Flavonoid-rich Scabiosa comosa inflorescence extract attenuates CCl4-induced hepatic fibrosis by modulating TGF-β-induced Smad3 phosphorylation

被引:15
作者
Ma, Yuehong [1 ]
Yuan, Hongwei [2 ]
Jin, Rong [1 ]
Bao, Xiaomei [3 ]
Wang, Haisheng [4 ]
Su, Xiaoli [5 ]
Mu, Meng Gen Si Li [1 ]
Liang, Jie [1 ]
Zhang, Jianyu [4 ]
Wu, Xingwei [6 ]
机构
[1] Inner Mongolia Med Univ, Sch Basic Med, Dept Pharmacol, Hohhot 010110, Peoples R China
[2] Inner Mongolia Med Univ, Sch Basic Med, Dept Pathol, Hohhot 010110, Peoples R China
[3] Inner Mongolia Med Univ, Sch Pharm, Dept Pharmaceut Engn, Hohhot 010110, Peoples R China
[4] Inner Mongolia Med Univ, Sch Basic Med, Dept Biochem, Hohhot 010110, Peoples R China
[5] Inner Mongolia Med Univ, Sch Basic Med, Lab Funct Sci, Hohhot 010110, Peoples R China
[6] Sichuan Prov Peoples Hosp, Dept Pharm, Chengdu 610072, Sichuan, Peoples R China
基金
中国国家自然科学基金;
关键词
Scabiosa comosa; Flavonoids; Liver fibrosis; TGF-beta; 1; Smad3; STELLATE CELL ACTIVATION; INDUCED LIVER FIBROSIS; INHIBITION; DIFFERENTIATION; ANTIOXIDANT; MECHANISMS; MICE;
D O I
10.1016/j.biopha.2018.06.118
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Scabiosa comosa inflorescence is a traditional Mongolian medicine in the treatment of liver diseases. In the study, we investigated the anti-fibrotic efficacy of flavonoid-rich Scabiosa comosa inflorescence extract (TF-SC) in a rat model of CCl4-induced hepatic fibrosis and explored its underlying mechanism in vitro and in vivo. Rats (Wistar, Male, weight 200-250 g) were injected intraperitoneally with CCl4 (1:1v/v in peanut oil, 2 mL/kg body weight) to induce liver fibrosis, followed by treatment with TF-SC or vehicle. In addition, transforming growth factor-beta 1 (TGF-beta 1)-activated hepatic stellate cells (HSCs) were used for measuring Smad3 phosphorylation. We found decrease in liver function and liver fibrosis markers in serums. Also, TF-SC decreased hydroxyproline content and collagen deposition in liver tissues. TF-SC also decreased the expression of alpha-SMA, collagen I and fibronectin in CCl4-induced hepatic fibrosis rats. Mechanistically, TF-SC attenuated liver fibrosis by selectively inhibiting Smad3 phosphorylation. In TGF-beta 1-stimulated HSCs, TF-SC blocked the interaction between Smad3 and TGF-beta type I receptor (T beta RI), suppressed subsequent phosphorylation and nuclear translocation of Smad3, and downregulated the transcription of fibrotic genes. In conclusion, the study demonstrated that TF-SC was an effective therapeutic agent for treatment of hepatic fibrosis, and provided a molecular basis through which TF-SC exerts its anti-fibrotic effects.
引用
收藏
页码:426 / 433
页数:8
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