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富含类黄酮的蓝蓟花序提取物通过调节 TGF-β诱导的 Smad 磷酸化来减轻 CCl 诱导的肝纤维化。

Flavonoid-rich Scabiosa comosa inflorescence extract attenuates CCl-induced hepatic fibrosis by modulating TGF-β-induced Smad phosphorylation.

机构信息

Department of Pharmacology, School of Basic Medicine, Inner Mongolia medical university, Hohhot, 010110, China.

Department of Pathology, School of Basic Medicine, Inner Mongolia medical university, Hohhot, 010110, China.

出版信息

Biomed Pharmacother. 2018 Oct;106:426-433. doi: 10.1016/j.biopha.2018.06.118. Epub 2018 Jul 11.

DOI:10.1016/j.biopha.2018.06.118
PMID:29990830
Abstract

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 CCl-induced hepatic fibrosis and explored its underlying mechanism in vitro and in vivo. Rats (Wistar, Male, weight 200-250 g) were injected intraperitoneally with CCl (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-β1 (TGF-β1)-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 α-SMA, collagen I and fibronectin in CCl4-induced hepatic fibrosis rats. Mechanistically, TF-SC attenuated liver fibrosis by selectively inhibiting Smad3 phosphorylation. In TGF-β1-stimulated HSCs, TF-SC blocked the interaction between Smad3 and TGF-β type I receptor (TβRI), suppressed subsequent phosphorylation and nuclear translocation of Smad3, and down-regulated 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.

摘要

毛蕊花糖苷是一种传统的蒙药,用于治疗肝脏疾病。在这项研究中,我们研究了富含黄酮类化合物的毛蕊花糖苷花序提取物(TF-SC)在 CCl 诱导的肝纤维化大鼠模型中的抗纤维化功效,并在体内和体外探讨了其潜在机制。大鼠(Wistar,雄性,体重 200-250g)经腹腔注射 CCl(1:1v/v 在花生油中,2mL/kg 体重)诱导肝纤维化,随后用 TF-SC 或载体进行治疗。此外,还使用转化生长因子-β1(TGF-β1)激活的肝星状细胞(HSCs)测量 Smad3 磷酸化。我们发现血清中肝功能和肝纤维化标志物降低。此外,TF-SC 降低了羟脯氨酸含量和肝组织中的胶原沉积。TF-SC 还降低了 CCl4 诱导的肝纤维化大鼠中α-SMA、胶原 I 和纤连蛋白的表达。机制上,TF-SC 通过选择性抑制 Smad3 磷酸化来减轻肝纤维化。在 TGF-β1 刺激的 HSCs 中,TF-SC 阻断了 Smad3 和 TGF-β 型 I 受体(TβRI)之间的相互作用,抑制了 Smad3 的随后磷酸化和核易位,并下调了纤维化基因的转录。总之,该研究表明 TF-SC 是治疗肝纤维化的有效治疗剂,并通过其发挥抗纤维化作用提供了分子基础。

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