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Resistance of metallothionein-III null mice to cadmium-induced acute hepatotoxicity

机译:金属硫蛋白-III无效小鼠对镉诱导的急性肝毒性的抵抗

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We examined the sensitivity of metallothionein (MT)-III null mice to cadmium (Cd)-induced acute hepatotoxicity. MT-I/II null mice were also used to compare Cd toxicities between MT-III null mice and MT-I/II null mice. Male MT-I/II null mice, MT-III null mice and wild-type mice were given s.c. injection of Cd (5-20 μmol/kg) and then the blood and liver were collected from each mouse under ether anesthesia at 2 days after the administration. Serum alanine aminotransferase (ALT) and aspartate aminotransferase (AST) activities elevated by injection of Cd were significantly higher in the MT-I/II null mice than in the wild-type mice. In the MT-III null mice, ALT and AST activities were not elevated following the injection of Cd. Further, marked morphological changes such as necrosis of hepatocytes, severe hemorrhage and congestion were observed by injection of Cd in both MT-I/II null mice and wild-type mice, whereas the degree of injury was found to be more extensive in MT-I/II null mice. In contrast, only occasional damage was observed in the liver of MT-III null mice treated with the same dose of Cd. These morphological observations were consistent with the results of ALT and AST activities. In the present study, it was clearly found that MT-III null mice were resistant to Cd hepatotoxicity, although MT-I/II null mice were sensitive to its toxicity. MT-III may be an accelerative factor in Cd-induced acute hepatotoxicity.
机译:我们检查了金属硫蛋白(MT)-III无效小鼠对镉(Cd)诱导的急性肝毒性的敏感性。还使用MT-I / II无效小鼠来比较MT-III无效小鼠和MT-I / II无效小鼠之间的Cd毒性。皮下注射雄性MT-I / II无效小鼠,MT-III无效小鼠和野生型小鼠。注射Cd(5-20​​μmol/ kg),然后在给药后2天,在乙醚麻醉下从每只小鼠收集血液和肝脏。注射Cd升高的血清丙氨酸氨基转移酶(ALT)和天冬氨酸氨基转移酶(AST)活性在MT-1 / II无效小鼠中显着高于野生型小鼠。在MT-III无效小鼠中,注射Cd后ALT和AST活性没有升高。此外,在MT-I / II无效小鼠和野生型小鼠中,注射Cd均观察到明显的形态学变化,例如肝细胞坏死,严重出血和充血,而在MT-I / II小鼠中观察到损伤程度更广泛I / II空小鼠。相反,在用相同剂量的Cd治疗的MT-III无效小鼠的肝脏中仅观察到偶尔的损伤。这些形态学观察与ALT和AST活性的结果一致。在本研究中,可以清楚地发现,MT-III无效小鼠对Cd肝毒性具有抵抗力,尽管MT-I / II无效小鼠对其毒性敏感。 MT-III可能是Cd诱导的急性肝毒性的促进因素。

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