Bujak Maro, Bujak Ivana Tartaro, Sobočanec Sandra, Mihalj Martina, Novak Sanja, Ćosić Anita, Levak Maja Tolušić, Kopačin Vjekoslav, Mihaljević Branka, Balog Tihomir, Drenjančević Ines, Loncar Mirela Baus
Laboratory for Biotechnology in Aquaculture, Division of Materials Chemistry, Ruđer Bošković Institute (IRB), Zagreb, Croatia.
Radiation Chemistry and Dosimetry Laboratory, Division of Materials Chemistry, IRB, Zagreb, Croatia.
Cell Physiol Biochem. 2018;47(2):827-841. doi: 10.1159/000490039. Epub 2018 May 22.
BACKGROUND/AIMS: Tff3 protein plays a well recognized role in the protection of gastrointestinal mucosa. The role of Tff3 in the metabolism is a new aspect of its function. Tff3 is one of the most affected liver genes in early diabetes and fatty liver rodent models. The aim of this study was to investigate the effect of Tff3 deficiency on lipid and carbohydrate metabolism and on markers of oxidative stress that accompanies metabolic deregulation.
Specific markers of health status were determined in sera of Tff3 deficient mice, including glucose level, functional glucose and insulin tolerance. Composition of fatty acids (FAs) was determined in liver and blood serum by using gas chromatography. Oxidative stress parameters were determined: lipid peroxidation level via determination of lipid hydroperoxide and thiobarbituric acid reactive substances (TBARS), antioxidative capacity (FRAP) and specific antioxidative enzyme activity. The expression of several genes and proteins related to the metabolism of lipids, carbohydrates and oxidative stress (CAT, GPx1, SOD2, PPARα, PPARγ, PPARδ, HNF4α and SIRT1) was determined.
Tff3 deficient mice showed better glucose utilization in the glucose and insulin test. Liver lipid metabolism is affected and increased formation of small lipid vesicles is noticed. Formation of lipid droplets is not accompanied by increased liver oxidative stress, although expression/activity of monitored enzymes is deregulated when compared with wild type mice. Tff3 deficient mice exhibit reduced expression of metabolism relevant SIRT1 and PPARγ genes.
Tff3 deficiency affects the profile and accumulation of FAs in the liver, with no obvious oxidative stress increase, although expression/activity of monitored enzymes is changed as well as the level of SIRT1 and PPARγ protein. Considering the strong downregulation of liver Tff3 in diabetic/obese mice, presence in circulation and regulation by food/insulin, Tff3 is an interesting novel candidate in metabolism relevant conditions.
背景/目的:三叶因子3(Tff3)蛋白在保护胃肠道黏膜方面发挥着公认的作用。Tff3在代谢中的作用是其功能的一个新方面。Tff3是早期糖尿病和脂肪肝啮齿动物模型中受影响最显著的肝脏基因之一。本研究的目的是探讨Tff3缺乏对脂质和碳水化合物代谢以及伴随代谢失调的氧化应激标志物的影响。
在Tff3基因缺陷小鼠的血清中测定健康状况的特定标志物,包括血糖水平、功能性葡萄糖和胰岛素耐受性。采用气相色谱法测定肝脏和血清中的脂肪酸(FAs)组成。测定氧化应激参数:通过测定脂质氢过氧化物和硫代巴比妥酸反应性物质(TBARS)来确定脂质过氧化水平、抗氧化能力(FRAP)和特定抗氧化酶活性。测定与脂质、碳水化合物和氧化应激代谢相关的几种基因和蛋白质(CAT、GPx1、SOD2、PPARα、PPARγ、PPARδ、HNF4α和SIRT1)的表达。
在葡萄糖和胰岛素试验中,Tff3基因缺陷小鼠表现出更好的葡萄糖利用能力。肝脏脂质代谢受到影响,观察到小脂质囊泡的形成增加。脂质滴的形成并未伴随肝脏氧化应激的增加,尽管与野生型小鼠相比,所监测酶的表达/活性失调。Tff3基因缺陷小鼠表现出与代谢相关的SIRT1和PPARγ基因表达降低。
Tff3缺乏影响肝脏中脂肪酸的分布和积累,尽管所监测酶的表达/活性以及SIRT1和PPARγ蛋白水平发生了变化,但氧化应激没有明显增加。考虑到糖尿病/肥胖小鼠肝脏中Tff3的强烈下调、其在循环中的存在以及受食物/胰岛素的调节,Tff3是代谢相关疾病中一个有趣且新颖的候选因子。