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葡萄籽原花青素提取物对硫代乙酰胺诱导的小鼠肝纤维化的改善作用。

Ameliorative effect of grape seed proanthocyanidin extract on thioacetamide-induced mouse hepatic fibrosis.

机构信息

MOE Key Laboratory of Molecular Animal Nutrition and Department of Veterinary Medicine, College of Animal Sciences, Zhejiang University, Hangzhou 310058, China.

出版信息

Toxicol Lett. 2012 Sep 18;213(3):353-60. doi: 10.1016/j.toxlet.2012.07.019. Epub 2012 Jul 31.

Abstract

The present study was designed to examine the effect of the grape seed proanthocyanidin extract (GSPE) on developing hepatic fibrosis that was induced by thioacetamide (TAA) in mice. Administration of TAA for 9 weeks led to a serious necrosis and apoptosis of the parenchymal cells, which resulted in an accumulation of excessive collagen in the liver and an increase of transformed hepatic stellate cells (HSCs). In addition, the mRNA expression of transforming growth factor β1 (TGF-β1), α-smooth muscle actin (α-SMA), as the marker of the activated HSCs, and α1-(I)-collagen were all up-regulated significantly when compared with the control. However, combined oral administration of GSPE at 100 mg/kg suppressed the mRNA expression of TGF-β1 and α-SMA, with decreased collagen accumulation as demonstrated by histomorphological evaluation and quantitative RT-PCR. The mRNA expression of the pro-inflammatory factors, including inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2), was remarkably enhanced by TAA treatment. However, their levels displayed a down-regulated trend beyond simultaneous GSPE treatment. Moreover, GSPE administration markedly suppressed lipid peroxidation. In conclusion, as a plant antioxidant, GSPE manifested effective hepatocellular protective action to ameliorate the developing liver fibrosis induced by chronic TAA administration in mice.

摘要

本研究旨在探讨葡萄籽原花青素提取物 (GSPE) 对硫代乙酰胺 (TAA) 诱导的小鼠肝纤维化形成的影响。TAA 给药 9 周导致实质细胞严重坏死和凋亡,导致肝脏内胶原过度积累和转化的肝星状细胞 (HSCs) 增加。此外,与对照组相比,转化生长因子 β1 (TGF-β1)、α-平滑肌肌动蛋白 (α-SMA)(作为活化的 HSCs 的标志物)和 α1-(I)-胶原的 mRNA 表达均显著上调。然而,GSPE 以 100mg/kg 的剂量口服给药可抑制 TGF-β1 和 α-SMA 的 mRNA 表达,组织形态学评价和定量 RT-PCR 显示胶原积累减少。TAA 处理可显著增强促炎因子诱导型一氧化氮合酶 (iNOS) 和环氧化酶-2 (COX-2) 的 mRNA 表达。然而,它们的水平在同时进行 GSPE 处理后呈下降趋势。此外,GSPE 给药可显著抑制脂质过氧化。综上所述,作为一种植物抗氧化剂,GSPE 表现出有效的肝细胞保护作用,可改善慢性 TAA 给药诱导的小鼠肝纤维化形成。

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