Department of Histology and Embryology, Faculty of Medicine, Trakya University, 22030 Edirne, Turkey.
J Mol Histol. 2010 Dec;41(6):395-402. doi: 10.1007/s10735-010-9301-7. Epub 2010 Oct 20.
The aim of this study was to evaluate the possible protective effects of quercetin (QE) against cholestatic oxidative stress and liver damage in the common bile duct ligated rats. A total of 24 male Wistar albino rats were divided into three groups: control, bile duct ligation (BDL) and BDL + received QE; each group contain 8 animals. The rats in QE treated groups were given QE (15 mg/kg) once a day intraperitoneally for 4 weeks starting 3 days prior to BDL operation. The changes demonstrating the bile duct proliferation and fibrosis in expanded portal tracts include the extension of proliferated bile ducts into lobules, mononuclear cells, and neutrophil infiltration into the widened portal areas were observed in BDL group. Treatment of BDL with QE attenuated alterations in liver histology. The alpha smooth muscle actin (α-SMA), transforming growth factor beta (TGF-β1) positive cells and the activity of TUNEL in the BDL were observed to be reduced with the QE treatment. The data indicate that QE attenuates BDL-induced cholestatic liver injury, bile duct proliferation, and fibrosis. The hepatoprotective effect of QE is associated with antioxidative potential.
本研究旨在评估槲皮素 (QE) 对胆总管结扎大鼠胆汁淤积性氧化应激和肝损伤的可能保护作用。总共 24 只雄性 Wistar 白化大鼠被分为三组:对照组、胆总管结扎 (BDL) 组和 BDL 加 QE 组;每组包含 8 只动物。QE 治疗组的大鼠在 BDL 手术前 3 天开始每天腹膜内给予 QE(15mg/kg)一次,持续 4 周。BDL 组中观察到扩张门脉区增生的胆管向小叶延伸、单核细胞和中性粒细胞浸润,显示出胆管增殖和纤维化的变化。用 QE 治疗 BDL 可减轻肝组织学改变。QE 治疗可降低 BDL 诱导的α平滑肌肌动蛋白 (α-SMA)、转化生长因子-β1 (TGF-β1) 阳性细胞和 TUNEL 活性。数据表明,QE 可减轻 BDL 诱导的胆汁淤积性肝损伤、胆管增殖和纤维化。QE 的保肝作用与抗氧化潜力有关。