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藏红花花瓣提取物处理对Caco-2/人白血病单核细胞共培养模型中细胞因子诱导的氧化应激和炎症的生物学反应

Biological Response of Treatment with Saffron Petal Extract on Cytokine-Induced Oxidative Stress and Inflammation in the Caco-2/Human Leukemia Monocytic Co-Culture Model.

作者信息

De Cecco Federica, Franceschelli Sara, Panella Valeria, Maggi Maria Anna, Bisti Silvia, Bravo Nuevo Arturo, D'Ardes Damiano, Cipollone Francesco, Speranza Lorenza

机构信息

Department of Medicine and Aging Sciences, University "G. d'Annunzio" Chieti-Pescara, Via dei Vestini 31, 66100 Chieti, Italy.

Uda-TechLab, Research Center, University "G. d'Annunzio" Chieti-Pescara, 66100 Chieti, Italy.

出版信息

Antioxidants (Basel). 2024 Oct 17;13(10):1257. doi: 10.3390/antiox13101257.

DOI:10.3390/antiox13101257
PMID:39456510
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11504373/
Abstract

The pathogenesis of Inflammatory Bowel Disease (IBD) involves complex mechanisms, including immune dysregulation, gut microbiota imbalances, oxidative stress, and defects in the gastrointestinal mucosal barrier. Current treatments for IBD often have significant limitations and adverse side effects, prompting a search for alternative therapeutic strategies. Natural products with anti-inflammatory and antioxidant properties have demonstrated potential for IBD management. There is increasing interest in exploring food industry waste as a source of bioactive molecules with healthcare applications. In this study, a co-culture system of Caco-2 cells and PMA-differentiated THP-1 macrophages was used to simulate the human intestinal microenvironment. Inflammation was induced using TNF-α and IFN-γ, followed by treatment with Saffron Petal Extract (SPE). The results demonstrated that SPE significantly attenuated oxidative stress and inflammation by downregulating the expression of pro-inflammatory mediators such as iNOS, COX-2, IL-1β, and IL-6 via modulation of the NF-κB pathway. Given that NF-κB is a key regulator of macrophage-driven inflammation, our findings support further investigation of SPE as a potential complementary therapeutic agent for IBD treatment.

摘要

炎症性肠病(IBD)的发病机制涉及复杂的机制,包括免疫失调、肠道微生物群失衡、氧化应激以及胃肠道黏膜屏障缺陷。IBD的现有治疗方法往往存在显著局限性和不良副作用,这促使人们寻找替代治疗策略。具有抗炎和抗氧化特性的天然产物已显示出治疗IBD的潜力。人们越来越有兴趣探索食品工业废料,将其作为具有医疗保健应用的生物活性分子来源。在本研究中,使用Caco-2细胞和经佛波酯(PMA)分化的THP-1巨噬细胞的共培养系统来模拟人类肠道微环境。使用肿瘤坏死因子-α(TNF-α)和干扰素-γ(IFN-γ)诱导炎症,随后用藏红花花瓣提取物(SPE)进行处理。结果表明,SPE通过调节核因子-κB(NF-κB)途径下调诱导型一氧化氮合酶(iNOS)、环氧化酶-2(COX-2)、白细胞介素-1β(IL-1β)和白细胞介素-6(IL-6)等促炎介质的表达,显著减轻了氧化应激和炎症。鉴于NF-κB是巨噬细胞驱动的炎症的关键调节因子,我们的研究结果支持进一步研究SPE作为IBD治疗的潜在辅助治疗剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb48/11504373/5b8512fae625/antioxidants-13-01257-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb48/11504373/98c65db124a2/antioxidants-13-01257-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb48/11504373/6327c3efb26e/antioxidants-13-01257-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb48/11504373/5b8512fae625/antioxidants-13-01257-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb48/11504373/98c65db124a2/antioxidants-13-01257-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb48/11504373/720bf307ac0d/antioxidants-13-01257-g002.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb48/11504373/c2983298d209/antioxidants-13-01257-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb48/11504373/58caea489d99/antioxidants-13-01257-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb48/11504373/1024ea5894fa/antioxidants-13-01257-g007.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb48/11504373/5b8512fae625/antioxidants-13-01257-g009.jpg

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