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通过上调过氧化物酶体增殖物激活受体α和抑制线粒体氧化损伤减轻代谢功能障碍相关脂肪性肝病

Alleviates Metabolic Dysfunction-Associated Steatotic Liver Disease by Upregulating Peroxisome Proliferator-Activated Receptor α and Inhibiting Mitochondrial Oxidative Damage.

作者信息

Ren Mingshi, Ren Jiayue, Zheng Jianmei, Sha Xiaotong, Lin Yining, Wu Feihua

机构信息

School of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing 211198, China.

出版信息

Antioxidants (Basel). 2024 Sep 20;13(9):1136. doi: 10.3390/antiox13091136.

Abstract

The most prevalent chronic liver disease, known as metabolic dysfunction-associated steatotic liver disease (MASLD), is characterized by an excessive accumulation of lipids and oxidative damage. , a natural herbal medicine widely used by Chinese folk, has antioxidative, anti-inflammatory, and lipid metabolism-regulating effects. Here, we explored the effect of extract (CGE) on MASLD using palmitic acid (PA)-induced hepatocytes and high-fat diet (HFD)-fed mice. In vitro, CGE could promote fatty acid oxidation and inhibit fatty acid synthesis and uptake to reduce lipid accumulation by regulating PPARα activation. Moreover, CGE could inhibit reactive oxygen species production and maintain mitochondrial homeostasis in PA-induced HepG2 cells. In vivo, animal study results indicated that CGE could effectively reduce lipid metabolism disorder, inhibit oxidative stress, and upregulate PPARα protein in the liver of HFD-fed mice. Molecular docking results also showed that active compounds isolated from CGE had low binding energy and highly stable binding with PPARα. In summary, these findings reveal that CGE may be a potential therapeutic candidate for MASLD and act by upregulating PPARα to reduce lipid accumulation and suppress mitochondrial oxidative damage.

摘要

最常见的慢性肝病,即代谢功能障碍相关脂肪性肝病(MASLD),其特征是脂质过度积累和氧化损伤。 ,一种在中国民间广泛使用的天然草药,具有抗氧化、抗炎和调节脂质代谢的作用。在此,我们使用棕榈酸(PA)诱导的肝细胞和高脂饮食(HFD)喂养的小鼠,探讨了 提取物(CGE)对MASLD的影响。在体外,CGE可通过调节PPARα激活来促进脂肪酸氧化,抑制脂肪酸合成和摄取,以减少脂质积累。此外,CGE可抑制PA诱导的HepG2细胞中活性氧的产生并维持线粒体稳态。在体内,动物研究结果表明,CGE可有效减轻高脂饮食喂养小鼠肝脏中的脂质代谢紊乱,抑制氧化应激,并上调PPARα蛋白。分子对接结果还表明,从CGE中分离出的活性化合物与PPARα具有低结合能和高度稳定的结合。总之,这些发现表明,CGE可能是MASLD的潜在治疗候选物,其作用机制是上调PPARα以减少脂质积累并抑制线粒体氧化损伤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a696/11428588/18d130a4c937/antioxidants-13-01136-g001.jpg

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