Physalis Peruviana Linnaeus 提取物对 Caco-2 肠上皮样细胞系炎症标志物表达的影响

IF 2.6 4区 医学 Q1 NUTRITION & DIETETICS Journal of the American Nutrition Association Pub Date : 2025-02-01 Epub Date: 2024-09-27 DOI:10.1080/27697061.2024.2406896
Daniela Moya, Karen Mirada, Matias Rivera, Miguel Arredondo
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引用次数: 0

摘要

目的:秘鲁苦蘵(Physalis Peruviana Linnaeus,PPL)是一种草本植物,具有多种生物活性化合物,具有抗炎特性。因此,这种水果可能成为慢性炎症性疾病(如炎症性肠病)的辅助疗法。本研究评估了 PPL 提取物对 Caco-2 细胞系炎症标志物表达的影响:方法:进行体外胃消化(50 克 PPL 果肉),得到一种提取物,用来挑战 Caco-2 细胞 24 小时和 72 小时。该提取物通过 LC-MS/MS 进行表征。然后,通过 qRT-PCR 测定 NF-kB、TLR4、IL-18 和 MCP-1 的相对 mRNA 表达量,通过 Luminex 免疫测定法测定 TNF-α、IL-6、IL-8、IL-18 和 MCP-1 的蛋白质水平:从提取物的表征中发现了具有生物活性潜力的化合物,如异硫氰酸盐、吲哚和香豆素。用 PPL 提取物(80 µg/ml)处理 Caco-2 细胞,尤其是 72 小时,可降低 IL-18 和 MCP-1 mRNA 的表达(p < 0.01),以及 IL-18(p < 0.01)、IL-8(p < 0.0001)和 MCP-1 (p < 0.01)的蛋白水平,但对 NF-kB p65(p = 0.09)和 TLR4(p = 0.20)mRNA 的表达没有影响:本研究的结果表明,定期食用 50 克 PPL 有可能成为治疗 IBD 的一种辅助疗法,从而改善这些患者的生活质量。
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Effects of an Extract of Physalis Peruviana Linnaeus on the Expression of Inflammatory Markers in the Caco-2 Intestinal Epithelium-like Cell Line.

Objective: Physalis Peruviana Linnaeus (PPL) is an herbaceous species characterized by a wide variety of bioactive compounds to which anti-inflammatory properties have been attributed. This makes this fruit a possible complementary therapy for diseases that involve chronic inflammation, such as inflammatory bowel diseases (IBD). In the present study, the effect of a PPL extract on the expression of inflammatory markers in the Caco-2 cell line was evaluated.

Methods: An in vitro gastric digest (50 g PPL pulp) was performed, obtaining an extract that was used to challenge Caco-2 cells for 24 and 72 hours. This extract was characterized by LC-MS/MS. Then, the relative mRNA expression of NF-kB, TLR4, IL-18 and MCP-1 was determined through qRT-PCR and the protein levels of TNF-α, IL-6, IL-8, IL-18 and MCP-1 through Luminex Immunoassay.

Results: From the characterization of the extract, compounds with bioactive potential such as isothiocyanates, indoles and coumarins were found. Treatment of Caco-2 cells with PPL extract (80 µg/ml), particularly for 72 hours, produced a reduction of IL-18 and MCP-1 mRNA expression (p < 0.01), in addition to IL-18 (p < 0.01), IL-8 (p < 0.0001) and MCP-1 (p < 0.01) protein levels, however, no effects on NF-kB p65 (p = 0.09) and TLR4 (p = 0.20) mRNA expression were observed.

Conclusion: The results obtained in this study open the possibility that the regular consumption of 50 g of PPL could constitute a possible complementary therapy for the treatment of IBD, improving the quality of life of these patients.

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