Curriculum in Toxicology, University of North Carolina, Chapel Hill, NC, USA.
Toxicology. 2011 Mar 15;281(1-3):48-55. doi: 10.1016/j.tox.2011.01.003. Epub 2011 Jan 13.
Perfluorononanoic acid (PFNA) is a fluorinated organic chemical found at low levels in the environment, but is detectable in humans and wildlife. The present study compared the pharmacokinetic properties of PFNA in two laboratory rodent species. Male and female Sprague-Dawley rats were given a single dose of PFNA by oral gavage at 1, 3, or 10mg/kg, and blood was collected from the tail vein at 1, 2, 3, 4, 7, 16, 21, 28, 35, 42 and 50 days after treatment. In addition, livers and kidneys were collected for PFNA analysis at the terminal time point. CD-1 mice were given a single oral dose of PFNA of 1 or 10mg/kg, and 4 males and 4 females were killed at similar time intervals; trunk blood, liver and kidney were collected. Serum and tissue concentrations of PFNA were determined by LC-MS/MS. Serum elimination of PFNA is by and large linear with exposure doses in the rat; however, like PFOA, a major sex difference in the rate of elimination is observed, with an estimated half-life of 30.6 days for males and 1.4 days for females. PFNA is stored preferentially in the liver but not in the kidneys. In the mouse, the rates of PFNA serum elimination are non-linear with exposure dose and are slightly faster in females than males, with terminal estimated serum half-life of 25.8-68.4 days and 34.3-68.9 days, respectively. PFNA is also stored preferentially in the mouse liver but not in the kidneys. Hepatic uptake appears to be more efficient and storage capacity greater in male mice than in females. These data suggest that (1) PFNA is more persistent in the mouse than in the rat; (2) there is a major sex difference in the serum elimination of PFNA in the rat, but much less so in the mouse; and (3) there is a significantly higher hepatic accumulation of PFNA in male mice than in females.
全氟壬酸(PFNA)是一种在环境中低水平存在的含氟有机化学物质,但可在人类和野生动物体内检测到。本研究比较了两种实验室啮齿动物物种中 PFNA 的药代动力学特性。雄性和雌性 Sprague-Dawley 大鼠经口灌胃给予 1、3 或 10mg/kg 的 PFNA 单一剂量,在治疗后 1、2、3、4、7、16、21、28、35、42 和 50 天从尾静脉采集血液。此外,在终末时间点采集肝脏和肾脏进行 PFNA 分析。CD-1 小鼠经口给予 1 或 10mg/kg 的 PFNA 单一剂量,4 只雄性和 4 只雌性在相似的时间间隔处死;采集胸血、肝脏和肾脏。通过 LC-MS/MS 测定血清和组织中 PFNA 的浓度。PFNA 在大鼠中的血清消除基本上呈线性与暴露剂量相关;然而,与 PFOA 一样,观察到消除率存在主要的性别差异,雄性的估计半衰期为 30.6 天,雌性为 1.4 天。PFNA 优先储存在肝脏中,但不在肾脏中。在小鼠中,PFNA 血清消除率与暴露剂量呈非线性关系,雌性比雄性略快,终末估计血清半衰期分别为 25.8-68.4 天和 34.3-68.9 天。PFNA 也优先储存在小鼠肝脏中,但不在肾脏中。肝摄取似乎在雄性小鼠中比在雌性小鼠中更有效,储存能力更大。这些数据表明:(1)PFNA 在小鼠中比在大鼠中更持久;(2)在大鼠中,PFNA 的血清消除存在主要的性别差异,但在小鼠中则较少;(3)雄性小鼠肝脏中 PFNA 的积累明显高于雌性。