Anti Helicobacter pylori activity and gastrointestinal protective effects of Terminalia bellirica: Mechanistic insights from in vitro and in vivo studies

IF 5.4 2区 医学 Q1 CHEMISTRY, MEDICINAL Journal of ethnopharmacology Pub Date : 2025-03-05 DOI:10.1016/j.jep.2025.119569
Yuanjing Zou , Bingyun Lu , Zhong Feng , Haobo Chen , Chuqiu Zhang , Chang Peng , Ling Ou , Ruixia Wei , Meicun Yao , Qingchang Chen , Ye Chen
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Abstract

Ethnopharmacological relevance

Terminalia bellirica (Gaertn.) Roxb. (Combretaceae) (T. bellirica) is a longstanding medicinal plant traditionally referenced in both Indian and Tibetan medical practices. Currently, approximately 50% of the global population is infected with Helicobacter pylori (H. pylori). To curb antibiotic overuse, asymptomatic patients might require alternative therapy to mitigate the intestinal side effects commonly associated with excessive antibiotic usage.

Aim of the study

Preliminary screening conducted by our team revealed that T. bellirica had excellent anti-H. pylori action in vitro. However, further research elucidating the mechanism behind T. bellirica's impact on H. pylori infection and its protective effects against related gastrointestinal diseases is yet to be explored.

Materials and methods

To assess the specific effect and underlying mechanism, we employed a comprehensive range of methodologies, including UPLC-MS/MS, in vitro and in vivo antibacterial assays, 5R 16S, molecular dynamics simulation and RT-qPCR.

Results

Phytochemical analysis revealed abundant phenolic contents in T. bellirica, including chebulagic acid, chebulinic acid, corilagin, gallic acid, and ellagic acid. In vitro antibacterial evaluations demonstrated significant efficacy of T. bellirica against H. pylori, with a minimum inhibitory concentration (MIC) of 160 μg/mL, effectively inhibiting critical bacterial defense such as urease, adhesion and gene vacA. In vivo animal experiments showed that in addition to its anti-H. pylori effect, T. bellirica exhibited mild influence on gastric microbiota, with the composition restoring to normal levels after administration.

Conclusions

T. bellirica exerts potent anti-H. pylori activity both in vitro and in vivo, indicating its potential as an alternative therapeutic strategy for managing H. pylori infections while exerting minimal impact on gastric microbial balance. Further studies are warranted to elucidate additional pathways involved and to validate its clinical applications.

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Terminalia bellirica 的抗幽门螺旋杆菌活性和胃肠道保护作用:来自体外和体内研究的机理启示。
民族药理学相关性:白莲属(Terminalia bellirica)Roxb。(combretacae) (T. bellirica)是一种长期存在的药用植物,传统上在印度和藏医实践中都有提及。目前,全球大约50%的人口感染了幽门螺杆菌(h.p ylori)。为了抑制抗生素的过度使用,无症状患者可能需要替代疗法来减轻通常与抗生素过度使用相关的肠道副作用。研究目的:经本课题组初步筛选,发现白僵菌具有优良的抗h。幽门螺杆菌的体外作用。然而,关于T. bellirica对幽门螺杆菌感染的影响及其对相关胃肠道疾病的保护作用的机制还有待进一步研究。材料和方法:为了评估其特异性作用和潜在机制,我们采用了一系列综合方法,包括UPLC-MS/MS,体外和体内抗菌试验,5r16s,分子动力学模拟和RT-qPCR。结果:植物化学分析显示,白莲属植物中含有丰富的酚类物质,包括车胆酸、车胆酸、芫花素、没食子酸和鞣花酸。体外抑菌试验表明,白杆菌对幽门螺杆菌具有显著的抑菌效果,其最低抑菌浓度(MIC)为160 μg/mL,可有效抑制细菌的关键防御功能,如脲酶、黏附酶和vacA基因。体内动物实验表明,除其抗h。在幽门螺杆菌作用下,贝利菌对胃微生物群的影响轻微,给药后其组成恢复到正常水平。结论:小黄霉具有较强的抗h。体外和体内幽门螺杆菌的活性,表明其作为控制幽门螺杆菌感染的替代治疗策略的潜力,同时对胃微生物平衡的影响最小。需要进一步的研究来阐明涉及的其他途径并验证其临床应用。
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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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