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姜黄素及其衍生物治疗肝脏疾病的最新进展

[Recent advances in curcumin and its derivatives for treatment of liver diseases].

作者信息

Sun Yong, Peng Ming-li

出版信息

Yao Xue Xue Bao. 2014 Nov;49(11):1483-90.

Abstract

Curcumin is a principal polyphenolic curcuminoid extracted from turmeric rhizome, which has been used for treating inflammation of joints, ulcers, jaundice and other disorders in Asian traditional medicine. In recent years, many studies have indicated that curcumin plays important roles in treatment of liver diseases. Curcumin attenuates liver injury and non-alcoholic fatty liver disease by lowering the release of inflammation cytokines, minimizing oxidative stress, enhancing the sensitivity of insulin and altering lipid metabolism. Curcumin shows potent anti-fibrosis activity, contributing to inhibit the activation of hepatic stellate cells and reduce the deposition of extracellular matrix by its regulation of PPAR-γ, NF-ΚB and TGF-β signaling pathways. Moreover, curcumin exhibits anti-cancer effect by inducing G2/M phase cell cycle arrest and apoptosis in several hepatoma cell lines. However, poor water solubility and low bioavailability of curcumin limit its clinical applications. To overcome its limited systemic bioavailability, many new approaches have been explored to deliver curcumin effectively. This article focuses on advances in the effects of curcumin and its derivatives for treatment of liver injury, non-alcoholic fatty liver disease, liver fibrosis and hepatocarcinoma.

摘要

姜黄素是从姜黄根茎中提取的一种主要的多酚类姜黄素,在亚洲传统医学中已被用于治疗关节炎症、溃疡、黄疸及其他病症。近年来,许多研究表明姜黄素在肝脏疾病的治疗中发挥着重要作用。姜黄素通过降低炎症细胞因子的释放、减少氧化应激、增强胰岛素敏感性及改变脂质代谢来减轻肝损伤和非酒精性脂肪性肝病。姜黄素具有强大的抗纤维化活性,通过调节PPAR-γ、NF-ΚB和TGF-β信号通路,有助于抑制肝星状细胞的活化并减少细胞外基质的沉积。此外,姜黄素通过诱导几种肝癌细胞系的G2/M期细胞周期阻滞和凋亡而表现出抗癌作用。然而,姜黄素的水溶性差和生物利用度低限制了其临床应用。为克服其有限的全身生物利用度,人们探索了许多新方法来有效递送姜黄素。本文重点介绍姜黄素及其衍生物在治疗肝损伤、非酒精性脂肪性肝病、肝纤维化和肝癌方面的研究进展。

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