赵双双, 邵荣光, 何红伟. 抗肝纤维化的潜在作用靶点J. 药学学报, 2014,49(10): 1365-1371.
引用本文: 赵双双, 邵荣光, 何红伟. 抗肝纤维化的潜在作用靶点J. 药学学报, 2014,49(10): 1365-1371.
ZHAO Shuang-shuang, SHAO Rong-guang, HE Hong-wei. Potential targets for anti-liver fibrosisJ. Acta Pharmaceutica Sinica, 2014,49(10): 1365-1371.
Citation: ZHAO Shuang-shuang, SHAO Rong-guang, HE Hong-wei. Potential targets for anti-liver fibrosisJ. Acta Pharmaceutica Sinica, 2014,49(10): 1365-1371.

抗肝纤维化的潜在作用靶点

Potential targets for anti-liver fibrosis

  • 摘要: 肝纤维化是肝脏内弥漫性细胞外基质特别是I型胶原α1过度沉积的病理过程,最终导致肝硬化或者肝功能衰竭。由于肝纤维化及肝硬化前期可以逆转,因此控制肝纤维化这一可逆的过程,对于肝硬化和肝功能衰竭的预防及治疗十分重要。本文在大量文献基础上,就潜在的抗肝纤维化靶点予以综述,包括致肝纤维化最重要的细胞因子之一TGF-β1以及近期发现的整合素αV等,旨在为预防或治疗肝纤维化提供新的途径。

     

    Abstract: Liver fibrosis is a pathological process of the excessive accumulation of extracellular matrix, especially collagen α1 (I) in liver. Ultimately, hepatic fibrosis leads to cirrhosis or hepatic failure. Liver fibrosis and early cirrhosis can be reversed, thus control of the development of liver fibrosis is very important for preventive treatment of cirrhosis and hepatic failure. This is a review of potential targets for anti-hepatic fibrosis based on plenty of publications, including TGF-β1 and integrin αV and so on, aimed at providing novel therapeutic targets in liver fibrosis.

     

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