Institut des Sciences de la Vie, UCLouvain, Croix du Sud 2/L7.05.08, 1348 Louvain-la-Neuve, Belgium.
Department of Pharmaceutical Sciences, Toxicological Center, Campus Drie Eiken, Universiteit Antwerpen, Universiteitsplein 1, 2610 Wilrijk, Belgium; Department of Chemistry, "Al. I. Cuza" University of Iasi, 700506 Iasi, Romania.
Environ Res. 2014 Jul;132:438-48. doi: 10.1016/j.envres.2014.04.016. Epub 2014 May 21.
Northern elephant seals (NES) (Mirounga angustirostris) from the Año Nuevo State Reserve (CA, USA) were longitudinally sampled during the post-weaning fast in order to study the mobilisation and redistribution of various classes of persistent organic pollutants (POPs), such as polybrominated diphenyl ethers (PBDEs), polychlorinated biphenyls (PCBs), dichlorodiphenyldichloroethylene (p,p'-DDE) and hexachlorobenzene (HCB) between blubber and blood. Inner and outer blubber layers were analysed separately. Organohalogenated compounds were detected in all blubber samples in the decreasing order of their concentrations: p,p'-DDE > PCBs ⪢ HCB > PBDEs. The concentrations of all studied compounds were homogeneously distributed in the blubber layer at early fast, since the concentrations of POPs were statistically not different in the inner and outer layers. With the progression of the fast, the concentrations of PBDEs, PCBs and p,p'-DDE increased more sharply in inner blubber than in outer blubber. As a result, their levels became significantly higher in inner blubber as compared to outer blubber at late fast. The rise of pollutant concentrations in blubber might result from a less efficient mobilisation than triglycerides and/or a reuptake by adipocytes of some of the pollutants released into the circulation. The mobilisation of pollutants from blubber was higher at late fast. An increase of pollutant concentrations was observed in serum between early and late fast. Lower halogenated congeners (i.e. tetra-CBs) were present in higher proportions in serum, whereas the higher halogenated congeners (i.e. hepta-CBs) were mainly found in the inner and outer blubber layers. The transfer ratios of both PBDEs and PCBs from inner blubber to serum decreased with the number of chlorine and bromine atoms. In addition, the distribution of both types of compounds between serum and blubber was strongly influenced by their lipophilic character (logKow values), with more lipophilic compounds being less efficiently released from blubber to serum.
来自加利福尼亚州阿尼奥尼奥图尔诺州立保护区的北方象海豹(Mirounga angustirostris)在哺乳期后快速期间被纵向采样,以研究各种持久性有机污染物(POPs)的动员和再分配,例如多溴二苯醚(PBDEs) 、多氯联苯(PCBs)、二氯二苯二氯乙烯(p,p'-DDE)和六氯苯(HCB)在脂肪和血液之间。内层和外层脂肪层分别进行了分析。所有脂肪样本中均检测到有机卤化物化合物,其浓度顺序为:p,p'-DDE>PCBs ⪢HCB>PBDEs。在早期快速时,所有研究化合物的浓度在脂肪层中均匀分布,因为 POPs 的浓度在内外层之间没有统计学差异。随着快速的进行,内层脂肪中 PBDEs、PCBs 和 p,p'-DDE 的浓度增加得比外层脂肪更快。因此,在内层脂肪中的含量在晚期快速时明显高于外层脂肪。脂肪中污染物浓度的升高可能是由于动员效率低于甘油三酯,和/或部分释放到循环中的污染物被脂肪细胞重新吸收。晚期快速时污染物从脂肪中的动员更高。在早期和晚期快速之间,血清中观察到污染物浓度增加。血清中存在更高比例的低卤代同系物(即四氯联苯),而高卤代同系物(即七氯联苯)主要存在于内层和外层脂肪层中。内层脂肪向血清中转移的 PBDEs 和 PCBs 的转移比随氯和溴原子的数量而降低。此外,两种类型的化合物在血清和脂肪之间的分布受到其亲脂性(logKow 值)的强烈影响,亲脂性化合物从脂肪向血清的释放效率较低。