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酒精性肝病大鼠肝脏中乙醛修饰和4-羟基壬烯醛修饰的蛋白质

Acetaldehyde-modified and 4-hydroxynonenal-modified proteins in the livers of rats with alcoholic liver disease.

作者信息

Li C J, Nanji A A, Siakotos A N, Lin R C

机构信息

Department of Medicine, Indiana University School of Medicine, Indianapolis, USA.

出版信息

Hepatology. 1997 Sep;26(3):650-7. doi: 10.1002/hep.510260317.

Abstract

Liver proteins form adducts with acetaldehyde and are modified by products of lipid peroxidation in alcohol-fed animals. It has been hypothesized that the formation of these modified liver proteins may contribute to liver injury in alcoholic liver disease. The present work was performed to determine the extent of protein modification in rats with experimental alcoholic liver disease. Rats were fed ethanol intragastrically with medium chain triglycerides (MCTs), palm oil, corn oil, or fish oil. The group fed MCTs and ethanol showed no liver injury, rats fed palm oil and ethanol showed only fatty liver, rats fed corn oil and ethanol showed fatty liver with moderate necrosis and inflammation, and rats fed fish oil and ethanol showed fatty liver with severe necrosis and inflammation. Antibodies were raised by using keyhole limpet hemocyanin modified in vitro by 4-hydroxynonenal (4-HNE) or acetaldehyde as immunogens. When liver extracts were examined by Western blot analysis, the intensities of the acetaldehyde-modified protein band (37 kd) in the alcohol-fed animals were significantly different among the ethanol-treated groups and correlated with plasma acetaldehyde concentrations. It was strongest in rats fed fish oil and ethanol, followed by rats fed palm oil and ethanol and rats fed corn oil and ethanol, whereas rats fed MCTs and ethanol showed the weakest intensity. The 37-kd protein-adetaldehyde adduct was located mainly in the pericentral region of the liver. No acetaldehyde adduct was detected in the control rats that were pair-fed with isocaloric amounts of dextrose. Western blot analysis using the anti-4-HNE antibody showed four distinctive bands (48, 45, 40, and 38 kd) in the liver extracts of alcohol-fed rats. Control animals showed only a weak 38-kd band. Although the intensities of the 48-, 40-, and 38-kd bands were similar among the different ethanol-treated groups, the intensity of the 45-kd band decreased from MCTs and ethanol > palm oil and ethanol > or = corn oil and ethanol > fish oil and ethanol. The data indicate that the degree of liver protein modification by acetaldehyde correlates well with the severity of liver injury in ethanol-fed rats, whereas modification by the lipid peroxidation product 4-HNE shows no correlation with the severity of liver injury.

摘要

在喂食酒精的动物中,肝脏蛋白质会与乙醛形成加合物,并被脂质过氧化产物修饰。据推测,这些修饰后的肝脏蛋白质的形成可能会导致酒精性肝病中的肝脏损伤。开展本研究以确定实验性酒精性肝病大鼠中蛋白质修饰的程度。给大鼠经胃内喂食乙醇,同时分别给予中链甘油三酯(MCTs)、棕榈油、玉米油或鱼油。喂食MCTs和乙醇的组未出现肝脏损伤,喂食棕榈油和乙醇的大鼠仅出现脂肪肝,喂食玉米油和乙醇的大鼠出现伴有中度坏死和炎症的脂肪肝,而喂食鱼油和乙醇的大鼠出现伴有严重坏死和炎症的脂肪肝。通过使用经4-羟基壬烯醛(4-HNE)或乙醛体外修饰的匙孔血蓝蛋白作为免疫原制备抗体。当通过蛋白质印迹分析检测肝脏提取物时,在喂食酒精的动物中,乙醛修饰的蛋白条带(37kd)的强度在不同乙醇处理组之间存在显著差异,并且与血浆乙醛浓度相关。在喂食鱼油和乙醇的大鼠中最强,其次是喂食棕榈油和乙醇的大鼠以及喂食玉米油和乙醇的大鼠,而喂食MCTs和乙醇的大鼠强度最弱。37kd的蛋白质-乙醛加合物主要位于肝脏的中央周围区域。在与等热量葡萄糖配对喂食的对照大鼠中未检测到乙醛加合物。使用抗4-HNE抗体进行的蛋白质印迹分析在喂食酒精的大鼠的肝脏提取物中显示出四条独特的条带(48、45、40和38kd)。对照动物仅显示出一条较弱的38kd条带。尽管在不同乙醇处理组中48kd、40kd和38kd条带的强度相似,但45kd条带的强度从MCTs和乙醇组>棕榈油和乙醇组≥玉米油和乙醇组>鱼油和乙醇组依次降低。数据表明,乙醛对肝脏蛋白质的修饰程度与喂食乙醇的大鼠肝脏损伤的严重程度密切相关,而脂质过氧化产物4-HNE的修饰与肝脏损伤的严重程度无关。

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