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短期暴露于富含脂肪或糖的能量匹配饮食对记忆、肠道微生物群以及大脑炎症和可塑性标志物的影响。

The effect of short-term exposure to energy-matched diets enriched in fat or sugar on memory, gut microbiota and markers of brain inflammation and plasticity.

机构信息

Department of Pharmacology, School of Medical Sciences, UNSW Australia, NSW 2052, Australia.

School of Medical Sciences, UNSW Australia, NSW 2052, Australia.

出版信息

Brain Behav Immun. 2016 Oct;57:304-313. doi: 10.1016/j.bbi.2016.07.151. Epub 2016 Jul 20.

Abstract

Short-term exposure to high-energy diets impairs memory but there is little data on the relative contributions of fat and sugar to these deficits or the mechanisms responsible. Here, we investigated how these different macronutrients affect memory, neuroinflammation and neuroplasticity markers and the gut microbiota. Rats were fed matched purified diets for 2weeks; Control, Sugar, Saturated Fatty Acid (SFA) or Polyunsaturated Fatty Acid (PUFA), which varied only in the percentage of energy available from sugar and the amount and type of fat. Rats consuming SFA and Sugar were impaired on hippocampal-dependent place recognition memory compared to Controls and PUFA rats, despite all rats consuming similar amounts of energy. All rats performed comparably on the object recognition task. Hippocampal and hypothalamic inflammatory markers were not substantially affected by the diets and there was no change in the neuroplasticity marker, brain-derived neurotrophic factor. Each of the diets significantly altered the microbial composition in distinct ways. Specifically, the relative abundance of 89 taxa differed significantly between groups with the majority of these changes accounted for by the Clostridiales order and within that, Lachnospiraceae and Ruminococcaceae. These taxa showed a range of macronutrient specific correlations with place memory. In addition, Distance based Linear Models found relationships between memory, inflammation-related hippocampal genes and the gut microbiota. In conclusion, our study shows that the macronutrient profile of the diet is crucial for diet-induced memory deficits and suggests a possible link between diet, the gut microbiota and hippocampal inflammatory genes.

摘要

短期暴露于高能量饮食会损害记忆,但关于脂肪和糖对这些缺陷的相对贡献或负责的机制的数据很少。在这里,我们研究了这些不同的宏量营养素如何影响记忆、神经炎症和神经可塑性标志物以及肠道微生物群。大鼠喂食匹配的纯化饮食 2 周;对照、糖、饱和脂肪酸(SFA)或多不饱和脂肪酸(PUFA),它们仅在糖的能量百分比和脂肪的量和类型上有所不同。与对照和 PUFA 大鼠相比,摄入 SFA 和糖的大鼠在海马依赖性位置识别记忆方面受损,尽管所有大鼠摄入的能量相似。所有大鼠在物体识别任务上的表现相当。饮食对海马和下丘脑炎症标志物没有明显影响,神经可塑性标志物脑源性神经营养因子也没有变化。每种饮食都以不同的方式显著改变了微生物组成。具体来说,89 个分类群的相对丰度在组间有显著差异,其中大多数变化归因于梭菌目,在该目中,lachnospiraceae 和 ruminococcaceae。这些分类群与位置记忆表现出一系列特定于宏量营养素的相关性。此外,基于距离的线性模型发现了记忆、与炎症相关的海马基因和肠道微生物群之间的关系。总之,我们的研究表明,饮食的宏量营养素谱对饮食诱导的记忆缺陷至关重要,并提示饮食、肠道微生物群和海马炎症基因之间可能存在联系。

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