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Cellular Aspects of Intestinal Lipoprotein Assembly in Psammomys Obesus: A Model of Insulin Resistance and Type 2 Diabetes

机译:Psammomys肥胖症肠道脂蛋白组装的细胞方面:胰岛素抵抗和2型糖尿病的模型。

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Although postprandial hypertriglyceridemia is a major contributing factor in the development of atherosclerosis, little information is available on the effect of insulin resistance and diabetes on intestinal fat transport. The aim of the present study was to examine intracellular events that govern lipid transport and apolipoprotein (apo) B-48-containing lipoprotein assembly in the small intestine of Psammomys obesus, a model of nutritionally induced insulin resistance and type 2 diabetes. Animals with normoglycemia/hyperinsulinemia and hyperglycemia/hyperinsulinemia exhibited high levels of triglycerides (TGs) in the plasma and intestine and postprandial plasma chylomicrons and apo B-48 compared with normoglycemicormoinsulinemic animals. In vitro studies, using cultured jejunal explants incubated with either [~(14)C]oleic acid or [~(35)S]methionine, revealed their higher efficiency in de novo TG synthesis, apo B-48 biogenesis, and TG-rich lipoprotein assembly. Accordingly, enhanced monoacylglycerol and diacylglyc-erol acyltransferase activity was also discernible and concomitant with an increased content of L-fatty acid binding protein and in vivo chylomicron production rates. However, both the I-fatty acid binding protein amount and the apo B-48 proteasomal degradative pathway were decreased. Overall, our findings show that the development of an insulin-resistant/diabetic state in Psammomys obesus triggers the whole intra-entero-cyte machinery, leading to lipoprotein assembly and favoring the intestinal oversecretion of apo B-48-lipo-proteins, which may contribute to characteristic hypertriglyceridemia.
机译:尽管餐后高甘油三酯血症是动脉粥样硬化发展的主要因素,但关于胰岛素抵抗和糖尿病对肠道脂肪运输的影响的信息很少。本研究的目的是检查细胞内事件,这些事件控制着脂肪诱导的小肠拟南芥(Psammomys obesus)小肠中的脂质运输和载脂蛋白(apo)B-48的脂蛋白装配,这是一种营养诱导的胰岛素抵抗和2型糖尿病的模型。具有正常血糖/高胰岛素血症和高血糖/高胰岛素血症的动物与正常血糖/正常胰岛素血症的动物相比,血浆,肠和餐后血浆乳糜微粒和apo B-48的甘油三酸酯(TG)含量较高。使用与[〜(14)C]油酸或[〜(35)S]蛋氨酸孵育的空肠外植体进行的体外研究显示,它们在从头合成TG,Apo B-48生物发生和富含TG方面效率更高。脂蛋白装配体。因此,也可以看出单酰基甘油和二酰基甘油-芥子酰基转移酶活性的增强,并且伴随着L-脂肪酸结合蛋白含量的增加和体内乳糜微粒的产生速率。然而,I-脂肪酸结合蛋白的量和载脂蛋白B-48蛋白酶体降解途径均降低。总体而言,我们的研究结果表明,在肥胖的沙门氏菌中胰岛素抵抗/糖尿病状态的发展会触发整个肠内细胞机制,导致脂蛋白组装并促进apo B-48-脂蛋白在肠道的过度分泌。导致特征性高甘油三酯血症。

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