Bn Swarnalatha, D'Souza Serena Stephen, Abraham Asha
Father George Albuquerque Pai Cell and Molecular Biology Laboratory, Department of Postgraduate Studies and Research in Biotechnology, St Aloysius College (Autonomous), Mangalore, Karnataka, India.
Endokrynol Pol. 2016;67(6):592-598. doi: 10.5603/EP.2016.0069.
Very few systematic studies are done during the onset and progression of metabolic syndrome in suitable animal models. In this paper we present the effect of High-Fat Simple Carbohydrate (HFSC) feed on the metabolic hormones in C57BL/6J mice to understand the sequence of events leading to impairment of glucose homeostasis.
One-month-old male C57BL/6J mice were fed with control (C group) and HFSC (T group) feed (n = 30 each) respectively for five months. The glucose tolerance was studied by Oral Glucose Tolerance Test (OGTT) whereas serum insulin and leptin were quantified using ELISA kits, and serum cortisol was quantified using CLIA kits.
Insulin resistance index and HOMA-IR levels were higher in the mice of group T as compared to age-matched mice of group C within one month and significantly higher after and five months of feeding. The total area under the glucose tolerance test curve (AUC) and the insulin curve (AUC ins) was found to significantly increase in the mice of T group as compared to the mice of C group as early as two months of feeding and was elevated after 5 months post feeding. Comparison of the Matsuda index revealed that pancreatic beta cell function was significantly lower in mice of T group as compared to mice of C group by five months of feeding. Leptin levels fluctuated during the 1st-4th month and by the 5th month significant hyperleptinaemia was detected. There was no significant change in cortisol levels in mice of group T as compared to mice of group C after five months of feeding.
HFSC feed induces insulin resistance by the first month and progressively impairs glucose tolerance, resulting in hyperleptinaemia by the fifth month in male C57BL/6J mice. (Endokrynol Pol 2016; 67 (6): 592-598).
在合适的动物模型中,针对代谢综合征的发病和进展开展的系统性研究非常少。在本文中,我们展示了高脂单糖(HFSC)饲料对C57BL/6J小鼠代谢激素的影响,以了解导致葡萄糖稳态受损的一系列事件。
分别给1月龄雄性C57BL/6J小鼠喂食对照(C组)和HFSC(T组)饲料(每组n = 30),持续5个月。通过口服葡萄糖耐量试验(OGTT)研究葡萄糖耐量,使用酶联免疫吸附测定(ELISA)试剂盒对血清胰岛素和瘦素进行定量,使用化学发光免疫分析(CLIA)试剂盒对血清皮质醇进行定量。
与年龄匹配的C组小鼠相比,T组小鼠在1个月内胰岛素抵抗指数和稳态模型评估胰岛素抵抗(HOMA-IR)水平更高,喂食后1个月及5个月时显著更高。早在喂食2个月时,与C组小鼠相比,T组小鼠的葡萄糖耐量试验曲线下总面积(AUC)和胰岛素曲线下总面积(AUC ins)就显著增加,喂食5个月后升高。松田指数比较显示,喂食5个月时,与C组小鼠相比,T组小鼠的胰腺β细胞功能显著更低。瘦素水平在第1至4个月波动,到第5个月时检测到显著的高瘦素血症。喂食5个月后,与C组小鼠相比,T组小鼠的皮质醇水平无显著变化。
HFSC饲料在第1个月就诱导雄性C57BL/6J小鼠产生胰岛素抵抗,并逐渐损害葡萄糖耐量,到第5个月导致高瘦素血症。(《内分泌学波兰文版》2016年;67(6):592 - 598)