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青黛通过改变肠道微生物群减轻葡聚糖硫酸钠诱导的大鼠结肠炎。

Indigo Naturalis Alleviates Dextran Sulfate Sodium-Induced Colitis in Rats via Altering Gut Microbiota.

作者信息

Sun Zhongmei, Li Junxiang, Dai Yi, Wang Wenting, Shi Rui, Wang Zhibin, Ding Panghua, Lu Qiongqiong, Jiang Hui, Pei Wenjing, Zhao Xingjie, Guo Yi, Liu Jiali, Tan Xiang, Mao Tangyou

机构信息

Graduate School, Beijing University of Chinese Medicine, Beijing, China.

Department of Gastroenterology, Dongfang Hospital, Beijing University of Chinese Medicine, Beijing, China.

出版信息

Front Microbiol. 2020 Apr 30;11:731. doi: 10.3389/fmicb.2020.00731. eCollection 2020.

DOI:10.3389/fmicb.2020.00731
PMID:32425906
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7203728/
Abstract

Ulcerative colitis is a gastrointestinal disorder intricately associated with intestinal dysbiosis, but effective treatments are currently limited. Indigo naturalis, a traditional Chinese medicine derived from indigo plants, has been widely used in the treatment of ulcerative colitis. However, the specific mechanisms have not yet been identified. Accordingly, in this study, we evaluated the effects and mechanisms of indigo naturalis on dextran sulfate sodium (DSS)-induced colitis in rats. Our results showed that indigo naturalis potently alleviated DSS-induced colitis in rats, and reversed DSS-induced intestinal dysbiosis using bacterial 16S rRNA amplicon sequencing. The protective effects of indigo naturalis were gut microbiota dependent, as demonstrated by antibiotic treatments and fecal microbiota transplantation. Depletion of the gut microbiota through a combination of antibiotic treatments blocked the anti-inflammatory effect of indigo naturalis on the DSS-induced colitis, and the recipients of the gut microbiota from indigo naturalis-treated rats displayed a significantly attenuated intestinal inflammation, which was actively responsive to therapeutic interventions with indigo naturalis. Notably, supplement with indigo naturalis greatly increased the levels of feces butyrate, which was positively correlated with the relative abundances of and . We further showed that indigo naturalis-dependent attenuation of colitis was associated with elevated expression of short-chain fatty acid-associated receptors GPR41 and GPR43. Collectively, these results suggested that indigo naturalis alleviates DSS-induced colitis in rats through a mechanism of the microbiota-butyrate axis, particularly alterations in and abundances, and target-specific microbial species may have unique therapeutic promise for ulcerative colitis.

摘要

溃疡性结肠炎是一种与肠道菌群失调复杂相关的胃肠道疾病,但目前有效的治疗方法有限。青黛,一种从靛蓝植物中提取的传统中药,已被广泛用于治疗溃疡性结肠炎。然而,其具体机制尚未明确。因此,在本研究中,我们评估了青黛对葡聚糖硫酸钠(DSS)诱导的大鼠结肠炎的影响及机制。我们的结果表明,青黛能有效减轻DSS诱导的大鼠结肠炎,并通过细菌16S rRNA扩增子测序逆转DSS诱导的肠道菌群失调。青黛的保护作用依赖于肠道微生物群,抗生素治疗和粪便微生物群移植证明了这一点。通过联合抗生素治疗耗尽肠道微生物群可阻断青黛对DSS诱导的结肠炎的抗炎作用,而接受来自青黛治疗大鼠的肠道微生物群的受体表现出明显减轻的肠道炎症,且对青黛的治疗干预有积极反应。值得注意的是,补充青黛可显著提高粪便丁酸盐水平,这与[具体菌种1]和[具体菌种2]的相对丰度呈正相关。我们进一步表明,青黛依赖的结肠炎减轻与短链脂肪酸相关受体GPR41和GPR43的表达升高有关。总体而言,这些结果表明,青黛通过微生物群 - 丁酸盐轴机制减轻DSS诱导的大鼠结肠炎,特别是[具体菌种1]和[具体菌种2]丰度的改变,并且特定的目标微生物物种可能对溃疡性结肠炎具有独特的治疗前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1d9/7203728/c2146ad18010/fmicb-11-00731-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1d9/7203728/b3e93c84a421/fmicb-11-00731-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1d9/7203728/f3990ca210fa/fmicb-11-00731-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1d9/7203728/51900ac2dc88/fmicb-11-00731-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1d9/7203728/2f0e2dee1c38/fmicb-11-00731-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1d9/7203728/ffb8ade23baf/fmicb-11-00731-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1d9/7203728/c2146ad18010/fmicb-11-00731-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1d9/7203728/b3e93c84a421/fmicb-11-00731-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1d9/7203728/f3990ca210fa/fmicb-11-00731-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1d9/7203728/51900ac2dc88/fmicb-11-00731-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1d9/7203728/2f0e2dee1c38/fmicb-11-00731-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1d9/7203728/ffb8ade23baf/fmicb-11-00731-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1d9/7203728/c2146ad18010/fmicb-11-00731-g006.jpg

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