• 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

基于气体摄取研究的吸入药代动力学。IV. 挥发性化合物的内源性产生。

Inhalation pharmacokinetics based on gas uptake studies. IV. The endogenous production of volatile compounds.

作者信息

Filser J G, Bolt H M

出版信息

Arch Toxicol. 1983 Feb;52(2):123-33. doi: 10.1007/BF00354772.

DOI:10.1007/BF00354772
PMID:6847378
Abstract

A pharmacokinetic description of production, distribution and metabolism of endogenous volatile compounds is presented. This description uses the "gas uptake model" of a closed recirculated atmosphere in which experimental animals are exposed. As an example, the production rates of acetone, under different conditions of stimulation by xenobiotics, are calculated from published experimental data. The theoretical descriptions may serve as a basis for treating the problem of hydrocarbon exhalation in toxicological experiments with compounds eliciting lipid peroxidation.

摘要

本文对内源性挥发性化合物的产生、分布和代谢进行了药代动力学描述。该描述采用了封闭循环大气的“气体吸收模型”,实验动物在其中暴露。例如,根据已发表的实验数据计算了在不同外源性物质刺激条件下丙酮的产生速率。这些理论描述可为处理在毒理学实验中由引发脂质过氧化的化合物导致的碳氢化合物呼出问题提供依据。

相似文献

1
Inhalation pharmacokinetics based on gas uptake studies. IV. The endogenous production of volatile compounds.基于气体摄取研究的吸入药代动力学。IV. 挥发性化合物的内源性产生。
Arch Toxicol. 1983 Feb;52(2):123-33. doi: 10.1007/BF00354772.
2
The closed chamber technique--uptake, endogenous production, excretion, steady-state kinetics and rates of metabolism of gases and vapors.密闭腔室技术——气体和蒸气的摄取、内源性生成、排泄、稳态动力学及代谢速率
Arch Toxicol. 1992;66(1):1-10. doi: 10.1007/BF02307263.
3
Increased acetone exhalation induced by metabolites of halogenated C1 and C2 compounds.卤代C1和C2化合物的代谢产物引起丙酮呼出增加。
Arch Toxicol. 1982 Jan;49(2):107-16. doi: 10.1007/BF00332358.
4
Inhalation pharmacokinetics based on gas uptake studies. II. Pharmacokinetics of acetone in rats.基于气体摄取研究的吸入药代动力学。II. 丙酮在大鼠体内的药代动力学。
Arch Toxicol. 1981 Jul;47(4):293-304. doi: 10.1007/BF00332395.
5
Development of an inhalation physiologically based pharmacokinetic (PBPK) model for 2,2, 4-trimethylpentane (TMP) in male Long-Evans rats using gas uptake experiments.建立吸入 2,2,4-三甲基戊烷(TMP)在雄性长耳大仓鼠体内生理药代动力学(PBPK)模型的研究。 使用气体摄取实验。
Inhal Toxicol. 2009 Dec;21(14):1176-85. doi: 10.3109/08958370903005751.
6
Toxicokinetic models for volatile industrial chemicals and reactive metabolites.
Toxicol Lett. 1995 Dec;82-83:357-66. doi: 10.1016/0378-4274(95)03566-4.
7
Inhalation pharmacokinetics based on gas uptake studies. I. Improvement of kinetic models.基于气体摄取研究的吸入药代动力学。I. 动力学模型的改进。
Arch Toxicol. 1981 Jul;47(4):279-92. doi: 10.1007/BF00332394.
8
Quantitative evaluation of ethane and n-pentane as indicators of lipid peroxidation in vivo.乙烷和正戊烷作为体内脂质过氧化指标的定量评估。
Arch Toxicol. 1983 Feb;52(2):135-47. doi: 10.1007/BF00354773.
9
Uptake of highly soluble gases in the epithelium of the conducting airways.高溶解性气体在传导气道上皮中的摄取。
Pflugers Arch. 1985 Dec;405(4):389-94. doi: 10.1007/BF00595693.
10
Inhalation pharmacokinetics based on gas uptake studies. III. A pharmacokinetic assessment in man of "peak concentrations" of vinyl chloride.基于气体摄取研究的吸入药代动力学。III. 人体中氯乙烯“峰值浓度”的药代动力学评估。
Arch Toxicol. 1981 Nov;48(4):213-28. doi: 10.1007/BF00319650.

引用本文的文献

1
Pharmacokinetic analysis of the chronic administration of the inert gases Xe and Ar using a physiological based model.使用基于生理学的模型对惰性气体氙气(Xe)和氩气(Ar)进行长期给药的药代动力学分析。
Med Gas Res. 2015 May 29;5:8. doi: 10.1186/s13618-015-0029-z. eCollection 2015.
2
Quantitative evaluation of ethane and n-pentane as indicators of lipid peroxidation in vivo.乙烷和正戊烷作为体内脂质过氧化指标的定量评估。
Arch Toxicol. 1983 Feb;52(2):135-47. doi: 10.1007/BF00354773.
3
Biological activation of 1,3-butadiene to vinyl oxirane by rat liver microsomes and expiration of the reactive metabolite by exposed rats.

