cell differentiation were studied in osteoclasts from C57BL/6 mice and in the MC3T3 pre-osteoblast cell line. PFOA exposed mice showed increased femoral periosteal area as well as decreased mineral density of tibias. Biomechanical properties of these bones were not affected. Bone PFOA concentrations were clearly elevated even at the age of 17months. In osteoblasts, low concentrations of PFOA increased osteocalcin (OCN) expression and calcium secretion, but at PFOA concentrations of 100μM and above osteocalcin (OCN) expression and calcium secretion were decreased. The number of osteoclasts was increased at all PFOA concentrations tested and resorption activity dose-dependently increased from 0.1-1.0μM, but decreased at higher concentrations. The results show that PFOA accumulates in bone and is present in bones until the old age. PFOA has the potential to influence bone turnover over a long period of time. Therefore bone is a target tissue for PFOA, and altered bone geometry and mineral density seem to persist throughout the life of the animal.
全氟辛酸(PFOA)是一种普遍存在且持久的环境化学物质,因其稳定性和降低表面张力的特性而被广泛使用。毒理学效应包括导致新生儿死亡和生殖毒性。在本研究中,怀孕的C57BL/6小鼠在整个孕期经口暴露于0.3mg PFOA/kg/天,对雌性后代在13或17月龄时进行研究。使用微型计算机断层扫描和三点弯曲分析股骨和胫骨的形态测量和生物力学特性,通过质谱法测定骨中PFOA浓度。在C57BL/6小鼠的破骨细胞和MC3T3前成骨细胞系中研究PFOA对骨细胞分化的影响。暴露于PFOA的小鼠股骨骨膜面积增加,胫骨矿物质密度降低。这些骨骼的生物力学特性未受影响。即使在17月龄时,骨中PFOA浓度也明显升高。在成骨细胞中,低浓度的PFOA增加骨钙素(OCN)表达和钙分泌,但在PFOA浓度为100μM及以上时,骨钙素(OCN)表达和钙分泌降低。在所有测试的PFOA浓度下破骨细胞数量均增加,吸收活性从0.1 - 1.0μM呈剂量依赖性增加,但在较高浓度时降低。结果表明,PFOA在骨中蓄积并在骨骼中一直存在至老年。PFOA有可能在很长一段时间内影响骨转换。因此,骨是PFOA的靶组织,骨几何形状和矿物质密度的改变似乎在动物的整个生命过程中持续存在。