McVey Neufeld Karen-Anne, Kay Sebastian, Bienenstock John
Department of Pathology and Molecular Medicine, McMaster University, Hamilton, ON, Canada.
Brain-Body Institute, St. Joseph's Healthcare at McMaster University, Hamilton, ON, Canada.
Front Neurosci. 2018 May 8;12:294. doi: 10.3389/fnins.2018.00294. eCollection 2018.
Currently, there is keen interest in the development of alternative therapies in the treatment of depression. Given the explosion of research focused on the microbiota-gut-brain axis, consideration has turned to the potential of certain probiotics to improve patient outcomes for those suffering from mood disorders. Here we examine the abilities of a known antidepressant, fluoxetine, and the probiotic JB-1™, to attenuate responses to two established criteria for depressive-like behavior in animal models, the tail suspension test (TST) and the corticosterone response to an acute restraint stressor. We examine two different strains of mice known to differ in the extent to which they express both anxiety-like behavior and measures of despair-BALB/c and Swiss Webster-with respectively high and normal behavioral phenotypes for each. While adult male BALB/c mice responded with increased antidepressive-like behavior to both fluoxetine and JB-1 in both the TST and the corticosterone stress response, SW mice did not respond to either treatment as compared to controls. These findings highlight the importance of investigating putative antidepressants in mouse strains known to express face validity for some markers of depression. Clinical studies examining the activity of JB-1 in patients suffering from mood disorders are warranted, as well as further pre-clinical work examining how interactions between host genotype and intestinal microbial alterations may impact behavioral responses. This study adds to the literature supporting the possibility that modifying the intestinal microbiota via probiotics represents a promising potential therapeutic breakthrough in the treatment of psychiatric disease.
目前,人们对开发抑郁症的替代疗法有着浓厚的兴趣。鉴于聚焦于微生物群-肠道-脑轴的研究激增,人们开始考虑某些益生菌改善情绪障碍患者预后的潜力。在此,我们研究了一种已知的抗抑郁药氟西汀和益生菌JB-1™减弱动物模型中两种既定的抑郁样行为标准反应的能力,即悬尾试验(TST)和对急性束缚应激源的皮质酮反应。我们研究了两种已知在表达焦虑样行为和绝望程度方面存在差异的小鼠品系——BALB/c和瑞士韦伯斯特小鼠,它们分别具有高和正常的行为表型。虽然成年雄性BALB/c小鼠在TST和皮质酮应激反应中对氟西汀和JB-1都表现出增强的抗抑郁样行为,但与对照组相比,SW小鼠对这两种治疗均无反应。这些发现凸显了在已知对某些抑郁症标志物具有表面效度的小鼠品系中研究假定抗抑郁药的重要性。有必要开展临床研究,考察JB-1在情绪障碍患者中的活性,以及进一步的临床前研究,考察宿主基因型与肠道微生物改变之间的相互作用如何影响行为反应。这项研究为文献增添了内容,支持了通过益生菌改变肠道微生物群可能代表着精神疾病治疗中有前景的潜在治疗突破这一可能性。