综合小肠微生物群和血清代谢组学揭示蒸酒缓解大黄所致腹泻的潜在机制

IF 4.2 2区 医学 Q2 IMMUNOLOGY Journal of Inflammation Research Pub Date : 2024-10-30 eCollection Date: 2024-01-01 DOI:10.2147/JIR.S479654
Ya-Ya Bai, Rui Tian, Yan Qian, Qiao Zhang, Chong-Bo Zhao, Yong-Gang Yan, Li Zhang, Shi-Jun Yue, Yu-Ping Tang
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引用次数: 0

摘要

背景:长期服用大黄(RH)通常会导致腹泻,用葡萄酒蒸煮可以缓解腹泻。然而,葡萄酒蒸煮缓解大黄引起的腹泻的具体机制仍不清楚:本研究旨在通过检测小肠菌群和血清代谢组学,揭示葡萄酒蒸煮缓解 RH 引起的腹泻的内在机制:采用超高效液相色谱-质谱法(UPLC-MS)检测主要的蒽醌和蒽酮成分。将 84 只 ICR 小鼠随机分为对照组、RH 组和红酒蒸 RH 组(PRH),连续 14 天分别给予 RH 和 PRH(1、4 和 8 克/千克,i.g)。使用苏木精-伊红染色进行组织病理学分析。测量了小肠中的炎症因子和紧密连接蛋白(Zonula occludens-1 (ZO-1)和occludin)的水平。使用 16S rRNA 测序分析小肠内容物,并使用 UPLC-MS 分析内源性代谢物:结果:PRH组主要蒽醌和蒽酮成分的含量下降。RH组和PRH组均出现不同程度的稀便和粪便含水量增加;RH组的影响更为严重。与对照组相比,RH 组造成小肠损伤、炎症细胞因子水平升高、ZO-1 和闭塞素表达下调,并诱导肠道微生物群(GM)失衡。乳酸杆菌的相对丰度下降,而志贺氏菌和链球菌的相对丰度上升。不过,PRH 的影响比 RH 轻微。甘油磷脂代谢途径参与了这种影响。炎症细胞因子和潜在代谢物(sn-甘油-3-磷乙醇胺)的水平与链球菌感染呈正相关,而 ZO-1 和闭塞素的水平与链球菌感染呈负相关。GM失衡和甘油磷脂代谢异常导致肠屏障功能受损和炎症因子释放,这可能是RH诱导腹泻的原因,但PRH的作用较弱:结论:PRH通过恢复GM平衡、减少ZO-1和闭塞素的表达以及减少炎症因子的释放,缓解了RH诱导的腹泻。这一机制可能与蒽醌含量减少有关。本研究首次通过小肠菌群和血清代谢组学探讨了蒸酒缓解 RH 引起的腹泻的机制。它为更广泛地临床使用 RH 及其更安全的应用提供了数据支持。
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Integrated Small Intestine Microbiota and Serum Metabolomics Reveal the Potential Mechanisms of Wine Steaming in Alleviating Rhubarb-Induced Diarrhea.

Background: Long-term use of rhubarb (RH) commonly leads to diarrhea, which can be alleviated by steaming with wine. However, the specific mechanism by which wine steaming alleviates RH-induced diarrhea remains unknown.

Objective: This study aims to reveal the underlying mechanisms of wine steaming in alleviating RH-induced diarrhea by examining small intestinal flora and serum metabolomics.

Methods: Major anthraquinone and anthrone components were detected using ultra-performance liquid chromatography-mass spectrometry (UPLC-MS). Eighty-four ICR mice were randomly divided into control, RH, and RH steamed with wine (PRH) groups and were administered RH and PRH (1, 4, and 8 g/kg, i.g). for 14 consecutive days. Histopathological analysis was performed using hematoxylin-eosin staining. Levels of inflammatory factors and tight junction proteins, zonula occludens-1 (ZO-1) and occludin, in the small intestine were measured. The small intestine content was analyzed using 16S rRNA sequencing, and UPLC-MS was used to analyze endogenous metabolites.

Results: Levels of major anthraquinone and anthrone components decreased in PRH. Both RH and PRH groups showed varying degrees of loose stools and increased fecal water rates; the RH group exhibited more severe effects. Compared with the control group, RH caused small intestine injuries, increased levels of inflammatory cytokines, downregulated the expression of ZO-1 and occludin, and induced gut microbiota (GM) imbalance. The relative abundance of Lactobacillus decreased, while the relative abundance of Shigella and Streptococcus increased. However, PRH had a milder impact than RH. The glycerophospholipid metabolic pathway was involved in this effect. The levels of inflammatory cytokines and potential metabolites (sn-glycero-3-phosphoethanolamine) were positively correlated with Streptococcus infection, while the levels of ZO-1 and occludin were negatively correlated with Streptococcus infection. GM imbalance and abnormal glycerophospholipid metabolism contributed to impaired intestinal barrier function and inflammatory factor release, which may underlie RH-induced diarrhea, though PRH had a weaker effect.

Conclusion: PRH alleviated RH-induced diarrhea by recovering GM balance, reducing ZO-1 and occludin expression, and decreasing the release of inflammatory factors. This mechanism may be linked to the reduced anthraquinone content. This study is the first to explore the mechanism of wine steaming in alleviating RH-induced diarrhea through small intestinal flora and serum metabolomics. It provides data to support the broader clinical use of RH and its safer application.

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来源期刊
Journal of Inflammation Research
Journal of Inflammation Research Immunology and Microbiology-Immunology
CiteScore
6.10
自引率
2.20%
发文量
658
审稿时长
16 weeks
期刊介绍: An international, peer-reviewed, open access, online journal that welcomes laboratory and clinical findings on the molecular basis, cell biology and pharmacology of inflammation.
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