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二乙基二硫代氨基甲酸盐和二硫化四乙基秋兰姆对小鼠锌代谢的影响。

Effects of diethyldithiocarbamate and tetraethylthiuram disulfide on zinc metabolism in mice.

作者信息

Sørensen J A, Andersen O

机构信息

Department of Environmental Medicine, Odense University, Denmark.

出版信息

Pharmacol Toxicol. 1989 Sep;65(3):209-13. doi: 10.1111/j.1600-0773.1989.tb01158.x.

Abstract

Chronic alcoholics with cirrhosis often develop symptoms of zinc deficiency. Tetraethylthiuram disulfide (TTD) is metabolized to two molecules of diethyldithiocarbamate (DDC). DDC chelates divalent metal ions, including zinc, by forming highly lipophilic neutral bis(dithiocarbamate)-metal complexes. DDC could therefore enhance the intestinal zinc uptake or increase the rate of zinc excretion. Accordingly, treatment of alcoholism with TTD could either aggravate or alleviate zinc deficiency. The present study investigated effects of DDC and TTD on intestinal zinc uptake and on the rate of zinc excretion in mice. When given as very high single oral doses, DDC and TTD increased the intestinal uptake of a single oral dose of zinc. When added to the diet and administered in lower doses, closer to those administered to humans for treatment of alcohol abuse, both compounds were without effect on the rate of excretion of the body's zinc stores. In a long-term experiment, where 65Zn was administered in the drinking water, these doses of TTD and DDC reduced the whole-body retention of 65Zn. No treatment changed the organ distribution of zinc in any of the experiments. In conclusion strong indications emerge from the present study that TTD treatment of alcoholism is more likely to reduce the intestinal zinc absorption than to enhance it as has been suggested by other authors. Thus, the widely used experimental model using single oral exposure to metal and chelator conceivably may give erroneous results, when used to predict effects of prolonged exposures.

摘要

患有肝硬化的慢性酗酒者常出现锌缺乏症状。二硫化四乙基秋兰姆(TTD)代谢生成两分子二乙基二硫代氨基甲酸盐(DDC)。DDC通过形成高度亲脂性的中性双(二硫代氨基甲酸盐)-金属络合物螯合二价金属离子,包括锌。因此,DDC可能会增强肠道对锌的吸收或提高锌的排泄速率。相应地,用TTD治疗酒精中毒可能会加重或缓解锌缺乏。本研究调查了DDC和TTD对小鼠肠道锌吸收及锌排泄速率的影响。当以非常高的单次口服剂量给药时,DDC和TTD增加了单次口服剂量锌的肠道吸收。当添加到饮食中并以较低剂量给药时,更接近用于治疗酒精滥用的人体给药剂量,这两种化合物对体内锌储备的排泄速率均无影响。在一项长期实验中,饮用水中添加了65Zn,这些剂量的TTD和DDC降低了65Zn在全身的潴留。在任何实验中,没有一种处理改变锌的器官分布。总之,本研究有力地表明,与其他作者所建议的相反,用TTD治疗酒精中毒更有可能降低肠道对锌的吸收,而不是增强吸收。因此,当用于预测长期接触的影响时,广泛使用的单次口服接触金属和螯合剂的实验模型可能会得出错误的结果。

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