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首页|期刊导航|动物学研究|C57BL/6J小鼠在构建2型糖尿病模型中体重和非空腹血糖浓度的异常变化

C57BL/6J小鼠在构建2型糖尿病模型中体重和非空腹血糖浓度的异常变化

牛屹东 梁蜀龙 王新生

动物学研究2007,Vol.28Issue(5):507-510,4.
动物学研究2007,Vol.28Issue(5):507-510,4.

C57BL/6J小鼠在构建2型糖尿病模型中体重和非空腹血糖浓度的异常变化

Abnormal Change in Body Weight and Non-Fasting Blood Glucose Levels of Mouse Strain C57BL/6J in Generating Type 2 Diabetes Model

牛屹东 1梁蜀龙 2王新生1

作者信息

  • 1. 北京大学人民医院,实验动物中心,北京,100044
  • 2. 北京大学,医学部基础医学院,北京,100083
  • 折叠

摘要

Abstract

The commercially available inbred obesity-prone C57BL/6J (B6) and outbred stock ICR mice (3-week old) purchased from a breeder of Beijing were weaned onto high-fat diet (HFD), HFD-3% fructose water (HFDF) and standard rodent chow, respectively. After exposure to the diets for six weeks, HFD and HFDF fed mice were injected intraperitoneaily with streptozotocin (STZ, 100mg/kg body weight) and kept on the same diet for next four weeks. Body weight was recorded weekly. Non-fasting blood glucose levels of HFD and HFDF fed mice were measured before and after STZ injections. The body weight of HFD-fed and HFDF-fed B6 mice were significantly lower than that of the control, but body weight of HFD-fed and HFDF-fed ICR mice were significantly higher than that of the control. After injection of STZ, blood glucose levels were above the stardardized criterion (11 mmol/L) for the diabetes mouse model in both HFD and HFDF fed ICR mice, but reverse in B6 mice. The type 2 diabetes model was generated successfully in ICR but not in B6 mice, regardless of whether fructose was supplied. The current results indicated that ICR mouse is still a useful and economical strain for HFD-induced/STZ-treated type 2 diabetes model, and that some variation may occur in the genetic composition among B6 mice bred by different breeders.

关键词

C57BL/6J小鼠/ICR小鼠/高脂饲料/链脲佐菌素/肥胖/2型糖尿病

Key words

C57BL/6J/ICR/High-fat diet/Streptozotocin/Obesity/Type 2 diabetes

分类

生物科学

引用本文复制引用

牛屹东,梁蜀龙,王新生..C57BL/6J小鼠在构建2型糖尿病模型中体重和非空腹血糖浓度的异常变化[J].动物学研究,2007,28(5):507-510,4.

基金项目

北京大学人民医院研究与发展基金(P886)Supported by Peking University People's Hospital Research and Development Foundation (P886) (P886)

动物学研究

OA北大核心CSCDCSTPCD

0254-5853

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