本文引用的文献

1
Characteristics of haloethylene-induced acetonemia in rats.大鼠中卤代乙烯诱导的丙酮血症的特征
Arch Toxicol. 1980 Jul;45(2):109-16. doi: 10.1007/BF01270908.
2
Determination of the kinetic constants for metabolism of inhaled toxicants in vivo using gas uptake measurements.利用气体摄取测量法测定体内吸入毒物代谢的动力学常数。
Toxicol Appl Pharmacol. 1980 Jun 15;54(1):100-16. doi: 10.1016/0041-008x(80)90011-3.
3
Inhalation pharmacokinetics based on gas uptake studies. III. A pharmacokinetic assessment in man of "peak concentrations" of vinyl chloride.
大鼠肝脏微粒体将1,3 - 丁二烯生物激活为乙烯基环氧乙烷以及暴露大鼠呼出活性代谢物的过程。
J Cancer Res Clin Oncol. 1983;106(2):112-6. doi: 10.1007/BF00395388.
4
Determination of alkanes in breath to monitor lipid peroxidation in the presence of volatile toxicants and metabolites. An optimized, automatic method.测定呼出气体中的烷烃以监测挥发性毒物和代谢物存在时的脂质过氧化。一种优化的自动方法。
Arch Toxicol. 1983 Jul;53(3):213-23. doi: 10.1007/BF00316505.
5
Inhalation pharmacokinetics based on gas uptake studies. VI. Comparative evaluation of ethylene oxide and butadiene monoxide as exhaled reactive metabolites of ethylene and 1,3-butadiene in rats.基于气体摄取研究的吸入药代动力学。VI. 大鼠体内环氧乙烷和一氧化丁二烯作为乙烯和1,3 - 丁二烯呼出的反应性代谢物的比较评估。
Arch Toxicol. 1984 Oct;55(4):219-23. doi: 10.1007/BF00341014.
6
Inhalation pharmacokinetics based on gas uptake studies. V. Comparative pharmacokinetics of ethylene and 1,3-butadiene in rats.基于气体摄取研究的吸入药代动力学。V. 大鼠体内乙烯和1,3 - 丁二烯的比较药代动力学。
Arch Toxicol. 1984 Oct;55(4):213-8. doi: 10.1007/BF00341013.
7
Metabolism and pharmacokinetics of vinyl acetate.
Arch Toxicol. 1985 Aug;57(3):191-5. doi: 10.1007/BF00290886.
8
Absence of lipid peroxidation as determined by ethane exhalation in rats treated with 2, 3, 7, 8-tetrachlorodibenzo-p-dioxin (TCDD).用乙烷呼出法测定经2,3,7,8-四氯二苯并对二恶英(TCDD)处理的大鼠体内脂质过氧化反应的缺失情况。
Arch Toxicol. 1985 Apr;57(1):13-6. doi: 10.1007/BF00286568.
9
Inhalation pharmacokinetics of 1,2-dichloroethane after different dietary pretreatments of male Sprague-Dawley rats.雄性斯普拉格-道利大鼠经不同饮食预处理后1,2-二氯乙烷的吸入药代动力学
Arch Toxicol. 1986 Oct;59(3):127-34. doi: 10.1007/BF00316320.
10
Species differences in butadiene metabolism between mice and rats evaluated by inhalation pharmacokinetics.通过吸入药代动力学评估小鼠和大鼠之间丁二烯代谢的种属差异。
Arch Toxicol. 1986 Apr;58(4):235-8. doi: 10.1007/BF00297112.
基于气体摄取研究的吸入药代动力学。III. 人体中氯乙烯“峰值浓度”的药代动力学评估。
Arch Toxicol. 1981 Nov;48(4):213-28. doi: 10.1007/BF00319650.
4
A physiologically based toxicokinetic description of the metabolism of inhaled gases and vapors: analysis at steady state.吸入气体和蒸气代谢的基于生理学的毒代动力学描述:稳态分析
Toxicol Appl Pharmacol. 1981 Sep 30;60(3):509-26. doi: 10.1016/0041-008x(81)90338-0.
5
Inhalation pharmacokinetics based on gas uptake studies. II. Pharmacokinetics of acetone in rats.基于气体摄取研究的吸入药代动力学。II. 丙酮在大鼠体内的药代动力学。
Arch Toxicol. 1981 Jul;47(4):293-304. doi: 10.1007/BF00332395.
6
Inhalation pharmacokinetics based on gas uptake studies. I. Improvement of kinetic models.基于气体摄取研究的吸入药代动力学。I. 动力学模型的改进。
Arch Toxicol. 1981 Jul;47(4):279-92. doi: 10.1007/BF00332394.
7
Monitoring lipid peroxidation by breath analysis: endogenous hydrocarbons and their metabolic elimination.通过呼吸分析监测脂质过氧化:内源性碳氢化合物及其代谢消除
Toxicol Appl Pharmacol. 1980 Dec;56(3):337-44. doi: 10.1016/0041-008x(80)90066-6.
8
Increased acetone exhalation induced by metabolites of halogenated C1 and C2 compounds.卤代C1和C2化合物的代谢产物引起丙酮呼出增加。
Arch Toxicol. 1982 Jan;49(2):107-16. doi: 10.1007/BF00332358.
9
Physiological roles of ketone bodies as substrates and signals in mammalian tissues.酮体在哺乳动物组织中作为底物和信号分子的生理作用。
Physiol Rev. 1980 Jan;60(1):143-87. doi: 10.1152/physrev.1980.60.1.143.
10
Quantitative evaluation of ethane and n-pentane as indicators of lipid peroxidation in vivo.乙烷和正戊烷作为体内脂质过氧化指标的定量评估。
Arch Toxicol. 1983 Feb;52(2):135-47. doi: 10.1007/BF00354773.