Translational Imaging Core, Center for Neuroscience and Regenerative Medicine, 4301 Jones Bridge Road, Bethesda, MD, 20814, USA.
Department of Anatomy, Physiology and Genetics, Uniformed Services University, 4301 Jones Bridge Road, Bethesda, MD, 20814, USA.
Neuroimage. 2019 Mar;188:419-426. doi: 10.1016/j.neuroimage.2018.12.033. Epub 2018 Dec 18.
Traumatic Brain Injury (TBI) affects approximately 2.5 million people in the United States, of which 80% are considered to be mild (mTBI). Previous studies have shown that cerebral glucose uptake and metabolism are altered after brain trauma and functional metabolic deficits observed following mTBI are associated with changes in cognitive performance. Imaging of glucose uptake using [F] Fluorodeoxyglucose (FDG) based Positron Emission Tomography (PET) with anesthesia during the uptake period demonstrated limited variability in results, but may have depressed uptake. Anesthesia has been found to interfere with blood glucose levels, and hence, FDG uptake. Conversely, forced cognitive testing during uptake may increase glucose demand in targeted regions, such as hippocampus, allowing for better differentiation of outcomes. Therefore, the objective of this study was to investigate the influence of a directed cognitive function task during the FDG uptake period on uptake measurements both in naïve rats and at 2 days after mild lateral fluid percussion (mLFP) TBI. Adult male Sprague Dawley rats underwent FDG uptake with either cognitive testing with the Novel Object Recognition (NOR) test or No Novel Object (NNO), followed by PET scans at baseline (prior to injury) and at 2days post mLFP. At baseline, FDG uptake in the right hippocampus was elevated in rats completing the NOR in comparison to the NNO (control group). Further, the NNO group rats demonstrated a greater fold change in the FDG uptake between baseline and post injury scans than the NOR group. Overall, these data suggest that cognitive activity during FDG uptake affects the regional uptake pattern in the brain, increasing uptake at baseline and suppressing the effects of injury.
创伤性脑损伤(TBI)影响美国约 250 万人,其中 80%被认为是轻度(mTBI)。先前的研究表明,脑创伤后葡萄糖摄取和代谢发生改变,mTBI 后观察到的功能代谢缺陷与认知表现的变化有关。使用 [F]氟脱氧葡萄糖(FDG)基于正电子发射断层扫描(PET)在摄取期间进行麻醉进行葡萄糖摄取成像显示结果的可变性有限,但摄取可能会被抑制。麻醉已被发现会干扰血糖水平,从而影响 FDG 摄取。相反,在摄取期间进行强制性认知测试可能会增加目标区域(如海马体)的葡萄糖需求,从而更好地区分结果。因此,本研究的目的是研究在 FDG 摄取期间进行定向认知功能测试对未受损伤的大鼠和轻度侧方液体打击(mLFP)TBI 后 2 天的摄取测量的影响。成年雄性 Sprague Dawley 大鼠接受 FDG 摄取,要么进行新物体识别(NOR)测试的认知测试,要么进行无新物体(NNO)测试,然后在基线(损伤前)和 mLFP 后 2 天进行 PET 扫描。在基线时,与进行 NNO(对照组)的大鼠相比,完成 NOR 的大鼠右侧海马体的 FDG 摄取增加。此外,与 NOR 组相比,NNO 组大鼠在基线和损伤后扫描之间的 FDG 摄取的变化幅度更大。总的来说,这些数据表明,FDG 摄取期间的认知活动会影响大脑的区域摄取模式,增加基线摄取并抑制损伤的影响。