Stranahan Alexis M, Norman Eric D, Lee Kim, Cutler Roy G, Telljohann Richard S, Egan Josephine M, Mattson Mark P
Cellular and Molecular Neurosciences Section, Laboratory of Neurosciences, National Institute on Aging Intramural Research Program, Baltimore, Maryland, USA.
Hippocampus. 2008;18(11):1085-8. doi: 10.1002/hipo.20470.
Overall dietary energy intake, particularly the consumption of simple sugars such as fructose, has been increasing steadily in Western societies, but the effects of such diets on the brain are poorly understood. Here, we used functional and structural assays to characterize the effects of excessive caloric intake on the hippocampus, a brain region important for learning and memory. Rats fed with a high-fat, high-glucose diet supplemented with high-fructose corn syrup showed alterations in energy and lipid metabolism similar to clinical diabetes, with elevated fasting glucose and increased cholesterol and triglycerides. Rats maintained on this diet for 8 months exhibited impaired spatial learning ability, reduced hippocampal dendritic spine density, and reduced long-term potentiation at Schaffer collateral--CA1 synapses. These changes occurred concurrently with reductions in levels of brain-derived neurotrophic factor in the hippocampus. We conclude that a high-calorie diet reduces hippocampal synaptic plasticity and impairs cognitive function, possibly through BDNF-mediated effects on dendritic spines.
在西方社会,总体饮食能量摄入量,尤其是果糖等单糖的消耗量一直在稳步增加,但此类饮食对大脑的影响却知之甚少。在此,我们运用功能和结构分析方法来描述热量摄入过多对海马体的影响,海马体是大脑中对学习和记忆至关重要的区域。喂食添加了高果糖玉米糖浆的高脂肪、高糖饮食的大鼠,其能量和脂质代谢出现了类似于临床糖尿病的变化,空腹血糖升高,胆固醇和甘油三酯增加。维持这种饮食8个月的大鼠表现出空间学习能力受损、海马体树突棘密度降低以及在Schaffer侧支-CA1突触处的长时程增强作用减弱。这些变化与海马体中脑源性神经营养因子水平的降低同时发生。我们得出结论,高热量饮食可能通过脑源性神经营养因子对树突棘的介导作用,降低海马体突触可塑性并损害认知功能。