Alwahsh Salamah Mohammad, Xu Min, Schultze Frank Christian, Wilting Jörg, Mihm Sabine, Raddatz Dirk, Ramadori Giuliano
Department Gastroenterology and Endocrinology, University Medical Center Goettingen, Goettingen, Germany.
Department of General, Visceral, and Pediatric Surgery, University Medical Center Goettingen, Goettingen, Germany.
PLoS One. 2014 Aug 7;9(8):e104220. doi: 10.1371/journal.pone.0104220. eCollection 2014.
Although both alcohol and fructose are particularly steatogenic, their long-term effect in the development of a metabolic syndrome has not been studied in vivo. Consumption of fructose generally leads to obesity, whereas ethanol can induce liver damage in the absence of overweight. Here, Sprague-Dawley rats were fed ad libitum for 28 days on five diets: chow (control), liquid Lieber-DeCarli (LDC) diet, LDC +30%J of ethanol (L-Et) or fructose (L-Fr), and LDC combined with 30%J ethanol and 30%J fructose (L-EF). Body weight (BW) and liver weight (LW) were measured. Blood and liver samples were harvested and subjected to biochemical tests, histopathological examinations, and RT-PCR. Alcohol-containing diets substantially reduced the food intake and BW (≤3rd week), whereas fructose-fed animals had higher LW than controls (P<0.05). Additionally, leukocytes, plasma AST and leptin levels were the highest in the fructose-administered rats. Compared to the chow and LDC diets, the L-EF diet significantly elevated blood glucose, insulin, and total-cholesterol levels (also vs. the L-Et group). The albumin and Quick-test levels were the lowest, whereas ALT activity was the highest in the L-EF group. Moreover, the L-EF diet aggravated plasma triglyceride and reduced HDL-cholesterol levels more than 2.7-fold compared to the sum of the effects of the L-Et and L-Fr diets. The decreased hepatic insulin clearance in the L-EF group vs. control and LDC groups was reflected by a significantly decreased C-peptide:insulin ratio. All diets except the control caused hepatosteatosis, as evidenced by Nile red and H&E staining. Hepatic transcription of insulin receptor substrate-1/2 was mainly suppressed by the L-Fr and L-EF diets. The L-EF diet did not enhance the mitochondrial β-oxidation of fatty acids (Cpt1α and Ppar-α expressions) compared to the L-Et or L-Fr diet. Together, our data provide evidence for the coaction of ethanol and fructose with a high-fat-diet on dyslipidemia and insulin resistance-accompanied liver damage.
尽管酒精和果糖都特别容易引发脂肪变性,但它们在代谢综合征发展过程中的长期影响尚未在体内进行研究。摄入果糖通常会导致肥胖,而乙醇在体重正常的情况下也会引发肝损伤。在此,将斯普拉格-道利大鼠随意喂食28天,采用五种饮食:普通饲料(对照)、液体利伯-德卡利(LDC)饮食、LDC + 30%乙醇(L-Et)或果糖(L-Fr),以及LDC与30%乙醇和30%果糖组合(L-EF)。测量体重(BW)和肝脏重量(LW)。采集血液和肝脏样本并进行生化检测、组织病理学检查和逆转录聚合酶链反应(RT-PCR)。含酒精的饮食显著减少食物摄入量和体重(至第3周),而喂食果糖的动物肝脏重量高于对照组(P<0.05)。此外,喂食果糖的大鼠白细胞、血浆天冬氨酸转氨酶(AST)和瘦素水平最高。与普通饲料和LDC饮食相比,L-EF饮食显著提高血糖、胰岛素和总胆固醇水平(与L-Et组相比也是如此)。白蛋白和奎克试验水平最低,而L-EF组丙氨酸转氨酶(ALT)活性最高。此外,与L-Et和L-Fr饮食的影响总和相比,L-EF饮食使血浆甘油三酯恶化,高密度脂蛋白胆固醇水平降低超过2.7倍。与对照组和LDC组相比,L-EF组肝脏胰岛素清除率降低,表现为C肽:胰岛素比值显著下降。除对照组外,所有饮食均导致肝脂肪变性,尼罗红和苏木精-伊红(H&E)染色可证明。胰岛素受体底物-1/2的肝脏转录主要受到L-Fr和L-EF饮食的抑制。与L-Et或L-Fr饮食相比,L-EF饮食并未增强脂肪酸的线粒体β-氧化(肉碱棕榈酰转移酶1α(Cpt1α)和过氧化物酶体增殖物激活受体α(Ppar-α)表达)。总之,我们的数据为乙醇和果糖与高脂肪饮食共同作用导致血脂异常和胰岛素抵抗相关肝损伤提供了证据。