首页> 外文期刊>International Journal of Obesity >Calcipotriol and iBRD9 reduce obesity in Nur77 knockout mice by regulating the gut microbiota, improving intestinal mucosal barrier function
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Calcipotriol and iBRD9 reduce obesity in Nur77 knockout mice by regulating the gut microbiota, improving intestinal mucosal barrier function

机译:Calcipotriol和IBRD9通过调节肠道微生物群,改善肠粘膜屏障功能,减少Nur77敲除小鼠的肥胖

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The orphan nuclear receptor Nur77 is an important factor regulating metabolism. Nur77 knockout mice become obese with age, but the cause of obesity in these mice has not been fully ascertained. We attempted to explain the cause of obesity in Nur77 knockout mice from the perspective of the gut microbiota and to investigate the inhibitory effect of calcipotriol combined with BRD9 inhibitor (iBRD9) on obesity. Eight-week-old wild-type mice and Nur77 knockout C57BL/6J mice were treated with calcipotriol combined with iBRD9 for 12 weeks. Mouse feces were collected and the gut microbiota was assessed by analyzing 16S rRNA gene sequences. The bacterial abundance difference was analyzed, and the intestinal mucosal tight junction protein, antimicrobial peptide, and inflammatory cytokine mRNA levels of the colon and serum LPS and inflammatory cytokine levels were measured. Calcipotriol combined with iBRD9 treatment reduced the body weight and body fat percentage in Nur77 knockout mice. In the gut microbiota of Nur77 knockout mice, the relative abundances of Lachnospiraceae and Prevotellaceae decreased, and Rikenellaceae increased; while Rikenellaceae decreased after treatment (p < 0.05). Correspondingly, the mRNA levels of intestinal mucosal tight junction proteins (occludin (Ocln), claudin3 (Cldn3)) in the colons of Nur77 knockout mice were significantly decreased, and they increased significantly after treatment (p < 0.001). The mRNA levels of inflammatory cytokines (tumor necrosis factor-(TNF-), interleukin-6 (IL-6), and interleukin-1(IL-1)) were significantly increased in Nur77 knockout mice, and TNF-and IL-6 levels were significantly decreased after treatment (p < 0.05, <0.01, or <0.001). The levels of serum LPS, TNF-, and IL-1in Nur77 knockout mice were significantly increased (p < 0.05). Serum LPS, TNF-, and IL-6 levels were significantly decreased after treatment (p < 0.05 or <0.01). Calcipotriol combined with iBRD9 can regulate the gut microbiota, improve intestinal mucosal barrier function, reduce LPS absorption into the blood, and alleviate obesity in Nur77 knockout mice.
机译:孤儿核受体NUR77是调节代谢的重要因素。 Nur77敲门鼠随着年龄的增长而变得肥胖,但这些小鼠的肥胖的原因尚未得到充分确定。我们试图从肠道微生物群的角度解释Nur77淘汰赛小鼠的肥胖原因,并探讨Calcipotriol联合BRD9抑制剂(IBRD9)对肥胖症的抑制作用。用Calcipotriol与IBRD9合并12周,用Calcipotriol治疗八周旧的野生型小鼠和NUR77敲除C57BL / 6J小鼠。收集小鼠粪便,通过分析16S rRNA基因序列来评估肠道微生物酵母。分析了细菌丰度差异,测定了结肠和血清LP和血清LPS和炎症细胞因子水平的肠粘膜紧密结蛋白,抗微生物肽和炎症细胞因子mRNA水平。 Calcipotriol联合IBRD9治疗减少了Nur77敲除小鼠的体重和体脂百分比。在Nur77敲除小鼠的Gut Microbiota中,Lachnospiraceae和Fvootellaceae的相对丰度降低,蓖麻植物增加;虽然治疗后Rikenellaceae降低(P <0.05)。相应地,Nur77敲除小鼠的冒号中肠粘膜紧密结蛋白的mRNA水平(OCCLUDIN(OCLUN),CLDN3))显着降低,处理后显着增加(P <0.001)。 NUR77敲除小鼠和TNF-and IL-6中,炎症细胞因子的mRNA水平(肿瘤坏死因子 - (TNF-),白细胞介素-6(IL-6)和白细胞介素-1(IL-1))显着增加处理后水平显着降低(P <0.05,<0.01或<0.001)。血清LPS,TNF-和IL-1IN NUR77敲除小鼠的水平显着增加(P <0.05)。处理后血清LPS,TNF-和IL-6水平显着降低(P <0.05或<0.01)。 Calcipotriol联合IBRD9可以调节肠道微生物群,改善肠道粘膜屏障功能,降低LPS吸收进入血液,并减轻Nur77敲除小鼠的肥胖。

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