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首页> 外文期刊>Macedonian Academy of Sciences and Arts: Section of Biological and Medical Sciences >SIX WEEK FOLLOW-UP OF METABOLIC EFFECTS INDUCED BY A HIGH-FAT DIET AND STREPTOZOTOCIN IN A RODENT MODEL OF TYPE 2 DIABETES MELLITUS
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SIX WEEK FOLLOW-UP OF METABOLIC EFFECTS INDUCED BY A HIGH-FAT DIET AND STREPTOZOTOCIN IN A RODENT MODEL OF TYPE 2 DIABETES MELLITUS

机译:2型糖尿病啮齿动物模型中高脂饮食和链脲佐菌素诱发的代谢作用六周随访

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摘要

This study was initiated to refine and characterize a nongenetic experimental model of type 2 diabetes mellitus and to follow up various metabolic parameters up to six weeks after diabetes induction. Male Wistar rats were divided into 4 groups: CON group – consumed standard rat chow and served as control; HFD group – consumed high-fat diet (45% calories as fat); STZ group-was injected once intraperitoneally with streptozotocin (35 mg/kg) on day 14, and DM-2 group – consumed high-fat diet and was injected with streptozotocin. The metabolic parameters were measured one week after streptozotocin injection (week 3) and at the end of the study (week 9). Our results confirm that HFD-group developed dyslipidaemia, obesity and insulin resistance. All metabolic parameters remained largely unaltered in STZ-group during the study. Only the combination of high-fat diet and streptozotocin (DM-2 group) induced type 2 diabetes that was characterized with moderate hyperglycaemia, insulin resistance, hypertriglyceridaemia, elevated free fatty acids, hypercholesterolaemia and increased plasma glucagon levels at the time of diabetes onset (week 3). The observed changes of the metabolic parameters after six additional weeks demonstrated an aggravated diabetic state, as confirmed from significantly increased fasting plasma glucose values, insufficient insulin secretion, severe hyperlipidaemia, increased glucagon levels, decreased serum adiponectin concentrations and significantly elevated urinary protein excretion. These results indicate that apart from its utility as a model of diabetes aetiology, this model could also be used for elucidating the role of the hormones adiponectin and glucagon in the progression of type 2 diabetes, as well as for investigating the diabetic complications.
机译:这项研究的开始是为了完善和表征2型糖尿病的非遗传实验模型,并在糖尿病诱导后6周内追踪各种代谢参数。将雄性Wistar大鼠分为4组:CON组–食用标准大鼠食物并作为对照组; HFD组–食用高脂饮食(45%的卡路里为脂肪); STZ组在第14天腹膜内注射链脲佐菌素(35 mg / kg),而DM-2组则进食高脂饮食,并注射链脲佐菌素。注射链脲佐菌素一周后(第3周)和研究结束时(第9周)测量代谢参数。我们的结果证实,HFD组会出现血脂异常,肥胖和胰岛素抵抗。在研究期间,STZ组的所有代谢参数基本保持不变。只有高脂饮食和链脲佐菌素(DM-2组)的组合才能诱发2型糖尿病,其特征是在糖尿病发作时表现为中度高血糖,胰岛素抵抗,高甘油三酸酯血症,游离脂肪酸升高,高胆固醇血症和血浆胰高血糖素水平升高(第3周)。在另外六周后观察到的代谢参数变化表明糖尿病状态恶化,这可通过空腹血糖值明显升高,胰岛素分泌不足,严重高脂血症,胰高血糖素水平升高,血清脂联素浓度降低和尿蛋白排泄量显着升高来证实。这些结果表明,除了将其用作糖尿病病因学模型外,该模型还可用于阐明激素脂联素和胰高血糖素在2型糖尿病进展中的作用,以及用于研究糖尿病并发症。

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