• 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

C-octamethylcyclotetrasiloxane(C-D4)在单次和重复吸入暴露后在 Fischer 344 和 Sprague Dawley CD 大鼠中的比较药代动力学研究。

Comparative pharmacokinetic studies of C-octamethylcyclotetrasiloxane (C-D4) in Fischer 344 and Sprague Dawley CD rats after single and repeated inhalation exposure.

机构信息

Dow Silicones Belgium SPRL, 7170 Seneffe, Belgium; Evonik Operations GmbH, 45127 Essen, Germany.

The Dow Chemical Company, Midland, MI 48674, United States; Du Pont, Midland, MI 48686, United States.

出版信息

Toxicol Lett. 2023 Jan 15;373:13-21. doi: 10.1016/j.toxlet.2022.10.008. Epub 2022 Nov 1.

DOI:10.1016/j.toxlet.2022.10.008
PMID:36332816
Abstract

Octamethylcyclotetrasiloxane (D4) is a high production volume chemical that has been subject to thorough toxicological investigations. Animal studies with the substance were conducted with either Fischer 344 or Sprague Dawley CD rats. While the pharmacokinetic fate of D4 in Fischer rats is well understood, little information exists on Sprague Dawley CD rats, where reproductive effects have been demonstrated. The objective of this study was to explore the pharmacokinetic behavior in both rats, and to identify potential strain-specific differences. Fischer and Sprague Dawley CD rats were exposed for six hours to 700 ppm of C-D4 vapor either with or without preceding 14-day exposure to non-radiolabeled D4. Time-course data in blood, tissues and excreta were obtained through 168 h post-exposure and analyzed for both total radioactivity and parent D4. The data confirm that repeated exposure results in increased metabolism in both rat strains, confirming the findings of earlier studies of auto-induction of CYP2B1/2 by D4. The results also indicate that D4 is subject to strain-specific pharmacokinetic behavior, and that Fischer rats appear to metabolize D4 to a greater extent than Sprague Dawley CD rats.

摘要

八甲基环四硅氧烷(D4)是一种高产量的化学品,已经进行了彻底的毒理学研究。该物质的动物研究使用 Fischer 344 或 Sprague Dawley CD 大鼠进行。虽然 D4 在 Fischer 大鼠中的药代动力学命运已经得到很好的理解,但关于 Sprague Dawley CD 大鼠的信息很少,其中已经证明了生殖效应。本研究的目的是探索两种大鼠的药代动力学行为,并确定潜在的品系特异性差异。Fischer 和 Sprague Dawley CD 大鼠在六小时内暴露于 700 ppm 的 C-D4 蒸气中,要么在暴露前 14 天接受非放射性标记的 D4 暴露,要么不接受。通过暴露后 168 小时获得血液、组织和排泄物中的时间过程数据,并对总放射性和母体 D4 进行分析。数据证实,重复暴露会导致两种大鼠的代谢增加,这证实了早期关于 D4 自身诱导 CYP2B1/2 的研究结果。结果还表明,D4 存在特定于品系的药代动力学行为,并且 Fischer 大鼠似乎比 Sprague Dawley CD 大鼠更能代谢 D4。

