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表没食子儿茶素-3-没食子酸酯(EGCG)作为治疗炎症性肠病辅助药物的潜力

The Potential of Epigallocatechin-3-gallate (EGCG) as Complementary Medicine for the Treatment of Inflammatory Bowel Disease.

作者信息

Schnur Sabrina, Hans Fabian, Dehne Annika, Osti Janina, Schneemann Malte-Ole, Schneider Marc, Hittinger Marius

机构信息

Department of Pharmacy, Biopharmaceutics and Pharmaceutical Technology, Saarland University, 66123 Saarbrücken, Germany.

Department of Drug Delivery, PharmBioTec Research and Development GmbH, 66123 Saarbrücken, Germany.

出版信息

Pharmaceuticals (Basel). 2023 May 14;16(5):748. doi: 10.3390/ph16050748.

Abstract

Complementary and alternative medicine has the potential to enrich conventional therapy to improve the treatment of various diseases. Patients that suffer from inflammatory bowel disease, which requires a constant need for medication, have to deal with the adverse effects of repeated application. Natural products such as Epigallocatechin-3-gallate (EGCG) possess the potential to improve symptoms of inflammatory diseases. We investigated the efficacy of EGCG on an inflamed co-culture model simulating IBD and compared it to the efficacies of four commonly applied active pharmaceutical ingredients. EGCG (200 µg/mL) strongly stabilized the TEER value of the inflamed epithelial barrier to 165.7 ± 4.6% after 4 h. Moreover, the full barrier integrity was maintained even after 48 h. This corresponds to the immunosuppressant 6-Mercaptopurin and the biological drug Infliximab. The EGCG treatment significantly decreased the release of the pro-inflammatory cytokines IL-6 (to 0%) and IL-8 (to 14.2%), similar to the effect of the corticosteroid Prednisolone. Therefore, EGCG has a high potential to be deployed as complementary medicine in IBD. In future studies, the improvement of EGCG stability is a key factor in increasing the bioavailability in vivo and fully harnessing the health-improving effects of EGCG.

摘要

补充和替代医学有潜力丰富传统疗法,以改善各种疾病的治疗。患有炎症性肠病的患者需要持续用药,不得不应对反复用药的不良反应。表没食子儿茶素-3-没食子酸酯(EGCG)等天然产物具有改善炎症性疾病症状的潜力。我们研究了EGCG对模拟炎症性肠病的炎症共培养模型的疗效,并将其与四种常用活性药物成分的疗效进行了比较。EGCG(200µg/mL)在4小时后将炎症上皮屏障的跨上皮电阻值强烈稳定至165.7±4.6%。此外,即使在48小时后,完整的屏障完整性仍得以维持。这与免疫抑制剂6-巯基嘌呤和生物药物英夫利昔单抗相当。EGCG治疗显著降低了促炎细胞因子IL-6(降至0%)和IL-8(降至14.2%)的释放,类似于皮质类固醇泼尼松龙的效果。因此,EGCG作为炎症性肠病的补充药物具有很大潜力。在未来的研究中,提高EGCG的稳定性是提高其体内生物利用度并充分发挥EGCG健康改善作用的关键因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5323/10224516/312522530565/pharmaceuticals-16-00748-g001.jpg

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