Section of Molecular Pharmacology and Toxicology, Laboratory of Membrane Biochemistry and Biophysics, National Institute on Alcohol Abuse and Alcoholism, NIH, Bethesda, MD.
Department of Food and Nutrition, Andong National University, Andong, South Korea.
Hepatology. 2021 Jun;73(6):2180-2195. doi: 10.1002/hep.30652. Epub 2019 May 31.
Fructose intake is known to induce obesity, insulin resistance, metabolic syndrome, and nonalcoholic fatty liver disease (NAFLD). We aimed to evaluate the effects of fructose drinking on gut leakiness, endotoxemia, and NAFLD and study the underlying mechanisms in rats, mice, and T84 colon cells. Levels of ileum junctional proteins, oxidative stress markers, and apoptosis-related proteins in rodents, T84 colonic cells, and human ileums were determined by immunoblotting, immunoprecipitation, and immunofluorescence analyses. Fructose drinking caused microbiome change, leaky gut, and hepatic inflammation/fibrosis with increased levels of nitroxidative stress marker proteins cytochrome P450-2E1 (CYP2E1), inducible nitric oxide synthase, and nitrated proteins in small intestine and liver of rodents. Fructose drinking significantly elevated plasma bacterial endotoxin levels, likely resulting from decreased levels of intestinal tight junction (TJ) proteins (zonula occludens 1, occludin, claudin-1, and claudin-4), adherent junction (AJ) proteins (β-catenin and E-cadherin), and desmosome plakoglobin, along with α-tubulin, in wild-type rodents, but not in fructose-exposed Cyp2e1-null mice. Consistently, decreased intestinal TJ/AJ proteins and increased hepatic inflammation with fibrosis were observed in autopsied obese people compared to lean individuals. Furthermore, histological and biochemical analyses showed markedly elevated hepatic fibrosis marker proteins in fructose-exposed rats compared to controls. Immunoprecipitation followed by immunoblot analyses revealed that intestinal TJ proteins were nitrated and ubiquitinated, leading to their decreased levels in fructose-exposed rats. Conclusion: These results showed that fructose intake causes protein nitration of intestinal TJ and AJ proteins, resulting in increased gut leakiness, endotoxemia, and steatohepatitis with liver fibrosis, at least partly, through a CYP2E1-dependent manner.
果糖摄入已知会导致肥胖、胰岛素抵抗、代谢综合征和非酒精性脂肪性肝病(NAFLD)。我们旨在评估果糖摄入对肠道通透性、内毒素血症和 NAFLD 的影响,并在大鼠、小鼠和 T84 结肠细胞中研究其潜在机制。通过免疫印迹、免疫沉淀和免疫荧光分析测定啮齿动物、T84 结肠细胞和人回肠中的回肠连接蛋白、氧化应激标志物和凋亡相关蛋白水平。果糖摄入导致微生物组变化、肠道通透性增加和肝炎症/纤维化,伴有氧化应激标志物蛋白细胞色素 P450-2E1(CYP2E1)、诱导型一氧化氮合酶和小肠和肝脏中硝化蛋白水平升高。果糖摄入显著升高血浆细菌内毒素水平,这可能是由于肠道紧密连接(TJ)蛋白(闭合蛋白 1、紧密连接蛋白、Claudin-1 和 Claudin-4)、黏着连接(AJ)蛋白(β-连环蛋白和 E-钙黏蛋白)和桥粒斑蛋白的水平降低,以及野生型啮齿动物中的α-微管蛋白,而不是在果糖暴露的 Cyp2e1 基因敲除小鼠中。一致地,与瘦个体相比,尸检肥胖个体中观察到肠道 TJ/AJ 蛋白减少和肝炎症伴纤维化。此外,与对照组相比,果糖暴露大鼠的肝纤维化标志物蛋白水平明显升高。免疫沉淀后免疫印迹分析显示,果糖暴露大鼠的肠道 TJ 蛋白发生硝化和泛素化,导致其水平降低。结论:这些结果表明,果糖摄入导致肠道 TJ 和 AJ 蛋白的蛋白质硝化,导致肠道通透性增加、内毒素血症和脂肪性肝炎伴肝纤维化,至少部分通过 CYP2E1 依赖性途径。