Antihyperalgesic properties of gut microbiota: Parabacteroides distasonis as a new probiotic strategy to alleviate chronic abdominal pain

益生菌 肠道菌群 内脏痛 医学 痛觉过敏 伤害感受器 炎症 神经调节 药理学 伤害 生物 刺激 内科学 细菌 免疫学 受体 遗传学
作者
Sandie Gervason,Mathieu Méleine,Stéphane Lolignier,Maëva Meynier,Valentine Daugey,A. Birer,Youssef Aissouni,Jean‐Yves Berthon,Denis Ardid,Edith Filaire,Frédéric A. Carvalho
出处
期刊:Pain [Lippincott Williams & Wilkins]
卷期号:165 (5): e39-e54 被引量:15
标识
DOI:10.1097/j.pain.0000000000003075
摘要

Abstract The potential role of gut microbiota in pain modulation is arousing an emerging interest since recent years. This study investigated neuromodulatory properties of gut microbiota to identify next-generation probiotics to propose alternative therapies for visceral pain management. Neuromodulation ability of 10 bacterial strains isolated from a healthy donor was assessed both on ND7/23 immortalized cell line and primary neuronal cells from rat dorsal root ganglia. This screening highlighted the neuroinhibitory property of Parabacteroides distasonis (F1-2) strain, supported both by its intracellular content and membrane fraction, which was further investigated in visceral pain mouse models. Oral administration of F1-2 resulted in a significant decrease of colonic hypersensitivity (CHS) in dextran sulfate sodium (0.5%) model associated with low-grade inflammation and a significant decrease of CHS in Citrobacter rodentium postinfectious models. No effect of F1-2 oral administration on CHS was observed in a neonatal maternal separation stress model. Antihyperalgesic effect unlikely involved modulation of inflammatory processes or restoration of intestinal barrier. Exploration of direct dialogue mechanisms between this strain and nervous system, assessed by calcium imaging experiments, revealed that F1-2 interacts directly with nociceptors by reducing activation level on capsaicin, inflammatory soup, and bradykinin stimulations. Our study provides new insights about bacteria–host interaction and places P distasonis as a potential therapeutic strategy in the treatment of visceral pain observed in leaky gut–associated pathologies.
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