Chen Li, Tang Junrui, Xia Yanglin, Wang Jie, Xia Li-Na
School of Health Preservation and Rehabilitation, Chengdu University of TCM, Shierqiao Road, Chengdu, 610075, Sichuan, People's Republic of China.
Key Laboratory of Traditional Chinese Medicine Regimen and Health Industry Development, State Administration of TCM, Chengdu, 610075, Sichuan, People's Republic of China.
Sci Rep. 2025 Jan 30;15(1):3826. doi: 10.1038/s41598-025-88291-y.
Despite the established link between chronic high salt diet (HSD) and an increase in gut inflammation, the effect of HSD on the integrity of the intestinal barrier remains understudied. The present study aims to investigate the impact of HSD on the intestinal barrier in rats, encompassing its mechanical, mucous, and immune components. Expression levels of intestinal tight junction proteins and mucin-2 (MUC2) in SD rats were analyzed using immunofluorescence. The expression area of goblet cell mucopolysaccharides was assessed through PAS staining. Additionally, serum D-lactic acid, SIgA, β-defensin, and colonic tissue cytokines were measured using ELISA. Rats fed with HSD exhibited decreased expression of tight junction proteins, particularly Occludin, resulting in impairment of the intestinal epithelial barrier and an elevated serum D-lactic acid level. Furthermore, a notable reduction in the expression of goblet cell mucopolysaccharides, along with lower β-defensin and MUC2 levels, was observed. Notably, the SIgA and immune-related cytokines were significantly reduced in the HSD group. HSD disrupts the intestinal barrier in rats, leading to increased permeability and the entry of inflammatory factors into the bloodstream. This finding suggests that HSD may contribute to the pathogenesis of various diseases.
尽管长期高盐饮食(HSD)与肠道炎症增加之间的关联已得到证实,但HSD对肠道屏障完整性的影响仍研究不足。本研究旨在探讨HSD对大鼠肠道屏障的影响,包括其机械、黏液和免疫成分。采用免疫荧光法分析SD大鼠肠道紧密连接蛋白和黏蛋白-2(MUC2)的表达水平。通过PAS染色评估杯状细胞黏多糖的表达面积。此外,使用ELISA检测血清D-乳酸、SIgA、β-防御素和结肠组织细胞因子。喂食HSD的大鼠紧密连接蛋白表达降低,尤其是闭合蛋白,导致肠上皮屏障受损,血清D-乳酸水平升高。此外,还观察到杯状细胞黏多糖表达显著降低,同时β-防御素和MUC2水平降低。值得注意的是,HSD组的SIgA和免疫相关细胞因子显著减少。HSD破坏大鼠肠道屏障,导致通透性增加和炎症因子进入血液。这一发现表明HSD可能促成各种疾病的发病机制。