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荷叶碱抑制培养的肝星状细胞激活和促进细胞凋亡:一种可能的分子机制。

Neferine inhibits cultured hepatic stellate cell activation and facilitates apoptosis: A possible molecular mechanism.

机构信息

Department of Gastroenterology, Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi 710004, China.

出版信息

Eur J Pharmacol. 2011 Jan 10;650(1):163-9. doi: 10.1016/j.ejphar.2010.10.025. Epub 2010 Oct 20.

Abstract

Neferine is a major alkaloid component of "Lian Zi Xin", embryos of the seeds of Nelumbo nucifera Gaertner, Nymphaeaceae. Previous studies have shown that neferine has an inhibitory effect on pulmonary fibrosis through its anti-inflammatory and anti-oxidative activities and inhibition of cytokines and NF-κB. However, it is unknown whether neferine also has an inhibitory effect on liver fibrosis through inhibition of TGF-β1 and collagen I and facilitation of apoptosis of hepatic stellate cells. This study examined the effects of neferine on cultured hepatic stellate (HSC-T6) cells and explored its possible action mechanisms by means of MTT assay, enzyme-linked immunosorbent assay, flow-cytometric annexin V-PI assay and Hoechst 33258 staining, as well as real-time PCR and western blotting. The results showed that neferine administration (2, 4, 6, 8 and 10μmol/l) significantly decreased the TGF-β1 and collagen I produced in HSC-T6 cells, and increased the HSC-T6 cell apoptosis in a dose-dependent manner. Neferine treatment for 48h at concentrations of 6 and 10μmol/l significantly increased Bax and caspase 3 mRNAs and proteins, and reduced Bcl2 and alpha-smooth muscle actin (α-SMA) mRNAs and proteins. Our data indicate that neferine efficiently inhibits cultured HSC-T6 cell activation and induces apoptosis by increasing Bax and caspase 3 expression via the mitochondrial pathway.

摘要

莲心碱是睡莲科莲属植物莲(Nelumbo nucifera Gaertner)种子的胚中主要的一种生物碱成分。先前的研究表明,莲心碱通过抗炎、抗氧化作用,抑制细胞因子和 NF-κB,对肺纤维化具有抑制作用。然而,莲心碱是否通过抑制 TGF-β1 和胶原 I 以及促进肝星状细胞凋亡对肝纤维化也具有抑制作用尚不清楚。本研究通过 MTT 检测、酶联免疫吸附检测、流式细胞术 Annexin V-PI 检测和 Hoechst 染色以及实时 PCR 和 Western blot 法,观察莲心碱对培养的肝星状细胞(HSC-T6)的作用,探讨其可能的作用机制。结果表明,莲心碱(2、4、6、8 和 10μmol/L)给药可显著降低 HSC-T6 细胞产生的 TGF-β1 和胶原 I,并呈剂量依赖性增加 HSC-T6 细胞凋亡。6 和 10μmol/L 的莲心碱处理 48h 可显著增加 Bax 和 caspase 3 的 mRNA 和蛋白水平,降低 Bcl2 和α-平滑肌肌动蛋白(α-SMA)的 mRNA 和蛋白水平。我们的数据表明,莲心碱通过增加 Bax 和 caspase 3 的表达,通过线粒体途径有效地抑制培养的 HSC-T6 细胞的激活,并诱导细胞凋亡。

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