• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

氟壬酸在大鼠和小鼠体内的比较药代动力学。

Comparative pharmacokinetics of perfluorononanoic acid in rat and mouse.

机构信息

Curriculum in Toxicology, University of North Carolina, Chapel Hill, NC, USA.

出版信息

Toxicology. 2011 Mar 15;281(1-3):48-55. doi: 10.1016/j.tox.2011.01.003. Epub 2011 Jan 13.

DOI:10.1016/j.tox.2011.01.003
PMID:21237237
Abstract

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.

摘要

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。

相似文献

1
Comparative pharmacokinetics of perfluorononanoic acid in rat and mouse.氟壬酸在大鼠和小鼠体内的比较药代动力学。
Toxicology. 2011 Mar 15;281(1-3):48-55. doi: 10.1016/j.tox.2011.01.003. Epub 2011 Jan 13.
2
NTP Toxicology and Carcinogenesis Studies of Pentachloroanisole (CAS No. 1825-21-4) in F344 Rats and B6C3F1 Mice (Feed Studies).五氯苯甲醚(CAS编号:1825-21-4)在F344大鼠和B6C3F1小鼠中的NTP毒理学与致癌性研究(饲料喂养研究)
Natl Toxicol Program Tech Rep Ser. 1993 Apr;414:1-284.
3
NTP Toxicology and Carcinogenesis Studies of Coumarin (CAS No. 91-64-5) in F344/N Rats and B6C3F1 Mice (Gavage Studies).香豆素(CAS编号91-64-5)在F344/N大鼠和B6C3F1小鼠中的NTP毒理学和致癌性研究(灌胃研究)
Natl Toxicol Program Tech Rep Ser. 1993 Sep;422:1-340.
4
NTP technical report on the toxicity studies of Dibutyl Phthalate (CAS No. 84-74-2) Administered in Feed to F344/N Rats and B6C3F1 Mice.美国国家毒理学计划关于邻苯二甲酸二丁酯(化学物质登记号84 - 74 - 2)经饲料给予F344/N大鼠和B6C3F1小鼠的毒性研究技术报告。
Toxic Rep Ser. 1995 Apr;30:1-G5.
5
Toxicology and Carcinogenesis Studies of Mercuric Chloride (CAS No. 7487-94-7) in F344 Rats and B6C3F1 Mice (Gavage Studies).氯化汞(CAS编号:7487-94-7)对F344大鼠和B6C3F1小鼠的毒理学和致癌性研究(灌胃研究)
Natl Toxicol Program Tech Rep Ser. 1993 Feb;408:1-260.
6
NTP Toxicology and Carcinogenesis Studies of Methyleugenol (CAS NO. 93-15-2) in F344/N Rats and B6C3F1 Mice (Gavage Studies).NTP对甲基丁香酚(CAS编号93-15-2)在F344/N大鼠和B6C3F1小鼠中的毒理学及致癌性研究(灌胃研究)
Natl Toxicol Program Tech Rep Ser. 2000 Jul;491:1-412.
7
NTP toxicology and carcinogenesis studies of 3,3',4,4',5-pentachlorobiphenyl (PCB 126) (CAS No. 57465-28-8) in female Harlan Sprague-Dawley rats (Gavage Studies).3,3',4,4',5-五氯联苯(PCB 126)(化学物质登记号:57465-28-8)对雌性哈兰斯普拉格-道利大鼠的NTP毒理学与致癌性研究(灌胃研究)
Natl Toxicol Program Tech Rep Ser. 2006 Jan(520):4-246.
8
Age effect on perfluorooctanoate (PFOA) plasma concentration in post-weaning rats following oral gavage with ammonium perfluorooctanoate (APFO).全氟辛酸铵(APFO)灌胃后,断奶后大鼠血浆中全氟辛酸(PFOA)浓度的年龄效应。
Toxicology. 2006 Aug 15;225(2-3):195-203. doi: 10.1016/j.tox.2006.06.002. Epub 2006 Jun 9.
9
NTP Toxicology and Carcinogenesis Studies of Salicylazosulfapyridine (CAS No. 599-79-1) in F344/N Rats and B6C3F1 Mice (Gavage Studies).柳氮磺胺吡啶(CAS编号:599-79-1)在F344/N大鼠和B6C3F1小鼠中的NTP毒理学与致癌性研究(灌胃研究)
Natl Toxicol Program Tech Rep Ser. 1997 May;457:1-327.
10
NTP technical report on the toxicity and metabolism studies of chloral hydrate (CAS No. 302-17-0). Administered by gavage to F344/N rats and B6C3F1 mice.国家毒理学计划关于水合氯醛(化学物质登记号:302-17-0)毒性和代谢研究的技术报告。通过灌胃法给予F344/N大鼠和B6C3F1小鼠。
Toxic Rep Ser. 1999 Aug(59):1-66, A1-E7.

