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首页> 外文期刊>The Journal of toxicological sciences >Mechanisms of cadmium-induced chronotoxicity in mice
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Mechanisms of cadmium-induced chronotoxicity in mice

机译:镉诱发小鼠慢性毒性的机制

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摘要

Biological defense factors show diurnal variations in their expression levels or activities. These variations can induce the different sensitivity to external toxicants of a day. We reported earlier that mice showed clear diurnal variation of cadmium (Cd)-induced toxicity, i.e., chronotoxicity. In this report, we investigated additional new evidences for the cadmium (Cd)-induced chronotoxicity, and considered the mechanisms contributed to this chronotoxicity. Male C57BL/6J mice were injected with CdCl_2 (6.4 mg/kg, one shot) intraperitoneally at 6 different time points of a day (zeitgeber time (ZT); ZT2, ZT6, ZT10, ZT14, ZT18 or ZT22) followed by monitoring the mortality until 14 days after the injection. We observed extreme difference in survival numbers: surprisingly, all mice died at ZT2 injection while all mice survived at ZT18 injection. Moreover, in non-lethal dose of Cd (4.5 mg/kg), the values of alanine aminotransferase (ALT) and aspartate aminotransferase (AST) used as indexes of hepatotoxicity markedly increased at ZT6 injection while mostly unchanged at ZT18 injection. To consider the mechanisms of this extreme diurnal variation, we examined biochemical studies and concluded that the diurnal variation was not caused by the differences in hepatic Cd level, basal hepatic metallothionein (MT) level, and induction level or induction speed of hepatic MT. We suggested that one of the candidate determination factors was glutathione. We believe that the "chronotoxicology" for metal toxicity may be classic, yet new viewpoint in modern toxicology field.
机译:生物防御因子的表达水平或活性表现出昼夜变化。这些变化会导致一天对外部有毒物质的敏感性不同。我们先前报道过,小鼠显示出镉(Cd)诱发的毒性(即慢性毒性)的明显昼夜变化。在本报告中,我们调查了镉(Cd)引起的慢性毒性的其他新证据,并考虑了造成这种慢性毒性的机制。在一天的6个不同时间点(zeitgeber时间(ZT); ZT2,ZT6,ZT10,ZT14,ZT18或ZT22)腹膜内注射CdCl_2(6.4 mg / kg,一次注射)给雄性C57BL / 6J小鼠,然后监测直至注射后14天死亡率。我们观察到存活数存在极大差异:令人惊讶的是,所有小鼠均在ZT2注射后死亡,而所有小鼠均在ZT18注射后存活。此外,在非致死剂量的Cd(4.5 mg / kg)中,用作肝毒性指标的丙氨酸氨基转移酶(ALT)和天冬氨酸氨基转移酶(AST)的值在ZT6注射时显着增加,而在ZT18注射时大部分保持不变。为了考虑这种极端的昼夜变化的机制,我们检查了生化研究,得出的结论是,昼夜变化不是由肝Cd水平,基础肝金属硫蛋白(MT)水平以及肝MT诱导水平或诱导速度的差异引起的。我们建议谷胱甘肽是候选决定因素之一。我们认为,金属毒性的“时变毒理学”可能是经典的,但却是现代毒理学领域的新观点。

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