高脂饮食对雄性小鼠肠道屏障的时间依赖性影响

C. S. Miranda, Daiana Araujo Santana-Oliveira, Isabela Macedo Lopes Vasques-Monteiro, Nathan Soares Dantas-Miranda, Jade Sancha de Oliveira Glauser, F. Silva-Veiga, Vanessa Souza-Mello
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摘要

背景 摄入过多饱和脂肪会损害肠道黏膜的完整性,导致低度炎症、黏膜完整性受损和肠道通透性增加,从而导致脂多糖(LPS)迁移到其他组织。目的 评估高脂饮食(HFD)(50% 的能量为脂肪)对 C57BL/6 小鼠肠道微生物群系分布、肠道屏障结构和保护的慢性影响(10 周和 16 周)。方法 将 40 只成年雄性小鼠分为四个营养组,其中字母指的是饮食类型(对照组和高脂饮食组或高脂饮食组),数字指的是饮食给药时间(以周为单位):对照组 10 周,HFD 组 10 周,对照组 16 周,HFD 组 16 周。牺牲后,进行生化、分子和立体学分析。结果 高频组体重超重、肠道菌群失调、闭塞素免疫染色逐渐降低、LPS浓度升高。HF16组每大肠面积的鹅口疮细胞数量和Mucin2表达量在摄入HFD 16周后逐渐减少,肠道超微结构完全紊乱。结论 长期摄入高氟日粮会导致超重、肠道菌群失调以及肠道屏障在 10 或 16 周后发生形态和功能改变。随着时间的推移,鹅口疮细胞数量密度和粘液分泌的减少已成为应对肥胖导致的肠道损伤的目标。
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Time-dependent impact of a high-fat diet on the intestinal barrier of male mice
BACKGROUND Excessive saturated fat intake compromises the integrity of the intestinal mucosa, leading to low-grade inflammation, impaired mucosal integrity, and increased intestinal permeability, resulting in the migration of lipopolysaccharide (LPS) to other tissues. AIM To evaluate the chronic effects (at 10 and 16 wk) of a high-fat diet (HFD) (with 50% energy as fat) on the phylogenetic gut microbiota distribution and intestinal barrier structure and protection in C57BL/6 mice. METHODS Forty adult male mice were divided into four nutritional groups, where the letters refer to the type of diet (control and HFD or HF) and the numbers refer to the period (in weeks) of diet administration: Control diet for 10 wk, HFD for 10 wk, control diet for 16 wk, and HFD for 16 wk. After sacrifice, biochemical, molecular, and stereological analyses were performed. RESULTS The HF groups were overweight, had gut dysbiosis, had a progressive decrease in occludin immunostaining, and had increased LPS concentrations. Dietary progression reduced the number of goblet cells per large intestine area and Mucin2 expression in the HF16 group, consistent with a completely disarranged intestinal ultrastructure after 16 wk of HFD intake. CONCLUSION Chronic HFD intake causes overweight, gut dysbiosis, and morphological and functional alterations of the intestinal barrier after 10 or 16 wk. Time-dependent reductions in goblet cell numerical density and mucus production have emerged as targets for countering obesity-driven intestinal damage.
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