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大黄素 8--葡萄糖苷通过调控 STAT3 信号通路对肝纤维化的肝保护作用。

Hepatoprotective Potency of Chrysophanol 8--Glucoside from L. against Hepatic Fibrosis via Regulation of the STAT3 Signaling Pathway.

机构信息

School of Pharmacy, Sungkyunkwan University, Suwon 16419, Korea.

Laboratory of Nuclear Magnetic Resonance, National Center for Inter-University Research Facilities (NCIRF), Seoul National University, Gwanak-gu, Seoul 08826, Korea.

出版信息

Int J Mol Sci. 2020 Nov 27;21(23):9044. doi: 10.3390/ijms21239044.

Abstract

Rhubarb is a well-known herb worldwide and includes approximately 60 species of the genus. One of the representative plants is , which is prescribed as official rhubarb due to its pharmacological potential in the Korean and Chinese pharmacopoeia. In our bioactive screening, we found out that the EtOH extract of inhibited hepatic stellate cell (HSC) activation by transforming growth factor β1 (TGF-β1). Chemical investigation of the EtOH extract led to the isolation of chrysophanol 8--glucoside, which was determined by structural analysis using NMR spectroscopic techniques and electrospray ionization mass spectrometry (ESIMS). To elucidate the effects of chrysophanol 8--glucoside on HSC activation, activated LX-2 cells were treated for 48 h with chrysophanol 8--glucoside, and α-SMA and collagen, HSC activation markers, were measured by comparative quantitative real-time PCR (qPCR) and western blotting analysis. Chrysophanol 8--glucoside significantly inhibited the protein and mRNA expression of α-SMA and collagen compared with that in TGF-β1-treated LX-2 cells. Next, the expression of phosphorylated SMAD2 (p-SMAD2) and p-STAT3 was measured and the translocation of p-STAT3 to the nucleus was analyzed by western blotting analysis. The expression of p-SMAD2 and p-STAT3 showed that chrysophanol 8--glucoside strongly downregulated STAT3 phosphorylation by inhibiting the nuclear translocation of p-STAT3, which is an important mechanism in HSC activation. Moreover, chrysophanol 8--glucoside suppressed the expression of p-p38, not that of p-JNK or p-Erk, which can activate STAT3 phosphorylation and inhibit MMP2 expression, the downstream target of STAT3 signaling. These findings provided experimental evidence concerning the hepatoprotective effects of chrysophanol 8--glucoside against liver damage and revealed the molecular basis underlying its anti-fibrotic effects through the blocking of HSC activation.

摘要

大黄是一种在世界范围内广泛应用的草药,包含约 60 个种。其中一种代表性植物是 ,由于其在韩国和中国药典中的药理学潜力而被规定为官方大黄。在我们的生物活性筛选中,我们发现,转化生长因子 β1(TGF-β1)通过转化生长因子 β1(TGF-β1)抑制肝星状细胞(HSC)激活的乙醇提取物。对乙醇提取物的化学研究导致分离出大黄素 8--葡萄糖苷,通过使用核磁共振波谱技术和电喷雾电离质谱(ESIMS)进行结构分析确定。为了阐明大黄素 8--葡萄糖苷对 HSC 激活的影响,用大黄素 8--葡萄糖苷处理激活的 LX-2 细胞 48 小时,并通过比较定量实时 PCR(qPCR)和 Western 印迹分析测量 HSC 激活标志物α-SMA 和胶原的表达。与 TGF-β1 处理的 LX-2 细胞相比,大黄素 8--葡萄糖苷显著抑制了α-SMA 和胶原的蛋白和 mRNA 表达。接下来,通过 Western 印迹分析测量磷酸化 SMAD2(p-SMAD2)和 p-STAT3 的表达,并分析 p-STAT3 向核内的转位。p-SMAD2 和 p-STAT3 的表达表明,大黄素 8--葡萄糖苷通过抑制 p-STAT3 的核内转位强烈地下调 STAT3 磷酸化,这是 HSC 激活的重要机制。此外,大黄素 8--葡萄糖苷抑制 p-p38 的表达,而不抑制 p-JNK 或 p-Erk 的表达,后者可以激活 STAT3 磷酸化并抑制 STAT3 信号通路的下游靶标 MMP2 的表达。这些发现为大黄素 8--葡萄糖苷对肝损伤的肝保护作用提供了实验证据,并通过阻断 HSC 激活揭示了其抗纤维化作用的分子基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8a4/7730872/a57218e38463/ijms-21-09044-g001.jpg

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