Effects and Mechanism of Supplemental Sini San on Hepatic Fibrosis in Rats
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Effects and Mechanism of Supplemental Sini San on Hepatic Fibrosis in Rats
Chinese Journal of Experimental Traditional Medical FormulaeVol. 18, Issue 18, Pages: 194-198(2012)
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Published:2012
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SHANG Li-zhi, WANG Fu, MIAO Xiao-ling, et al. Effects and Mechanism of Supplemental Sini San on Hepatic Fibrosis in Rats[J]. Chinese journal of experimental traditional medical formulae, 2012, 18(18): 194-198.
DOI:
SHANG Li-zhi, WANG Fu, MIAO Xiao-ling, et al. Effects and Mechanism of Supplemental Sini San on Hepatic Fibrosis in Rats[J]. Chinese journal of experimental traditional medical formulae, 2012, 18(18): 194-198.DOI:
Effects and Mechanism of Supplemental Sini San on Hepatic Fibrosis in Rats
3.5 g ·kg-1)。采用酸性水解法检测肝组织羟脯氨酸(HYP)含量;放射免疫法(RIA)检测肝组织白介素-1(IL-1)和肿瘤坏死因子-α(TNF-α)含量;原位杂交、免疫组化法分别检测肝组织转化生长因子-β1 (TGF-β1)和α-平滑肌肌动蛋白(α-SMA)mRNA与蛋白表达。 结果: 与模型组比较
四逆散加味中剂量组大鼠肝组织羟脯氨酸(478.32±42.35) vs (327.09±39.41) μg ·L-1
P<0.01; IL-1(0.58±0.89) vs (0.35±0.47) μg ·L-1(P<0.05); TNF-α(4.82±0.49) vs (4.21±0.45) μg ·L-1(P<0.05)
含量均显著降低
TGF-β1 mRNA(9.92±2.57) vs (5.27±1.39)
(P<0.01)和α-SMA mRNA(12.87±0.39) vs (6.33±0.72)
(P<0.01)及其蛋白表达显著减弱(均P<0.01)。 结论: 四逆散加味有明显的抗肝纤维化作用
其机制可能与抑制TGF-β1和α-SMA基因表达有关。
Abstract
Objective: To investigate the protective effects and its mechanism of Supplemental Sini San(SNS) on hepatic fibrosis in rats. Method: The immunohepatic fibrosis model was induced by intraperitoneal injection of porcine serum. Eighty Wister rats were divided into eight groups:normal control
model control
Sini San Jiawei(SNSJW) high-dose
mediate-dose and low-dose
prevention and SNS group. Except the normal control groups
all the other groups were injected with pig's serum without inactivation into abdominal cavity
twice per week and 0.5 mL each time
persisting for 10 weeks. The prevention groups were orally given with the medicines(SNSJW 7 g · kg-1
10 weeks)at the same time models wasduplicated
the other treatment groups were dealed with just as the prevention groups 6 weeks later
lasted for 4 weeks. The dose was following:SNS group 4 g · kg-1
SNSJW high-dose group 14 g · kg-1
mediate-dose group 7 g · kg-1
low-dose group 3.5 g · kg-1. The changes of hepatic fibrosis were detected. The content of liver tissue interleukin-1(IL-1) and tumor necrosis factor-alpha (TNF-α)were tested by RIA. In situ hybridization assay and immunohistochemical S-P method were used to detect the expression of transforming growth factor-β1(TGF-β1) mRNA and α-smoth muscle actin(α-SMA) mRNA and there protein in hepatic fibrosis tissues. Result: Compared with model group in SNSJW mediate-dose group
the content of HYP
IL-1
TNF-α in liver tissue was depressed significantly
the expression of TGF-β1 and α-SMA genes was significantly lower in SNSJW mediate-dose group. Conclusion: Supplemental SNS has an action on hepatic fibrosis in rats. The mechanism is related with its inhibiting the expression of TGF-β1 and α-SMA genes in rats liver.