Lozada Luis E, Desai Abhishek, Kevala Karl, Lee Ji-Won, Kim Hee-Yong
Department of Pediatrics, Walter Reed National Military Medical Center, Bethesda, MD; and.
Laboratory of Molecular Signaling, National Institute on Alcohol Abuse and Alcoholism, NIH, Bethesda, MD.
J Nutr. 2017 Sep;147(9):1624-1630. doi: 10.3945/jn.117.254607. Epub 2017 Aug 2.
Premature infants are deprived of prenatal accumulation of brain docosahexaenoic acid [DHA (22:6n-3)], an omega-3 fatty acid [ω-3 FA (n-3 FA)] important for proper development of cognitive function. The resulting brain DHA deficit can be reversed by ω-3 FA supplementation. The objective was to test whether there is a critical period for providing ω-3 FA to correct cognitive deficits caused by developmental ω-3 FA deprivation in mice. Twelve timed-pregnant mice [embryonic day 14 (E14), C57/BL6NCr] were fed an ω-3 FA-deficient diet containing 0.04% α-linolenic acid [ALA (18:3n-3)], and their offspring were fed the same deficient diet (Def group) or changed to an ω-3 FA-adequate diet containing 3.1% ALA at 3 wk, 2 mo, or 4 mo of age. In parallel, 3 E14 pregnant mice were fed the adequate diet and their offspring were fed the same diet (Adeq group) throughout the experiment. Brain FA composition, learning and memory, and hippocampal synaptic protein expression were evaluated at 6 mo by gas chromatography, the Morris water maze test, and western blot analysis, respectively. Maternal dietary ω-3 FA deprivation decreased DHA by >50% in the brain of their offspring at 3 wk of age. The Def group showed significantly worse learning and memory at 6 mo than those groups fed the adequate diet. These pups also had decreased hippocampal expression of postsynaptic density protein 95 (43% of Adeq group), Homer protein homolog 1 (21% of Adeq group), and synaptosome-associated protein of 25 kDa (64% of Adeq group). Changing mice to the adequate diet at 3 wk, 2 mo, or 4 mo of age restored brain DHA to the age-matched adequate concentration. However, deficits in hippocampal synaptic protein expression and spatial learning and memory were normalized only when the diet was changed at 3 wk. Developmental deprivation of brain DHA by dietary ω-3 FA depletion in mice may have a lasting impact on cognitive function if not corrected at an early age.
早产婴儿缺乏产前大脑二十二碳六烯酸(DHA,22:6n - 3)的积累,DHA是一种对认知功能正常发育很重要的ω-3脂肪酸(ω-3 FA,n-3 FA)。由此导致的大脑DHA缺乏可通过补充ω-3 FA来逆转。本研究目的是测试是否存在一个关键时期,通过提供ω-3 FA来纠正小鼠发育性ω-3 FA缺乏所导致的认知缺陷。将12只怀孕的定时受孕小鼠(胚胎期第14天,E14,C57/BL6NCr)喂食含0.04%α-亚麻酸(ALA,18:3n - 3)的ω-3 FA缺乏饮食,其后代喂食相同的缺乏饮食(缺陷组),或在3周龄、2月龄或4月龄时改为含3.1% ALA的ω-3 FA充足饮食。同时,3只E14怀孕小鼠喂食充足饮食,其后代在整个实验过程中也喂食相同饮食(充足组)。分别在6月龄时通过气相色谱法、莫里斯水迷宫试验和蛋白质免疫印迹分析来评估大脑脂肪酸组成、学习和记忆以及海马突触蛋白表达。母体饮食中ω-3 FA缺乏使后代3周龄时大脑中的DHA减少超过50%。缺陷组在6月龄时的学习和记忆能力明显比喂食充足饮食的组差。这些幼崽海马中突触后致密蛋白95(为充足组的43%)、荷马蛋白同源物1(为充足组的21%)和25 kDa突触体相关蛋白(为充足组的64%)的表达也降低。在3周龄、2月龄或4月龄时将小鼠饮食改为充足饮食可使大脑DHA恢复到与年龄匹配的充足浓度。然而,只有在3周龄时改变饮食,海马突触蛋白表达以及空间学习和记忆的缺陷才能恢复正常。小鼠饮食中ω-3 FA消耗导致的大脑DHA发育性缺乏如果在早期未得到纠正,可能会对认知功能产生持久影响。