Excretion of PFOA and PFOS in Male Rats During a Subchronic Exposure

被引:60
作者
Cui, Lin [1 ]
Liao, Chun-yang [1 ]
Zhou, Qun-fang [1 ]
Xia, Tong-mei [2 ]
Yun, Zhao-jun [1 ]
Jiang, Gui-bin [1 ]
机构
[1] Chinese Acad Sci, Ecoenvironm Sci Res Ctr, State Key Lab Environm Chem & Ecotoxicol, Beijing 100085, Peoples R China
[2] Univ Sci & Technol Beijing, Sch Appl Sci, Dept Biol, Beijing 100083, Peoples R China
基金
中国国家自然科学基金;
关键词
PERFLUOROOCTANOIC ACID; PERFLUOROALKYL ACIDS; DISPOSITION; TOXICITY; PHARMACOKINETICS; FLUOROCHEMICALS; ELIMINATION; SULFONATE; MONKEYS;
D O I
10.1007/s00244-009-9336-5
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Perfluorinated compounds (PFCs), a class of synthetic surfactants that are widely used, have become global environmental contaminants because of their high persistence and bioaccumulation. An increasing number of studies have described the pharmacokinetics of PFCs following in vivo exposure, however, few papers have focused on the excretion of these compounds during a period of consecutive exposure. In this study, the excretions of perfluorooctanoic acid (PFOA) and perfluorooctane sulfonate (PFOS) in male Sprague-Dawley rats gavaged consecutively for 28 days were investigated and compared. The faster elimination rate in urine compared to feces indicated that urinary excretion is the primary clearance route in rats for either PFOA or PFOS. During the first 24 h after administration of PFOA (5 and 20 mg/kg body weight/day), about 24.7-29.6% of the oral dose was excreted through urine and feces, while for PFOS, the excretion amounts were only 2.6-2.8% of the total gavaged doses (5 and 20 mg/kg body weight/day). The excretion rates of both PFCs increased with increasing exposure doses. The higher elimination rate of PFOA through excretion indicated its lower accumulation in rats, thus inducing possible lower toxicities compared to PFOS.
引用
收藏
页码:205 / 213
页数:9
相关论文
共 30 条
  • [1] [Anonymous], 2003, 7473 DUPONT
  • [2] Austin ME, 2003, ENVIRON HEALTH PERSP, V111, P1485, DOI 10.1289/ehp.6128
  • [3] Mechanisms of extrahepatic tumor induction by peroxisome proliferators in male CD rats
    Biegel, LB
    Hurtt, ME
    Frame, SR
    O'Connor, JC
    Cook, JC
    [J]. TOXICOLOGICAL SCIENCES, 2001, 60 (01) : 44 - 55
  • [4] Toxicity of ammonium perfluorooctanoate in male cynomolgus monkeys after oral dosing for 6 months
    Butenhoff, J
    Costa, G
    Elcombe, C
    Farrar, D
    Hansen, K
    Iwai, H
    Jung, R
    Kennedy, G
    Lieder, P
    Olsen, G
    Thomford, P
    [J]. TOXICOLOGICAL SCIENCES, 2002, 69 (01) : 244 - 257
  • [5] Pharmacokinetics of perfluorooctanoate in cynomolgus monkeys
    Butenhoff, JL
    Kennedy, GL
    Hinderliter, PM
    Lieder, PH
    Jung, R
    Hansen, KJ
    Gorman, GS
    Noker, PE
    Thomford, PJ
    [J]. TOXICOLOGICAL SCIENCES, 2004, 82 (02) : 394 - 406
  • [6] Studies on the Toxicological Effects of PFOA and PFOS on Rats Using Histological Observation and Chemical Analysis
    Cui, Lin
    Zhou, Qun-fang
    Liao, Chun-yang
    Fu, Jian-jie
    Jiang, Gui-bin
    [J]. ARCHIVES OF ENVIRONMENTAL CONTAMINATION AND TOXICOLOGY, 2009, 56 (02) : 338 - 349
  • [7] GIBSON SJ, 1979, AR2260455 USEPA
  • [8] Global distribution of perfluorooctane sulfonate in wildlife
    Giesy, JP
    Kannan, K
    [J]. ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2001, 35 (07) : 1339 - 1342
  • [9] Perfluorochemical surfactants in the environment
    Giesy, JP
    Kannan, K
    [J]. ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2002, 36 (07) : 146A - 152A
  • [10] Gene expression profiles in rat liver treated with perfluorooctanoic acid (PFOA)
    Guruge, KS
    Yeung, LWY
    Yamanaka, N
    Miyazaki, S
    Lam, PKS
    Giesy, JP
    Jones, PD
    Yamashita, N
    [J]. TOXICOLOGICAL SCIENCES, 2006, 89 (01) : 93 - 107