Department of Psychiatry and Behavioral Neurobiology, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Department of Neuroscience, Southern Research, Birmingham, Alabama, USA.
Obesity (Silver Spring). 2020 Dec;28(12):2347-2356. doi: 10.1002/oby.22983. Epub 2020 Oct 11.
This study aimed to investigate both the long-term and short-term impacts of high-fat diets (HFD) or high-sucrose diets (HSD) on the normal diurnal pattern of cognitive function, protein expression, and the molecular clock in mice.
This study used both 6-month and 4-week feeding strategies by providing male C57BL/6J mice access to either a standard chow, HFD, or HSD. Spatial working memory and synaptic plasticity were assessed both day and night, and hippocampal tissue was measured for changes in NMDA and AMPA receptor subunits (GluN2B, GluA1), as well as molecular clock gene expression.
HFD and HSD both disrupted normal day/night fluctuations in spatial working memory and synaptic plasticity. Mice fed HFD altered their food intake to consume more calories during the day. Both diets disrupted normal hippocampal clock gene expression, and HFD reduced GluN2B levels in hippocampal tissue.
Taken together, these results suggest that both HFD and HSD induce a loss of day/night performance in spatial working memory and synaptic plasticity as well as trigger a cascade of changes that include disruption to the hippocampal molecular clock.
本研究旨在探究高脂肪饮食(HFD)或高蔗糖饮食(HSD)对正常昼夜节律认知功能、蛋白表达和分子钟的长期和短期影响。
本研究采用 6 个月和 4 周的喂养策略,让雄性 C57BL/6J 小鼠分别摄入标准食物、HFD 或 HSD。分别在白天和晚上评估空间工作记忆和突触可塑性,并测量海马组织中 NMDA 和 AMPA 受体亚基(GluN2B、GluA1)以及分子钟基因表达的变化。
HFD 和 HSD 均破坏了空间工作记忆和突触可塑性的正常昼夜波动。喂食 HFD 的小鼠改变了它们的进食习惯,在白天摄入更多的热量。两种饮食均破坏了正常的海马时钟基因表达,HFD 降低了海马组织中 GluN2B 水平。
综上所述,这些结果表明,HFD 和 HSD 均可导致空间工作记忆和突触可塑性的昼夜表现丧失,并引发一系列变化,包括破坏海马分子钟。