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瑞因通过肠道微生物群调节宿主嘌呤代谢进而改善实验性结肠炎。

Rhein modulates host purine metabolism in intestine through gut microbiota and ameliorates experimental colitis.

机构信息

Jiangsu Key Laboratory for Pharmacolgy and Safety Evaluation of Chinese Materia Medica, School of Pharmacy, Nanjing University of Chinese Medicine, Nanjing 210023, PR China.

State Key Laboratory Cultivation Base for TCM Quality and Efficacy, Nanjing University of Chinese Medicine, Nanjing University of Chinese Medicine, Nanjing 210023, PR China.

出版信息

Theranostics. 2020 Aug 29;10(23):10665-10679. doi: 10.7150/thno.43528. eCollection 2020.

Abstract

Gut microbiota, which plays a crucial role in inflammatory bowel diseases (IBD), might have therapeutic benefits for ulcerative colitis or Crohn's disease. Targeting gut microbiota represents a new treatment strategy for IBD patients. Rhein is one of the main components of rhubarb and exhibits poor oral bioavailability but still exerts anti-inflammatory effects in some diseases. Therefore, we investigated the effect of rhein on colitis and studied its possible mechanisms. The chronic mouse colitis model was induced by four rounds of 2% dextran sulfate sodium (DSS) treatment. The mice were treated with 50 mg/kg and 100 mg/kg rhein daily, body weight, colon length, histological score, inflammatory cytokines in serum or intestine, and fecal lipocalin 2 concentration were determined. Th17 cell, Th1 cell and Th2 cell infiltration in the mesenteric lymph node were analyzed by flow cytometry. Metabolic profiles were collected by non-targeted metabolomics and key metabolic pathways were identified using MetaboAnalyst 4.0. We also assessed intestinal barrier permeability and performed 16s rDNA sequencing. was cultured, and fecal microbiota transplantation (FMT) was employed to evaluate the contribution of gut microbiota. Rhein could significantly alleviate DSS-induced chronic colitis. Uric acid was identified as a crucial modulator of colitis and rhein treatment led to decreased uric acid levels. We determined that rhein changed purine metabolism indirectly, while the probiotic was involved in the regulation of host metabolism. Uric acid resulted in a worsened intestinal barrier, which could be rescued by rhein. We further confirmed that rhein-treated gut microbiota was sufficient to relieve DSS-induced colitis by FMT. We showed that rhein could modulate gut microbiota, which indirectly changed purine metabolism in the intestine and subsequently alleviated colitis. Our study has identified a new approach to the clinical treatment of colitis.

摘要

肠道微生物群在炎症性肠病(IBD)中发挥着关键作用,可能对溃疡性结肠炎或克罗恩病有治疗益处。针对肠道微生物群代表了 IBD 患者的一种新的治疗策略。大黄酸是大黄的主要成分之一,口服生物利用度差,但在某些疾病中仍具有抗炎作用。因此,我们研究了大黄酸对结肠炎的影响及其可能的机制。采用 4 轮 2%葡聚糖硫酸钠(DSS)处理诱导慢性小鼠结肠炎模型。用 50mg/kg 和 100mg/kg 大黄酸每天处理小鼠,测定体重、结肠长度、组织学评分、血清或肠道中的炎症细胞因子和粪便脂联素 2 浓度。通过流式细胞术分析肠系膜淋巴结中的 Th17 细胞、Th1 细胞和 Th2 细胞浸润。通过非靶向代谢组学收集代谢谱,并使用 MetaboAnalyst 4.0 确定关键代谢途径。我们还评估了肠道屏障通透性并进行了 16s rDNA 测序。培养 ,并进行粪便微生物群移植(FMT)以评估肠道微生物群的贡献。大黄酸可显著缓解 DSS 诱导的慢性结肠炎。尿酸被确定为结肠炎的关键调节剂,大黄酸治疗导致尿酸水平降低。我们确定大黄酸间接改变嘌呤代谢,而益生菌 参与宿主代谢的调节。尿酸导致肠道屏障恶化,大黄酸可挽救。我们进一步证实,大黄酸处理的肠道微生物群通过 FMT 足以缓解 DSS 诱导的结肠炎。我们表明,大黄酸可以调节肠道微生物群,这间接改变肠道中的嘌呤代谢,从而缓解结肠炎。我们的研究为结肠炎的临床治疗提供了一种新方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e61b/7482825/436ec0f34197/thnov10p10665g001.jpg

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