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通过调节代谢途径和氧化应激改善肝脂肪变性、肥胖和血糖。

Ameliorates Hepatic Steatosis, Obesity, and Blood Glucose via Modulation of Metabolic Pathways and Oxidative Stress.

作者信息

Lee Sang-Seop, Lee Sang-Hoon, Kim So-Yeon, Lee Ga-Young, Han Seung-Yun, Lee Bong-Ho, Yoo Yung-Choon

机构信息

Department of Microbiology, College of Medicine, Konyang University, Daejon 32992, Republic of Korea.

Department of Anatomy, College of Medicine, Konyang University, Daejon 32992, Republic of Korea.

出版信息

Int J Mol Sci. 2025 May 26;26(11):5103. doi: 10.3390/ijms26115103.

Abstract

Obesity and metabolic dysfunction-associated steatotic liver disease (MASLD) are major contributors to the rise in metabolic disorders, particularly in developed countries. Despite the need for effective therapies, natural product-based interventions remain underexplored. This study investigated the therapeutic effects of , a type of brown algae, hot water extract (EB-WE) in ameliorating obesity and MASLD using high-fat diet (HFD)-induced ICR mice for an acute obesity model (4-week HFD feeding) and C57BL/6 mice for a long-term MASLD model (12-week HFD feeding). EB-WE administration significantly reduced body and organ weights and improved serum lipid markers, such as triglycerides (TG), total cholesterol (T-CHO), HDL (high-density lipoprotein), LDL (low-density lipoprotein), adiponectin, and apolipoprotein A1 (ApoA1). mRNA expression analysis of liver and skeletal muscle tissues revealed that EB-WE upregulated and while downregulating and suppressing lipogenic signaling. Additionally, EB-WE activated brown adipose tissue through and contributing to fatty liver alleviation. Western blot analysis of liver tissues demonstrated that EB-WE enhanced AMPK phosphorylation and modulated lipid metabolism by upregulating PGC-1α and UCP-1 and downregulating PPAR-γ, C/EBP-α, and FABP4 proteins. It also reduced oxidation markers, such as OxLDL (oxidized low-density lipoprotein) and ApoB (apolipoprotein B), while increasing ApoA1 levels. EB-WE suppressed lipid peroxidation by modulating oxidative stress markers, such as SOD (superoxide dismutase), CAT (catalase), GSH (glutathione), and MDA (malondialdehyde), in liver tissues. Furthermore, EB-WE regulated the glucose regulatory pathway in the liver and muscle by inhibiting the expression of , and while increasing the expression of and . Tentative liquid chromatography-tandem mass spectrometry (LC-MS/MS) analysis for EB-WE identified bioactive compounds, such as pyropheophorbide A and digiprolactone, which are known to have antioxidant or metabolic regulatory activities. These findings suggest that EB-WE improves obesity and MASLD through regulation of metabolic pathways, glucose homeostasis, and antioxidant activity, making it a promising candidate for natural product-based functional foods and pharmaceuticals targeting metabolic diseases.

摘要

肥胖和代谢功能障碍相关脂肪性肝病(MASLD)是代谢紊乱增加的主要原因,尤其是在发达国家。尽管需要有效的治疗方法,但基于天然产物的干预措施仍未得到充分探索。本研究使用高脂饮食(HFD)诱导的ICR小鼠作为急性肥胖模型(4周高脂饮食喂养),C57BL/6小鼠作为长期MASLD模型(12周高脂饮食喂养),研究了一种褐藻热水提取物(EB-WE)在改善肥胖和MASLD方面的治疗效果。给予EB-WE可显著降低体重和器官重量,并改善血清脂质标志物,如甘油三酯(TG)、总胆固醇(T-CHO)、高密度脂蛋白(HDL)、低密度脂蛋白(LDL)、脂联素和载脂蛋白A1(ApoA1)。肝脏和骨骼肌组织的mRNA表达分析表明,EB-WE上调了[相关基因名称1]和[相关基因名称2],同时下调了[相关基因名称3]并抑制脂肪生成信号。此外,EB-WE通过[相关机制1]和[相关机制2]激活棕色脂肪组织,有助于减轻脂肪肝。肝脏组织的蛋白质印迹分析表明,EB-WE增强了AMPK磷酸化,并通过上调PGC-1α和UCP-1以及下调PPAR-γ、C/EBP-α和FABP4蛋白来调节脂质代谢。它还降低了氧化标志物,如氧化型低密度脂蛋白(OxLDL)和载脂蛋白B(ApoB),同时增加了ApoA1水平。EB-WE通过调节肝脏组织中的氧化应激标志物,如超氧化物歧化酶(SOD)、过氧化氢酶(CAT)、谷胱甘肽(GSH)和丙二醛(MDA),抑制脂质过氧化。此外,EB-WE通过抑制[相关基因名称4]、[相关基因名称5]和[相关基因名称6]的表达,同时增加[相关基因名称7]和[相关基因名称8]的表达,调节肝脏和肌肉中的葡萄糖调节途径。对EB-WE进行的液相色谱-串联质谱(LC-MS/MS)初步分析鉴定出了具有抗氧化或代谢调节活性的生物活性化合物,如焦脱镁叶绿酸A和双环内酯。这些发现表明,EB-WE通过调节代谢途径、葡萄糖稳态和抗氧化活性来改善肥胖和MASLD,使其成为基于天然产物的针对代谢疾病的功能性食品和药物的有前途的候选物。

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