Department of Food Science, Faculty of Food Science and Technology, Universiti Putra Malaysia, 43400, Serdang, Selangor, Malaysia.
Laboratory of Natural Products, Institute of Bioscience, Universiti Putra Malaysia, 43400, Serdang, Selangor, Malaysia.
J Physiol Biochem. 2018 Aug;74(3):403-416. doi: 10.1007/s13105-018-0631-3. Epub 2018 May 15.
Diabetes mellitus (DM) is a chronic disease that can affect metabolism of glucose and other metabolites. In this study, the normal- and obese-diabetic rats were compared to understand the diabetes disorders of type 1 and 2 diabetes mellitus. This was done by evaluating their urine metabolites using proton nuclear magnetic resonance (H NMR)-based metabolomics and comparing with controls at different time points, considering the induction periods of obesity and diabetes. The biochemical parameters of the serum were also investigated. The obese-diabetic model was developed by feeding the rats a high-fat diet and inducing diabetic conditions with a low dose of streptozotocin (STZ) (25 mg/kg bw). However, the normal rats were induced by a high dose of STZ (55 mg/kg bw). A partial least squares discriminant analysis (PLS-DA) model showed the biomarkers of both DM types compared to control. The synthesis and degradation of ketone bodies, tricarboxylic (TCA) cycles, and amino acid pathways were the ones most involved in the variation with the highest impact. The diabetic groups also exhibited a noticeable increase in the plasma glucose level and lipid profile disorders compared to the control. There was also an increase in the plasma cholesterol and low-density lipoprotein (LDL) levels and a decline in the high-density lipoprotein (HDL) of diabetic rats. The normal-diabetic rats exhibited the highest effect of all parameters compared to the obese-diabetic rats in the advancement of the DM period. This finding can build a platform to understand the metabolic and biochemical complications of both types of DM and can generate ideas for finding targeted drugs.
糖尿病(DM)是一种慢性疾病,可影响葡萄糖和其他代谢物的代谢。在这项研究中,通过评估正常和肥胖糖尿病大鼠的尿液代谢物,比较了 1 型和 2 型糖尿病的糖尿病紊乱,使用基于质子核磁共振(H NMR)的代谢组学并与对照进行比较,在不同的时间点考虑肥胖和糖尿病的诱导期。还研究了血清的生化参数。通过用高脂肪饮食喂养大鼠并使用低剂量链脲佐菌素(STZ)(25mg/kg bw)诱导糖尿病条件来建立肥胖糖尿病模型,而正常大鼠则用高剂量 STZ(55mg/kg bw)诱导。偏最小二乘判别分析(PLS-DA)模型显示与对照相比,两种 DM 类型的生物标志物。酮体、三羧酸(TCA)循环和氨基酸途径的合成和降解是与变化最相关的途径。与对照组相比,糖尿病组的血浆葡萄糖水平和脂质谱紊乱也明显增加。糖尿病大鼠的血浆胆固醇和低密度脂蛋白(LDL)水平升高,高密度脂蛋白(HDL)水平下降。与肥胖糖尿病大鼠相比,正常糖尿病大鼠在 DM 期间的所有参数中表现出最高的影响。这一发现可以为理解两种类型的 DM 的代谢和生化并发症提供一个平台,并为寻找有针对性的药物提供思路。