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消除内质网压力:肥胖症中调节内质网应激的营养策略。

Unstressing the Reticulum: Nutritional Strategies for Modulating Endoplasmic Reticulum Stress in Obesity.

机构信息

Pathology Post Graduate Program, Fluminense Federal University (UFF), Niterói, RJ, 24070-090, Brazil.

Cardiovascular Sciences Post Graduate Program, Fluminense Federal University (UFF), Niterói, RJ, 24070-090, Brazil.

出版信息

Mol Nutr Food Res. 2024 Oct;68(20):e2400361. doi: 10.1002/mnfr.202400361. Epub 2024 Oct 4.

Abstract

The progression of obesity involves several molecular mechanisms that are closely associated with the pathophysiological response of the disease. Endoplasmic reticulum (ER) stress is one such factor. Lipotoxicity disrupts endoplasmic reticulum homeostasis in the context of obesity. Furthermore, it induces ER stress by activating several signaling pathways via inflammatory responses and oxidative stress. ER performs crucial functions in protein synthesis and lipid metabolism; thus, triggers such as lipotoxicity can promote the accumulation of misfolded proteins in the organelle. The accumulation of these proteins can lead to metabolic disorders and chronic inflammation, resulting in cell death. Thus, alternatives, such as flavonoids, amino acids, and polyphenols that are associated with antioxidant and anti-inflammatory responses have been proposed to attenuate this response by modulating ER stress via the administration of nutrients and bioactive compounds. Decreasing inflammation and oxidative stress can reduce the expression of several ER stress markers and improve clinical outcomes through the management of obesity, including the control of body weight, visceral fat, and lipid accumulation. This review explores the metabolic changes resulting from ER stress and discusses the role of nutritional interventions in modulating the ER stress pathway in obesity.

摘要

肥胖的进展涉及几种与疾病病理生理反应密切相关的分子机制。内质网(ER)应激就是其中的一个因素。脂肪毒性破坏了肥胖情况下内质网的内稳态。此外,它通过炎症反应和氧化应激激活几种信号通路诱导内质网应激。内质网在蛋白质合成和脂质代谢中发挥重要作用;因此,脂肪毒性等触发因素可以促进细胞器中错误折叠蛋白质的积累。这些蛋白质的积累可导致代谢紊乱和慢性炎症,从而导致细胞死亡。因此,有人提出了一些替代方法,如类黄酮、氨基酸和多酚,它们通过调节营养物质和生物活性化合物的内质网应激,与抗氧化和抗炎反应相关联,从而减轻这种反应。通过控制体重、内脏脂肪和脂质积累来减轻炎症和氧化应激,可以降低几种内质网应激标志物的表达,并改善肥胖症的临床结局。本综述探讨了内质网应激引起的代谢变化,并讨论了营养干预在肥胖症内质网应激途径调节中的作用。

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