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Protein synthesis is associated with high-speed dynamics and broad-band stability of functional hubs in the brain

机译:蛋白质合成与大脑中功能枢纽的高速动力学和宽带稳定性有关

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摘要

L-[1-11C]leucine PET can be used to measure in vivo protein synthesis in the brain. However, the relationship between regional protein synthesis and on-going neural dynamics is unclear. We use a graph theoretical approach to examine the relationship between cerebral protein synthesis (rCPS) and both static and dynamical measures of functional connectivity (measured using resting state functional MRI, R-fMRI). Our graph theoretical analysis demonstrates a significant positive relationship between protein turnover and static measures of functional connectivity. We compared these results to simple measures of metabolism in the cortex using [18F]FDG PET). Whilst some relationships between [18F]FDG binding and graph theoretical measures was present, there remained a significant relationship between protein turnover and graph theoretical measures, which were more robustly explained by L-[1-11C]Leucine than [18F]FDG PET. This relationship was stronger in dynamics at a faster temporal resolution relative to dynamics measured over a longer epoch. Using a Dynamic connectivity approach, we also demonstrate that broad-band dynamic measures of Functional Connectivity (FC), are inversely correlated with protein turnover, suggesting greater stability of FC in highly interconnected hub regions is supported by protein synthesis. Overall, we demonstrate that cerebral protein synthesis has a strong relationship independent of tissue metabolism to neural dynamics at the macroscopic scale.
机译:L- [1- 11 C]亮氨酸PET可用于测量大脑中的体内蛋白质合成。但是,尚不清楚区域蛋白合成与持续的神经动力学之间的关系。我们使用图论的方法来检查脑蛋白合成(rCPS)与功能连接的静态和动态度量(使用静止状态功能MRI,R-fMRI测量)之间的关系。我们的图形理论分析表明蛋白质更新和功能连接的静态措施之间的显着正相关。我们将这些结果与使用[ 18 F] FDG PET的皮质中新陈代谢的简单测量值进行了比较。尽管存在[ 18 F] FDG绑定与图理论值之间的某些关系,但蛋白质周转率与图理论值之间仍存在显着关系,L- [1- 11 C]亮氨酸比[ 18 F] FDG PET高。相对于在较长时期内测得的动力学,这种关系在以更快的时间分辨率的动力学中更强。使用动态连通性方法,我们还证明了功能连通性(FC)的宽带动态度量与蛋白质更新成反比,这表明蛋白质合成可以支持高度互连的集线器区域中FC的更大稳定性。总的来说,我们证明了脑蛋白合成在宏观范围内与组织代谢和神经动力学有密切的关系。

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