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益生菌补充对代谢综合征患者肠道通透性的影响:一项开放标签、随机先导研究。

The influence of probiotic supplementation on gut permeability in patients with metabolic syndrome: an open label, randomized pilot study.

机构信息

Division of Transplantation Surgery, Department of Surgery, Medical University of Graz, Graz, Austria.

出版信息

Eur J Clin Nutr. 2012 Oct;66(10):1110-5. doi: 10.1038/ejcn.2012.103. Epub 2012 Aug 8.


DOI:10.1038/ejcn.2012.103
PMID:22872030
Abstract

BACKGROUND/OBJECTIVES: Obesity and metabolic disorders are linked to inflammation via gut microbiota and/or gut permeability. Gut-derived endotoxin triggers inflammation leading to metabolic syndrome (MetS) and contributing to oxidative stress. We intended to investigate the effect of Lactobacillus casei Shirota on gut permeability, presence of endotoxin and neutrophil function in MetS. SUBJECTS/METHODS: Patients with MetS were randomized to receive 3 × 6.5 × 10⁹ CFU L. casei Shirota (probiotic group) or not for 3 months. Gut permeability was assessed by a differential sugar absorption method and by determination of diaminooxidase serum levels, endotoxin by an adapted limulus amoebocyte lysate assay, neutrophil function and toll-like receptor (TLR) expression by flow cytometry and ELISA was used to detect lipopolysaccharide-binding protein (LBP) and soluble CD14 (sCD14) levels. RESULTS: Twenty-eight patients and 10 healthy controls were included. Gut permeability was significantly increased in MetS compared with controls but did not differ between patient groups. None of the patients were positive for endotoxin. LBP and sCD14 levels were not significantly different from healthy controls. High-sensitive C-reactive protein and LBP levels slightly but significantly increased after 3 months within the probiotics group. Neutrophil function and TLR expression did not differ from healthy controls or within the patient groups. CONCLUSIONS: Gut permeability of MetS patients was increased significantly compared with healthy controls. L. casei Shirota administration in the MetS patients did not have any influence on any parameter tested possibly due to too-short study duration or underdosing of L. casei Shirota.

摘要

背景/目的:肥胖和代谢紊乱通过肠道菌群和/或肠道通透性与炎症有关。肠道来源的内毒素触发炎症,导致代谢综合征(MetS),并导致氧化应激。我们旨在研究干酪乳杆菌 Shirota 对 MetS 患者肠道通透性、内毒素存在和中性粒细胞功能的影响。 受试者/方法:MetS 患者被随机分为 3 组,每组接受 3×6.5×10⁹ CFU L. casei Shirota(益生菌组)或不接受 3 个月。肠道通透性通过差异糖吸收法和血清二胺氧化酶水平测定、内毒素通过改良鲎阿米巴细胞溶解物测定、中性粒细胞功能和 Toll 样受体(TLR)表达通过流式细胞术和 ELISA 进行检测,用于检测脂多糖结合蛋白(LBP)和可溶性 CD14(sCD14)水平。 结果:共纳入 28 例患者和 10 例健康对照者。与对照组相比,MetS 患者的肠道通透性明显增加,但两组患者之间无差异。没有患者内毒素检测呈阳性。LBP 和 sCD14 水平与健康对照组无显著差异。益生菌组患者的高敏 C 反应蛋白和 LBP 水平在 3 个月内略有但显著升高。中性粒细胞功能和 TLR 表达与健康对照组或患者组之间无差异。 结论:与健康对照组相比,MetS 患者的肠道通透性明显增加。在 MetS 患者中给予干酪乳杆菌 Shirota 治疗对任何测试参数均无影响,可能是由于研究时间太短或干酪乳杆菌 Shirota 剂量不足。

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引用本文的文献

[1]
Serum lipopolysaccharide binding protein (LBP) and metabolic syndrome: a systematic review and meta-analysis.

Diabetol Metab Syndr. 2025-7-16

[2]
Therapeutic Strategies to Modulate Gut Microbial Health: Approaches for Chronic Metabolic Disorder Management.

Metabolites. 2025-2-13

[3]
Intestinal Barrier Impairment, Preservation, and Repair: An Update.

Nutrients. 2024-10-15

[4]
Effect of Probiotics on Improving Intestinal Mucosal Permeability and Inflammation after Surgery.

Gut Liver. 2025-3-15

[5]
Biomarkers of intestinal permeability are associated with inflammation in metabolically healthy obesity but not normal-weight obesity.

Am J Physiol Heart Circ Physiol. 2024-11-1

[6]
The potential preventive effect of probiotics, prebiotics, and synbiotics on cardiovascular risk factors through modulation of gut microbiota: A review.

Food Sci Nutr. 2024-5-29

[7]
Silybin restores glucose uptake after tumour necrosis factor-alpha and lipopolysaccharide stimulation in 3T3-L1 adipocytes.

Adipocyte. 2024-12

[8]
Randomized clinical trial evaluating the efficacy of synbiotic supplementation on serum endotoxin and trimethylamine N-oxide levels in patients with dyslipidaemia.

Arch Med Sci Atheroscler Dis. 2024-2-1

[9]
The Efficacy of ssp. Supplementation in Managing Body Weight and Blood Lipids of People with Overweight: A Randomized Pilot Trial.

Metabolites. 2024-2-16

[10]
Position statement on nutrition therapy for overweight and obesity: nutrition department of the Brazilian association for the study of obesity and metabolic syndrome (ABESO-2022).

Diabetol Metab Syndr. 2023-6-9

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