Glenn Melissa J, Kirby Elizabeth D, Gibson Erin M, Wong-Goodrich Sarah J, Mellott Tiffany J, Blusztajn Jan K, Williams Christina L
Psychology and Neuroscience, Duke University, Durham, NC, USA.
Brain Res. 2008 Oct 27;1237:110-23. doi: 10.1016/j.brainres.2008.08.049. Epub 2008 Aug 28.
Supplemental choline in the maternal diet produces a lasting enhancement in memory in offspring that resists age-related decline and is accompanied by neuroanatomical, neurophysiological and neurochemical changes in the hippocampus. The present study was designed to examine: 1) if prenatal choline supplementation alters behaviors that contribute to risk or resilience in cognitive aging, and 2) whether, at old age (25 months), prenatally choline-supplemented rats show evidence of preserved hippocampal plasticity. A longitudinal design was used to look at exploration of an open field, with and without objects, at 1 and 24 months of age in male and female rats whose mothers were fed a diet supplemented with choline (SUP; 5 mg/kg choline chloride) or not supplemented (CON; 1.1 mg/kg choline chloride) on embryonic days 12-17. Aging caused a significant decline in open field exploration that was more pronounced in males but interest in novel objects was maintained in both sexes. Prenatal choline supplementation attenuated, but did not prevent age-related decline in exploration in males and increased object exploration in young females. Following behavioral assessment, rats were euthanized to assess markers of hippocampal plasticity. Aged SUP males and females had more newly proliferated cells in the hippocampal dentate gyrus and protein levels of vascular endothelial growth factor (VEGF) and neurotrophin-3 (NT-3) were significantly elevated in female SUP rats in comparison to all other groups. Taken together, these findings provide the first evidence that prenatal choline supplementation causes changes in exploratory behaviors over the lifespan and preserves some features of hippocampal plasticity that can be seen even at 2 years of age.
母体饮食中补充胆碱可使后代的记忆力得到持久增强,这种增强能抵抗与年龄相关的衰退,并伴有海马体的神经解剖学、神经生理学和神经化学变化。本研究旨在探讨:1)产前补充胆碱是否会改变导致认知衰老风险或恢复力的行为;2)在老年(25个月)时,产前补充胆碱的大鼠是否表现出海马体可塑性保留的证据。采用纵向设计,观察在胚胎期第12至17天,其母亲喂食补充胆碱(SUP;5 mg/kg氯化胆碱)或未补充胆碱(CON;1.1 mg/kg氯化胆碱)饮食的雄性和雌性大鼠在1个月和24个月大时对有无物体的旷场探索情况。衰老导致旷场探索显著下降,雄性更为明显,但两性对新物体的兴趣均得以维持。产前补充胆碱可减轻雄性大鼠与年龄相关的探索能力下降,但不能预防这种下降,且增加了年轻雌性大鼠对物体的探索。行为评估后,对大鼠实施安乐死以评估海马体可塑性的标志物。与所有其他组相比,老年SUP雄性和雌性大鼠海马齿状回中新生细胞更多,雌性SUP大鼠中血管内皮生长因子(VEGF)和神经营养因子-3(NT-3)的蛋白质水平显著升高。综上所述,这些发现首次证明产前补充胆碱会导致整个生命周期内探索行为的变化,并保留海马体可塑性的一些特征,甚至在2岁时也能观察到。