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首页> 外文期刊>Behavioural Brain Research: An International Journal >Absence of gut microbiota influences lipopolysaccharide-induced behavioral changes in mice
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Absence of gut microbiota influences lipopolysaccharide-induced behavioral changes in mice

机译:肠道菌群的缺乏影响脂多糖诱导的小鼠行为改变

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摘要

Changes in the microbiota composition of gastrointestinal tract are emerging as potential players in the physiopathology of neuropsychiatric disorders. In the present work we evaluated the relationship between the absence of gut microbiota and neuroinflammatory mechanisms in a murine model of LPS-induced behavioral alterations. Germ-free (GF) or conventional male mice received a single i.p. injection of lipopolysaccharide (LPS i.p.; 0.83 mg/Kg) or PBS, and after 24 h they were tested for depressive-like behaviors (forced swimming test, tail suspension test - TST, or sucrose preference test - SPT). After behavioral evaluation, animals were analyzed for possible changes in neuroplasticity by means of BDNF, NGF and cytokines levels in prefrontal cortex and hippocampus, and the expression of Iba-1 (microglial activation marker) in the hippocampus, and the cellular activity marker, Delta FosB, in the dorsal raphe nucleus. In conventional mice, LPS induced depressive-like behaviors. LPS-induced changes were followed by up-regulation of the expression of TNF and Iba-1 in the hippocampus. The same effects were not observed in GF mice. Behavioral effects of LPS were not observed in GF mice submitted to TST. GF mice present a lower response to the anhedonia-like effect induced by LPS when compared to conventional animals (SPT). There was up-regulation of Delta FosB in the dorsal raphe nucleus in the absence of gut microbiota, events not influenced by LPS treatment. Our results suggest that gut-microbiota interactions influence depressive-like behaviors, raphe nucleus activation and activation of pro-inflammatory mechanisms within the hippocampus. (C) 2016 Elsevier B.V. All rights reserved.
机译:胃肠道微生物群组成的变化正在成为神经精神疾病的生理病理学的潜在参与者。在目前的工作中,我们评估了LPS诱导的行为改变的小鼠模型中肠道菌群的缺乏与神经炎症机制之间的关系。无胚芽(GF)或常规雄性小鼠接受一次腹膜内注射。注射脂多糖(LPS i.p .; 0.83 mg / Kg)或PBS,并在24小时后对他们进行类似抑郁的行为测试(强迫游泳测试,尾部悬挂测试-TST或蔗糖偏爱测试-SPT)。进行行为评估后,通过前额叶皮层和海马中的BDNF,NGF和细胞因子水平以及海马中Iba-1的表达(小胶质激活标记)和细胞活性标记Delta分析动物的神经可塑性变化FosB,在背缝核中。在常规小鼠中,LPS引起抑郁样行为。 LPS诱导的变化后,海马中TNF和Iba-1的表达上调。在GF小鼠中未观察到相同的作用。在提交TST的GF小鼠中未观察到LPS的行为效应。与常规动物(SPT)相比,GF小鼠对LPS诱发的类似快感性痴呆的反应较低。在不存在肠道菌群的情况下,背沟核中的Delta FosB上调,该事件不受LPS处理的影响。我们的研究结果表明肠道菌群相互作用影响抑郁样行为,缝核激活和海马内促炎机制的激活。 (C)2016 Elsevier B.V.保留所有权利。

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