Cadmium toxicity and distribution in metallothionein-I and -II deficient transgenic mice.

C C Conrad, C A Walter, A Richardson, M A Hanes, D T Grabowski
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引用次数: 13

Abstract

To date, numerous correlative studies have implicated metallothionein in the detoxification of heavy metals and in the regulation of metal distribution within an organism. In the present study cadmium-binding proteins (metallothionein equivalents), cadmium acute toxicity, and cadmium distribution in tissues and subcellular fractions were compared in metallothionein-I and -II deficient (MT-/-) mice and the parental strain carrying intact metallothionein genes (MT+/+) to determine if the absence of metallothionein altered any of these parameters. In an uninduced state, MT-/- mice expressed lower levels of cadmium-binding proteins relative to MT+/+ mice in several tissues. Administration of zinc enhanced the levels of cadmium-binding proteins in liver, small intestine, kidney, pancreas, and male sex organs, but not in cecum or brain of MT+/+ mice compared to zinc pretreated MT-/- mice. The cadmium LD50 was similar for MT-/-, MT+/+, and zinc-pretreated MT-/- mice (15-17 mumol CdCl2/kg body weight delivered i.p.). However, zinc-pretreated MT+/+ mice had a cadmium LD50 of 58-63 mumol CdCl2/kg body weight. Over two-thirds of cadmium was found in liver, cecum, small intestine, and kidney in both MT+/+ and MT-/- mice; therefore, metallothionein levels do not appear to play a major role in the tissue distribution of cadmium. However, after zinc pretreatment, MT+/+ mice accumulated more cadmium in the liver and less in other tissues, whereas the amount of cadmium in the liver was not altered by zinc pretreatment in MT-/- mice. In general, the cytosolic/particulate ratio of cadmium was significantly higher in tissues of noninduced MT+/+ mice relative to MT-/- mice. This difference was accentuated after zinc pretreatment. Together these results indicate that basal levels of metallothionein do not protect from the acute toxicity of a single i.p. cadmium challenge. Furthermore, it does not appear that the cytosolic compartmentalization of cadmium is correlated with reduced toxicity.

镉在金属硫蛋白i和-II缺乏转基因小鼠中的毒性和分布。
迄今为止,许多相关研究都表明金属硫蛋白与重金属解毒和调节金属在生物体中的分布有关。在本研究中,比较了金属硫蛋白i和- ii缺陷(MT-/-)小鼠和携带完整金属硫蛋白基因(MT+/+)的亲本菌株中镉结合蛋白(金属硫蛋白当量)、镉急性毒性以及镉在组织和亚细胞组分中的分布,以确定金属硫蛋白缺失是否改变了这些参数。在非诱导状态下,MT-/-小鼠在一些组织中表达的镉结合蛋白水平低于MT+/+小鼠。与锌预处理的MT-/-小鼠相比,锌处理提高了MT+/+小鼠肝脏、小肠、肾脏、胰腺和男性性器官中的镉结合蛋白水平,但在盲肠和脑中没有。MT-/-、MT+/+和锌预处理的MT-/-小鼠的镉LD50相似(15-17 μ mol CdCl2/kg体重)。而经锌预处理的MT+/+小鼠镉LD50为58 ~ 63 μ mol CdCl2/kg体重。在MT+/+和MT-/-小鼠的肝脏、盲肠、小肠和肾脏中发现了超过三分之二的镉;因此,金属硫蛋白水平似乎在镉的组织分布中不起主要作用。然而,锌预处理后,MT+/+小鼠肝脏中镉的积累较多,其他组织中镉的积累较少,而MT-/-小鼠肝脏中镉的含量未受锌预处理的影响。总体而言,非诱导MT+/+小鼠组织中镉的胞质/颗粒比明显高于MT-/-小鼠。这种差异在锌预处理后更明显。综上所述,这些结果表明,金属硫蛋白的基础水平并不能保护小鼠免受单口镉的急性毒性。此外,镉的细胞质区隔化似乎与毒性降低无关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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