Engle James R, Machado Christopher J, Permenter Michele R, Vogt Julie A, Maurer Andrew P, Bulleri Alicia M, Barnes Carol A
Evelyn F. McKnight Brain Institute and.
Division of Neural Systems, Memory and Aging, University of Arizona, Tucson, Arizona 85724.
J Neurosci. 2016 Nov 30;36(48):12217-12227. doi: 10.1523/JNEUROSCI.4116-15.2016.
The ability to navigate through space involves complex interactions between multiple brain systems. Although it is clear that spatial navigation is impaired during aging, the networks responsible for these altered behaviors are not well understood. Here, we used a within-subject design and [F]FDG-microPET to capture whole-brain activation patterns in four distinct spatial behaviors from young and aged rhesus macaques: constrained space (CAGE), head-restrained passive locomotion (CHAIR), constrained locomotion in space (TREADMILL), and unconstrained locomotion (WALK). The results reveal consistent networks activated by these behavior conditions that were similar across age. For the young animals, however, the coactivity patterns were distinct between conditions, whereas older animals tended to engage the same networks in each condition. The combined observations of less differentiated networks between distinct behaviors and alterations in functional connections between targeted regions in aging suggest changes in network dynamics as one source of age-related deficits in spatial cognition.
We report how whole-brain networks are involved in spatial navigation behaviors and how normal aging alters these network patterns in nonhuman primates. This is the first study to examine whole-brain network activity in young or old nonhuman primates while they actively or passively traversed an environment. The strength of this study resides in our ability to identify and differentiate whole-brain networks associated with specific navigational behaviors within the same nonhuman primate and to compare how these networks change with age. The use of high-resolution PET (microPET) to capture brain activity of real-world behaviors adds significantly to our understanding of how active circuits critical for navigation are affected by aging.
在空间中导航的能力涉及多个脑系统之间的复杂相互作用。虽然很明显衰老过程中空间导航会受损,但负责这些行为改变的神经网络尚不清楚。在此,我们采用受试者内设计和[F]FDG-微PET来捕捉年轻和老年恒河猴在四种不同空间行为中的全脑激活模式:受限空间(笼中)、头部固定被动运动(椅上)、空间受限运动(跑步机)和自由运动(行走)。结果显示,这些行为条件激活的一致网络在不同年龄组中相似。然而,对于年轻动物,不同条件下的共激活模式是不同的,而老年动物在每种条件下倾向于激活相同的网络。在不同行为之间网络分化减少以及衰老过程中目标区域之间功能连接改变的综合观察结果表明,网络动态变化是空间认知中与年龄相关缺陷的一个来源。
我们报告了全脑网络如何参与空间导航行为以及正常衰老如何改变非人类灵长类动物的这些网络模式。这是第一项在年轻或老年非人类灵长类动物主动或被动穿越环境时检查全脑网络活动的研究。本研究的优势在于我们能够在同一非人类灵长类动物中识别和区分与特定导航行为相关的全脑网络,并比较这些网络如何随年龄变化。使用高分辨率PET(微PET)来捕捉现实世界行为中的脑活动,极大地增进了我们对导航关键活性回路如何受衰老影响的理解。