• 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

Metabolism and distribution of [2,3-14C]acrolein in Sprague-Dawley rats.

作者信息

Parent R A, Caravello H E, Sharp D E

机构信息

Consultox Ltd., Damariscotta, ME 04543, USA.

出版信息

J Appl Toxicol. 1996 Sep-Oct;16(5):449-57. doi: 10.1002/(SICI)1099-1263(199609)16:5<449::AID-JAT369>3.0.CO;2-9.

DOI:10.1002/(SICI)1099-1263(199609)16:5<449::AID-JAT369>3.0.CO;2-9
PMID:8889798
Abstract

The metabolism and disposition of [2,3-14C]acrolein was studied in Sprague-Dawley rats after oral or intravenous dosing. Four groups of ten rats (five male and five female) were dosed with radiolabeled acrolein intravenously at 2.5 mg kg-1 (Group 2), orally by gavage at 2.5 mg kg-1, either as a single dose (Group 3) or after 14 daily doses of unlabeled acrolein (Group 4), or orally by gavage at 15 mg kg-1 (Group 5). Urine, feces, expired air and organic volatiles were collected for 7 days, after which the animals were sacrificed and tissues collected. All samples were analyzed for total radioactivity. After 7 days, the excretory patterns of male and female rats were almost identical. Urinary excretion was highest in the intravenously dosed animals (66-69%) and lowest in the Group 5 animals (36-40%), whereas the reverse was true for feces (< 2% for i.v. Group 2 animals and 28-30% for the Group 5 animals). Carbon dioxide expiration was comparable (26-31%) across all groups. Tissue concentrations of radioactivity were minimal in all groups (< 1.2%), but concentrations of radioactivity were highest in the intravenous Group 2 animals. The time course of excretion for all groups was similar with the exception of the high-dose animal group, which showed a pronounced delay in excretion during the first 12 h.

摘要

相似文献

1
Metabolism and distribution of [2,3-14C]acrolein in Sprague-Dawley rats.
J Appl Toxicol. 1996 Sep-Oct;16(5):449-57. doi: 10.1002/(SICI)1099-1263(199609)16:5<449::AID-JAT369>3.0.CO;2-9.
2
Metabolism and distribution of [2,3-14C]acrolein in Sprague-Dawley rats. II. Identification of urinary and fecal metabolites.
Toxicol Sci. 1998 Jun;43(2):110-20. doi: 10.1006/toxs.1998.2462.
3
Disposition of 2-mercaptobenzothiazole and 2-mercaptobenzothiazole disulfide in rats dosed intravenously, orally, and topically and in guinea pigs dosed topically.2-巯基苯并噻唑和2-巯基苯并噻唑二硫化物在大鼠静脉注射、口服和局部给药以及豚鼠局部给药后的处置情况。
J Toxicol Environ Health. 1989;27(1):65-84. doi: 10.1080/15287398909531279.
4
Effects of dose, strain, and dosing vehicle on methacrylonitrile disposition in rats and identification of a novel-exhaled metabolite.剂量、菌株及给药载体对大鼠体内甲基丙烯腈处置的影响以及一种新型呼出代谢物的鉴定
Drug Metab Dispos. 1992 Sep-Oct;20(5):643-52.
5
Toxicokinetics of 14C-endosulfan in male Sprague-Dawley rats following oral administration of single or repeated doses.单次或重复口服给药后,雄性斯普拉格-道利大鼠体内14C-硫丹的毒代动力学
Environ Toxicol. 2005 Oct;20(5):533-41. doi: 10.1002/tox.20142.
6
Disposition of [14C]gamma-cyclodextrin in germ-free and conventional rats.[14C]γ-环糊精在无菌大鼠和普通大鼠体内的处置情况。
Regul Toxicol Pharmacol. 1998 Apr;27(2):150-8. doi: 10.1006/rtph.1998.1219.
7
NTP Toxicology and Carcinogenesis Studies of 1-Amino-2,4-Dibromoanthraquinone (CAS No. 81-49-2) in F344/N Rats and B6C3F1 Mice (Feed Studies).1-氨基-2,4-二溴蒽醌(CAS编号:81-49-2)在F344/N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. 1996 Aug;383:1-370.
8
NTP Technical Report on the comparative toxicity studies of allyl acetate (CAS No. 591-87-7), allyl alcohol (CAS No. 107-18-6) and acrolein (CAS No. 107-02-8) administered by gavage to F344/N rats and B6C3F1 mice.NTP关于经口给予F344/N大鼠和B6C3F1小鼠乙酸烯丙酯(CAS编号:591-87-7)、烯丙醇(CAS编号:107-18-6)和丙烯醛(CAS编号:107-02-8)的比较毒性研究技术报告。
Toxic Rep Ser. 2006 Jul(48):1-73, A1-H10.
9
Disposition and metabolism of the new hypocholesterolemic compound S-8921 in rats and dogs.新型降胆固醇化合物S-8921在大鼠和犬体内的处置与代谢
Arzneimittelforschung. 1998 Oct;48(10):995-1006.
10
Pharmacokinetics of ethylene glycol. I. Plasma disposition after single intravenous, peroral, or percutaneous doses in female Sprague-Dawley rats and CD-1 mice.乙二醇的药代动力学。I. 雌性斯普拉格-道利大鼠和CD-1小鼠单次静脉注射、口服或经皮给药后的血浆处置情况
Drug Metab Dispos. 1996 Aug;24(8):911-21.

