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Mechanisms Underlying Microbial-Mediated Changes in Social Behavior in Mouse Models of Autism Spectrum Disorder

机译:自闭症谱系疾病小鼠模型中微生物介导的社会行为变化的机制

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Currently, there are no medications that effectively treat the core symptoms of Autism Spectrum Disorder (ASD). We recently found that the bacterial species Lactobacillus (L.) reuteri reverses social deficits in maternal high-fat-diet offspring. However, whether the effect of L. reuteri on social behavior is generalizable to other ASD models and its mechanism(s) of action remains unknown. Here, we found that treatment with L. reuteri selectively rescues social deficits in genetic, environmental, and idiopathic ASD models. Interestingly, the effects of L. reuteri on social behavior are not mediated by restoring the composition of the host's gut microbiome, which is altered in all of these ASD models. Instead, L. reuteri acts in a vagus nerve-dependent manner and rescues social interaction-induced synaptic plasticity in the ventral tegmental area of ASD mice, but not in oxytocin receptor-deficient mice. Collectively, treatment with L. reuteri emerges as promising non-invasive microbial-based avenue to combat ASD-related social dysfunction.
机译:目前,没有药物有效地治疗自闭症谱系疾病(ASD)的核心症状。我们最近发现细菌物种乳酸杆菌(L.)Reuteri扭转了母体高脂饮食后代的社会赤字。然而,L. REUTERI对社会行为的影响是概遍的,其他ASD模型及其行动机制仍然未知。在这里,我们发现与L. Reuteri的治疗选择性地拯救了遗传,环境和特发性ASD模型的社会缺陷。有趣的是,L. Reuteri对社会行为的影响不是通过恢复主机肠道微生物组的组成,这在所有这些ASD模型中改变。相反,L. Reuteri以迷走神经依赖性的方式起作用,并拯救社会相互作用诱导的ASD小鼠的腹侧突触面积,但不在催产素受体缺陷小鼠中。统称,与L. Reuteri的治疗结果作为有前途的非侵入性微生物的途径,以打击与其相关的社会功能障碍。

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