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纸质出版日期:2013
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夏星, 覃洪含, 王勤, 等. 三叶香茶菜防治大鼠肝纤维化作用机制研究[J]. 中国实验方剂学杂志, 2013,19(19):238-241.
XIA Xing, QIN Hong-han, WANG Qin, et al. Study on Therapeutic Mechanism of on Rat Hepatic Fibrosis[J]. Chinese journal of experimental traditional medical formulae, 2013, 19(19): 238-241.
夏星, 覃洪含, 王勤, 等. 三叶香茶菜防治大鼠肝纤维化作用机制研究[J]. 中国实验方剂学杂志, 2013,19(19):238-241. DOI: 10.11653/syfj2013190238.
XIA Xing, QIN Hong-han, WANG Qin, et al. Study on Therapeutic Mechanism of on Rat Hepatic Fibrosis[J]. Chinese journal of experimental traditional medical formulae, 2013, 19(19): 238-241. DOI: 10.11653/syfj2013190238.
目的: 探讨三叶香茶菜防治大鼠肝纤维化的作用机制。方法: 大鼠每3 d接受一次背部sc 40%CCl4花生油(首次5 mL·kg-1
其余为3 mL·kg-1)
连续8周引发肝纤维化模型
造模同时每日分别给予三叶香茶菜提取物20
40
80 g·kg-1灌胃。给药8周后取血
ELISA法测定大鼠血清中Ⅲ型前胶原(proeollagen type Ⅲ
PCIII)、透明质酸(hyaluronic acid
HA)、金属蛋白酶组织抑制因子-1(tissue inhibitor of metalloproteinase-1
TIMP-1)、基质金属蛋白酶-2(matrix metal oproteinase-2
MMP-2)及肝脏中转化生长因子-β1(transforming growth Factor-β1
TGF-β1)含量;Masson染色病理切片观察肝脏胶原纤维生成。结果: 模型组血清中HA
PCIII
TGF-1及TIMP-1含量较正常组显著升高(P<0.01)
且MMP-2浓度显著下降(P<0.01)。与模型组比较
三叶香茶菜高、中剂量组能显著降低大鼠血清HA
PCIII
TIMP-1的含量
提高MMP-2含量(P<0.01);并能显著降低肝组织TGF-β1水平(P<0.01)。三叶香茶菜低剂量组能显著降低大鼠血清HA
PCIII含量(P<0.05);并有降低血清TIMP-1及肝组织TGF-β1水平
提高MMP-2含量的趋势。结论: 三叶香茶菜能有效减轻慢性肝损伤大鼠肝纤维化程度
其作用机制可能与调节TGF-β1水平
控制肝星状细胞释放TIMP-1及MMP-2有关。
Objective: To investigate the mechanism of Rabdosia ternifolia on hepatic fibrosis in rats. Method: Rat hepatic fibrosis model was produced by back subcutaneous injection of 40% carbon tetrachloride(CCl4) peanut oil
once every three days
for eight consecutive weeks
at the same time the rats were given R. ternifolia extract at 20
40
80 g·kg-1 with gavage. Take blood After 8 weeks of administration
serum were collect
and the ELISA method was used for the determination of serum proeollagen type Ⅲ (PCIII)
hyaluronic acid (HA)
tissue inhibitor of metalloproteinase-1 (TIMP-1)
matrix metal oproteinase-2 (MMP-2) and liver transforming growth factor-β1 (TGF-β1) concentration. The liver collagen fiber formation was observed by Masson staining. Result: Serum HA
PCIII
TGF-β1 and TIMP-1 concentration were significantly raised in model group rats than normal group rats (P<0.01)
while MMP-2 was significantly decreased (P<0.01). R. ternifolia at high
medium dosage significantly reduced the content of HA
PCIII
TIMP-1
as well as increased the content of MMP-2 in serum (P<0.01); and the extract significantly reduced TGF-β1 level in liver (P<0.01). The R. ternifolia at low dosage significantly reduces the levels of serum HA
PCIII content (P<0.05); it also demonstrated a trend of decreasing serum TIMP-1 and liver TGF-β1 content
increasing of the content of MMP-2
but the difference with the model group is not significant. Conclusion: R. ternifolia effectively alleviated the degree of the chronic liver injury in liver fibrosis rat
the mechanism may be related to the regulation of TGF-β1 level and the controlling of the release of the TIMP-1 and MMP-2 in hepatic stellate cells.
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