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纸质出版日期:2018
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林小凤, 廖凌虹, 陈继承, 等. 平胃散对糖脂代谢紊乱小鼠血脂血糖和HNF-1表达的影响[J]. 中国实验方剂学杂志, 2018,24(16):103-108.
LIN Xiao-feng, LIAO Ling-hong, CHEN Ji-cheng, et al. Effect of Pingweisan on Blood Lipid, Blood Glucose and HNF-1 Expression in Mice with Glycolipid Metabolism Disorder[J]. Chinese journal of experimental traditional medical formulae, 2018, 24(16): 103-108.
林小凤, 廖凌虹, 陈继承, 等. 平胃散对糖脂代谢紊乱小鼠血脂血糖和HNF-1表达的影响[J]. 中国实验方剂学杂志, 2018,24(16):103-108. DOI: 10.13422/j.cnki.syfjx.20181623.
LIN Xiao-feng, LIAO Ling-hong, CHEN Ji-cheng, et al. Effect of Pingweisan on Blood Lipid, Blood Glucose and HNF-1 Expression in Mice with Glycolipid Metabolism Disorder[J]. Chinese journal of experimental traditional medical formulae, 2018, 24(16): 103-108. DOI: 10.13422/j.cnki.syfjx.20181623.
目的:观察平胃散对高脂饮食诱导的糖脂代谢紊乱小鼠血脂、血糖和肝细胞核因子-1β(hepatocyte nuclear factor-1β,HNF-1β/TCF2)表达的影响,探讨平胃散调节糖脂代谢可能存在的分子机制。方法: 40只SPF级C57BL/6J成年雄性小鼠随机分为正常组(n=8)和造模组(n=32),分别以普通饲料和高脂饲料喂养10周。第11周起,将造模组随机分为模型组,平胃散组(6 g·kg-1·d-1),二甲双胍组(300 mg·kg-1·d-1)和辛伐他汀组(2 mg·kg-1·d-1),每组8只。正常组及模型组只给予相同体积蒸馏水,即各组灌胃10 mL·kg-1·d-1,通过药物干预4周。喂养期间对体质量、腹围、血脂、血糖和胰岛素进行连续监测。干预结束后取肝脏和肾脏组织检测HNF-1β的mRNA和蛋白表达。结果:第10周末,与正常组比较,造模组体质量,腹围,胆固醇(TC),甘油三酯(TG),低密度脂蛋白(LDL-C),高密度脂蛋白(HDL-C)和空腹血糖(FPG)均明显升高(P<0.05),空腹胰岛素(FINS)明显降低(P<0.05)。用药4周后,与正常组比较,模型组体质量、腹围、血脂和口服葡萄糖耐量试验(OGTT)4个时间段血糖均显著升高(P<0.01),FINS,HNF-1β的mRNA和蛋白相对表达量均降低(P<0.05)。与模型组比较,平胃散组体质量,腹围,TC,TG和OGTT 4个时间段血糖均降低(P<0.05),FINS,HNF-1β的mRNA和蛋白相对表达量均升高(P<0.05),二甲双胍组体质量,腹围,TC,TG,LDL-C,OGTT 4个时间段血糖均降低(P<0.05),FINS,HNF-1β的mRNA和蛋白相对表达量均升高(P<0.05),辛伐他汀组体质量、腹围、血脂均显著降低(P<0.01),FINS,HNF-1β的mRNA和蛋白相对表达量均升高(P<0.05)。结论:高脂饮食喂养10周即可建立良好的糖脂代谢紊乱小鼠模型,平胃散可能通过调节HNF-1β的表达来调节血脂和血糖水平。
Objective: To observe the effect of Pingweisan on blood lipid
blood glucose and hepatocyte nuclear factor-1β(HNF-1β/TCF2) expression in mice with glycolipid metabolism disorder induced by high-fat diet
in order to explore the possible molecular mechanism of Pingweisan in regulating glucose and lipid metabolism in mice. Method: A total of 40 specific pathogen free (SPF) C57BL/6J adult male mice were randomly divided into normal group (n=8) and model group (n=32)
which were respectively fed with normal diet and high-fat diet for 10 weeks. Since the 11th week
the model group was randomly divided into model group (n=8)
Pingweisan group (n=8)
metformin group (n=8) and simvastatin group (n=8). The Pingweisan group was given Pingweisan 6 000 mg·kg-1·d-1
the metformin group was given metformin 300 mg·kg-1·d-1
the simvastatin group was given simvastatin 2 mg·kg-1·d-1
and the normal group and model group were given the same volume of distilled water only; that is to say
each group was given by gavage 10 mL·kg-1·d-1 for 4 weeks. During feeding
body weight
abdominal circumference
blood lipids
blood glucose and insulin were continuously monitored. After the intervention
liver and kidney tissues were taken to detect the mRNA and protein expression of HNF-1β. Result: At the end of the 10th week
compared with the normal group
the weight
abdominal circumference
total cholesterol (TC)
triglyceride (TG)
low-density lipoprotein cholesterol (LDL-C)
high-density lipoprotein cholesterol (HDL-C) and fasting plasma glucose (FPG) of the model group increased (P<0.05)
while fasting insulin (FINS) decreased (P<0.05). After 4 weeks of treatment
compared with the normal group
the body weight
abdominal circumference
blood lipid and 4 hours of blood glucose of oral glucose tolerance test (OGTT) of the model group were significantly increased (P<0.01). Relative mRNA and protein expressions of FINS and HNF-1β were decreased (P<0.05). Compared with the model group
the weight
abdominal circumference
TC
TG
and OGTT 4 hours of blood glucose of the Pingweisan group were all decreased (P<0.05)
whereas the relative mRNA and protein expressions of FINS and HNF-1β were all increased (P<0.05). The body weight
abdominal circumference
TC
TG
LDL-C
OGTT 4 hours of blood glucose of the metformin group were all decreased (P<0.05)
and the relative mRNA and protein expressions of FINS and HNF-1β were all increased (P<0.05). The body weight
abdominal circumference and the blood lipid of the simvastatin group were significantly decreased (P<0.01)
and the relative mRNA and protein expressions of FINS and HNF-1β were increased (P<0.05). Conclusion: After 10 weeks of high-fat diet
a mouse model of glycolipid metabolism disorder can be established. Pingweisan can regulate the blood lipid and blood glucose levels by regulating the expression of HNF-1β.
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