含有 P. acidilatici 和 L. plantarum 的鸡尾酒益生菌治疗耐力跑运动员肠胃不适的安全性和有效性:随机双盲交叉临床试验。

Sarah Lennon, Thomas Lackie, Adriana Miltko, Zoey C Kearns, Maxime R Paquette, Richard J Bloomer, Anyou Wang, Marie van der Merwe
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引用次数: 0

摘要

益生菌越来越多地被用于治疗与胃肠道损伤和渗透性有关的疾病,包括运动引起的胃肠道不适。本研究评估了益生菌在改变肠道环境和减轻耐力跑运动员胃肠道症状方面的安全性和有效性。在一项双盲交叉研究中,16 名跑步者被随机分配到每天补充含有酸性乳杆菌和植物乳杆菌的鸡尾酒益生菌或安慰剂的环境中,为期 4 周。研究人员收集了空腹血液和粪便样本,用于测量肠道渗透性指标、免疫参数和微生物组分析。在治疗前后进行了跑步机跑步测试;参与者在27°C的温度下以65-70%的VO2max速度跑步,最长时间为90分钟或直到出现疲劳/胃肠道症状。跑步测试后采集血液样本。对健康人来说,补充四周的益生菌不会改变健康参数,尽管仅在益生菌治疗中观察到天门冬氨酸氨基转移酶(AST)水平略有下降(P=0.05)。肠道症状(GIS)、肠道渗透性相关参数(iFABP、LBP、zonulin 和细胞因子)以及肠道微生物含量均未因补充益生菌而发生变化。赛后对 GIS 和肠道相关参数的测量结果在各组之间并无差异;然而,由于在赛跑过程中没有充分诱导 GIS,因此缺乏可测量的功能结果,这就混淆了所观察到的无差异现象。在目前的研究条件下,益生菌的使用是安全的,而且不会影响肠道或免疫相关参数,也不会影响健康人群的肠道症状。益生菌可能会减少组织损伤,但还需要进行更多的研究。
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Safety and efficacy of a probiotic cocktail containing P. acidilactici and L. plantarum for gastrointestinal discomfort in endurance runners: randomized double-blinded crossover clinical trial.

Probiotics are increasingly used to treat conditions associated with gastrointestinal injury and permeability, including exercise-induced gastrointestinal discomfort. This study assessed safety and efficacy of a probiotic in altering the intestinal milieu and mitigating gastrointestinal symptoms (GIS) in endurance runners. In a double blind, crossover study, 16 runners were randomized to 4 weeks of daily supplementation with a probiotic cocktail containing Pediococcus acidilactici bacteria and Lactobacillus plantarum or placebo. Fasting blood and stool samples were collected for measurement of gut permeability markers, immune parameters, and microbiome analyses. Treadmill run tests were performed before and after treatment; participants ran at 65%-70% of VO2max at 27 °C for a maximum of 90 min or until fatigue/GIS developed. A blood sample was collected after the treadmill run test. In healthy individuals, 4 weeks of probiotic supplementation did not alter health parameters, although a marginal reduction in aspartate aminotransferase levels was observed with probiotic treatment only (p = 0.05). GIS, gut permeability-associated parameters (intestinal fatty acid binding protein, lipopolysaccharide binding protein, zonulin, and cytokines), and intestinal microbial content were not altered by the probiotic supplementation. Post-run measurements of GIS and gut-associated parameters did not differ between groups; however, the observed lack of differences is confounded by an absence of measurable functional outcome as GIS was not sufficiently induced during the run. Under the current study conditions, the probiotic was safe to use, and did not affect gut- or immune-associated parameters, or intestinal symptoms in a healthy population. The probiotic might reduce tissue damage, but more studies are warranted.

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