XIAO Wang, ZENG Jian-hong, CHEN Xu. Hypoglycemic Effect of Polysaccharides on Type 2 Diabetes Mellitus Rats[J]. Chinese journal of experimental traditional medical formulae, 2015, 21(21): 144-147.
DOI:
XIAO Wang, ZENG Jian-hong, CHEN Xu. Hypoglycemic Effect of Polysaccharides on Type 2 Diabetes Mellitus Rats[J]. Chinese journal of experimental traditional medical formulae, 2015, 21(21): 144-147. DOI: 10.13422/j.cnki.syfjx.2015210144.
Hypoglycemic Effect of Polysaccharides on Type 2 Diabetes Mellitus Rats
Objective: To investigate the hypoglycemic effect of Curcuma kwangsiensis polysaccharide (CKP) on type 2 diabetes mellitus (T2DM) rats. Method: T2DM models were induced through high-sucrose and high-fat diet combined with low-dose abdominal injection of streptozotocin(STZ
45 mg·kg-1).The successfully modeled rats were randomly divided into 4 groups:T2DM model group
CKP low dosage group (CKP-LG)
CKP middle dosage group (CKP-MG) and CKP high dosage group (CKP-HG). Another 10 normal rats were selected as normal group. CKP groups with different dosages (0.5
1.0
2.5 g·kg-1·d-1) were ig administered continuously for 6 weeks
once a day. The model group and normal group received ig normal saline of the same volume. After 6 weeks of administration
fasting blood glucose(FBG)
insulin (INS)
total cholesterol (TC)
and triglyceride (TG) levels were detected in rats
and pathological change of pancreas was evaluated by hematoxylin and eosin(HE) staining and immunohistochemistry
Fas protein expressions of pancreatic β cells were detected. Result: Compared with the normal rats
FBG
TG
and TC levels were increased significantly in rats of model group
and pancreas Fas protein expressions were increased
with statistically significant difference (P<0.05
P<0.01)
Compared with the model group
CKP groups could reduce FBG
TC and TG levels of T2DM rats
and reduce pancreas Fas protein expressions and reduce apoptosis of pancreatic β cells
with significant difference (P<0.05
P<0.01). Conclusion: The hypoglycemic effect of CKP on T2DM rats may be achieved by protecting pancreatic β cells and reducing their apoptosis.