脂肪肝
体内
自愈水凝胶
动物模型
体外
细胞外基质
生物医学工程
组织工程
化学
药理学
医学
生物化学
病理
生物
生物技术
内科学
有机化学
疾病
作者
Ji Jiang,Yanfei Tan,Amin Liu,Rentai Yan,Yanzhe Ma,Likun Guo,Jing Sun,Zhenzhen Guo,Hongsong Fan
标识
DOI:10.1016/j.colsurfb.2021.111980
摘要
In alcoholic liver disease (ALD) research, animal models, as one of the most popular methods to explore pathology and therapeutic drug screening, show the limitations of expensive cost and ethic, as well as long modeling time. To minimize the use of animal models in ALD research, an artificial liver model has been developed by incorporating HepG2 cells into hydrogel matrix based on difunctional hyaluronan and collagen. And on this basis an alcohol-induced ALD model in vitro by adding alcohol in the engineering process has been established. Results showed that the construct exhibited a simulated synthetic and metabolic liver function thanks to the bionic fibrillar and viscoelastic characteristics of hydrogels. And the in vitro alcohol-induced ALD model was also proved to be successfully established, even presenting equal results with ALD mice. Furthermore, epigallocatechin gallate (EGCG) as an intervention on ALD was confirmed in both in vitro and in vivo model. The findings indicate our simple artificial liver model is not only highly predictive but also easy to apply to drug screening and implantation studies, suggesting a promising alternative to animal models. Moreover, as the main active ingredient of tea, EGCG's effective intervention and reversal effect on fatty liver provides support for the theory that green tea could prevent alcoholic fatty liver.
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