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自旋捕获剂α-苯基-N-叔丁基硝酮(PBN)在大鼠体内的排泄、代谢及组织分布

Excretion, metabolism and tissue distribution of a spin trapping agent, alpha-phenyl-N-tert-butyl-nitrone (PBN) in rats.

作者信息

Chen G M, Bray T M, Janzen E G, McCay P B

机构信息

Department of Nutritional Sciences, University of Guelph, Ontario, Canada.

出版信息

Free Radic Res Commun. 1990;9(3-6):317-23. doi: 10.3109/10715769009145690.

Abstract

The objective of this study is using radiolabelled PBN to determine the tissue distribution, excretion, and metabolism of PBN in rats in order to evaluate the effective time to trap free radical in appropriate tissue(s). Our results demonstrated that PBN is rapidly absorbed when it is injected intraperitoneally in the animal. PBN can be used as an effective spin trapping agent for a variety of tissues since it is evenly distributed among a wide range of tissues measured. Since there is no difference in the tissue concentrations and distribution pattern of PBN at 15, 30 and 60 min after injection of PBN, it is appropriate to choose any of these time intervals to terminate the experiment and extract the spin adduct. The excretion of PBN, however, is slow. The majority of the radioactivity (70%) was excreted by the first 3 days. Only 5.7% of radioactivity was collected from 3 to 14 days. The remaining 25% of the radioactivity may be in the form of expired 14CO2. Trace amounts of radioactivity were recovered in the feces. PBN has probably only one major form of metabolite excreted in the urine. A small amount of the parent compound, however, was also excreted in the urine. The chemical structure of the metabolite(s) is still unknown.

摘要

本研究的目的是使用放射性标记的PBN来确定PBN在大鼠体内的组织分布、排泄和代谢情况,以便评估在适当组织中捕获自由基的有效时间。我们的结果表明,将PBN腹腔注射到动物体内后,它能迅速被吸收。由于PBN在所测量的广泛组织中分布均匀,因此它可作为多种组织的有效自旋捕获剂。由于在注射PBN后15、30和60分钟时,PBN的组织浓度和分布模式没有差异,所以选择这些时间间隔中的任何一个来终止实验并提取自旋加合物都是合适的。然而,PBN的排泄较慢。大部分放射性(70%)在前3天排出。从第3天到第14天仅收集到5.7%的放射性。其余25%的放射性可能以呼出的14CO2形式存在。粪便中回收了微量放射性。PBN在尿液中排泄的代谢物可能只有一种主要形式。不过,尿液中也排泄出少量的母体化合物。代谢物的化学结构仍然未知。

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