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莪术通过调节肠道菌群和代谢物减轻 DSS 诱导的结肠炎。

Rhizoma Attenuates DSS-Induced Colitis by Regulating Intestinal Flora and Metabolites.

机构信息

College of Pharmacy, Hubei University of Chinese Medicine, Wuhan 430065, P. R. China.

Center for Hubei TCM Processing Technology Engineering, Wuhan 430065, P. R. China.

出版信息

Am J Chin Med. 2022;50(2):525-552. doi: 10.1142/S0192415X22500203. Epub 2022 Feb 3.

DOI:10.1142/S0192415X22500203
PMID:35114907
Abstract

(Thunb.) DC. is a herb widely used traditionally for the treatment of gastrointestinal diseases such as gastric ulcer, spleen deficiency, and diarrhea. In China, people fry raw (SCZ) together with wheat bran to make bran-fried (FCZ). Ancient Chinese texts have documented that FCZ can enhance the function of regulating the intestines and stomach. Nevertheless, the effect and mechanism of SCZ and FCZ on ulcerative colitis (UC) are still unclear. The aim of this study was to compare the therapeutic effects of SCZ and FCZ and their mechanisms on dextran sulfate sodium (DSS)-induced UC in mice. The chemical constituents of SCZ and FCZ were analyzed using high-performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) with six reference compounds. The effects of SCZ and FCZ were investigated based on their effects on weight loss, disease activity index (DAI) score, colon length shortening, goblet cell loss, and pathological changes using the colons from a mouse model of DSS-induced UC. The effects of SCZ and FCZ on levels of the inflammatory cytokines (tumor necrosis factor-[Formula: see text], interleukin-6, interleukin-1[Formula: see text], mucoprotein (MUC2), tight protein (ZO-1, occludin), and the activation of macrophages were determined using immunohistochemistry (IHC) and immunofluorescence (IF). 16s RNA sequencing technology was used to detect the composition of the intestinal flora in each group. Nontargeted metabonomics was used to detect the serum metabolite levels of mice in each group. Pearson analysis was used to determine the correlation between the intestinal flora, metabolites, and pathological indices. Reverse transcription-polymerase chain reaction was used to detect the genes of different metabolite-related enzymes. A pseudogerm free (PGF) mouse model was used to verify whether the effect of SCZ and FCZ in UC depends on the regulation of intestinal flora. SCZ and FCZ could inhibit weight loss and decrease the DAI score, colon length shortening, goblet cell loss, and the extent of pathological changes in the colons of mice with DSS-induced colitis. Moreover, SCZ and FCZ inhibited the decrease in MUC2, ZO-1, occludin, production of pro-inflammatory factors, and activation of pro-inflammatory macrophages in colonic tissue. The effect of FCZ was better than that of SCZ. SCZ and FCZ not only inhibited the abundance of harmful bacteria and increased the abundance of beneficial bacteria, but also regulated the metabolism of disease-related metabolites such as amino acid and cholesterol metabolism. Both preparations inhibited the gene expression (Slc6A7, PRODH, Sdsl, HMGCR, SREBP-2) of different metabolite-related enzymes. In the PGF mouse model, the above effects were not observed. Rhizoma Atractylodes was effective in alleviating DSS-induced UC in mice, and FCZ was found to be superior to SCZ. The mechanism of action of FCZ and SCZ is mainly related to the regulation of intestinal flora and their associated metabolites.

摘要

(Thunb.)DC. 是一种草药,传统上广泛用于治疗胃肠道疾病,如胃溃疡、脾虚和腹泻。在中国,人们将生 (SCZ) 和麦麸一起炒制成麸炒 (FCZ)。古代文献记载,FCZ 能增强调节肠胃的功能。然而,SCZ 和 FCZ 对溃疡性结肠炎(UC)的作用和机制仍不清楚。本研究旨在比较 SCZ 和 FCZ 对葡聚糖硫酸钠(DSS)诱导的 UC 小鼠的治疗效果及其机制。采用高效液相色谱-串联质谱法(HPLC-MS/MS)结合 6 种对照化合物分析 SCZ 和 FCZ 的化学成分。通过观察 DSS 诱导 UC 小鼠的体重减轻、疾病活动指数(DAI)评分、结肠缩短、杯状细胞丢失和组织病理学变化,研究 SCZ 和 FCZ 的作用。采用免疫组化(IHC)和免疫荧光(IF)技术检测 SCZ 和 FCZ 对炎症细胞因子(肿瘤坏死因子-[Formula: see text]、白细胞介素-6、白细胞介素-1[Formula: see text]、粘蛋白(MUC2)、紧密蛋白(ZO-1、occludin)和巨噬细胞活化的影响。采用 16s RNA 测序技术检测各组肠道菌群组成。采用非靶向代谢组学检测各组小鼠血清代谢物水平。采用 Pearson 分析确定肠道菌群、代谢物与病理指标的相关性。采用逆转录-聚合酶链反应检测不同代谢物相关酶的基因。采用无菌(PGF)小鼠模型验证 SCZ 和 FCZ 在 UC 中的作用是否依赖于肠道菌群的调节。SCZ 和 FCZ 可抑制体重减轻,降低 DAI 评分、结肠缩短、杯状细胞丢失和 DSS 诱导结肠炎小鼠结肠组织的病理变化程度。此外,SCZ 和 FCZ 抑制了 MUC2、ZO-1、occludin 的减少、促炎因子的产生和促炎巨噬细胞的激活。FCZ 的作用优于 SCZ。SCZ 和 FCZ 不仅抑制了有害菌的丰度,增加了有益菌的丰度,还调节了疾病相关代谢物(如氨基酸和胆固醇代谢)的代谢。两种制剂均抑制了不同代谢物相关酶的基因表达(Slc6A7、PRODH、Sdsl、HMGCR、SREBP-2)。在 PGF 小鼠模型中,未观察到上述作用。白术对 DSS 诱导的 UC 小鼠有缓解作用,且 FCZ 优于 SCZ。FCZ 和 SCZ 的作用机制主要与肠道菌群及其相关代谢物的调节有关。

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