Singla Bhupesh
Pharmaceutical Sciences, The University of Tennessee Health Science Center, Memphis, TN 38103, United States.
World J Gastroenterol. 2024 Dec 14;30(46):4964-4968. doi: 10.3748/wjg.v30.i46.4964.
The prevalence of metabolic dysfunction-associated steatotic liver disease (MASLD) has increased significantly in recent decades and is projected to increase further due to the rising obesity rates. MASLD patients are at higher risk of developing advanced liver diseases "cirrhosis and hepatocellular carcinoma" as well as liver- or cardiovascular-related mortality. Existing lipid-lowering therapies failed to reduce the risk of mortality in these patients. Therefore, there is an urgent need for pharmacotherapies that can control and even reverse this disease. Fanlian Huazhuo Formula (FLHZF) is a combination herbal preparation, and its various individual constituents regulate hepatic lipid metabolism, adipose tissue inflammation, and gut microbiota. Despite, these useful effects, limited information is available on its benefits in diet-induced hepatosteatosis. In this article, we discuss the research findings recently published about the therapeutic effects of FLHZF in suppressing MASLD development and underlying mechanisms. Utilizing a series of and experiments, the authors demonstrated for the first time that FLHZF suppresses MASLD in male mice possibly by inhibiting hepatic lipogenesis pathways and reducing hepatocyte death. This study paves the way for future investigations aimed at investigating FLHZF's role in inhibiting lipogenesis particularly using radioactively-labeled glucose and acetate, and governing hepatocyte mitochondrial function, gut microbiome profile, and its effects in other models of MASLD, and female mice.
近几十年来,代谢功能障碍相关脂肪性肝病(MASLD)的患病率显著上升,并且由于肥胖率的不断上升,预计还会进一步增加。MASLD患者发生晚期肝病(肝硬化和肝细胞癌)以及肝脏或心血管相关死亡率的风险更高。现有的降脂疗法未能降低这些患者的死亡风险。因此,迫切需要能够控制甚至逆转这种疾病的药物治疗方法。翻莲化浊方(FLHZF)是一种复方草药制剂,其各种成分可调节肝脏脂质代谢、脂肪组织炎症和肠道微生物群。尽管有这些有益作用,但关于其在饮食诱导的肝脂肪变性中的益处的信息有限。在本文中,我们讨论了最近发表的关于FLHZF在抑制MASLD发展及其潜在机制方面的治疗效果的研究结果。通过一系列实验,作者首次证明FLHZF可能通过抑制肝脏脂肪生成途径和减少肝细胞死亡来抑制雄性小鼠的MASLD。这项研究为未来的研究铺平了道路,这些研究旨在研究FLHZF在抑制脂肪生成中的作用,特别是使用放射性标记的葡萄糖和乙酸盐,以及调节肝细胞线粒体功能、肠道微生物群谱,及其在其他MASLD模型和雌性小鼠中的作用。