引用本文的文献

1
Human gut bacteria bioaccumulate per- and polyfluoroalkyl substances.人类肠道细菌会生物累积全氟和多氟烷基物质。
Nat Microbiol. 2025 Jul;10(7):1630-1647. doi: 10.1038/s41564-025-02032-5. Epub 2025 Jul 1.
2
Estimation of species- and sex-specific PFAS pharmacokinetics in mice, rats, and non-human primates using a Bayesian hierarchical methodology.使用贝叶斯分层方法估计小鼠、大鼠和非人灵长类动物中特定物种和性别的全氟烷基和多氟烷基物质(PFAS)药代动力学。
Toxicol Appl Pharmacol. 2025 Jun;499:117336. doi: 10.1016/j.taap.2025.117336. Epub 2025 Apr 8.
3
Exposure to Long- and Short-Chain Per- and Polyfluoroalkyl Substances in Mice and Ovarian-Related Outcomes: An and Study.
小鼠暴露于长链和短链全氟和多氟烷基物质及其与卵巢相关的结局:一项……研究(原文中“An and Study”表述不完整,可能影响更准确翻译)
Environ Health Perspect. 2025 May;133(5):57024. doi: 10.1289/EHP14876. Epub 2025 May 28.
4
Associations of cord blood concentrations of perfluoroalkyl substances with autistic traits in Singaporean children: The growing up in Singapore towards healthy outcomes study.新加坡儿童脐带血中全氟烷基物质浓度与自闭症特征的关联:新加坡健康成长研究
Chemosphere. 2025 Feb;371:144040. doi: 10.1016/j.chemosphere.2024.144040. Epub 2025 Jan 8.
5
An oat fiber intervention for reducing PFAS body burden: A pilot study in male C57Bl/6 J mice.一项关于降低全氟烷基和多氟烷基物质(PFAS)体内负荷的燕麦纤维干预研究:对雄性C57Bl/6 J小鼠的初步研究。
Toxicol Appl Pharmacol. 2025 Feb;495:117188. doi: 10.1016/j.taap.2024.117188. Epub 2024 Dec 6.
6
Effects of Per- and Polyfluoroalkylated Substances on Female Reproduction.全氟和多氟烷基物质对雌性生殖的影响。
Toxics. 2024 Jun 25;12(7):455. doi: 10.3390/toxics12070455.
7
A Machine Learning Model to Estimate Toxicokinetic Half-Lives of Per- and Polyfluoro-Alkyl Substances (PFAS) in Multiple Species.一种用于估计多种物种中全氟和多氟烷基物质(PFAS)毒代动力学半衰期的机器学习模型。
Toxics. 2023 Jan 20;11(2):98. doi: 10.3390/toxics11020098.
8
Perfluoroalkyl Mixture Exposure in Relation to Fetal Growth: Potential Roles of Maternal Characteristics and Associations with Birth Outcomes.全氟烷基混合物暴露与胎儿生长的关系:母体特征的潜在作用及与出生结局的关联
Toxics. 2022 Oct 28;10(11):650. doi: 10.3390/toxics10110650.
9
Tubeimoside-1: A review of its antitumor effects, pharmacokinetics, toxicity, and targeting preparations.土贝母苷甲:其抗肿瘤作用、药代动力学、毒性及靶向制剂的综述
Front Pharmacol. 2022 Jul 15;13:941270. doi: 10.3389/fphar.2022.941270. eCollection 2022.
10
Internal Relative Potency Factors for the Risk Assessment of Mixtures of Per- and Polyfluoroalkyl Substances (PFAS) in Human Biomonitoring.人类生物监测中评估全氟和多氟烷基物质 (PFAS) 混合物风险的内部相对效力因素。
Environ Health Perspect. 2022 Jul;130(7):77005. doi: 10.1289/EHP10009. Epub 2022 Jul 26.