Assessment of Fructosamine 3-kinase in Type 2 Diabetic Patients and Its Relation to Some Biochemical Variables

Tamara E Abdulrahman, Rafad Mohammed
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Abstract

It took over 30 years for first description of the synthesis of fructosamines and this was conducted through non-enzymatic protein-glucose reactions (also known as glycation). Fructosamines in mammalian cells has not been known until recently. It transforms spontaneously into advanced glycation end products. The discovery of fructosamine 3-kinase, which is a novel enzyme, in human reveals the existence of a previously unknown intracellular metabolism of these substances. Protein-bound fructosamines are phosphorylated by fructosamine 3-kinase with high affinity on a third carbon atom of the deoxyfructose moiety and this results in fructosamine 3-phosphates. These later substances are unstable and spontaneously break down into inorganic phosphate and 3-deoxyglucosone, regenerating the unglycated amine in the process. The fact that many prokaryotic and eukaryotic genomes contain proteins connected to fructosamine 3-kinase shows that this 'deglycation' process is not exclusive to mammals. The current study aims at determining the normal values of fructoseamine 3-kinase enzyme in the control group as well as in the group of patients with type II diabetes (the experimental group). The relationship of enzyme  activity with some biochemical variables was also studied in patients with type 2 diabetes, due to the association of these variables with high blood sugar, as shown by previous studies. The Research dealt with the investigation of Fructosamine 3-Kinase activity and some biochemical variables for (136) Type 2 diabetes patients. The results indicated that there was a significant increase in Fructosamine 3-Kinase activity in type 2 diabetes patients (253 ng/l) in comparison to the control group. The normal value of enzyme in the control group was (181ng/l) and the activity of the enzyme in control group individuals was not affected by age and sex. The research also showed a significant decrease in the level of iron, zinc, chromium and sodium as well as a significant increase in the potassium level in patients with type 2 diabetes compared to the control group individuals. Additionally, the research predicted that there is a significant decrease in the levels of vitamins C and E. Also, it was shown that there was a significant increase in malondialdehyde level and a myeloperoxidase activity in type 2 diabetes patients. Activity of FN3K increased in type 2 diabetes compared to the control group individuals. It was noted that the activity of FN3K in the control group was not affected by age or sex.
2型糖尿病患者果糖胺3-激酶的测定及其与生化指标的关系
首次描述果糖胺的合成花了30多年的时间,这是通过非酶蛋白质-葡萄糖反应(也称为糖基化)进行的。哺乳动物细胞中的果糖胺直到最近才为人所知。它自发地转化为晚期糖基化终产物。果糖胺3-激酶是一种新的酶,它的发现揭示了这些物质在细胞内代谢的存在,这是以前未知的。蛋白结合的果糖胺被具有高亲和力的果糖胺3-激酶磷酸化在脱氧果糖部分的第三个碳原子上,这就产生了果糖胺3-磷酸。这些后期的物质是不稳定的,会自发地分解成无机磷酸盐和3-脱氧葡萄糖酮,并在此过程中再生无糖基化胺。事实上,许多原核生物和真核生物的基因组都含有与果糖胺3-激酶相关的蛋白质,这表明这种“去糖基化”过程并非哺乳动物所独有。本研究旨在测定对照组和2型糖尿病患者组(实验组)果糖胺3-激酶的正常值。在2型糖尿病患者中,酶活性与一些生化变量的关系也被研究,因为这些变量与高血糖有关联,如以往的研究所示。本研究对136例2型糖尿病患者的果糖胺3-激酶活性和一些生化指标进行了调查。结果表明,与对照组相比,2型糖尿病患者的果糖胺3-激酶活性显著增加(253 ng/l)。对照组酶的正常值为(181ng/l),对照组个体酶的活性不受年龄和性别的影响。研究还显示,与对照组相比,2型糖尿病患者的铁、锌、铬和钠含量显著降低,钾含量显著增加。此外,该研究预测,维生素C和e的水平显著下降。此外,研究表明,2型糖尿病患者的丙二醛水平和髓过氧化物酶活性显著增加。与对照组相比,2型糖尿病患者的FN3K活性增加。值得注意的是,对照组中FN3K的活性不受年龄和性别的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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