Jiang Ling, Yi Rong, Chen Huan, Wu Shuwu
Department of Endocrinology and Metabolism, People's Hospital of Yichun City, Yichun, Jiangxi, People's Republic of China.
Anim Biotechnol. 2025 Dec;36(1):2442351. doi: 10.1080/10495398.2024.2442351. Epub 2024 Dec 24.
The natural flavonoid quercetin, which exhibits a range of biological activities, has been implicated in liver disease resistance in recent research. study attesting to quercetin's protective effect against metabolic-associated fatty liver disease (MAFLD) is inadequate, however. Here, our investigation explored the potential benefits of quercetin in preventing MAFLD in C57BL/6 mice fed a high-fat diet (HFD). The results revealed that quercetin ameliorated the aberrant enhancement of body and liver weight. The hepatic histological anomalie induced by MAFLD were also mitigated by quercetin. HFD-induced imbalance in serum LDL, HDL, AST, ALT, TG, and LDH was mitigated by quercetin. Mechanically, we found that quercetin improved lipid metabolism by reducing lipogenesis proteins including ACC, FASN, and SREBP-1c and enhancing β-oxidation proteins including PPARα and CPT1A. study demonstrated that quercetin regulated hepatic lipid metabolism by targeting SREBP-1c and PPARα. Additionally, quercetin enhanced the antioxidant capacity in HFD-treated mice by downregulating Nrf2 and HO-1 expressions and upregulating SOD and GPX1 expressions. The hyper-activation of inflammation was also restored by quercetin via eliminating the phosphorylation of IκBα and NF-κB p65. Collectively, our observations highlight that quercetin exerts hepatoprotective properties in MAFLD mice by regulating hepatic lipid metabolism, oxidative stress and inflammatory response.
天然黄酮类化合物槲皮素具有一系列生物活性,在最近的研究中被认为与肝脏疾病抗性有关。然而,证明槲皮素对代谢相关脂肪性肝病(MAFLD)具有保护作用的研究并不充分。在此,我们的研究探讨了槲皮素在预防高脂饮食(HFD)喂养的C57BL/6小鼠发生MAFLD方面的潜在益处。结果显示,槲皮素改善了体重和肝脏重量的异常增加。槲皮素还减轻了MAFLD诱导的肝脏组织学异常。槲皮素减轻了HFD诱导的血清低密度脂蛋白(LDL)、高密度脂蛋白(HDL)、天冬氨酸转氨酶(AST)、丙氨酸转氨酶(ALT)、甘油三酯(TG)和乳酸脱氢酶(LDH)失衡。从机制上讲,我们发现槲皮素通过减少包括乙酰辅酶A羧化酶(ACC)、脂肪酸合酶(FASN)和固醇调节元件结合蛋白-1c(SREBP-1c)在内的脂肪生成蛋白,并增强包括过氧化物酶体增殖物激活受体α(PPARα)和肉碱/有机阳离子转运体1A(CPT1A)在内的β-氧化蛋白,从而改善脂质代谢。一项研究表明,槲皮素通过靶向SREBP-1c和PPARα来调节肝脏脂质代谢。此外,槲皮素通过下调核因子E2相关因子2(Nrf2)和血红素加氧酶-1(HO-1)的表达,并上调超氧化物歧化酶(SOD)和谷胱甘肽过氧化物酶1(GPX1)的表达,增强了HFD处理小鼠的抗氧化能力。槲皮素还通过消除IκBα和核因子κB p65(NF-κB p65)的磷酸化来恢复炎症的过度激活。总的来说,我们的观察结果表明,槲皮素通过调节肝脏脂质代谢、氧化应激和炎症反应,对MAFLD小鼠发挥肝脏保护作用。