引用本文的文献

1
Origin and Fate of Acrolein in Foods.食品中丙烯醛的来源与去向
Foods. 2022 Jul 3;11(13):1976. doi: 10.3390/foods11131976.
2
Metabolic Investigation on the Interaction Mechanism between Dietary Dihydrochalcone Intake and Lipid Peroxidation Product Acrolein Reduction.膳食二氢查尔酮摄入与脂质过氧化产物丙烯醛还原的相互作用机制的代谢研究。
Mol Nutr Food Res. 2022 May;66(9):e2101107. doi: 10.1002/mnfr.202101107. Epub 2022 Mar 3.
3
Comparing the preclinical risk profile of inhalable candidate and potential candidate modified risk tobacco products: A bridging use case.
比较可吸入候选和潜在候选的改良风险烟草产品的临床前风险概况:一个过渡用例。
Toxicol Rep. 2020 Sep 12;7:1187-1206. doi: 10.1016/j.toxrep.2020.09.004. eCollection 2020.
4
Gut Microbial Glycerol Metabolism as an Endogenous Acrolein Source.肠道微生物甘油代谢作为内源性丙烯醛的来源。
mBio. 2018 Jan 16;9(1):e01947-17. doi: 10.1128/mBio.01947-17.
5
Metabolic fate of endogenous molecular damage: Urinary glutathione conjugates of DNA-derived base propenals as markers of inflammation.内源性分子损伤的代谢命运:DNA衍生碱基丙烯醛的尿谷胱甘肽缀合物作为炎症标志物
Proc Natl Acad Sci U S A. 2015 Sep 1;112(35):E4845-53. doi: 10.1073/pnas.1503945112. Epub 2015 Aug 17.
6
Molecular mechanism of acrylamide neurotoxicity: lessons learned from organic chemistry.丙烯酰胺神经毒性的分子机制:从有机化学中得到的启示。
Environ Health Perspect. 2012 Dec;120(12):1650-7. doi: 10.1289/ehp.1205432. Epub 2012 Oct 11.
7
Acrolein consumption induces systemic dyslipidemia and lipoprotein modification.丙烯醛摄入会引发全身性血脂异常和脂蛋白修饰。
Toxicol Appl Pharmacol. 2010 Feb 15;243(1):1-12. doi: 10.1016/j.taap.2009.12.010. Epub 2009 Dec 23.
8
Acrolein activates matrix metalloproteinases by increasing reactive oxygen species in macrophages.丙烯醛通过增加巨噬细胞中的活性氧来激活基质金属蛋白酶。
Toxicol Appl Pharmacol. 2009 Apr 15;236(2):194-201. doi: 10.1016/j.taap.2009.01.024. Epub 2009 Feb 7.
9
Role of endoplasmic reticulum stress in acrolein-induced endothelial activation.内质网应激在丙烯醛诱导的内皮细胞激活中的作用。
Toxicol Appl Pharmacol. 2009 Jan 1;234(1):14-24. doi: 10.1016/j.taap.2008.09.019. Epub 2008 Oct 7.
10
A comparative 90-day toxicity study of allyl acetate, allyl alcohol and acrolein.乙酸烯丙酯、烯丙醇和丙烯醛的90天毒性对比研究。
Toxicology. 2008 Nov 20;253(1-3):79-88. doi: 10.1016/j.tox.2008.08.014. Epub 2008 Sep 4.