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阐明非酒精性脂肪性肝病:发病机制、分子机制、模型和新兴治疗方法。

Shedding light on non-alcoholic fatty liver disease: Pathogenesis, molecular mechanisms, models, and emerging therapeutics.

机构信息

Department of Pharmaceutical Sciences, College of Pharmacy and Health Sciences, St. John's University, Queens, NY 11439, USA.

Department of Pharmaceutical Sciences, College of Pharmacy and Health Sciences, St. John's University, Queens, NY 11439, USA.

出版信息

Life Sci. 2023 Jan 1;312:121185. doi: 10.1016/j.lfs.2022.121185. Epub 2022 Nov 12.

Abstract

Nonalcoholic fatty liver disease (NAFLD) is the most common chronic liver disorder globally impacting an estimated 25% of the population associated with severe consequences such as cirrhosis, hepatocellular carcinoma (HCC), and overall mortality. Fatty liver disease is triggered through multiple pathways, but the most prominent cause is either diabetes or obesity, or a combination of both. Therefore, hepatic glucose, insulin and fatty acid signaling becomes a dire need to understand which is well elaborated in this review. This review summarizes the popular two-hit pathogenesis of NAFLD, the molecular mechanisms underlying hepatic insulin resistance. As fatty liver disease gets advanced, it requires in-vitro as well as in-vivo models closer to disease progression in humans for better understanding the pathological state and identifying a novel therapeutic target. This review summarizes in-vitro (2D cell-culture/co-culture, 3D spheroid/organoid/liver-on-a-chip) models as well as in-vivo (genetically/dietary/chemically induced fatty liver disease) research models. Fatty liver disease research has gathered lots of attention recently since there is no FDA approved therapy available so far. However, there have been numerous promising targets to treat fatty liver disease including potential therapeutic targets under clinical trials are listed in this review.

摘要

非酒精性脂肪性肝病 (NAFLD) 是全球最常见的慢性肝脏疾病,估计影响全球 25%的人口,可导致严重后果,如肝硬化、肝细胞癌 (HCC) 和总体死亡率。脂肪性肝病是通过多种途径引发的,但最主要的原因是糖尿病或肥胖症,或两者兼有。因此,了解肝脏葡萄糖、胰岛素和脂肪酸信号转导就成为当务之急,这在本综述中得到了详细阐述。

本综述总结了 NAFLD 的流行双打击发病机制,以及肝胰岛素抵抗的分子机制。随着脂肪性肝病的进展,需要更接近人类疾病进展的体外和体内模型,以更好地了解病理状态并确定新的治疗靶点。本综述总结了体外(2D 细胞培养/共培养、3D 球体/类器官/芯片上肝脏)模型以及体内(遗传、饮食、化学诱导的脂肪性肝病)研究模型。

由于目前尚无获得 FDA 批准的治疗方法,脂肪性肝病研究最近受到了广泛关注。然而,已经有许多有前途的治疗脂肪性肝病的靶点,包括正在临床试验中的潜在治疗靶点都在本综述中列出。

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