Institute of Molecular Genetics and Genetic Engineering, University of Belgrade, Belgrade, Serbia.
Appl Environ Microbiol. 2013 Sep;79(18):5735-44. doi: 10.1128/AEM.01807-13. Epub 2013 Jul 12.
The present study was carried out to test the colonic mucosal response of rats to oral supplementation with Lactobacillus fermentum BGHI14 and to correlate the tissue reaction to trinitrobenzenesulfonate (TNBS)-induced colitis with mucosal barrier alterations caused by bacterial ingestion. An immune cell-mediated reaction of healthy colonic tissue was noticed after bacterial feeding. After prolonged bacterial treatment, the observed reaction had retreated to normality, but the mRNA levels of proinflammatory cytokines interleukin-1β (IL-1β) and tumor necrosis factor alpha (TNF-α) remained elevated. These data point to the chronic low-grade inflammation that could be caused by long-term probiotic consumption. Although no detrimental effects of bacterial pretreatment were noticed in colitic rats, at least in the acute state of disease, the results obtained in our study point to the necessity of reassessment of existing data on the safety of probiotic preparations. Additionally, probiotic effects in experimental colitis models might depend on time coordination of disease induction with treatment duration.
本研究旨在测试大鼠口服补充发酵乳杆菌 BGHI14 对结肠黏膜的反应,并将组织对三硝基苯磺酸(TNBS)诱导的结肠炎的反应与细菌摄入引起的黏膜屏障改变相关联。在细菌喂养后,健康结肠组织出现免疫细胞介导的反应。经过长时间的细菌处理后,观察到的反应已经恢复正常,但促炎细胞因子白细胞介素-1β(IL-1β)和肿瘤坏死因子-α(TNF-α)的 mRNA 水平仍然升高。这些数据表明可能由长期益生菌消耗引起的慢性低度炎症。尽管在结肠炎大鼠中没有注意到细菌预处理的有害影响,至少在疾病的急性状态下,我们的研究结果表明有必要重新评估现有关于益生菌制剂安全性的数据。此外,益生菌在实验性结肠炎模型中的作用可能取决于疾病诱导与治疗持续时间的时间协调。