Nielsen J B, Andersen H L, Sørensen J A, Andersen O
Department of Environmental Medicine, Odense University, Denmark.
Pharmacol Toxicol. 1992 Apr;70(4):262-7. doi: 10.1111/j.1600-0773.1992.tb00468.x.
During the last 5 years, the site of gastrointestinal absorption of inorganic mercury has been attempted identified mainly by experiments using perfused intestinal segments in vitro or in situ. The present investigation will discuss the localization of the absorption site for mercuric chloride based on a completely undisturbed in vivo experimental model in mice. As the mice were allowed to eat their normal diet during the experimental period, the present results would independently add to existing knowledge on intestinal absorption sites for inorganic mercury. The mice were given 203Hg labelled mercuric chloride orally, either through stomach tube or in the drinking water, and were killed after various time intervals. Mercury was localized and quantified in various segments of the gastrointestinal tract by gamma-counting. Time course analysis of the segmental deposition of mercury demonstrated that the deposition mainly takes place in the proximal jejunum and suggested that a larger part of the jejunum than previously reported is involved in absorption of mercury. Using this in vivo model, tetraethylthiuram disulfide was demonstrated to increase the intestinal deposition and absorption without changing the site of deposition.
在过去5年中,主要通过体外或原位灌注肠段实验试图确定无机汞在胃肠道的吸收部位。本研究将基于完全未受干扰的小鼠体内实验模型,探讨氯化汞吸收部位的定位。由于在实验期间允许小鼠食用正常饮食,本研究结果将独立地补充有关无机汞肠道吸收部位的现有知识。通过胃管或饮水给小鼠口服203Hg标记的氯化汞,并在不同时间间隔后处死。通过γ计数对胃肠道各段中的汞进行定位和定量。汞在各段沉积的时间进程分析表明,沉积主要发生在空肠近端,提示参与汞吸收的空肠部分比先前报道的要大。利用该体内模型,已证明二硫化四乙秋兰姆能增加肠道沉积和吸收,但不改变沉积部位。