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首页> 外文期刊>Lipids in Health Disease >Hepatic lipid profile in mice fed a choline-deficient, low-methionine diet resembles human non-alcoholic fatty liver disease
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Hepatic lipid profile in mice fed a choline-deficient, low-methionine diet resembles human non-alcoholic fatty liver disease

机译:小鼠肝脂肪型喂养胆碱,低甲硫氨酸饮食类似于人的非酒精脂肪肝病

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Emerging data support a role for lipids in non-alcoholic steatohepatitis (NASH) and hepatocellular carcinoma (HCC) in humans. With experimental models such data can be challenged or validated. Mice fed a low-methionine, choline-deficient (LMCD) diet develop NASH and, when injected with diethylnitrosamine (DEN), HCC. Here, lipidomic analysis was used to elucidate whether the NASH and HCC associated lipid derangements resemble the lipid profile of the human disease. Lipids were measured in the liver of mice fed a control or a LMCD diet for 16?weeks. DEN was injected at young age to initiate hepatocarcinogenesis. DEN treatment associated changes of the lipid composition and the tumor lipidome were evaluated. LMCD diet fed mice accumulated ceramides and triacylglycerols in the liver. Phospholipids enriched with monounsaturated fatty acids were also increased, whereas hepatic cholesterol levels remained unchanged in the LMCD model. Phosphatidylcholine and lysophosphatidylcholine concentrations declined in the liver of LMCD diet fed mice. The changes of most lipids associated with LMCD diet feeding were similar between water and DEN injected mice. Several polyunsaturated (PU) diacylglycerol species were already low in the liver of DEN injected mice fed the control diet. Tumors developed in the liver of LMCD diet fed mice injected with DEN. The tumor specific lipid profile, however, did not resemble the decrease of ceramides and PU phospholipids, which was consistently described in human HCC. Triacylglycerols declined in the cancer tissues, which is in accordance with a low expression of lipogenic enzymes in the tumors. The LMCD model is suitable to study NASH associated lipid reprogramming. Hepatic lipid profile was modestly modified in the DEN injected mice suggesting a function of these derangements in carcinogenesis. Lipid composition of liver tumors did not resemble the human HCC lipidome, and most notably, lipogenesis and triacylglycerol levels were suppressed.
机译:新兴数据支持人类中非酒精脂肪性炎(NASH)和肝细胞癌(HCC)的脂质作用。使用实验模型,此类数据可能受到挑战或验证。小鼠喂养低蛋氨酸,胆碱缺陷(LMCD)饮食发育肿瘤,当注射用二乙基硝基胺(DEN),HCC时。这里,利用脂质体分析来阐明纳什和HCC相关的脂质紊乱是否类似于人类疾病的脂质概况。在小鼠的肝脏中测量脂质,喂食对照或LMCD饮食16?周。在年轻时注射DEN以启动肝癌发生。评估DEN治疗相关变化脂质组合物和肿瘤脂质体。 LMCD饮食喂养小鼠累积的酰胺和肝脏中的三酰基甘油。富含单不饱和脂肪酸的磷脂也升高,而LMCD模型中肝胆水平保持不变。磷脂酰胆碱和溶血磷脂酰胆碱浓度下降在喂食小鼠的肝脏肝脏中。与LMCD饮食喂养相关的大多数脂质的变化在水和DEN注射的小鼠之间相似。在喂养对照饮食的Den注入小鼠的肝脏中,几种多不饱和(PU)二酰基甘油物种已经很低。在LMCD饮食肝脏肝脏中产生的肿瘤喂食小鼠注射巢穴。然而,肿瘤特异性脂质谱不会类似于神经酰胺和PU磷脂的减少,这在人HCC中始终描述。三酰基甘油在癌组织中下降,这与肿瘤中脂质酶的低表达。 LMCD模型适用于研究NASH相关的脂质重编程。肝脂肪曲线在注射小鼠中,在癌细胞发生中的这种紊乱的函数中进行了温和的修饰。肝脏肿瘤的脂质组合物不像人HCC脂质体,最值得注意的是,抑制脂肪生成和三酰基甘油水平。

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