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紫贻贝()作为一种治疗肥胖的潜在功能性食品来源。

Purple Butter Clam () as a Potential Functional Food Source for Obesity Treatment.

机构信息

Department of Food and Nutrition, Pukyong National University, Busan, Republic of Korea.

National Marine Biodiversity of Korea (MABIK), Seochun, Korea.

出版信息

J Med Food. 2024 Nov;27(11):1038-1049. doi: 10.1089/jmf.2024.k.0169. Epub 2024 Oct 9.

Abstract

extract (SPE) is a highly consumable seafood worldwide with known health-related benefits. However, there are no reports of its' anti-obesity effect. This study explores the potential of SPE for anti-obesity effects by modulating adipogenesis and lipolysis. SPE reduced intracellular lipid and triglyceride accumulation while increasing free glycerol release in adipocytes. SPE inhibited lipogenesis protein expressions and increased the phosphorylation of hormone-sensitive lipase and Adenosine monophosphate-activated protein kinase (AMPK) to promote lipolysis. In addition, SPE suppressed adipogenesis by downregulating protein expression of key adipogenic markers, peroxisome proliferator-activated receptor gamma (PPARγ), CCAAT/enhancer-binding protein α (C/EBPα), and sterol regulatory element-binding protein 1 (SREBP1) via Wnt/β-catenin signaling. SPE augmented the heme oxygenase-1 (HO-1) expression. Thus, pharmacological intervention with Zinc protoporphyrin (ZnPP-HO-1 antagonist) was employed to validate the HO-1 role. The presence of ZnPP increased the lipid accumulation and reduced the free glycerol release. At the molecular level, adipogenic transcription factors (PPARγ, C/EBPα, and SREBP1) expressions were restored in the presence of ZnPP. GC-MS analysis revealed that SPE was comprised of several fatty acids, contributing to its anti-obesity activity. SPE is an effective nutraceutical that can be used to reduce the progression of obesity. HO-1 expression during adipogenesis might be the mechanism of action for the anti-obesity effect of SPE.

摘要

鱼胶原蛋白肽(SPE)是一种在全球范围内消费很高的海鲜,具有已知的与健康相关的益处。然而,目前尚无关于其抗肥胖作用的报道。本研究通过调节脂肪生成和脂肪分解来探索 SPE 具有抗肥胖作用的潜力。SPE 减少了脂肪细胞内的脂质和甘油三酯积累,同时增加了游离甘油的释放。SPE 抑制了脂肪生成蛋白的表达,增加了激素敏感脂肪酶和腺苷一磷酸激活蛋白激酶(AMPK)的磷酸化,以促进脂肪分解。此外,SPE 通过下调关键脂肪生成标记物过氧化物酶体增殖物激活受体γ(PPARγ)、CCAAT/增强子结合蛋白α(C/EBPα)和固醇调节元件结合蛋白 1(SREBP1)的蛋白表达来抑制脂肪生成,通过 Wnt/β-连环蛋白信号通路。SPE 增加了血红素加氧酶-1(HO-1)的表达。因此,采用锌原卟啉(ZnPP-HO-1 拮抗剂)进行药理学干预来验证 HO-1 的作用。ZnPP 的存在增加了脂质积累,减少了游离甘油的释放。在分子水平上,ZnPP 的存在恢复了脂肪生成转录因子(PPARγ、C/EBPα 和 SREBP1)的表达。GC-MS 分析表明,SPE 由几种脂肪酸组成,这有助于其抗肥胖活性。SPE 是一种有效的营养保健品,可用于减缓肥胖的进展。HO-1 表达在脂肪生成过程中可能是 SPE 抗肥胖作用的作用机制。

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