Newton Isabel G, Forbes M Elizabeth, Linville M Constance, Pang Hui, Tucker Elizabeth W, Riddle David R, Brunso-Bechtold Judy K
Department of Neurobiology and Anatomy, Medical Center Boulevard, Wake Forest University School of Medicine, Winston-Salem, NC 27157-1010, USA.
Neurobiol Aging. 2008 Sep;29(9):1308-18. doi: 10.1016/j.neurobiolaging.2007.03.009. Epub 2007 Apr 11.
Caloric restriction (CR) attenuates aging-related degenerative processes throughout the body. It is less clear, however, whether CR has a similar effect in the brain, particularly in the hippocampus, an area important for learning and memory processes that often are compromised in aging. In order to evaluate the effect of CR on synapses across lifespan, we quantified synapses stereologically in the middle molecular layer of the dentate gyrus (DG) of young, middle aged and old Fischer 344 x Brown Norway rats fed ad libitum (AL) or a CR diet from 4 months of age. The results indicate that synapses are maintained across lifespan in both AL and CR rats. In light of this stability, we addressed whether aging and CR influence neurotransmitter receptor levels by measuring subunits of NMDA (NR1, NR2A and NR2B) and AMPA (GluR1, GluR2) receptors in the DG of a second cohort of AL and CR rats across lifespan. The results reveal that the NR1 and GluR1 subunits decline with age in AL, but not CR rats. The absence of an aging-related decline in these subunits in CR rats, however, does not arise from increased levels in old CR rats. Instead, it is due to subunit decreases in young CR rats to levels that are sustained in CR rats throughout lifespan, but that are reached in AL rats only in old age.
热量限制(CR)可减轻全身与衰老相关的退行性过程。然而,CR在大脑中是否有类似作用尚不清楚,尤其是在海马体中,海马体是对学习和记忆过程很重要的区域,而这些过程在衰老过程中常常受损。为了评估CR对整个生命周期突触的影响,我们对自由摄食(AL)或从4月龄开始采用CR饮食的年轻、中年和老年Fischer 344×Brown Norway大鼠齿状回(DG)中层分子层的突触进行了立体定量分析。结果表明,在AL和CR大鼠中,突触在整个生命周期内都得以维持。鉴于这种稳定性,我们通过测量另一组AL和CR大鼠整个生命周期DG中NMDA(NR1、NR2A和NR2B)和AMPA(GluR1、GluR2)受体的亚基,来研究衰老和CR是否会影响神经递质受体水平。结果显示,在AL大鼠中,NR1和GluR1亚基随年龄下降,但在CR大鼠中并非如此。然而,CR大鼠中这些亚基没有出现与衰老相关的下降,并非是因为老年CR大鼠中这些亚基水平升高。相反,这是由于年轻CR大鼠中这些亚基水平下降至CR大鼠在整个生命周期中维持的水平,而AL大鼠仅在老年时才达到这一水平。