Lin Yun-Lian, Lee Ting-Fang, Huang Yeh-Jeng, Huang Yi-Tsau
National Research Institute of Chinese Medicine, National Yang-Ming University, Taipei, Taiwan.
J Gastroenterol Hepatol. 2006 Aug;21(8):1257-65. doi: 10.1111/j.1440-1746.2006.04326.x.
Platelet-derived growth factor (PDGF) is a very potent mitogen for hepatic stellate cells (HSC) in hepatic fibrogenesis. Ligusticum chuanxiong Hort. (LC), a traditional Chinese herb used for cerebrovascular diseases, has been shown to exert anti-inflammatory and free radical scavenging effects. The aims of the present study were to investigate the effects of LC extract on the proliferation-related biomarkers in a rat HSC cell line (HSC-T6) stimulated with PDGF.
DNA synthesis via bromodeoxyuridine (BrdU) incorporation, cell cycle related proteins and apoptosis markers were determined to evaluate the inhibitory effects of LC.
The results revealed that LC extract (25-100 microg/mL) concentration-dependently decreased the PDGF-induced cell proliferation as well as alpha-smooth muscle actin expression in HSC. The inhibitory activity of LC on HSC was associated with: (i) inhibition of BrdU incorporation; (ii) induction of apoptosis with the activation of caspase-3, up-regulation of cell cycle inhibitory proteins p21 and p27, and down-regulation of cell cycle stimulatory proteins cyclins D1 and D2; and (iii) increased phosphorylation of mitogen-activated protein kinases (JNK). LC at the studied concentrations showed no direct cytotoxicity on primary hepatocytes.
The results suggest that LC significantly inhibited PDGF-activated HSC proliferation, possibly through apoptotic mechanisms and the potential of LC as an antifibrotic agent warrants further investigation.
血小板衍生生长因子(PDGF)是肝纤维化过程中肝星状细胞(HSC)的一种非常有效的促有丝分裂原。川芎,一种用于治疗脑血管疾病的传统中药,已被证明具有抗炎和清除自由基的作用。本研究的目的是探讨川芎提取物对血小板衍生生长因子刺激的大鼠肝星状细胞系(HSC-T6)中增殖相关生物标志物的影响。
通过溴脱氧尿苷(BrdU)掺入法测定DNA合成、细胞周期相关蛋白和凋亡标志物,以评估川芎的抑制作用。
结果显示,川芎提取物(25 - 100μg/mL)浓度依赖性地降低了血小板衍生生长因子诱导的肝星状细胞增殖以及α-平滑肌肌动蛋白的表达。川芎对肝星状细胞的抑制活性与以下因素有关:(i)抑制BrdU掺入;(ii)通过激活半胱天冬酶-3诱导凋亡,上调细胞周期抑制蛋白p21和p27,下调细胞周期刺激蛋白细胞周期蛋白D1和D2;(iii)丝裂原活化蛋白激酶(JNK)磷酸化增加。在所研究浓度下,川芎对原代肝细胞无直接细胞毒性。
结果表明,川芎显著抑制血小板衍生生长因子激活的肝星状细胞增殖,可能通过凋亡机制,川芎作为抗纤维化药物的潜力值得进一步研究。