研究报告

合生元对盐酸洛哌丁胺诱导便秘小鼠肠道菌群和短链脂肪酸的影响

  • 卢少帅 ,
  • 马微微 ,
  • 张紫薇 ,
  • 徐瑞鑫 ,
  • 黄莉莉
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  • 1(黑龙江中医药大学 药学院,黑龙江 哈尔滨,150006)
    2(长春金赛药业有限责任公司,吉林 长春,130015)
第一作者:硕士研究生(黄莉莉教授为通信作者,E-mail:908668195@qq.com)

收稿日期: 2025-09-18

  修回日期: 2026-01-06

  网络出版日期: 2026-09-10

基金资助

国家自然科学基金项目(32472302);黑龙江省自然科学基金-联合引导(LH2019H106);黑龙江省省属本科高校“优秀青年教师基础研究计划”(YQJH2023152)

Modulation of gut microbiota and short-chain fatty acids by a specific synbiotic in mice with loperamide hydrochloride-induced constipation

  • LU Shaoshuai ,
  • MA Weiwei ,
  • ZHANG Ziwei ,
  • XU Ruixin ,
  • HUANG Lili
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  • 1(College of Pharmacy, Heilongjiang University of Chinese Medicine, Harbin 150006, China)
    2(Changchun Jinsai Pharmaceutical Co.Ltd., Changchun 130015, China)

Received date: 2025-09-18

  Revised date: 2026-01-06

  Online published: 2026-09-10

摘要

基于前期研究证实该合生元具有润肠通便功能的基础,该研究旨在从微生态角度深入探究由植物乳植杆菌CCFM8661、动物双歧杆菌乳亚种XLTG11与低聚木糖(xylooligosaccharide,XOS)组成的合生元对便秘小鼠肠道菌群结构及短链脂肪酸(short chain fatty acids,SCFAs)代谢的调节作用,并分析其剂量-效应关系。根据前期功能实验确定的剂量范围,将ICR小鼠分为空白组、模型组及低、中、高剂量合生元组。灌胃14 d后建立便秘模型,收集粪便样本进行宏基因组测序和SCFAs分析。合生元干预能剂量依赖性地调节肠道菌群结构,各剂量组均提升了双歧杆菌属(Bifidobacterium)、粪杆菌属(Faecalibaculum)等有益菌属丰度,并降低了丁酸单胞菌属(Butyricimonas)等菌属丰度。α和β多样性分析显示,中剂量干预在恢复菌群多样性和群落结构方面表现出最佳趋势,而高剂量干预则引起了ACE指数与Obs指数的显著降低(P<0.05)。SCFAs分析表明,低剂量与中剂量组接近于空白组,高剂量组发生了显著变化。该合生元可通过重塑肠道菌群结构及影响SCFAs代谢缓解便秘。综合菌群结构稳态与代谢功能指标,中剂量(3×106 CFU+2 mg XOS)显示出更优的调节潜力。

本文引用格式

卢少帅 , 马微微 , 张紫薇 , 徐瑞鑫 , 黄莉莉 . 合生元对盐酸洛哌丁胺诱导便秘小鼠肠道菌群和短链脂肪酸的影响[J]. 食品与发酵工业, 2026 , 52(16) : 80 -88 . DOI: 10.13995/j.cnki.11-1802/ts.044538

Abstract

Previous studies confirmed the laxative effect of this synbiotic.Building on this, this study investigated its dose-dependent effects on gut microbiota and short-chain fatty acids (SCFAs) in constipated mice from a microecological perspective.A synbiotic containing Lactiplantibacillus plantarum CCFM8661, Bifidobacterium animalis subsp.lactis XLTG11, and xylooligosaccharides (XOS) was administered to ICR mice at low, medium, and high doses for 14 days.Constipation was then induced with loperamide hydrochloride.Fecal samples were analyzed via metagenomic sequencing and SCFA profiling.Synbiotic intervention dose-dependently modulated gut microbiota.All doses increased beneficial genera like Bifidobacterium and Faecalibaculum while reducing Butyricimonas.Medium-dose intervention best restored microbial diversity and structure, whereas high-dose significantly lowered ACE and observed species indices (P<0.05).SCFA profiles in low- and medium-dose groups resembled the blank group, but the high-dose group showed significant changes.This synbiotic alleviates constipation by remodeling gut microbiota and regulating SCFA metabolism.The medium dose (3×106 CFU+2 mg XOS) demonstrated optimal regulatory potential by balancing microbiota structure and metabolic function.

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