白葡萄酒渣减轻高血糖诱导的 Caco-2 细胞损伤和氧化应激

Foods 2023 Pub Date : 2023-10-13 DOI:10.3390/foods2023-15000
Víctor Gutiérrez-González, Gisela Gerardi, P. Muñiz, M. Cavia-Saiz
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引用次数: 0

摘要

:高血糖是代谢综合征的一个重要风险因素,导致心血管疾病和糖尿病的发生。高血糖会通过葡萄糖氧化和蛋白质糖基化增加 ROS(活性氧)的产生,从而导致细胞损伤。我们之前的研究强调了葡萄酒渣产品(一种酿酒副产品)的抗氧化特性及其调节氧化应激的能力。本研究的目的是评估 wWPPs 对高血糖 Caco-2 细胞氧化应激的保护作用。在正常血糖或高血糖(35 mM 葡萄糖)条件下,用从胃肠消化(WPGI)和结肠发酵(WPF)中获得的 1.5 µ g GAE/mL wWPP 生物可利用部分对 Caco-2 细胞进行处理。处理 24 小时后,对细胞活力、氧化应激生物标志物以及参与细胞氧化平衡的转录因子和酶的表达进行了评估。高血糖导致细胞活力降低 30%,而 WPF 处理后细胞活力恢复到正常血糖水平。生物可接受性馏分能够抵消高血糖诱导的肠细胞氧化应激,这体现在羰基和 MDA 水平的显著下降(分别为 10% 和 40%)。此外,WPGI 和 WPF 预处理还显著降低了高血糖诱导的 NF-κ B 过表达(15% 至 53%),从而调节了氧化还原活性。总之,WWPP 的生物可接受性组分,尤其是 WPF,在减轻高血糖诱导的氧化应激和提高 Caco-2 细胞活力方面表现出了巨大的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
White Wine Pomace Mitigates Hyperglycemia-Induced Cell Damage and Oxidative Stress in Caco-2 Cells
: Hyperglycemia is a significant risk factor in metabolic syndrome, contributing to the development of cardiovascular diseases and diabetes mellitus. Hyperglycemia increases ROS (reactive oxygen species) production via glucose oxidation and protein glycosylation, leading to cell damage. Our previous studies have highlighted the antioxidant properties of wine pomace products (wWPPs), a co-product of winemaking, and their ability to modulate oxidative stress. The objective of this study was to evaluate the protective effect of wWPPs against oxidative stress in hyperglycemic Caco-2 cells. They were treated with 1.5 µ g GAE/mL of wWPP bioaccessible fractions, obtained from gastrointestinal digestion (WPGI) and colonic fermentation (WPF), under normoglycemic or hyperglycemic (35 mM glucose) conditions. After 24 h of treatment, cell viability, oxidative stress biomarkers and the expression of transcription factors and enzymes involved in cellular oxidation balance were evaluated. Hyperglycemia induced a 30% reduction in cell viability, which was restored to normoglycemic levels by WPF treatment. The bioaccessible fractions were able to counteract hyperglycemia-induced oxidative stress in intestinal cells, as evidenced by significant decreases in carbonyl groups and MDA levels (10 and 40%, respectively). Furthermore, hyperglycemia-induced NF-κ B overexpression was also significantly reduced by WPGI and WPF pre-treatment (between 15 and 53%), modulating the redox activity. In conclusion, the bioaccessible fractions of wWPP, particularly WPF, demonstrated significant potential in mitigating hyperglycemia-induced oxidative stress and enhancing cell viability in Caco-2 cells.
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