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小鼠体内N-[14C]乙基-N-亚硝基脲的组织分布及转归研究。

Studies on the tissue-disposition and fate of N-[14C]ethyl-N-nitrosourea in mice.

作者信息

Johansson-Brittebo E, Tjälve H

出版信息

Toxicology. 1979 Aug;13(3):275-85. doi: 10.1016/s0300-483x(79)80031-1.

Abstract

The tissue-disposition and fate of N-[14C]ethyl-N-nitrosourea has been studied in mice. A large part of the injected N-[14C]ethyl-N-nitrosourea radioactivity was found to be exhaled as 14CO2. Whole-body autoradiography showed evenly distributed radioactivity in most tissues shortly after the administration of N-[14C]ethyl-N-nitrosourea which probably is due to the homogeneously distributed substance and the non-enzymatically formed ethyl-carbonium ions which have reacted with the tissues. The blood-brain barrier seemed to have a capacity to partially prevent the uptake of the substance in the central nervous system. A high radioactivity was observed in the liver, which may imply that N-[14C]ethyl-N-nitrosourea is enzymatically decomposed in this tissue. An observed labelling of kidneys may be connected with urinary excretion of radioactivity. The radioactivity in the liver and kidney decreased at later survival intervals and a distribution pattern appeared, which was characterized by a labelling of tissues with a high protein or steroid synthesis and of fat containing tissues. The distribution pattern corresponded to the one seen after the administration of [14C]acetaldehyde and is probably due to normal biosynthetic incorporation of radioactivity in the 2-carbon pool. Pretreatments with pyrazole, nialamide and diethyldithiocarbamate caused a marked inhibition of the exhalation of 14CO2 and of the incorporation of radioactivity in the liver. This effect may be directed towards the decomposition of N-[14C]ethyl-N-nitrosourea itself, but an effect on the metabolism of formed 2-carbon fragments is also possible. The incorporation of radioactivity in other tissues was not influenced by the pretreatments.

摘要

已对N-[¹⁴C]乙基-N-亚硝基脲在小鼠体内的组织分布和归宿进行了研究。发现注射的N-[¹⁴C]乙基-N-亚硝基脲放射性的很大一部分以¹⁴CO₂的形式呼出。全身放射自显影显示,在给予N-[¹⁴C]乙基-N-亚硝基脲后不久,大多数组织中的放射性分布均匀,这可能是由于该物质分布均匀以及与组织发生反应的非酶促形成的乙基碳正离子所致。血脑屏障似乎有能力部分阻止该物质在中枢神经系统中的摄取。在肝脏中观察到高放射性,这可能意味着N-[¹⁴C]乙基-N-亚硝基脲在该组织中被酶分解。观察到的肾脏标记可能与放射性物质的尿液排泄有关。在后期存活时间,肝脏和肾脏中的放射性降低,并出现了一种分布模式,其特征是蛋白质或类固醇合成高的组织以及含脂肪组织被标记。这种分布模式与给予[¹⁴C]乙醛后所见的模式一致,可能是由于放射性在二碳池中正常的生物合成掺入。用吡唑、尼亚酰胺和二乙二硫代氨基甲酸盐进行预处理可显著抑制¹⁴CO₂的呼出以及肝脏中放射性的掺入。这种作用可能针对N-[¹⁴C]乙基-N-亚硝基脲本身的分解,但对形成的二碳片段的代谢也可能有影响。预处理对其他组织中放射性的掺入没有影响。

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