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改性蒙脱石负载益生菌增强定植于黏液缺失肠道并高效清除活性氧用于结肠炎治疗

Modified montmorillonite armed probiotics with enhanced on-site mucus-depleted intestinal colonization and HS scavenging for colitis treatment.

机构信息

Institute of Brain Science and Disease, School of Basic Medicine, Shandong Provincial Key Laboratory of Pathogenesis and Prevention of Neurological Disorders, Qingdao University, Qingdao 266021, PR China; School of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou 450001, PR China.

School of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou 450001, PR China.

出版信息

J Control Release. 2024 Oct;374:140-153. doi: 10.1016/j.jconrel.2024.07.071. Epub 2024 Aug 14.

DOI:10.1016/j.jconrel.2024.07.071
PMID:39117113
Abstract

Inflammatory bowel diseases (IBD) are often associated with dysregulated gut microbiota and excessive inflammatory microenvironment. Probiotic therapy combined with inflammation management is a promising approach to alleviate IBD, but the efficacy is hindered by the inferior colonization of probiotics in mucus-depleted inflammatory bowel segments. Here, we present modified montmorillonite armed probiotic Escherichia coli Nissle 1917 (MMT-Fe@EcN) with enhanced intestinal colonization and hydrogen sulfide (HS) scavenging for synergistic alleviation of IBD. The montmorillonite layer that can protect EcN against environmental assaults in oral delivery and improve on-site colonization of EcN in the mucus-depleted intestinal segment due to its strong adhesive capability and electronegativity, with a 22.6-fold increase in colonization efficiency compared to EcN. Meanwhile, MMT-Fe@EcN can manage inflammation by scavenging HS, which allows for enhancing probiotic viability and colonization for restoring the gut microbiota. As a result, MMT-Fe@EcN exhibits extraordinary therapeutic effects in the dextran sulfate sodium-induced mouse colitis models, including alleviating intestinal inflammation and restoring disrupted intestinal barrier function, and gut microbiota. These findings provide a promising strategy for clinical IBD treatment and potentially other mucus-depletion-related diseases.

摘要

炎症性肠病(IBD)常与肠道菌群失调和过度炎症微环境有关。益生菌治疗联合炎症管理是缓解 IBD 的一种很有前途的方法,但由于益生菌在黏液耗竭的炎症肠段中的定植能力差,其疗效受到限制。在这里,我们提出了一种经过改良的蒙脱石武装益生菌大肠杆菌 Nissle 1917(MMT-Fe@EcN),它具有增强的肠道定植能力和硫化氢(HS)清除能力,可协同缓解 IBD。蒙脱石层可以保护 EcN 免受口服递送过程中的环境攻击,并由于其强大的粘附能力和电负性,提高 EcN 在黏液耗竭肠段中的原位定植能力,定植效率比 EcN 提高了 22.6 倍。同时,MMT-Fe@EcN 可以通过清除 HS 来管理炎症,从而提高益生菌的活力和定植能力,以恢复肠道菌群。结果,MMT-Fe@EcN 在葡聚糖硫酸钠诱导的小鼠结肠炎模型中表现出了非凡的治疗效果,包括缓解肠道炎症和恢复受损的肠道屏障功能和肠道菌群。这些发现为临床 IBD 治疗提供了一种很有前途的策略,也可能为其他与黏液耗竭相关的疾病提供了一种策略。

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