HUANG Qi, LIAO Xin, WU Qin, et al. Effects of Alkaloids on Blood Glucose and Gene Expression of IRS-2 and IGF-1 in Liver of Rats with Diabetes[J]. Chinese journal of experimental traditional medical formulae, 2014, 20(19): 155-158.
HUANG Qi, LIAO Xin, WU Qin, et al. Effects of Alkaloids on Blood Glucose and Gene Expression of IRS-2 and IGF-1 in Liver of Rats with Diabetes[J]. Chinese journal of experimental traditional medical formulae, 2014, 20(19): 155-158. DOI: 10.13422/j.cnki.syfjx.2014190155.
Objective: To investigate effects of Dendrobium nobile Lindl. alkaloids (DNLA) on blood glucose and gene expression of insulin receptor substrate 2(IRS-2) and insulin-like growth factor 1(IGF-1) in liver of rats with diabetes. Method: Male Spragye-Dawley rats were fed with high-fat diet for 6 weeks. Then streptozotocin(STZ) 40 mg·kg-1 was injected intraperitoneally once to induce diabetic rat model. Diabetic rats were randomly divided into model group
metformin (metformin 100 mg·kg-1) and DNLA 20
40
80 mg·kg-1 group. And normal control group was fed with basal feed. After intragastric administration of metformin
DNLA and isopyknic distilled water daily for 4 weeks to rats of metformin group
DNLA group and normal control group respectively
the fasting plasma glucose (FPG) and fasting insulin (FINS) were determined
and homeostasis model assessment of insulin resistance (HOMA-IR) were calculated. The expressions of IRS-2 mRNA and IGF-1 mRNA in liver were determined by real time RT-PCR. Result: Compared with the normal control group
the levels of FPG
FINS
HOMA-IR were significantly increased (P<0.05). The FPG
FINS and HOMA-IR were significantly decreased in the metformin group and DNLA 40
80 mg·kg-1 group compared with those in the model group(P<0.05). Contents of IRS-2 mRNA and IGF-1 mRNA in model group were decreased; compared with model group
contents of IRS-2 mRNA and IGF-1 mRNA in the metformin group and DNLA 40
80 mg·kg-1 group were increased. Conclusion: DNLA can significantly decrease the levels of FPG of diabetic rats
and its mechanism may be related with enhancing the expressional levels of IRS-2 mRNA and IGF-1 mRNA in liver