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糖尿病 KK-A(y) 小鼠对乙酰氨基酚诱导的氧化性肝损伤高度敏感。

Diabetic KK-A(y) mice are highly susceptible to oxidative hepatocellular damage induced by acetaminophen.

机构信息

Department of Gastroenterology, Juntendo University School of Medicine, Tokyo, Japan.

出版信息

Am J Physiol Gastrointest Liver Physiol. 2010 Aug;299(2):G329-37. doi: 10.1152/ajpgi.00361.2009. Epub 2010 Jun 10.

Abstract

Despite pathophysiological similarities to alcoholic liver disease, susceptibility to acetaminophen hepatotoxicity in metabolic syndrome-related nonalcoholic steatohepatitis (NASH) has not been well elucidated. In this study, therefore, we investigated acetaminophen-induced liver injury in KK-A(y) mice, an animal model of metabolic syndrome. Twelve-week-old male KK-A(y) and C57Bl/6 mice were injected intraperitoneally with 300 or 600 mg/kg acetaminophen, and euthanized 6 h later. Liver histology was assessed, and hepatic expression of 4-hydroxy-2-nonenal was detected by immunohistochemistry. Levels of reduced glutathione were determined spectrophotometrically. Phosphorylation of c-Jun NH(2)-terminal kinase (JNK) was analyzed by Western blotting. Hepatocytes were isolated from both strains by collagenase perfusion, and cell death and oxidative stress were measured fluorometrically by use of propidium iodide and 5-(and-6)-chloromethyl-2'7'-dichloro-dihydrofluorescein diacetate acetyl ester, respectively. Acetaminophen induced more severe necrosis and apoptosis of hepatocytes in KK-A(y) mice than in C57Bl/6 mice and significantly increased serum alanine aminotransferase levels in KK-A(y) mice. Acetaminophen-induction of 4-hydroxy-2-nonenal in the liver was potentiated, whereas the levels of reduced glutathione in liver were lower in KK-A(y) mice. Acetaminophen-induced phosphorylation of JNK in the liver was also enhanced in KK-A(y) mice. Exposure to 20 microM tert-butyl hydroperoxide did not kill hepatocytes isolated from C57Bl/6 mice but induced cell death and higher oxidative stress in hepatocytes from KK-A(y) mice. These results demonstrated that acetaminophen toxicity is increased in diabetic KK-A(y) mice mainly due to enhanced oxidative stress in hepatocytes, suggesting that metabolic syndrome-related steatohepatitis is an exacerbating factor for acetaminophen-induced liver injury.

摘要

尽管代谢综合征相关非酒精性脂肪性肝炎(NASH)与酒精性肝病在病理生理学上有相似之处,但对乙酰氨基酚肝毒性的易感性尚未得到充分阐明。因此,在这项研究中,我们研究了代谢综合征动物模型 KK-A(y) 小鼠中的乙酰氨基酚诱导的肝损伤。将 12 周龄雄性 KK-A(y) 和 C57Bl/6 小鼠经腹腔注射 300 或 600mg/kg 乙酰氨基酚,6 小时后安乐死。通过免疫组织化学检测肝组织中 4-羟基-2-壬烯醛的表达,通过分光光度法测定还原型谷胱甘肽的水平。通过 Western blot 分析 c-Jun NH(2)-末端激酶(JNK)的磷酸化。通过胶原酶灌注从两种品系中分离肝细胞,并通过碘化丙啶和 5-(和-6)-氯甲基-2'7'-二氯二氢荧光素二乙酸乙酰酯分别测量细胞死亡和氧化应激的荧光。与 C57Bl/6 小鼠相比,乙酰氨基酚在 KK-A(y) 小鼠中引起更严重的肝细胞坏死和凋亡,并显著增加 KK-A(y) 小鼠的血清丙氨酸氨基转移酶水平。肝中 4-羟基-2-壬烯醛的乙酰氨基酚诱导增强,而 KK-A(y) 小鼠肝中还原型谷胱甘肽的水平降低。肝中 JNK 的乙酰氨基酚诱导磷酸化也在 KK-A(y) 小鼠中增强。暴露于 20µM 叔丁基过氧化物不会杀死从 C57Bl/6 小鼠分离的肝细胞,但会诱导来自 KK-A(y) 小鼠的肝细胞死亡和更高的氧化应激。这些结果表明,糖尿病 KK-A(y) 小鼠中乙酰氨基酚的毒性增加主要是由于肝细胞中的氧化应激增强,这表明代谢综合征相关的脂肪性肝炎是加重乙酰氨基酚肝损伤的一个因素。

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