ZHU Tie-chui. Inhibitory Effects of Cassia Seed on the Renal Fibrosis in Diabetic Rats[J]. Chinese journal of experimental traditional medical formulae, 2012, 18(24): 315-319.
ZHU Tie-chui. Inhibitory Effects of Cassia Seed on the Renal Fibrosis in Diabetic Rats[J]. Chinese journal of experimental traditional medical formulae, 2012, 18(24): 315-319.DOI:
Objective:To explore the anti-fibrosis effects of Cassia seed on the renal fibrosis in diabetic rats and its possible mechanisms. Method: Seventy rats were randomly divided into model group (n=60) and normal control group (n=10). Fasted for 12 h
the model group rats were left intraperitoneal injected 55 mg·kg-1 of streptozotocin to induce diabetes. Control rats were given equal volume of normal saline. The model-established rats were randomly divided into 5 groups: diabetic model group(NS
4 mL·kg-1)
captopril group (10 mg·kg-1)
low
medium and high dose Cassia seed groups (1
5
10 g·kg-1). After eight weeks of treatment
fasting blood glucose
serum creatine
24 h urine protein (U Pro)
clearance rate of creatine were detected. The morphology was observed
and the mRNA expression of transforming growth factor β1(TGF-β1) and connective tissue growth factor(CTGF) were detected by RT-PCR. The protein expression of Smad3 and Smad6 were detected by western blot. Result: Compared with normal control group
fasting blood glucose
serum creatine
24 h urine protein (U Pro) were significantly increased (P<0.05)
as well as the mRNA expression of TGF-β1 and CTGF and the protein expression of Smad3 were significantly increased (P<0.05)
but clearance rate of creatine and the protein expression of Smad6 were significantly decreased (P<0.05) in diabetic model group. Compared with diabetic model group
there were obvious improvements after the treatment of Cassia seed (P<0.05)
in addition
the renal pathological changes were also improved. Conclusion: Cassia seed has protective effect against the renal fibrosis induced by STZ in rats
the mechanisms may be related to its ability of down-regulating TGF-β1