Center for Geroscience, Brain Health, and Metabolism (GERO), Santiago, Chile; Department of Biology, Faculty of Sciences, Universidad de Chile, Santiago, Chile.
The Buck Institute for Research on Aging, Novato, CA, USA.
Cell Rep Med. 2024 Jun 18;5(6):101593. doi: 10.1016/j.xcrm.2024.101593. Epub 2024 Jun 5.
Aging compromises brain function leading to cognitive decline. A cyclic ketogenic diet (KD) improves memory in aged mice after long-term administration; however, short-term effects later in life and the molecular mechanisms that govern such changes remain unclear. Here, we explore the impact of a short-term KD treatment starting at elderly stage on brain function of aged mice. Behavioral testing and long-term potentiation (LTP) recordings reveal that KD improves working memory and hippocampal LTP. Furthermore, the synaptosome proteome of aged mice fed a KD long-term evidence changes predominantly at the presynaptic compartment associated to the protein kinase A (PKA) signaling pathway. These findings were corroborated in vivo by western blot analysis, with high BDNF abundance and PKA substrate phosphorylation. Overall, we show that a KD modifies brain function even when it is administered later in life and recapitulates molecular features of long-term administration, including the PKA signaling pathway, thus promoting synaptic plasticity at advanced age.
衰老会损害大脑功能,导致认知能力下降。周期性生酮饮食(KD)在长期给药后可改善老年小鼠的记忆力;然而,其在生命后期的短期作用以及控制这些变化的分子机制尚不清楚。在这里,我们探讨了从老年期开始进行短期 KD 治疗对老年小鼠大脑功能的影响。行为测试和长时程增强(LTP)记录显示 KD 可改善工作记忆和海马体 LTP。此外,长期接受 KD 喂养的老年小鼠突触体蛋白质组学证据表明,主要在前突触区发生变化,与蛋白激酶 A(PKA)信号通路有关。这些发现通过 Western blot 分析在体内得到了证实,BDNF 丰度增加和 PKA 底物磷酸化。总的来说,我们表明,KD 即使在生命后期给药也能调节大脑功能,并再现长期给药的分子特征,包括 PKA 信号通路,从而在高龄时促进突触可塑性。