相似文献

1
Comparative pharmacokinetic studies of C-octamethylcyclotetrasiloxane (C-D4) in Fischer 344 and Sprague Dawley CD rats after single and repeated inhalation exposure.C-octamethylcyclotetrasiloxane(C-D4)在单次和重复吸入暴露后在 Fischer 344 和 Sprague Dawley CD 大鼠中的比较药代动力学研究。
Toxicol Lett. 2023 Jan 15;373:13-21. doi: 10.1016/j.toxlet.2022.10.008. Epub 2022 Nov 1.
2
A 28-day whole-body inhalation study to evaluate octamethylcyclotetrasiloxane (D4) absorption/distribution in two rat strains.一项为期 28 天的全身吸入研究,评估两种大鼠品系中八甲基环四硅氧烷(D4)的吸收/分布情况。
Toxicol Lett. 2022 Nov 1;370:53-65. doi: 10.1016/j.toxlet.2022.09.001. Epub 2022 Sep 12.
3
Inhalation toxicology of octamethylcyclotetrasiloxane (D4) following a 3-month nose-only exposure in Fischer 344 rats.八甲基环四硅氧烷(D4)对Fischer 344大鼠进行为期3个月的仅经鼻吸入染毒后的吸入毒理学研究
Int J Toxicol. 2002 Jan-Feb;21(1):39-53. doi: 10.1080/10915810252826000.
4
Effects of chronic exposure to octamethylcyclotetrasiloxane and decamethylcyclopentasiloxane in the aging female Fischer 344 rat.长期暴露于八甲基环四硅氧烷和十甲基环五硅氧烷对老年雌性费希尔344大鼠的影响。
Toxicol Lett. 2017 Oct 20;279 Suppl 1:54-74. doi: 10.1016/j.toxlet.2017.08.016. Epub 2017 Aug 23.
5
Evaluation of octamethylcyclotetrasiloxane (D4) as an inducer of rat hepatic microsomal cytochrome P450, UDP-glucuronosyltransferase, and epoxide hydrolase: a 28-day inhalation study.八甲基环四硅氧烷(D4)作为大鼠肝微粒体细胞色素P450、UDP-葡萄糖醛酸转移酶和环氧水解酶诱导剂的评价:一项为期28天的吸入研究。
Toxicol Sci. 1998 Jan;41(1):29-41. doi: 10.1006/toxs.1997.2398.
6
Physiological modeling reveals novel pharmacokinetic behavior for inhaled octamethylcyclotetrasiloxane in rats.生理建模揭示了大鼠吸入八甲基环四硅氧烷的新型药代动力学行为。
Toxicol Sci. 2001 Apr;60(2):214-31. doi: 10.1093/toxsci/60.2.214.
7
Incorporation of a recirculating mobile lipid pool description into the cyclic volatile siloxane (cVMS) PBPK model captures terminal clearance of D after repeated inhalation exposure in F344 and SD Rats.将循环流动脂质池描述纳入环状挥发性硅氧烷(cVMS)的生理药代动力学(PBPK)模型,可捕捉F344和SD大鼠反复吸入暴露后D的终末清除率。
Toxicol Lett. 2023 Feb 15;375:29-38. doi: 10.1016/j.toxlet.2022.12.014. Epub 2022 Dec 31.
8
Biological relevance of effects following chronic administration of octamethylcyclotetrasiloxane (D4) in Fischer 344 rats.八甲基环四硅氧烷(D4)长期给药对Fischer 344大鼠影响的生物学相关性。
Toxicol Lett. 2017 Oct 20;279 Suppl 1:42-53. doi: 10.1016/j.toxlet.2017.01.010. Epub 2017 Jan 18.
9
Toxicology and humoral immunity assessment of octamethylcyclotetrasiloxane (D4) following a 28-day whole body vapor inhalation exposure in Fischer 344 rats.在Fischer 344大鼠中进行28天全身蒸汽吸入暴露后,对八甲基环四硅氧烷(D4)的毒理学和体液免疫评估。
Drug Chem Toxicol. 1999 Nov;22(4):655-77. doi: 10.3109/01480549908993174.
10
Repeated inhalation exposure to octamethylcyclotetrasiloxane produces hepatomegaly, transient hepatic hyperplasia, and sustained hypertrophy in female Fischer 344 rats in a manner similar to phenobarbital.反复吸入八甲基环四硅氧烷会使雌性Fischer 344大鼠出现肝肿大、短暂性肝脏增生以及持续性肥大,其方式与苯巴比妥类似。
Toxicol Appl Pharmacol. 2001 Apr 15;172(2):83-92. doi: 10.1006/taap.2000.9110.

引用本文的文献

1
Kinetically-derived maximal dose (KMD) confirms lack of human relevance for high-dose effects of octamethylcyclotetrasiloxane (D4).动力学推导的最大剂量(KMD)证实八甲基环四硅氧烷(D4)的高剂量效应与人体无关。
Arch Toxicol. 2025 Feb;99(2):611-621. doi: 10.1007/s00204-024-03914-z. Epub 2025 Jan 12.