Miranda Carolline Santos, Santana-Oliveira Daiana Araujo, Vasques-Monteiro Isabela Lopes, Dantas-Miranda Nathan Soares, Glauser Jade Sancha de Oliveira, Silva-Veiga Flavia Maria, Souza-Mello Vanessa
Department of Anatomy, Rio de Janeiro State University, Rio de Janeiro 20551030, Brazil.
World J Methodol. 2024 Mar 20;14(1):89723. doi: 10.5662/wjm.v14.i1.89723.
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.
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.
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.
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 expression in the HF16 group, consistent with a completely disarranged intestinal ultrastructure after 16 wk of HFD intake.
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.
饱和脂肪摄入过多会损害肠黏膜的完整性,导致低度炎症、黏膜完整性受损以及肠道通透性增加,从而使脂多糖(LPS)迁移至其他组织。
评估高脂饮食(HFD,脂肪供能占50%)对C57BL/6小鼠肠道微生物群系统发育分布、肠道屏障结构及保护作用的慢性影响(10周和16周时)。
将40只成年雄性小鼠分为四个营养组,字母代表饮食类型(对照和HFD或HF),数字代表饮食给予的时间段(周):10周对照饮食、10周HFD、16周对照饮食、16周HFD。处死后,进行生化、分子和体视学分析。
HF组体重超标,存在肠道菌群失调,闭合蛋白免疫染色逐渐减少,LPS浓度升高。饮食进程使每单位大肠面积杯状细胞数量减少,且在HF16组中表达减少,这与摄入HFD 16周后肠道超微结构完全紊乱一致。
长期摄入HFD在10周或16周后会导致体重超标、肠道菌群失调以及肠道屏障形态和功能改变。杯状细胞数量密度和黏液分泌随时间的减少已成为对抗肥胖驱动的肠道损伤的靶点。