Effects of excessive Platycodon grandiflorus root on gut microbiota and host co-metabolism in mice

IF 5.4 2区 医学 Q1 CHEMISTRY, MEDICINAL Journal of ethnopharmacology Pub Date : 2025-04-09 Epub Date: 2025-03-08 DOI:10.1016/j.jep.2025.119577
Shasha Han , Zichen Luo , Shihang Bao , Zihan Xiao , Weichen Xu , Tong Xie , Chen Shi , Jin Wang , Jinjun Shan
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Abstract

Ethnopharmacological relevance

Platycodon grandiflorus root, is a widely used herb in East Asia for treating respiratory diseases, but research on its oral safety is limited.

Aim of the study

This study examines the potential adverse gastrointestinal reactions resulting from excessive consumption of Platycodon grandiflorus root (PR) and its effects on gut microbiota and host co-metabolism.

Materials and methods

This study evaluated the effects of different doses (1.5, 4.5, and 7.5 g/kg/day) of PR on ICR mice through gavage. Select the 7.5 g/kg/day dosage group and the control group to assess intestinal morphology and conduct histopathological studies. Examine inflammation-related factors and tight junction proteins using WB, qPCR, and ELISA. Additionally, perform 16S rDNA sequencing and metabolomic analyses to evaluate changes in gut microbiota and endogenous metabolites. Finally, the clearance of gut microbiota with antibiotics, the effects of excessive PR on mice were investigated.

Results

Excessive intake of PR can lead to mortality in mice, as well as symptoms such as intestinal flatulence and slowed intestinal transit, suggesting the occurrence of chronic intestinal pseudo-obstruction accompanied by endotoxemia. It altered both α-diversity and β-diversity in the gut microbiota of mice, with increased relative abundances of Pseudomonadota, Verrucomicrobiota, Escherichia-Shigella, Akkermansia, Bacteroides, and Klebsiella, closely linked to intestinal obstruction and bacterial overgrowth. Excessive intake of PR also resulted in metabolic disturbances in mice, particularly in the levels of metabolites such as bate-hydroxybutyrate, 5,6-dihydrouracil, uridine, isoleucine, mannitol, bate-alanine, L-cysteine, L-tyrosine, and orotic acid, which may provide insights into the side effects associated with excessive consumption of PR. Clearing the gut microbiota significantly mitigated adverse effects on the intestines and restored metabolite levels.

Conclusions

This study demonstrates that excessive PR induces gut microbiota and metabolic disruption in normal mice, with the overgrowth of Gram-negative bacteria releasing LPS that impair smooth muscle contraction, leading to adverse effects such as chronic intestinal pseudo-obstruction.

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过量桔梗根对小鼠肠道菌群及宿主共代谢的影响。
民族药理学相关性:桔梗是东亚地区广泛用于治疗呼吸系统疾病的草药,但对其口服安全性的研究有限。研究目的:探讨过量食用桔梗(Platycodon grandflorus root, PR)可能引起的胃肠道不良反应及其对肠道菌群和宿主共代谢的影响。材料与方法:本研究通过灌胃的方法评价不同剂量(1.5、4.5、7.5 g/kg/d)的PR对ICR小鼠的影响。选取7.5 g/kg/天剂量组和对照组,评估肠道形态,进行组织病理学研究。使用WB、qPCR和ELISA检测炎症相关因子和紧密连接蛋白。此外,进行16S rDNA测序和代谢组学分析,以评估肠道微生物群和内源性代谢物的变化。最后,研究了抗生素对小鼠肠道菌群的清除作用以及过量PR对小鼠肠道菌群的影响。结果:过量摄入PR可导致小鼠死亡,并出现肠道胀气、肠道运输缓慢等症状,提示存在慢性假性肠梗阻并伴有内毒素血症。它改变了小鼠肠道微生物群α-多样性和β-多样性,增加了假单胞菌、Verrucomicrobiota、Escherichia-Shigella、Akkermansia、Bacteroides和Klebsiella的相对丰度,与肠道阻塞和细菌过度生长密切相关。过量摄入PR还会导致小鼠代谢紊乱,特别是在代谢物水平方面,如蝙蝠-羟基丁酸、5,6-二氢尿嘧啶、尿苷、异亮氨酸、甘露醇、蝙蝠-丙氨酸、l -半胱氨酸、l -酪氨酸和山梨酸,这可能为过量摄入PR相关的副作用提供了见解。清除肠道微生物群显著减轻了对肠道的不良影响,并恢复了代谢物水平。结论:本研究表明,过量的PR可引起正常小鼠肠道菌群和代谢紊乱,革兰氏阴性菌过度生长,释放LPS损害平滑肌收缩,导致慢性肠道假性梗阻等不良反应。
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来源期刊
Journal of ethnopharmacology
Journal of ethnopharmacology 医学-全科医学与补充医学
CiteScore
10.30
自引率
5.60%
发文量
967
审稿时长
77 days
期刊介绍: The Journal of Ethnopharmacology is dedicated to the exchange of information and understandings about people''s use of plants, fungi, animals, microorganisms and minerals and their biological and pharmacological effects based on the principles established through international conventions. Early people confronted with illness and disease, discovered a wealth of useful therapeutic agents in the plant and animal kingdoms. The empirical knowledge of these medicinal substances and their toxic potential was passed on by oral tradition and sometimes recorded in herbals and other texts on materia medica. Many valuable drugs of today (e.g., atropine, ephedrine, tubocurarine, digoxin, reserpine) came into use through the study of indigenous remedies. Chemists continue to use plant-derived drugs (e.g., morphine, taxol, physostigmine, quinidine, emetine) as prototypes in their attempts to develop more effective and less toxic medicinals.
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