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芽菜影响 Huh7 细胞和高脂饮食诱导肥胖小鼠的甘油三酯代谢。

Sprouts Affect Triglyceride Metabolism in Huh7 Cells and High-Fat Diet-Induced Obese Mice.

机构信息

Department of Herbology, College of Korean Medicine, Daegu Haany University, Daegu, Republic of Korea.

Research Center for Herbal Convergence on Liver Disease, Daegu Haany University, Gyeongsan-si, Gyeongsangbuk-do, Republic of Korea.

出版信息

J Med Food. 2024 Aug;27(8):728-739. doi: 10.1089/jmf.2023.k.0246. Epub 2024 May 29.

Abstract

Lipolysis is the hydrolysis of triglycerides (TGs), commonly known as fats. Intracellular lipolysis of TG is associated with adipose triglyceride lipase (ATGL), which provides fatty acids during times of metabolic need. The aim of this study was to determine whether L. Stapf () sprouts (CS) can alleviate obesity through lipolysis. Overall, we investigated the potential of CS under and conditions and confirmed the underlying mechanisms. Huh7 cells were exposed to free fatty acids (FFAs), and C57BL/6J mice were fed a 60% high-fat diet. When FFA were introduced into Huh7 cells, the intracellular TG levels increased within the Huh7 cells. However, CS treatment significantly reduced intracellular TG levels. Furthermore, CS decreased the expression of and mRNA and downregulated the mutant (I148M) mRNA. Notably, CS significantly upregulated ATGL expression. CS treatment at a dose of 200 mg/kg/day resulted in a significant and dose-dependent decrease in body weight gain and epididymal adipose tissue weight. Specifically, the group treated with CS (200 mg/kg/day) exhibited a significant modulation of serum lipid biomarkers. In addition, CS ameliorated histological alterations in both the liver and adipose tissues. In summary, CS efficiently inhibited lipid accumulation through the activation of the lipolytic enzyme ATGL coupled with the suppression of enzymes involved in TG synthesis. Consequently, CS show promise as a potential anti-obesity agent.

摘要

脂肪分解是甘油三酯(TGs)的水解,通常被称为脂肪。细胞内的 TG 脂肪分解与脂肪甘油三酯脂肪酶(ATGL)有关,它在代谢需要时提供脂肪酸。本研究旨在确定 L. Stapf () 芽(CS)是否可以通过脂肪分解来减轻肥胖。总的来说,我们研究了 CS 在 和 条件下的潜力,并证实了其潜在的机制。在 Huh7 细胞中暴露于游离脂肪酸(FFAs),并用 60%高脂肪饮食喂养 C57BL/6J 小鼠。当 FFA 被引入 Huh7 细胞时,细胞内 TG 水平在 Huh7 细胞内增加。然而,CS 处理显著降低了细胞内 TG 水平。此外,CS 降低了 和 mRNA 的表达,并下调了突变体 (I148M) mRNA。值得注意的是,CS 显著上调了 ATGL 的表达。CS 以 200mg/kg/天的剂量治疗导致体重增加和附睾脂肪组织重量的显著和剂量依赖性下降。具体来说,用 CS(200mg/kg/天)治疗的组表现出对血清脂质生物标志物的显著调节。此外,CS 改善了肝和脂肪组织的组织学改变。总之,CS 通过激活与 TG 合成相关的酶的抑制作用,有效地抑制了脂质积累,通过激活脂肪分解酶 ATGL。因此,CS 有望成为一种潜在的抗肥胖药物。

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