Goyal Manu S, Vlassenko Andrei G, Blazey Tyler M, Su Yi, Couture Lars E, Durbin Tony J, Bateman Randall J, Benzinger Tammie L-S, Morris John C, Raichle Marcus E
Mallinckrodt Institute of Radiology, Washington University School of Medicine, St. Louis, MO 63110, USA; Department of Neurology, Washington University School of Medicine, St. Louis, MO 63110, USA; Knight Alzheimer's Disease Research Center, Washington University School of Medicine, St. Louis, MO 63110, USA.
Mallinckrodt Institute of Radiology, Washington University School of Medicine, St. Louis, MO 63110, USA; Knight Alzheimer's Disease Research Center, Washington University School of Medicine, St. Louis, MO 63110, USA.
Cell Metab. 2017 Aug 1;26(2):353-360.e3. doi: 10.1016/j.cmet.2017.07.010.
The normal aging human brain experiences global decreases in metabolism, but whether this affects the topography of brain metabolism is unknown. Here we describe PET-based measurements of brain glucose uptake, oxygen utilization, and blood flow in cognitively normal adults from 20 to 82 years of age. Age-related decreases in brain glucose uptake exceed that of oxygen use, resulting in loss of brain aerobic glycolysis (AG). Whereas the topographies of total brain glucose uptake, oxygen utilization, and blood flow remain largely stable with age, brain AG topography changes significantly. Brain regions with high AG in young adults show the greatest change, as do regions with prolonged developmental transcriptional features (i.e., neoteny). The normal aging human brain thus undergoes characteristic metabolic changes, largely driven by global loss and topographic changes in brain AG.
正常衰老的人类大脑会出现整体代谢下降,但这是否会影响大脑代谢的拓扑结构尚不清楚。在此,我们描述了基于正电子发射断层扫描(PET)对20至82岁认知正常成年人的脑葡萄糖摄取、氧利用和血流的测量。与年龄相关的脑葡萄糖摄取下降超过氧利用下降,导致脑有氧糖酵解(AG)丧失。虽然全脑葡萄糖摄取、氧利用和血流的拓扑结构随年龄增长基本保持稳定,但脑AG拓扑结构发生了显著变化。年轻成年人中AG高的脑区变化最大,具有延长发育转录特征(即幼态持续)的区域也是如此。因此,正常衰老的人类大脑会经历特征性的代谢变化,这在很大程度上是由脑AG的整体丧失和拓扑结构变化驱动的。