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首页> 外文期刊>Toxicology and Applied Pharmacology >Age-related change in cadmium-induced hepatotoxicity in Wistar rats: role of Kupffer cells and neutrophils.
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Age-related change in cadmium-induced hepatotoxicity in Wistar rats: role of Kupffer cells and neutrophils.

机译:镉诱导的Wistar大鼠肝毒性的年龄相关变化:库普弗细胞和中性粒细胞的作用。

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The hepatotoxicity of cadmium was studied in 1-, 2-, and 6-month-old male Wistar rats. Liver damage, indicated by the increase in serum alanine aminotransferase activity 24 h after sc administration of 3 and 6 mg/kg cadmium, was observed only in 6-month-old rats. Dose-dependent increases in the cadmium content of the liver were similar for all three age groups. Basal and induced metallothionein contents were higher in livers of 1-month-old rats than in those of 2- and 6-month-old rats. In contrast, the basal glutathione content of the liver was higher in 6-month-old rats than in 1- and 2-month-old rats, and glutathione content increased slightly in all three age groups after cadmium administration. Thus, the higher susceptibility to cadmium-induced hepatotoxicity in 6-month-old rats seemed not to be explained by differences in cadmium uptake or by the metallothionein and glutathione contents of the liver. Inactivation of Kupffer cells with gadolinium chloride or depletion of neutrophils with cyclophosphamide relieved cadmium hepatotoxicity only in 6-month-old rats. In addition, 6-month-old rats were more susceptible than 2-month-old rats to lipopolysaccharide-induced hepatotoxicity. The results suggest that age-associated changes in Kupffer cell function and infiltration of neutrophils are important determinants of cadmium-induced hepatotoxicity in rats. Copyright 1998 Academic Press.
机译:在1、2和6个月大的雄性Wistar大鼠中研究了镉的肝毒性。仅在6个月大的大鼠中观察到肝损伤,这是在皮下注射3和6 mg / kg镉后24小时血清丙氨酸氨基转移酶活性增加所表明的。在所有三个年龄组中,肝脏中镉含量的剂量依赖性增加均相似。 1月龄大鼠肝脏的基础和诱导金属硫蛋白含量高于2月龄和6月龄大鼠的肝脏。相比之下,6个月大的大鼠肝脏的基础谷胱甘肽含量高于1个月和2个月大的大鼠,并且在施用镉后的所有三个年龄组中,谷胱甘肽的含量均略有增加。因此,在6个月大的大鼠中,镉引起的肝毒性敏感性更高,似乎不能通过镉吸收差异或肝脏中金属硫蛋白和谷胱甘肽含量的差异来解释。仅在6个月大的大鼠中,用氯化g灭活Kupffer细胞或用环磷酰胺灭活嗜中性白细胞可减轻镉的肝毒性。此外,6个月大的老鼠比2个月大的老鼠更易受到脂多糖诱导的肝毒性。结果表明,与年龄相关的库普弗细胞功能变化和中性粒细胞浸润是镉诱导大鼠肝毒性的重要决定因素。版权所有1998学术出版社。

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