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预防性给予氧化镁可预防葡聚糖硫酸钠诱导的小鼠结肠损伤。

Prophylactic Administration of Magnesium Oxide Prevents Dextran Sulfate Sodium-Induced Colonic Injury in Mice.

机构信息

Department of Environmental Biochemistry, Division of Biological Sciences, Kyoto Pharmaceutical University.

Technical Development Division, Ako Kasei, Co., Ltd.

出版信息

Biol Pharm Bull. 2022;45(9):1312-1320. doi: 10.1248/bpb.b22-00278.

Abstract

We previously demonstrated that per os administration and ad libitum ingestion of a magnesium chloride (MgCl) solution had a prophylactic effect on dextran sulfate sodium (DSS)-induced colitis in mice, magnesium being considered to play a role in this preferable action. Magnesium oxide (MgO) is a commercially available magnesium formulation, but whether or not it prevents development of colitis is unknown. In this study, we investigated the effect of MgO administration on development of colitis in DSS-treated male C57BL/6J mice. Experimental colitis was induced by ad libitum ingestion of 1% (w/v) DSS, and the colitis severity was evaluated by disease activity index (DAI) scores, histological assessment and colonic expression of inflammatory cytokines. A 1 mg/mL MgO solution was administered to mice through ad libitum ingestion from a day before DSS treatment to the end of the experimental period of 12 d. In addition, the effects of DSS, MgO and their combination on the gut microbiota were investigated by 16S ribosomal RNA metagenome analysis. DSS-induced elevation of DAI scores was partially but significantly decreased by MgO administration, while MgO administration had no apparent effect on the shortened colonic length, elevated mRNA expression of colonic interleukin-1β and tumor necrosis factor-α, increased accumulation of colonic mast cells, or altered features of the gut microbiota in DSS-treated mice. Overall, we demonstrated that MgO had a prophylactic effect on the development of colitis in DSS-treated mice by preventing histological colonic damage, but not colonic inflammation or alteration of the gut microbiota.

摘要

我们之前证明,经口给予并随意摄入氯化镁(MgCl)溶液对葡聚糖硫酸钠(DSS)诱导的小鼠结肠炎具有预防作用,镁被认为在此优选作用中发挥作用。氧化镁(MgO)是一种市售的镁制剂,但它是否能预防结肠炎的发生尚不清楚。在这项研究中,我们研究了 MgO 给药对 DSS 处理的雄性 C57BL/6J 小鼠结肠炎发展的影响。通过随意摄入 1%(w/v)DSS 诱导实验性结肠炎,并通过疾病活动指数(DAI)评分、组织学评估和结肠炎性细胞因子表达来评估结肠炎的严重程度。通过随意摄入,从 DSS 处理前一天到实验结束的 12 天内,将 1mg/mL 的 MgO 溶液给予小鼠。此外,通过 16S 核糖体 RNA 宏基因组分析研究了 DSS、MgO 及其组合对肠道微生物群的影响。MgO 给药部分但显著降低了 DSS 诱导的 DAI 评分升高,而 MgO 给药对缩短的结肠长度、结肠白细胞介素-1β和肿瘤坏死因子-αmRNA 表达升高、结肠肥大细胞积累增加或 DSS 处理小鼠的肠道微生物群特征没有明显影响。总体而言,我们证明了 MgO 通过防止组织学结肠损伤对 DSS 处理小鼠的结肠炎发展具有预防作用,但对结肠炎症或肠道微生物群的改变没有作用。

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