针对急性胰腺炎的肠道微生物动力学和治疗策略

Prachi Mehta , Dipankar Saha , Trishna Das , Bhrigu Kumar Das
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摘要

背景:急性胰腺炎(AP)是一种以突然腹痛为特征的严重炎症,可升级为全身性炎症和器官衰竭。肠道微生物群的改变,包括致病菌如肠杆菌科的过度生长和双歧杆菌水平的降低,与氧化应激增加、细菌易位和肠道屏障功能受损有关,加剧了全身炎症和疾病的严重程度。最近的研究强调了植物成分和微生物组调节在调节ap相关炎症途径中的潜力。目的探讨肠道微生物群和植物化学物质在急性胰腺炎调控中的作用,并评估营养干预、益生菌和乳酸林格液对急性胰腺炎管理的影响。方法使用“急性胰腺炎”、“肠道微生物组”、“植物化学物质”和“营养管理”等关键词,在多个数据库中对截至2024年10月发表的英文研究进行了全面的文献检索。结果槲皮素、大黄素、山奈酚等关键植物化学物质可有效调节AP患者的脂肪酶和淀粉酶水平。对照试验表明,营养调节和纳米姜黄素的补充显著减轻了疼痛,改善了临床结果。肠道微生物组也调节与AP相关的关键代谢途径,影响炎症和疾病进展。结论肠道微生物组显著影响胰腺炎症、酶调节和AP进展。通过植物药物、微生物组靶向治疗和营养策略解决氧化应激和肠道生态失调,为AP的管理提供了有希望的途径。需要进一步研究阐明这些干预措施的机制和潜在的临床应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Targeting the gut microbiome dynamics and treatment strategies in acute pancreatitis

Background

Acute pancreatitis (AP) is a severe inflammatory condition characterized by sudden abdominal pain that may escalate to systemic inflammation and organ failure. Alterations in the gut microbiome, including overgrowth of pathogenic bacteria like Enterobacteriaceae and reduced levels of Bifidobacterium, have been linked to increased oxidative stress, bacterial translocation, and compromised intestinal barrier function, exacerbating systemic inflammation and disease severity. Recent research highlights the potential of phytoconstituents and microbiome modulation in regulating AP-associated inflammatory pathways.

Objective

This review examines the roles of the gut microbiome and phytochemicals in AP regulation and evaluates the impact of nutritional interventions, probiotics, and Ringer's lactate solution on AP management.

Method

A comprehensive literature search was conducted across multiple databases for studies published in English up to October 2024, using keywords like 'acute pancreatitis', 'gut microbiome', 'phytochemicals', and 'nutritional management'.

Results

Key phytochemicals, such as Quercetin, Rhein, and Kaempferol, effectively regulate lipase and amylase levels in AP patients. Controlled trials indicated that nutritional regulation and nano-curcumin supplementation significantly alleviated pain and improved clinical outcomes. The gut microbiome also modulated critical metabolic pathways related to AP, influencing inflammation and disease progression.

Conclusion

The gut microbiome significantly impacts pancreatic inflammation, enzyme regulation, and AP progression. Addressing oxidative stress and gut dysbiosis through phytomedicines, microbiome-targeted therapies, and nutritional strategies presents promising avenues for AP management. Further research is necessary to elucidate these interventions' mechanisms and potential clinical applications.
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