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Pectic polysaccharides from unripe and mature kiwifruit alleviate ulcerative colitis by modulating gut microbiota and restoring the intestinal barrier

文献类型： 外文期刊

作者： Jiang, Kai-Xin 1 ; Geng, Jin-Lei 1 ; Yuan, Qin 2 ; Li, Jie 3 ; Liu, Wen 2 ; Liu, Hong-Yan 3 ; Hu, Yi-Chen 1 ; Zou, Liang 1 ; Wang, Shengpeng 2 ; Wu, Ding-Tao 1 ;

作者机构： 1.Chengdu Univ, Minist Agr & Rural Affairs, Sch Food & Biol Engn, Key Lab Coarse Cereal Proc, Chengdu 610106, Sichuan, Peoples R China

2.Univ Macau, Inst Chinese Med Sci, State Key Lab Qual Res Chinese Med, Macau, Peoples R China

3.Chinese Acad Agr Sci, Inst Urban Agr, Natl Agr Sci & Technol Ctr, Res Ctr Plants & Human Hlth, Chengdu 610213, Peoples R China

4.Chengdu Agr Coll, Chengdu 611130, Sichuan, Peoples R China

5.Univ Macau, Macao Ctr Res & Dev Chinese Med, Macau, Peoples R China

6.Chengdu Univ, Inst Adv Study, Chengdu 610106, Sichuan, Peoples R China

关键词： Kiwifruit pectic polysaccharide; Rhamnogalacturonan I; Intestinal inflammation; Intestinal barrier function; Gut microbiota

期刊名称：FOOD BIOSCIENCE （ 影响因子：5.9； 五年影响因子：6.1 ）

ISSN： 2212-4292

年卷期： 2025 年 71 卷

页码：

收录情况： SCI

摘要： Thinned unripe kiwifruit, a significant byproduct of commercial kiwifruit production, contains abundant pectic polysaccharides comparable to mature kiwifruit. Although acidic heteropolysaccharides from mature kiwifruit exhibit potent anti-inflammatory activity, the protective effects of unripe kiwifruit-derived pectic polysaccharides against ulcerative colitis (UC) remain unclear, ultimately limiting their potential utilizations. Therefore, to bridge this knowledge gap and facilitate their utilization, the chemical structures and anti-UC effects of two pectic polysaccharides, TKP (from unripe kiwifruit) and MKP (from mature kiwifruit), were systematically studied and compared. Results demonstrated that TKP and MKP share nearly identical primary chemical structures, predominantly comprising homogalacturonan (HG) and rhamnogalacturonan I (RG-I) domains. Particularly, TKP exhibited a longer side chain length (14.37 vs. 8.21) and higher RG-I content (73.62 mol % vs. 50.02 mol%) than MKP. Furthermore, both TKP and MKP significantly alleviated dextran sulfate sodium (DSS)-induced UC in mice. Notably, TKP exhibited superior effects to MKP in several aspects, such as enhanced butyrate production, more effective restoration of goblet cell populations, enhanced upregulation of tight junction protein ZO-1, and greater reduction in pro-inflammatory cytokines (IL-1 beta, IL-6, and TNF-alpha). Both TKP and MKP effectively suppressed pathogenic bacteria (e.g., Escherichia-Shigella and Oscillibacter) while promoted beneficial bacteria (e.g., Akkermansia and Bacteroides). Notably, TKP significantly and selectively enhanced Paraprevotella growth, an effect not observed within MKP. These differential effects between TKP and MKP may be linked to their structural differences. Collectively, these findings provide valuable insights to develop TKP as a promising functional food or ingredient for preventing and ameliorating intestinal inflammatory disorders.

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